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Cat. No. | Product Name | ||
---|---|---|---|
L8800 | 药物片段库 | 1119 compounds | |
1119 种药物片段分子,是FBDD 方法新药筛选的有力工具; | |||
L4200 | FDA 上市药物库 | 1729 compounds | |
1729 个FDA 批准药物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L2151 | 化疗药物库 | 48 compounds | |
48 个肿瘤化疗药物,可以用于高通量和高内涵筛选; | |||
L1000 | 上市药物库 | 2808 compounds | |
2808 个上市药物化合物集合,可用于高通量筛选和高内涵筛选; | |||
L9200 | 药物功能重定位化合物库 | 4630 compounds | |
4630 种全球上市药物和临床药物的独特集合,可用于高通量筛选和高内涵筛选,是老药新用、新的药物靶点筛选和细胞诱导的有效工具。 | |||
L2150 | 抗癌药物库 | 3080 compounds | |
3080 个具有抗癌活性小分子的独特集合,生物活性已经临床前实验证实,可用于高通量、高内涵筛选; | |||
L4210 | NMPA中国上市药物库 | 1270 compounds | |
1270 个 NMPA 中国上市药物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L2110 | 抗癌上市药物库 | 1779 compounds | |
1779 个具有抗癌活性小分子的独特集合,所有化合物都经过了严格的临床前研究和临床试验,由FDA、EMA 或NMPA 批准上市,可用于高通量、高内涵筛选。 | |||
L5800 | 药物代谢杂质库 | 197 compounds | |
197 种药物异构体/代谢产物的特有集合,可用于高通量、高内涵筛选; | |||
L2152 | 靶向治疗药物库 | 119 compounds | |
119 个肿瘤靶向治疗药物,可以用于高通量和高内涵筛选; | |||
L1010 | FDA上市及药典收录分子库 | 3158 compounds | |
3158 个上市及药典分子集合,可用于高通量筛选和高内涵筛选; | |||
L6160 | Ro5类药天然产物库 | 2703 compounds | |
2703 种符合 RO5原则的天然产物单体集合,可以用于高通量和高内涵筛选; | |||
L9210 | 儿童药物库 | 972 compounds | |
972 种儿童药物的独特集合,可用于高通量筛选和高内涵筛选 | |||
L5510 | 肝脏毒性化合物库 | 1001 compounds | |
1001 个肝脏毒性化合物的特有集合,可用于高通量、高内涵筛选,是毒理学研究的良好工具; | |||
L1020 | EMA 上市药物库 | 657 compounds | |
657个EMA批准药物的独特集合,可用于高通量筛选和高内涵筛选 | |||
L5610 | Golden骨架库 | 10000 compounds | |
多样性好,从160万个小分子中挑选而出,10000 个化合物,5000种骨架结构; | |||
LF9000 | 半胱氨酸靶向共价抑制剂库 | 3400 compounds | |
It contains over 3,400 potential covalent modifiers. | |||
L5600 | Mini骨架库 | 5000 compounds | |
多样性好,从一百多万个小分子中挑选而出,5000 个化合物代表5000 种骨架结构; | |||
L9410 | 共价抑制剂库 | 1920 compounds | |
1920 种小分子的独特集合,包含已发现的共价抑制剂以及包含某些共价反应基团常见弹头的分子,如氯乙酰基,2-氯丙酰基,丙烯酰基,1-丙-2-炔基,1-丁-2-炔基,酮羰基,二硫键等,可以用于共价抑制剂药物研发; | |||
DF4000 | Smart共价片段化合物库 | 511 compounds | |
ChemDiv’s Smart Library of Covalent Fragments contains 799 compounds | |||
LF1000 | 多样性核心预制库 | 50000 compounds | |
For your convenience, there are Diversity Sets of 5,000, 10,000, 15,000, and 20,000 compounds with no structure overlap. | |||
L6900 | 稀有天然产物库 | 693 compounds | |
693 种稀有天然产物的集合,可以用于高通量和高内涵筛选; | |||
VM1400 | 多样性核心库Part2 | 25920 compounds | |
分子量<500,主要集中于250-450之间,方便后续的改造优化; | |||
L4900 | 心血管毒性化合物库 | 131 compounds | |
131 种心血管毒性化合物的独特集合,可用于毒理学研究; | |||
DF1000 | 片段化合物库 | 11269 compounds | |
ChemDiv’s Fragments Library contains 11,269 compounds. | |||
L7820 | 高溶解性微型片段化合物库 | 1081 compounds | |
高溶解性微型片段化合物库由 1081 个低分子量片段组成。 | |||
L7830 | 高溶解性片段药效团化合物库 | 985 compounds | |
高溶解性片段药效团库包含985 个片段小分子。 | |||
BN1100 | 二代高端片段化合物库 | 1139 compounds | |
The 2nd Generation Premium Fragment Library contains 1166 compounds. | |||
L9230 | ReFRAME 相关化合物库 | 3210 compounds | |
3210 化合物的独特集合,可用于高通量筛选和高内涵筛选 | |||
L1500 | GPCR靶点分子库 | 1940 compounds | |
1940 种与 G 蛋白及其耦联受体相关的生物活性小分子化合物,所有小分子都具有良好的生物和药理活性,部分是 FDA 批准的上市药物; | |||
L1580 | GPCR库Plus | 338 compounds | |
338 种GPCR 靶向、结构新颖的化合物; | |||
L7840 | 高溶解性卤化片段化合物库 | 796 compounds | |
高溶解性卤化片段库包含796 个卤化片段化合物。 | |||
L6010 | 天然产物库 | 3840 compounds | |
3840 种天然产物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L9100 | 磷酸酶抑制剂化合物库 | 79 compounds | |
79 种已知活性的磷酸酶抑制剂的集合,可用于化合物筛选、化学基因组学、药理分析等方面; | |||
L4020 | NO PAINS 化合物库 | 9384 compounds | |
TargetMol NO PAINS 化合物库包含 9384 个剔除了PAINS 的小分子活性化合物,可用于新药研发,信号通路研究,老药新用等研究。 | |||
L2570 | 人代谢物化合物库 | 4454 compounds | |
4454 种人代谢物的独特集合,用于高通量、高内涵筛选; | |||
L4150 | 新颖已知活性精选库 | 989 compounds | |
989 种百里挑一的活性化合物; | |||
L9850 | 口服活性化合物库 | 2427 compounds | |
2427 种口服活性化合物独特集合,可用于高通量筛选和高内涵筛选 | |||
L1800 | 抗感染化合物库 | 2938 compounds | |
2938 种具有抗感染活性的化合物的特有集合,包括抗细菌、抗真菌、抗巨细胞病毒、抗HIV、抗SARS、抗流感等活性; | |||
L4010 | 已知活性化合物库 | 22555 compounds | |
22555 个已知活性化合物的集合,可用于高通量筛选、高内涵筛选、细胞诱导和靶点确认; | |||
L4600 | 植物来源化合物库 | 3048 compounds | |
3048 个植物来源天然产物的独特集合,来自277类植物的精心之选; | |||
L4000 | 经典已知活性库 | 14439 compounds | |
14439 个已知活性化合物的集合,可用于高通量筛选、高内涵筛选、细胞诱导和靶点确认; | |||
L3400 | 临床期小分子药物库 | 3404 compounds | |
3404 个临床期化合物集合,可用于高通量筛选和高内涵筛选; | |||
L4510 | 抗寄生虫库 | 419 compounds | |
419 种具有抗寄生虫活性的小分子化合物; | |||
L2200 | 酪氨酸激酶分子库 | 1016 compounds | |
1016 种酪氨酸激酶抑制剂的独特集合,可用于高通量筛选和高内涵筛选; | |||
L6110 | 生物碱类天然产物库 | 500 compounds | |
500 种生物碱类天然产物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L1710 | 抗COVID-19化合物库 | 1133 compounds | |
1133 种对SARS-CoV-2有抑制作用或潜在抑制作用的化合物集合,可用于高通量和高内涵筛选; | |||
L2300 | 离子通道库 | 931 compounds | |
931 种与离子通道相关的生物活性小分子化合物的特有集合,用于离子通道相关的疾病和药物研究,可用于高通量筛选和高内涵筛选; | |||
L6700 | 抗癌天然产物库 | 1772 compounds | |
1772 种已知活性天然产物的独特集合,是肿瘤药物开发、抗癌先导化合物筛选等领域的有力工具,可用于HTS 和HCS。 | |||
L2500 | 人内源代谢化合物库 | 499 compounds | |
499 种内源性生物活性化合物的独特集合,用于高通量、高内涵筛选; | |||
L1700 | 抗病毒库 | 1040 compounds | |
1040 种具有抗病毒活性的化合物的特有集合,是筛选新型抗病毒药的有效工具;可用于高通量筛选和高内涵筛选; | |||
L6000 | 高通量筛选天然产物库 | 4533 compounds | |
4533 种天然产物的独特集合,是药物开发、药理研究、干细胞分化、指纹图谱研究、质量研究等领域的有力工具,可用于HTS 和HCS; | |||
L9840 | 抗阿尔茨海默症化合物库 | 986 compounds | |
986 种阿尔茨海默症相关的化合物集合,可用于高通量和高内涵筛选; | |||
L4520 | 抗菌活性库 | 904 compounds | |
904 种具有抗菌活性的化合物,是抗菌药物研发的有力工具; | |||
L9900 | 药用辅料化合物库 | 182 compounds | |
182 种 FDA 批准药品中的非活性成分集合 | |||
L4710 | 非甾体类抗炎化合物库 | 530 compounds | |
530 种非甾体类的抗炎相关化合物,可用于高通量和高内涵筛选; | |||
L7800 | 高溶解性片段库 | 2728 compounds | |
2728 种片段分子合集,数量适中,是 FBDD 方法新药筛选的有力工具。 | |||
L6810 | 中药单体化合物库 | 2755 compounds | |
2755 种中药来源的单体化合物,是药物开发、药理研究等领域的有力工具; | |||
L5700 | 精选片段库 | 246 compounds | |
246 个片段小分子的独特集合,可用于基于片段的筛选和药物发现(FBDD); | |||
L2190 | 抗肺癌化合物库 | 1702 compounds | |
1702 种与肺癌相关的化合物,可以用于抗肺癌药物研发和药理研究; | |||
L4400 | 抗生素库 | 692 compounds | |
692 个具有抗菌活性化合物的独特集合,是医药研究的优良工具库和药物筛选的有效载体; | |||
L5300 | 线粒体靶向库 | 812 compounds | |
812 种具有潜在或确定线粒体靶向活性的化合物,以促进针对线粒体的药物研究; | |||
L9830 | 抗帕金森病化合物库 | 857 compounds | |
857 种帕金森病相关的化合物集合,可用于高通量和高内涵筛选; | |||
L8100 | 细胞周期化合物库 | 677 compounds | |
677 种细胞周期相关的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L6600 | 胃肠炎天然产物库 | 219 compounds | |
219 种胃肠炎相关的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L8000 | 干细胞分化化合物库 | 1197 compounds | |
1197 种干细胞分化信号通路相关的生物活性小分子化合物的特有集合,可用于高通量、高内涵筛选; | |||
L9600 | 多肽分子库 | 791 compounds | |
791 种多肽类分子,可用于多肽药物开发及信号转导通路和作用机制研究; | |||
L5900 | 血脑屏障通透化合物库 | 509 compounds | |
509 个 CNS-Penetrant 生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L7870 | 可溶性羧酸片段化合物库 | 1806 compounds | |
可溶性羧酸片段库包含 1806 个化合物 | |||
L6030 | 天然产物衍生物虚筛化合物库 | 163000 compounds | |
16.3万种天然产物衍生物,并且在持续增加中; | |||
L2180 | 抗肿瘤库Plus | 1468 compounds | |
1468 种抗肿瘤相关、结构新颖的化合物; | |||
L1400 | MAPK 抑制剂库 | 365 compounds | |
365 种与MAPK 信号通路相关的生物活性小分子化合物的特有集合,可用于高通量筛选和高内涵筛选; | |||
L3600 | 细胞因子抑制剂库 | 604 compounds | |
604 个与细胞因子紧密相关的化合物集合,是高通量、高内涵筛选的良好载体; | |||
CB1100 | EXP多样性库 | 50000 compounds | |
For hit finding across different targets, against novel targets, or for the discovery of new chemical series against existing targets, ChemBridge offers up to 150,000 DIVERSet Library compounds in economical, pre-plated format. The DIVERSet Libraries are suitable for biochemical assays, phenotypic and other cell based assays, and assays using model organisms such as bacteria, yeast, c. elegans, zebrafish, or arabidopsis. DIVERSet Libraries have been used across many disease areas resulting in hu... | |||
L5200 | 抗代谢疾病化合物库 | 1544 compounds | |
1544 个代谢疾病相关的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L2193 | 抗肝癌化合物库 | 1787 compounds | |
1787 种与肝癌相关的化合物,可以用于抗肝癌药物研发和药理研究; | |||
LF9100 | 丝氨酸靶向共价抑制剂库 | 2700 compounds | |
Over 2,700 small-molecule screening compounds in the library. | |||
L1900 | 抗糖尿病库 | 683 compounds | |
683 种生物活性小分子化合物; | |||
L9300 | 大环化合物库 | 210 compounds | |
210 种活性已知的大环化合物,用于高通量、高内涵筛选; | |||
L1600 | 激酶抑制剂库 | 2720 compounds | |
2720 种激酶抑制剂/调节剂的独特集合,用于特定靶向激酶,可用于高通量筛选和高内涵筛选; | |||
L6800 | 中国药典收录天然产物库 | 2051 compounds | |
2051 种中国药典收录的天然产物,是药物开发、药理研究等领域的有力工具; | |||
L9240 | 农药化合物库 | 270 compounds | |
270种农药相关化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
DF4500 | 多样性核心库Part1 | 50000 compounds | |
绝大部分分子量<500,主要集中于250-450之间,方便后续的改造优化; | |||
L4500 | 抗真菌库 | 252 compounds | |
252 个抗真菌活性化合物的独特集合,包含作用于真菌相关靶点的化合物和临床中用于真菌类疾病的药物,是相关疾病药物筛选的有效工具。 | |||
L8700 | 铁死亡化合物库 | 779 compounds | |
779 种与铁死亡通路相关的化合物,可用于高通量和高内涵筛选; | |||
L2610 | 神经递质受体化合物库 | 1513 compounds | |
1513 种与神经递质受体相关的化合物,用于高通量、高内涵筛选; | |||
DO1200 | 药物靶点库 | 53200 compounds | |
数量多,含53200种小分子化合物,是高通量筛选的有力工具; | |||
L2510 | 脂代谢化合物库 | 492 compounds | |
492 个脂代谢相关的化合物集合,可用于高通量和高内涵筛选; | |||
L6730 | 抗病毒中药单体化合物库 | 268 compounds | |
268 种具有抗病毒活性的中药单体集合,是药物开发、药理研究的有效工具; | |||
L4660 | 神经疾病库Plus | 1246 compounds | |
1246 种神经系统相关、结构新颖的化合物; | |||
L5500 | 毒性化合物库 | 262 compounds | |
262 个细胞毒性化合物的特有集合,可用于高通量、高内涵筛选。 | |||
L6710 | 中药抗炎分子库 | 1246 compounds | |
1246 种具有抗炎活性或靶向炎症相关靶点的中药单体集合,是药物开发、药理研究的有效工具; | |||
L6610 | 抗感染天然产物库 | 1060 compounds | |
1060 个抗感染相关的天然产物集合,是药物开发、药理研究的有效工具; | |||
L6100 | 天然多酚类化合物库 | 635 compounds | |
635 个天然多酚化合物的独特集合,可用于高通量、高内涵筛选; | |||
L2010 | 高选择性抑制剂库 | 575 compounds | |
575种具有高选择性的抑制剂集合 | |||
L2501 | 人内源代谢化合物库 Plus | 1283 compounds | |
1283种内源性生物活性化合物的独特集合,用于高通量、高内涵筛选。 | |||
L6020 | 天然产物单体化合物库 | 16627 compounds | |
16627 种精选天然产物集合,结构多样,遍布多种动植物与微生物; | |||
L1510 | 核受体化合物库 | 531 compounds | |
531 个核受体作用化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L1100 | 蛋白酶抑制剂库 | 343 compounds | |
343 种已知的小分子蛋白酶抑制剂的特有集合,可用于高通量筛选和高内涵筛选; | |||
L2191 | 抗乳腺癌化合物库 | 1939 compounds | |
1939 种与乳腺癌相关的化合物,可以用于抗乳腺癌药物研发和药理研究; | |||
L9610 | 环肽库 | 80 compounds | |
80 种环肽分子,可用于高通量和高内涵筛选; | |||
L7600 | 趋化因子抑制剂库 | 59 compounds | |
59 种趋化因子或其受体抑制剂的独特集合,可用于高通量筛选和高内涵筛选; | |||
L6001 | Mini真菌代谢天然产物筛选库 | Inquiry | |
L9001 | 食品添加剂化合物库 | 425 compounds | |
425种食品添加剂的集合 | |||
L9810 | 抗纤维化化合物库 | 1180 compounds | |
1180 种潜在的抗纤维化分子,是研究纤维化的有效工具,可以用于高通量筛选和高内涵筛选; | |||
L3500 | 组蛋白修饰化合物库 | 469 compounds | |
469 个组蛋白修饰相关的小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L2170 | 肿瘤免疫治疗小分子化合物库 | 449 compounds | |
449 种靶向肿瘤免疫治疗靶点的小分子,可用于高通量和高内涵筛选,是研究肿瘤免疫治疗的有力工具; | |||
L6150 | 天然产物共价化合物库 | 583 compounds | |
提供产品的生物学信息和药物学信息,为筛选提供理论方向和研究基础; | |||
L2192 | 抗胰腺癌化合物库 | 2238 compounds | |
2238 种与胰腺癌相关的化合物,可以用于高通量和高内涵筛选; | |||
L2630 | 神经元分化化合物库 | 672 compounds | |
672 种与神经元分化相关的化合物,可以用于神经系统疾病药物研发 | |||
L2160 | 抗癌活性化合物库 | 3188 compounds | |
3188 种具有抗肿瘤活性的化合物的特有集合,用于高通量、高内涵筛选; | |||
L2100 | 抗癌化合物库 | 7234 compounds | |
7234 种肿瘤相关的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L6300 | 药食同源库 | 1290 compounds | |
1290 个药食同源化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L6620 | 抗寄生虫天然产物库 | 253 compounds | |
253 个抗寄生虫相关的天然产物集合,是药物开发、药理研究的有效工具; | |||
L8200 | 抗衰老化合物库 | 3279 compounds | |
3279 个抗衰老化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L2800 | 5-羟色胺分子库 | 268 compounds | |
268 种生物活性小分子化合物,用于高通量、高内涵筛选; | |||
L6230 | 苗药化合物库 | 534 compounds | |
534种苗族特色药材的天然产物分子,可用于高通量和高内涵筛选 | |||
L3700 | JAK-STAT 化合物库 | 252 compounds | |
252 个 JAK/STAT 靶点相关的小分子化合物的独特集合,用于高通量、高内涵筛选; | |||
L4800 | 血管生成库 | 1353 compounds | |
1353 个高潜力的抑制或促进血管生成的小分子集合,可用于药物靶点开发、血管生成机理研究的高通量筛选,高内涵筛选; | |||
L2195 | 抗前列腺癌化合物库 | 2070 compounds | |
2070 种与前列腺癌相关的化合物,可以用于高通量和高内涵筛选 | |||
L4100 | TGF-β/Smad靶点化合物库 | 184 compounds | |
184 个 TGF-β/Smad 靶点相关的小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L8110 | 细胞重编程化合物库 | 1813 compounds | |
1813 种重编程信号通路相关的生物活性小分子化合物的特有集合,可用于高通量、高内涵筛选 | |||
DO2200 | 共价抑制剂库CD | 12000 compounds | |
数量多:超过12000种共价结合化合物,并且数量在持续增加; | |||
L1720 | 核苷类化合物库 | 334 compounds | |
334 种核苷类化合物,包括核苷酸、核苷酸类似物及衍生物等,适用于抗病毒、抗肿瘤、抗真菌、抗抑郁等药物的研发; | |||
L7500 | 凝血与抗凝化合物库 | 144 compounds | |
144 个化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L2140 | 癌细胞分化化合物库 | 406 compounds | |
406 个诱导肿瘤细胞分化化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L1110 | 微管靶向化合物库 | 142 compounds | |
142 种靶向微管的分子集合,用于高通量筛选和高内涵筛选; | |||
L7900 | 成骨分子库 | 317 compounds | |
317 种成骨相关的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L2130 | 抗癌细胞代谢库 | 1268 compounds | |
1268 种癌细胞代谢相关的生物活性小分子化合物的特有集合,用于肿瘤相关的研究以及抗肿瘤药物的筛选,用于高通量、高内涵筛选; | |||
L2540 | 肠道微生物代谢化合物库 | 614 compounds | |
614 种肠道微生物代谢物的集合,可以用于高通量和高内涵筛选; | |||
L1310 | 细胞骨架化合物库 | 759 compounds | |
759 种细胞骨架相关的化合物,可以用于高通量和高内涵筛选; | |||
L6400 | 海洋天然产物库 | 144 compounds | |
144 种海洋来源的单体化合物,是药物开发、药理研究等领域的有力工具; | |||
L4700 | 免疫/炎症分子化合物库 | 4720 compounds | |
4720 种具有抗炎症活性的化合物的特有集合,可用于高通量筛选和高内涵筛选; | |||
L5100 | 含氟化合物库 | 574 compounds | |
574 个含氟化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L3100 | 造血毒性小分子库 | 101 compounds | |
101 种生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L2521 | 糖酵解化合物库 | 555 compounds | |
555 种糖酵解相关的活性化合物,可用于高通量和高内涵筛选 | |||
L9500 | 表型筛选靶点鉴定库 | 1796 compounds | |
1796 种靶点明确的已知活性化合物,适合表型筛选; | |||
L4300 | Wnt/Hedgehog/Notch 通路化合物库 | 237 compounds | |
237 个Wnt & Hedgehog & Notch 靶点相关的生物活性小分子化合物的特有集合,用于相关通路的研究及药物的筛选,可用于高通量、高内涵筛选。 | |||
L7110 | 抗高血压化合物库 | 678 compounds | |
678 种高血压相关的小分子,用于高通量和高内涵筛选; | |||
L7100 | 抗肥胖化合物库 | 2247 compounds | |
2247 个抗肥胖化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L6210 | 藏药化合物库 | 747 compounds | |
747 种藏药来源的天然产物分子集合,可以用于高通量和高内涵筛选; | |||
L6220 | 蒙药化合物库 | 950 compounds | |
950 种蒙药来源的天然产物分子集合,可以用于高通量和高内涵筛选; | |||
L9400 | PPI抑制剂库 | 485 compounds | |
485 种已知活性的 PPI 相关的抑制剂,可用于高通量、高内涵筛选; | |||
L6500 | 微生物天然产物库 | 685 compounds | |
685 种微生物来源的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L2194 | 抗结直肠癌化合物库 | 1545 compounds | |
1545 种与结直肠癌相关的化合物,可以用于高通量和高内涵筛选; | |||
L1610 | FDA 上市激酶抑制剂库 | 263 compounds | |
263种靶向激酶的上市药物集合,用于特定靶向激酶,可用于高通量筛选和高内涵筛选; | |||
L6200 | 瑶药化合物库 | 221 compounds | |
221 种瑶药来源的天然产物分子集合,可以用于高通量和高内涵筛选; | |||
L9000 | 细胞凋亡化合物库 | 1760 compounds | |
1760 种与凋亡相关的生物活性小分子化合物的特有集合,多用于研究肿瘤发生发展机制和抗癌药物筛选等。可用于高通量筛选和高内涵筛选; | |||
L1300 | PI3K/Akt/mTOR 化合物库 | 420 compounds | |
420 种与PI3K/Akt/mTOR 相关的生物活性小分子化合物的特有集合,用于PI3K/Akt/mTOR 相关研究以及高通量、高内涵筛选; | |||
L2196 | 抗卵巢癌化合物库 | 1867 compounds | |
1867 种与卵巢癌相关的化合物,可以用于抗卵巢癌药物研发和药理研究 | |||
L2550 | 谷氨酰胺代谢化合物库 | 565 compounds | |
565 种谷氨酰胺代谢相关的分子,可以用于高通量和高内涵筛选; | |||
L6820 | 烟草单体化合物库 | 747 compounds | |
747种烟草单体化合物的独特集合,可用于高通量筛选和高内涵筛选 | |||
L6740 | 抗结直肠癌中药单体化合物库 | 382 compounds | |
382 种抗结直肠癌相关的中药单体集合,是药物开发、药理研究的有效工具; | |||
L6720 | 抗COVID-19中药单体库 | 1147 compounds | |
根据抗新冠肺炎疫情过程中应用于临床治疗的中药方剂,收集了1147 种相关中药来源的单体化合物,可用于高通量和高内涵筛选,是抗新冠病毒药物研发的良好工具; | |||
L8500 | HIF-1化合物库 | 1336 compounds | |
1336 个HIF-1相关小分子的独特集合,可用于缺血性疾病、癌症等相关领域的药物开发和药理研究; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4661 |
PKG drug G1
|
PKA | Tyrosine Kinase/Adaptors |
PKG drug G1 靶向作用于PKG Iα。它通过 C42 PKGIα 非依赖性机制,促进血管舒张以及血压降低。 | |||
T23757 |
Ascorbic acid, rutoside drug combination
Rutinoscorbin,Rutascorbin,Ruta C 60,Cerutin |
Others | Others |
Ascorbic acid, rutoside drug combination is used for treating diabetic retinopathy. | |||
T15058 |
DBCO-amine
|
ADC Linker | Antibody-drug Conjugate/ADC Related |
DBCO-amine 是一种可切割的 ADC 接头,用于合成抗体-药物偶联物。 | |||
T15098 |
Deruxtecan
|
Others; Drug-Linker Conjugates for ADC | Antibody-drug Conjugate/ADC Related; Others |
Deruxtecan 是一种 ADC 药物-接头偶联物,由 DX-8951 (DXd) 的衍生物和马来酰亚胺-GGFG 肽接头组成,用于合成 DS-8201 和 U3-1402。 | |||
T9014 |
SKI-178
|
Apoptosis; S1P Receptor | Apoptosis; GPCR/G Protein |
SKI-178 是一种鞘氨醇激酶-1(SphK1)和 SphK2抑制剂,以 CDK1 依赖性方式诱导人急性髓性白血病细胞凋亡。 | |||
T22334 |
FMOC-3VVD-OH
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Fmoc-3VVD-OH 是一种可降解的 ADC 连接剂,用于合成抗体-药物偶联物。 | |||
T16218 |
N-Boc-PEG5-bromide
|
Others; PROTAC Linker; ADC Linker | Antibody-drug Conjugate/ADC Related; Others; PROTAC |
N-Boc-PEG5-bromide 是 PROTAC 的 linker,属于 PEG 类和 Alkyl/ether 类.它也是可降解的 ADC 连接桥,用于抗体药物结合物的合成。 | |||
T8547 |
DCBA
|
Drug Metabolite | Metabolism |
DCBA 是驱虫剂 N-N-diethyl-meta-toluamide (DEET) 的代谢物。尿液中 DCBA 的浓度是评估 DEET 暴露程度的指标。 | |||
T17389 |
AMAS
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
AMAS 是一种不可裂解的异双功能交联剂,具有 NHS 酯和马来酰亚胺基团,可实现含胺和巯基分子的共价结合。 | |||
T15179 |
DTSSP Crosslinker
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
DTSSP Crosslinker 是一种可降解的 ADC linker,可用于合成抗体-药物偶联物 (ADCs)。 | |||
T13621 |
CNDAC hydrochloride
|
Nucleoside Antimetabolite/Analog; Others; Drug Metabolite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Others |
CNDAC hydrochloride 是一种核苷类似物,是沙帕他滨的代谢物。 | |||
T3540 |
IMR-1A
|
Gamma-secretase; Drug Metabolite | Metabolism; Neuroscience; Proteases/Proteasome; Stem Cells |
IMR-1A 是 IMR-1 的酸代谢物。IMR-1A 是 Notch 抑制剂,IC50=0.5 μM。IMR-1A 相对于 IMR-1 的效力提高了 50 倍。 | |||
T4346 |
SPDB
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
SPDB 是一种可降解的 ADC 连接剂,可用于合成抗体偶联药物。它是一个与 DM4 偶联物相连的小片段,利用二硫键与抗体偶联。 | |||
T15176 |
DSS Crosslinker
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
DSS Crosslinker 是一种不可切割的 ADC 连接剂,用于合成抗体-药物偶联物。 | |||
T18723 |
Succinic anhydride
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Succinic anhydride 中的环状酸酐和不可裂解的 ADC 接头。它可以与化合物 4 反应,将前药连接到靶向多肽的胺或羟基 1 基团。 | |||
T14933 |
Cetaben
|
Others | Others |
Cetaben 是不依赖 PPARα 的过氧化物酶体增殖物。它可有效降低胆固醇和甘油三酸酯的浓度,是一种非纤维化降血脂药。 | |||
T37514 |
Hydroxy Dimetridazole
|
Drug Metabolite | Metabolism |
Hydroxy Dimetridazole 是Dimetridazol 的羟基化代谢产物。Dimetridazol 是一种硝基咪唑类药物,可用于对抗原生动物感染。 | |||
T0150 |
Hydroxyhexamide
乙酸己脲,(±)-Hydroxyhexamid |
Potassium Channel; Drug Metabolite | Membrane transporter/Ion channel; Metabolism |
Hydroxyhexamide ((±)-Hydroxyhexamid) 是Acetohexamide 的活性代谢物, 可用作降血糖药。 | |||
T12490 |
Pitavastatin lactone
|
Others; HMG-CoA Reductase | Metabolism; Others |
Pitavastatin lactone 是 Pitavastatin 在人体中的主要代谢产物。Pitavastatin 是 HMG-CoA 还原酶竞争性抑制剂。 | |||
T13131 |
Tert-Buthyl Pitavastatin
|
HMG-CoA Reductase | Metabolism |
tert-Buthyl Pitavastatin 是 Pitavastatin 的代谢产物。其中Pitavastatin 是HMG-CoA 还原酶抑制剂。 | |||
T15171 |
DSG Crosslinker
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
DSG Crosslinker 是用于合成抗体偶联药物的 linker,可降解。 | |||
T6741 |
SPDP
SPDP Crosslinker |
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
SPDP 是一种短链交联剂,用于通过 NHS 酯和吡啶基二硫醇反应基团与半胱氨酸巯基形成可切割(可还原)的二硫键,实现胺与巯基的共轭。它是一种可降解的 ADC 连接剂,可用于合成抗体偶联药物。 | |||
T17693 |
Boc-Val-Cit-PAB
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Boc-Val-Cit-PAB 是一种可切割的 ADC 接头,用于抗体-药物偶联物的合成。 | |||
T4989 |
Fosfomycin Tromethamine
|
Antibacterial; Antibiotic | Microbiology/Virology |
Fosfomycin tromethamine 是一种能透过血脑屏障的广谱抗生素,不可逆地抑制细胞壁合成的早期阶段。它对多种细菌具有杀菌活性,包括耐多药、广泛耐药和耐全药细菌。 | |||
T18479 |
NH-bis(C1-Boc)
亚氨基二乙酸二异丁酯 |
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Boc-NH-C6-Br 是一种不可切割的接头,用于抗体-药物偶联物。 | |||
T18867 |
Val-Cit-PAB-MMAE
|
Drug-Linker Conjugates for ADC | Antibody-drug Conjugate/ADC Related |
Val-Cit-PAB-MMAE 是 ADC 的药物-接头偶联物。它包含 ADC 接头(肽 Val-Cit-PAB)和有效的微管蛋白抑制剂 MMAE。 | |||
T15175 |
DSP Crosslinker
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
DSP Crosslinker 是一种可降解的 ADC 连接剂,用于合成可用于合成抗体偶联药物。 | |||
T8924 |
MFCD28987368
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
MFCD28987368 是一种可以被降解的 ADC linker,可用于抗体偶联药物 (ADC)的合成。 | |||
T10138 |
4-Desmethoxy Omeprazole
|
Drug Metabolite | Metabolism |
4-Desmethoxy Omeprazole 是 Omeprazole 的活性代谢物。Omeprazole 是质子泵抑制剂。Omeprazole 竞争性抑制 CYP2C19 活性,Ki=2 - 6 μM。Omeprazole 还抑制革兰氏阴性菌和革兰氏阳性菌生长。 | |||
T18308 |
MC-Gly-Gly-Phe
|
ADC Linker | Antibody-drug Conjugate/ADC Related |
MC-Gly-Gly-Phe 是一种用于抗体-药物偶联物的可切割接头。 | |||
T17952 |
Fmoc-Gly-Gly-OH
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Fmoc-Gly-Gly-OH 是一种可切割的 ADC 接头,用于合成抗体-药物偶联物。 | |||
T18728 |
Sulfo-SMCC sodium
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Sulfo-SMCC sodium 是一种异双功能、不可裂解的 ADC 交联剂,带有 N-羟基琥珀酰亚胺酯和马来酰亚胺基团,分别与伯胺和巯基反应。 | |||
T17983 |
Fmoc-Val-Cit-PAB-MMAE
|
Others; Drug-Linker Conjugates for ADC | Antibody-drug Conjugate/ADC Related; Others |
Fmoc-Val-Cit-PAB-MMAE 由 ADC 接头 (Fmoc-Val-Cit-PAB) 和强效微管蛋白抑制剂 (MMAE) 组成。 它是一种用于 ADC 的药物-接头偶联物。 | |||
T9344 |
3-Amino-2-oxazolidinone
|
Others; Endogenous Metabolite | Metabolism; Others |
3-Amino-2-oxazolidinone 是一种呋喃唑烷酮的代谢物 (metabolite),可用作检测呋喃唑烷酮残留的一个指标。 | |||
T16045 |
Methotrexate metabolite
DAMPA,甲喋呤杂质E |
Antifolate; Drug Metabolite | Cell Cycle/Checkpoint; Metabolism |
Methotrexate metabolite (DAMPA) (DAMPA)是 Methotrexate 的活性代谢物。Methotrexate 具有拮抗叶酸 (folic acid) 的作用,被用作免疫抑制剂。 | |||
T18868 |
Val-Cit
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Val-Cit 是一种可切割的 ADC 接头,用于合成抗体-药物偶联物。 | |||
T22278 |
BOC-Dap-NE
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Boc-Dap-NE 是一种二肽,用作一种可降解的 ADC 连接剂,可用于合成抗体偶联药物。 | |||
T37600 |
Dasatinib N-oxide
|
Others; Bcr-Abl | Angiogenesis; Cytoskeletal Signaling; Others; Tyrosine Kinase/Adaptors |
Dasatinib N-oxide 是 Dasatinib 的一种次要代谢物。Dasatinib 是口服有效的Src/Bcr-Abl 抑制剂。 | |||
T17372 |
Ald-Ph-NHS ester
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Ald-Ph-NHS ester 是用于抗体-药物偶联的不可切割接头。 | |||
T16031 |
McMMAF
Maleimidocaproyl monomethylauristatin F |
Microtubule Associated; Drug-Linker Conjugates for ADC | Antibody-drug Conjugate/ADC Related; Cytoskeletal Signaling |
McMMAF 是一种保护基团共轭的 MMAF。它是一种具有马来酰亚胺基己酰基接头(MC 接头)的 MMAF 衍生物, MMAF 是一种有效的微管蛋白聚合抑制剂。它可与抗体或其他蛋白质或生物聚合物结合。 | |||
T4678 |
Fmoc-Val-Cit-PAB
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Fmoc-Val-Cit-PAB 是一种可降解的抗体-药物偶联的连接剂。 | |||
T18540 |
Phe-Lys(Trt)-PAB
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Phe-Lys(Trt)-PAB 是一种组织蛋白酶可裂解的 ADC 接头,用于合成抗体-药物偶联物。 | |||
T16225 |
N-Hydroxysulfosuccinimide sodium
|
ADC Linker | Antibody-drug Conjugate/ADC Related |
N-Hydroxysulfosuccinimide sodium 是一种不可降解的 ADC 连接剂,用于合成抗体-药物偶联物。 | |||
T17691 |
Boc-Val-Cit-OH
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Boc-Val-Cit-OH 是一种可切割的 ADC 接头,用于合成抗体-药物偶联物。 | |||
T8722 |
iKIX1
|
Antifungal | Microbiology/Virology |
iKIX1 是一种 Pdr1 依赖性基因激活。 它在体外和在播散性和泌尿道光滑念珠菌感染的动物模型中使耐药的光滑念珠菌对唑类抗真菌剂重新敏感。它可研究多药耐药性和光滑念珠菌感染。 | |||
T17213 |
Val-cit-PAB-OH
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Val-cit-PAB-OH 是可降解ADC 连接剂。 | |||
T38953 |
Azido-C6-OH
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Azido-C6-OH 是可降解的 ADC linker,可用于合成抗体偶联药物。 | |||
T3131 |
Fosfomycin calcium
Phosphomycin calcium salt,Fosmicin,磷霉素钙 |
Antibacterial; Antibiotic | Microbiology/Virology |
Fosfomycin calcium (Phosphomycin calcium salt) 是一种能透过血脑屏障的广谱抗生素,不可逆地抑制细胞壁合成的早期阶段。它对多种细菌具有杀菌活性,包括耐多药、广泛耐药和耐全药细菌。 | |||
T17692 |
Boc-Val-Cit-PAB-PNP
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Boc-Val-Cit-PAB-PNP 是一种可切割的 ADC 接头,用于合成抗体-药物偶联物。 | |||
T18318 |
MC-Val-Ala-PAB-PNP
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
MC-Val-Ala-PAB-PNP 是一种用于合成抗体偶联药物的 linker,可降解。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T13539 |
Allopurinol riboside
|
Others; Endogenous Metabolite; Parasite; Drug Metabolite | Metabolism; Microbiology/Virology; Others |
Allopurinol riboside 是别嘌醇的代谢产物,具有抗寄生虫作用。 Allopurinol riboside 竞争性抑制嘌呤核苷磷酸化酶对肌苷的作用,Ki 为 277 μM。 | |||
Fr13756 |
Isonicotinic acid
|
Endogenous Metabolite; Drug Metabolite | Metabolism |
Isonicotinic acid 是 Isoniazid 的代谢产物。Isoniazid 通过肼解转化为 Isonicotinic acid。 Isoniazid 向 Isonicotinic acid 的生物转化可以通过细胞色素 P450 酶催化。 | |||
T8115 |
Menthofuran
|
Others | Others |
Menthofuran 是一种天然产品。 | |||
TN4660 |
Niranthin
|
Anti-infection; HBV; PAFR; Topoisomerase | DNA Damage/DNA Repair; GPCR/G Protein; Microbiology/Virology |
Niranthin 是一种木脂素,具有广泛的药理活性。它是L. donovaniIB 拓扑异构酶的非竞争性抑制剂,可用于研究耐药利什曼病的治疗。 | |||
TN6512 |
Tectol
|
Transferase; Parasite | Metabolism; Microbiology/Virology |
Tectol 是从Lippia sidoides 中分离的,对人白血病细胞株 HL60 和 CEM 具有显著的抑制作用。它是法尼基转移酶抑制剂,在人和布氏锥虫的IC50分别为 2.09 和 1.73 μM。它具有抗疟原虫活性,是一种中等活性的生长抑制剂,IC50 为 3.44±0.20μM。 | |||
TN1740 |
Homoeriodictyol
高胜草酚,高圣草酚 |
5-HT Receptor; transporter; Sodium Channel; Drug Metabolite | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Homoeriodictyol 是 Eriocitrin 的代谢物,属于黄酮类。Eriocitrin 是强效抗氧化剂。 | |||
T9784 |
Docosanedioic acid
|
PROTAC Linker; ADC Linker | Antibody-drug Conjugate/ADC Related; PROTAC |
Docosanedioic acid 可以作为ADC linker 或PROTAC linker,用于合成抗体偶联药物或合成 PROTAC。 | |||
T8175 |
DL-Laudanosine
Laudanosine,DL-劳丹素 |
Others; Drug Metabolite | Metabolism; Others |
DL-Laudanosine (Laudanosine) 是 Atracurium 和 Cisatracurium 的代谢物,它能够透过血脑屏障,引起兴奋和癫痫。 | |||
T12095 |
Monomethyl fumarate
|
GPR; Drug Metabolite | Endocrinology/Hormones; GPCR/G Protein; Metabolism |
Monomethyl fumarate 是 Dimethyl fumarate 的活性代谢产物。Monomethyl fumarate 是一种 GPR109A 激动剂。Monomethyl fumarate 是一种 GPR109A 激动剂具有用于多种神经保护途径和其他视网膜疾病模型的潜力。 | |||
T4820 |
Maleimide
马来酰亚胺,2,5-Pyrroledione |
Others | Others |
Maleimide (2,5-Pyrroledione) 可用于制备荧光探针,主要用于硫醇分析物的特异性检测。它也可用于制备用于癌症研究的抗体-药物偶联物 (ADC)。 | |||
T4000 |
(±)-Equol
Equol,(±)-雌马酚,(R,S)-Equol |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Drug Metabolite | Endocrinology/Hormones; Metabolism |
(±)-Equol ((R,S)-Equol) 是 equol 的外消旋体。它对 ERα 和 ERβ 的 EC50s of 分别为 200 和 74 nM。Equol 是大豆异黄酮黄豆苷和大豆黄素的代谢产物。 | |||
T8262 |
Fosfomycin sodium
Fosfomycin Disodium,磷霉素钠 |
Antibacterial; Antibiotic | Microbiology/Virology |
Fosfomycin sodium 是一种能透过血脑屏障的广谱抗生素,不可逆地抑制细胞壁合成的早期阶段。它对多种细菌具有杀菌活性,包括耐多药、广泛耐药和耐全药的细菌。 | |||
TN1742 |
Homovanillyl alcohol
高香草醇,4-羟基-3-甲氧基苯乙醇 |
TNF; Drug Metabolite | Apoptosis; Metabolism |
Homovanillyl alcohol 是羟基酪醇的生物代谢物。Hydroxytyrosol 是存在于原始橄榄油和葡萄酒中的酚类化合物。它能够保护红细胞免受氧化损伤,并对心血管具有保护作用。 | |||
T2149 |
Vinburnine
Eburnalritardo,L-Eburnamonine,长春布宁,Vincamone,(-)-Eburnamonine,(-)-Vincamone |
Others; Drug Metabolite | Metabolism; Others |
Vinburnine (Eburnalritardo) 是一种长春花生物碱,是长春胺的代谢物和是血管扩张剂。 | |||
T8149 |
Dobutamine hydrochloride
盐酸多巴酚丁胺,Dobutamine (hydrochloride) |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Dobutamine hydrochloride (Dobutamine(hydrochloride)) 是一种合成的儿茶酚胺,可作用于肾上腺素能受体α1-AR、β1-AR 和β2-AR,是一种选择性的 β1-AR 受体激动剂,对 α1-AR 和 β2-AR 作用相对较弱。它能够增加心输出量,矫正低灌注。 | |||
T16338 |
Norgestimate metabolite Norelgestromin
17-Deacetyl norgestimate,17-Deacylnorgestimate,甲基孕酮 |
Drug Metabolite | Metabolism |
Norgestimate metabolite Norelgestromin (17-Deacylnorgestimate) 是norgestimate 的一种活性代谢物。它是用于避孕贴片的甾体孕激素,与雌激素乙炔雌二醇结合使用。 | |||
T7174 |
Urolithin A
尿石素A,3,8-二羟基-6H-二苯并[B,D]吡喃-6-酮 |
Apoptosis; Reactive Oxygen Species; DNA/RNA Synthesis; Endogenous Metabolite; Autophagy; Drug Metabolite | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; NF-κB |
Urolithin A 是一种鞣花酸的肠道微生物代谢产物,可诱导自噬和凋亡,抑制细胞周期进程,抑制DNA 合成,具有抗炎、抗增殖和抗氧化的特性。 | |||
T6293 |
Mycophenolate Mofetil
TM-MMF,吗替麦考酚酯,RS 61443 |
Apoptosis; Dehydrogenase; Drug Metabolite | Apoptosis; Metabolism |
Mycophenolate Mofetil (TM-MMF) 是 Mycophenolic acid 的吗啉乙酯前药。它通过抑制肌苷一磷酸脱氢酶抑制从头嘌呤合成,显示出选择性淋巴细胞抗增殖作用。 | |||
T8183 |
Deslanoside
洋地黄,去乙酰西地兰,Desacetyllanatoside C,Deacetyllanatoside C |
ATPase; Drug Metabolite | Membrane transporter/Ion channel; Metabolism |
Deslanoside (Desacetyllanatoside C) 是一种快速作用的强心苷,可抑制Na-K-ATPase 膜泵,导致细胞内钠和钙浓度增加。它用于研究充血性心力衰竭和因折返机制引起的室上性心律失常,并在研究慢性心房颤动时控制心室率。 | |||
T0983 |
Penicillamine
青霉胺,d-penicillamin,Dimethyl Cysteine,D-青霉胺,Artamine,D-(-)-Penicillamine |
Antibiotic | Microbiology/Virology |
Penicillamine (Artamine) 是一种 penicillin 的代谢降解产物,是一种螯合剂,可作用于威尔逊氏病。 | |||
T0617 |
Nicotinamide N-oxide
Nicotinamide-N-oxide,Nicotinamide 1-oxide,N-氧代烟酰胺,烟酰胺-N-氧化物,1-oxynicotinamide |
c-Myc; Endogenous Metabolite; CXCR; Drug Metabolite | Autophagy; Cell Cycle/Checkpoint; GPCR/G Protein; Immunology/Inflammation; Metabolism |
Nicotinamide N-oxide (Nicotinamide 1-oxide) 是生物体内烟酰胺分解代谢物,是高效选择性CXCR2受体拮抗剂。 | |||
T4710 |
3-Methoxytyramine hydrochloride
3-O-methyl Dopamine hydrochloride,3-O-methyl Dopamine hydrochloride),3-O-甲基多巴胺盐酸盐 |
Others; Endogenous Metabolite; Drug Metabolite | Metabolism; Others |
3-Methoxytyramine hydrochloride (3-O-methyl Dopamine hydrochloride) 是多巴胺的无活性代谢物,能够活化痕量胺相关受体1 。 | |||
T5320 |
Tulipalin A
α-methylene-γ-butyrolactone,2-Methylenebutyrolactone,2-甲烯基丁内酯 |
Others; Drug Metabolite | Metabolism; Others |
Tulipalin A (α-methylene-γ-butyrolactone) 是来源于郁金香鳞茎的有毒糖苷。Tulipalin A 是引起过敏性接触皮炎的致敏性致敏物 (causative allergen),在低剂量影响免疫细胞的功能,例如 Jurkat T 细胞。 | |||
T17143 |
Toyocamycin
丰加霉素,Vengicide |
Apoptosis; Others; IRE1; Antibiotic; Antifungal | Apoptosis; Cell Cycle/Checkpoint; Microbiology/Virology; Others |
Toyocamycin (Vengicide) 是放线菌类产生的腺苷类似物,为 X 盒结合蛋白 1 (XBP1) 抑制剂,抑制 IRE1α 诱导的 ATP 依赖性 XBP1 mRNA 的断裂,IC50值为 80 nM。它还诱导凋亡。 | |||
T13808 |
p-Coumaric Acid Ethyl Ester
对香豆酸乙酯,Ethyl (E)-p-hydroxycinnamate,Ethyl trans-4-hydroxycinnamate |
Others; Drug Metabolite | Metabolism; Others |
p-Coumaric Acid Ethyl Ester (Ethyl (E)-p-hydroxycinnamate) 是 p-Coumaric acid 的乙酯形式。p-Coumaric Acid 是一种免疫抑制剂, 能够用于自身免疫性炎性疾病 (如类风湿关节炎) 的研究。 | |||
T3797 |
Isosilybin
Isosilybinin,Isosilibinin,异水飞蓟宾,Silymarin,Silybin B,Q-100795 |
P450 | Metabolism |
Isosilybin (Isosilibinin) 是一种类黄酮,来源于乳蓟;能够抑制CYP3A4诱导(IC50:74 μM)。 | |||
T3212 |
Digoxigenin
地谷新配基,异羟基洋地黄毒苷元 |
Others | Others |
Digoxigenin, a therapeutic drug belonging to the group of cardiac glycosides, is widely used in the management of congestive heart failure and other cardiac diseases | |||
T3669 |
Curcumenol
(+)-Curcumenol,莪术醇 |
P450 | Metabolism |
Curcumenol ((+)-Curcumenol) 提取具有药用价值的 Curcuma zedoaria,是高效的 CYP3A4抑制剂(IC50=12.6 μM),具有神经抗肿瘤、保护、抗炎、和保肝的作用。它在 LPS 刺激的 BV-2 小胶质细胞中,抑制 Akt 介导的 NF-κB 活化及 p38 MAPK 信号通路。 | |||
TWO2771 |
2-Adamantanol
2-金刚烷醇,Adamantan-2-Ol,2-Hydroxyadamantane |
Others | Others |
2-Adamantanol (2-Hydroxyadamantane) 用于合成抗过敏药物Mizolastine。 | |||
T1468 |
Lornoxicam
Ro 13-9297,Chlortenoxicam,TS110,氯诺昔康 |
COX; Endogenous Metabolite | Immunology/Inflammation; Metabolism; Neuroscience |
Lornoxicam (Chlortenoxicam) 是一种新型非甾体抗炎药,是高活性 COX-1 和 COX-2 抑制剂,IC50 分别为 5 和 8 nM。 | |||
T3327 |
Artemotil
SM-227,β-Arteether,Beta-Arteether,蒿乙醚,Arteether,(+)-Arteether |
CXCR; CCR; Parasite | Autophagy; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology |
Artemotil (SM-227) 是一种新型的速效抗疟药,可研究耐Plasmodium falciparum 的恶性疟原虫疟疾,IC50值为 1.61 nM。 | |||
T6S2243 |
Alisol A 24-acetate
Alisol A 24-monoacetate,Alisol A monoacetate,泽泻醇A24-醋酸酯 |
Others | Others |
Alisol A 24-acetate (Alisol A monoacetate) 是一种天然产物。 | |||
T5567 |
Tetradecanedioic acid
十四烷二酸,Tetradecanedicarboxylate |
Others; Endogenous Metabolite | Metabolism; Others |
Tetradecanedioic acid (Tetradecanedicarboxylate) 是一种长链脂肪酸,属于内源性代谢物的一种。它能够作为有机阴离子转运多肽介导的药物-药物相互作用的候选生物标志物。 | |||
T3820 |
Iridin
野鸢尾苷,Lridin |
Others | Others |
Iridin (Lridin) 是抑制异黄酮化合物,从Iris milesii 中提取得到。 | |||
T10147 |
4-Hydroxymephenytoin
(+/-)-4'-Hydroxymephenytoin |
Others; Drug Metabolite | Metabolism; Others |
4-Hydroxymephenytoin ((+/-)-4'-Hydroxymephenytoin) 是抗癫痫药 mephenytoin 的代谢产物。Mephenytoin 是 CYP2C19的配体。 | |||
T7936 |
Benzopinacole
|
Others | Others |
Benzopinacole 是一种抗阿米巴药物,可作为中间体合成多种化合物。 | |||
T0681 |
Rifampicin
Rifamycin AMP,利福平,Rimactane,Rifampin |
Influenza Virus; DNA/RNA Synthesis; Antibacterial; Antibiotic; Antifection | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Rifampicin (Rifamycin AMP) 是广谱抗生素,可抵抗细菌病原体以及具有抗流感病毒活性。 | |||
T4S0647 |
Butylphthalide
丁基苯酞,3-Butylphthalide,3-n-Butylphathlide,3-n-Butylphthalide |
Others | Others |
Butylphthalide (3-Butylphthalide) 是一种抗脑缺血药物,最初分离自芹菜种中,对中风动物模型有效。 | |||
T2959 |
Ginsenoside Rh2
20(S)-Rh2,20S-Ginsenoside Rh2,人参皂苷Rh2,20(S)-Ginsenoside Rh2,人参皂苷 Rh2 |
Apoptosis; EGFR; Caspase; Endogenous Metabolite | Angiogenesis; Apoptosis; JAK/STAT signaling; Metabolism; Proteases/Proteasome; Tyrosine Kinase/Adaptors |
Ginsenoside Rh2 (20(S)-Ginsenoside Rh2) 诱导caspase-8和caspase-9活化。它以多途径方式诱导癌细胞凋亡。 | |||
T1381 |
Milbemycin oxime
|
Others; Antibiotic; Parasite | Microbiology/Virology; Others |
Milbemycin oxime 是一种大环内酯,具有广谱抗寄生虫活性。它由 Milbemycin A4 和 A3 组成。它可结合谷氨酸门控的氯离子通道,可作用于肠道线虫,肺和心脏蠕虫。 | |||
T22286 |
Cyanosafracin B
Cyanoquinonamine,氰基番红菌素 B,CBR28-1 |
Others | Others |
Cyanosafracin B (Cyanoquinonamine) 是一种合成 Phthalascidin Pt-650 及 Ecteinascidin ET-743 的起始原料。 | |||
T0254 |
Probucol
DH-581,普罗布考 |
Virus Protease; ABC; Lipid | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology |
Probucol (DH-581) 是一种抗高脂血症药物,可通过增加 LDL 分解代谢率来降低血液中的胆固醇水平。 | |||
T4S0051 |
Coptisine sulfate
|
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Coptisine Sulfate 是一种从黄连中分离到的生物碱,是非竞争性的IDO 抑制剂,Ki=为 5.8 μM,IC50=6.3 μM。 | |||
T3S2381 |
Perillene
3-Isohexenylfuran,紫苏烯,Perillen |
Others; Antibacterial | Microbiology/Virology; Others |
Perillene (3-Isohexenylfuran) 是促进肠蠕动的药物中的活性成分,它对金黄色葡萄球菌和大肠杆菌具有很强的抗药性。 | |||
T1285 |
Anethole trithione
茴三硫,Anetholtrithion |
Others; AChR | Neuroscience; Others |
Anethole trithione (Anetholtrithion) 是硫杂环胆碱,是一种胆汁分泌刺激剂,可增强唾液分泌并增加 mAChR 受体,用于口干症的研究。 | |||
TN3967 |
Epieriocalyxin A
|
ERK; BCL; ROS; Caspase; DNA/RNA Synthesis; JNK | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; MAPK; Proteases/Proteasome |
Epieriocalyxin A 可以抑制 Caco-2 结肠癌细胞的生长。它可能是未来结肠癌治疗的潜在药物。 | |||
TQ0152 |
Dalfopristin
RP54476,达福普汀 |
Antibacterial; Antibiotic | Microbiology/Virology |
Dalfopristin (RP54476) 是一种半合成的链霉素抗生素。 Quinupristin/Dalfopristin (Q/D) 用于治疗耐多药粪肠球菌感染。 | |||
TN1296 |
5-Feruloylquinic acid
5-O-Feruloylquinic acid,5-FQA,5-O-阿魏酰奎尼酸 |
Tyrosinase; Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair; Proteases/Proteasome |
5-Feruloylquinic acid (5-FQA) 表现出抗氧化作用和酪氨酸酶抑制作用。 | |||
T3021 |
Bulleyaconitine A
草乌甲素,Bulleyaconi cine A |
Sodium Channel | Membrane transporter/Ion channel |
Bulleyaconitine A (Bulleyaconi cine A) 是一种分离自乌头属植物的抗炎活性化合物,也可用于缓解疼痛的研究。 | |||
T5132 |
9-dihydro-13-acetylbaccatin III
13-乙酰基-9-羟基巴卡丁 III,13-Acetyl-9-dihydrobaccatin III,9-DHAB III |
Apoptosis | Apoptosis |
9-dihydro-13-acetylbaccatin III (9-DHAB III) 是一种制备紫杉醇类似物的中间体。 | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-02062 |
SULT1A1 Protein, Human, Recombinant (His)
HAST1/HAST2,PST,P-PST,ST1A1,STP,sulfotransferase family, cyt... |
Human | E. coli |
Sulfate conjugation catalyzed by cytosolic sulfotransferase (SULT) enzymes. The SULTs are Phase II drug-metabolizing enzymes that catalyze the addition of a sulfuryl moiety to both endogenous compounds, including steroids and neurotransmitters, and certain xenobiotics, including N-hydroxy-2-acetylaminoflourine and phenolic compounds, like alpha-naphthol. SULTs may be involved in the individual genetic disposition, species differences, and organotropisms for toxicological effects of chemicals. Pa... | |||
TMPY-05321 |
CYP3A4 Protein, Human, Recombinant (His)
P450C3,P450PCN1,CYPIIIA4,CP34,cytochrome P450 family 3 subfa... |
Human | E. coli |
CYP3A4 is an important member of the cytochrome P450 enzyme superfamily, with 33 allelic variants. Human cytochrome P450 3A4 (CYP3A4) is an important drug metabolizing enzyme involved in a number of drug-drug and food-drug interactions. Systemic inflammation has been linked to suppressed CYP3A4 activity. | |||
TMPY-02271 |
TRXR1/TXNRD1 Protein, Human, Recombinant (aa 161-647, His)
thioredoxin reductase 1,TR1,TXNR,TR,TRXR1,GRIM-12 |
Human | E. coli |
Thioredoxin reductase 1 (TXNRD1) which is a selenocysteine-containing protein is overexpressed in many malignancies. TXNRD1 plays a key role in regulating cell growth and transformation, and protects cells against oxidative damage. We investigated the association between TXNRD1 polymorphisms and ATDH susceptibility. Moreover, TXNRD1 is an essential selenium-containing enzyme involved in detoxification of reactive oxygen species (ROS) and redox signaling. And genetic variations in TXNRD1 favor th... | |||
TMPH-03139 |
MDR1 Protein, Plasmodium falciparum, Recombinant (His & SUMO)
Chloroquine resistance protein,MDR1,Multidrug resis... |
Plasmodium falciparum | E. coli |
Energy-dependent efflux pump responsible for decreased drug accumulation in multidrug-resistant cells. MDR1 Protein, Plasmodium falciparum, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 54.2 kDa and the accession number is P13568. | |||
TMPK-01308 |
TAG-72 Protein, Canine, Recombinant (His)
mRNA-methyltransferase,mRNA (guanine-N(7))-methyltransferase... |
Canine | E. coli |
The guanine-N7 methyltransferase domain of vaccinia virus mRNA capping enzyme is a heterodimer composed of a catalytic subunit and a stimulatory subunit. Cap (guanine-N7) methylation is an essential step in eukaryal mRNA synthesis and a potential target for antiviral, antifungal, and antiprotozoal drug discovery. | |||
TMPK-00806 |
GHR/Growth Hormone R Protein, Human, Recombinant (His)
GHR/BP,GH receptor,GHBP,GHR |
Human | HEK293 Cells |
Pegvisomant, a growth hormone receptor (GHR) antagonist, is a well-known drug that was designed to treat acromegaly. However, recent studies have indicated that the GHR is a "moonlighting" protein that may exhibit dual functions based on its localization in the plasma membrane and nucleus. | |||
TMPK-01039 |
FcRH5/FcRL5 Protein, Mouse, Recombinant (His)
CD307e,FcRL5,BXMAS1MGC119592,IFGP5,FcRH5,BXMAS1,CD307,DKFZp6... |
Mouse | HEK293 Cells |
FcRH5 is a cell surface marker enriched on malignant plasma cells when compared to other hematologic malignancies and normal tissues. DFRF4539A is an anti-FcRH5 antibody-drug conjugated to monomethyl auristatin E (MMAE), a potent anti-mitotic agent. FcRH5/FcRL5 Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with C-His tag. The predicted molecular weight is 53.7 kDa and the accession number is Q68SN8-1. | |||
TMPK-00759 |
IgG1 Fc Protein, Human, Recombinant
Igh-4,VH7183,IgG1,RGD1359539 |
Human | HEK293 Cells |
IgG1 is most abundant in serum among the four IgG subclasses (IgG1, 2, 3 and 4) and binds to Fc receptors (FcγR) on phagocytic cells with high affinity. Fc fragment is demonstrated to mediate phagocytosis, trigger inflammation, and target Ig to particular tissues.IgG1 Fc was reported has a novel role as a potential anti-inflammatory drug for treatment of human autoimmune diseases. | |||
TMPK-00618 |
FcRH5/FcRL5 Protein, Human, Recombinant (His)
FcR-like protein 5,CD307,BXMAS1,FcRH5,IFGP5,CD307e,FcRL5 |
Human | HEK293 Cells |
FcRH5 is a cell surface marker enriched on malignant plasma cells when compared to other hematologic malignancies and normal tissues. DFRF4539A is an anti-FcRH5 antibody-drug conjugated to monomethyl auristatin E (MMAE), a potent anti-mitotic agent. FcRH5/FcRL5 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with C-His tag. The predicted molecular weight is 92.38 kDa and the accession number is AAK93971. | |||
TMPK-01145 |
FcRH5/FcRL5 Protein, Human, Recombinant (His & Avi), Biotinylated
CD307,FcRL5,FcR-like protein 5,FCRH5MGC119593,DKFZp667F216,B... |
Human | HEK293 Cells |
FcRH5 is a cell surface marker enriched on malignant plasma cells when compared to other hematologic malignancies and normal tissues. DFRF4539A is an anti-FcRH5 antibody-drug conjugated to monomethyl auristatin E (MMAE), a potent anti-mitotic agent. FcRH5/FcRL5 Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian cells with N-His-Avi tag. The predicted molecular weight is 94.19 kDa and the accession number is Q96RD9-1. | |||
TMPK-00619 |
FcRH5/FcRL5 Protein (Primary Amine Labeling), Human, Recombinant (His), Biotinylated
IFGP5,CD307,FCRH5MGC119593,FLJ00397,DKFZp667E2019,BXMAS1MGC1... |
Human | HEK293 Cells |
FcRH5 is a cell surface marker enriched on malignant plasma cells when compared to other hematologic malignancies and normal tissues. DFRF4539A is an anti-FcRH5 antibody-drug conjugated to monomethyl auristatin E (MMAE), a potent anti-mitotic agent. FcRH5/FcRL5 Protein (Primary Amine Labeling), Human, Recombinant (His), Biotinylated is expressed in HEK293 mammalian cells with C-His tag. The predicted molecular weight is 92.38 kDa and the accession number is AAK93971. | |||
TMPK-00483 |
PCSK9 Protein, Cynomolgus, Recombinant (His)
PCSK9 |
Cynomolgus | HEK293 Cells |
Proprotein convertase subtilisin/kexin type 9 (PCSK9) is an enzyme encoded by the PCSK9 gene in humans on chromosome 1.The first two PCSK9 inhibitors, alirocumab and evolocumab, were approved as once every two week injections, by the U.S. Food and Drug Administration in 2015 for lowering LDL-particle concentrations when statins and other drugs were not sufficiently effective or poorly tolerated. | |||
TMPJ-01426 |
SARS-CoV-2 NSP2 Protein (His)
SARS-CoV 2 nsp2,SARS-CoV 2 p65 homolog |
SARS-CoV-2 | E. coli |
The positive-stranded RNA genome of the coronaviruses is translated from ORF1 to yield polyproteins that are proteolytically processed into intermediate and mature nonstructural proteins (nsps). SARS-CoV 2 polyproteins incorporate 16 protein domains (nsps). The putative non-structural protein 2 (nsp2) of SARS-CoV plays an important role in viral transcription and replication, and is an attractive target for anti-SARS drug development. | |||
TMPK-00407 |
AXL Protein, Human, Recombinant (His & Avi)
AXL oncogene,Axl,EC 2.7.10.1,Tyro7,UFO,ARK,EC 2.7.10,AI32364... |
Human | HEK293 Cells |
Axl, a member of the TAM (Tyro3, Axl, Mer) family, and its inhibitors can specifically break the kinase signaling nodes, allowing advanced patients to regain drug sensitivity with improved therapeutic efficacy. Overexpression and activation of Axl receptor tyrosine kinase have been widely accepted to promote cell proliferation, chemotherapy resistance, invasion, and metastasis in several human cancers, such as lung, breast, and pancreatic cancers. AXL Protein, Human, Recombinant (His & Avi) is e... | |||
TMPK-01384 |
SARS PLpro/papain-like protease Protein (His)
Papain-like Protease,PL-PRO,Replicase polyprotein 1a,pp1a,PL... |
SARS | E. coli |
The coronaviral proteases, papain-like protease (PLpro) and 3C-like protease (3CLpro), are attractive antiviral drug targets because they are essential for coronaviral replication. Although the primary function of PLpro and 3CLpro are to process the viral polyprotein in a coordinated manner, PLpro has the additional function of stripping ubiquitin and ISG15 from host-cell proteins to aid coronaviruses in their evasion of the host innate immune responses. SARS PLpro/papain-like protease Protein (... | |||
TMPK-00472 |
AXL Protein, Cynomolgus, Recombinant (His)
Tyro7,JTK11,AI323647,AXL oncogene,EC 2.7.10.1,EC 2.7.10,UFO,... |
Cynomolgus | HEK293 Cells |
Axl, a member of the TAM (Tyro3, Axl, Mer) family, and its inhibitors can specifically break the kinase signaling nodes, allowing advanced patients to regain drug sensitivity with improved therapeutic efficacy. Overexpression and activation of Axl receptor tyrosine kinase have been widely accepted to promote cell proliferation, chemotherapy resistance, invasion, and metastasis in several human cancers, such as lung, breast, and pancreatic cancers. AXL Protein, Cynomolgus, Recombinant (His) is ex... | |||
TMPY-03458 |
Sorcin/SRI Protein, Human, Recombinant
sorcin,SCN,CP22,V19,CP-22 |
Human | Baculovirus Insect Cells |
Sorcin was originally identified in multidrug-resistant cells. It is a calcium-binding protein. Sorcin modulates excitation-contraction coupling in the heart, contributes to calcium homeostasis in the heart sarcoplasmic reticulum. Sorcin is overexpressed in the multi-drug resistant chinese hamster ovary cell line CHRC5 and a variety of multidrug-resistant tumor cell lines, but overexpression is not a sufficient or necessary condition for the acquisition of the multidrug-resistant phenotype. Sorc... | |||
TMPK-00954 |
Hyaluronidase 2/HYAL2 Protein, Human, Recombinant (His)
LuCa-2,Hyaluronidase 2,LUCA2,HYAL2,Hyal-2,Hyaluronidase-2 |
Human | HEK293 Cells |
Hyaluronidases, a family of enzymes that are able to degrade hyaluronic acid (HA), are employed in medicine to increase drug diffusion and reverse the effects of HA filler injections. Hyaluronidases are able to dissolve subcutaneous nodules or to correct excessive quantities of injected filler. Upregulation of hyaluronidase 2 (HYAL2), one of somatic hyaluronidase (HAase), was demonstrated in granulation tissue during the healing of equine superficial digital flexor tendon injuries. Hyaluronidase... | |||
TMPK-00410 |
AXL Protein (Primary Amine Labeling), Human, Recombinant (hFc), Biotinylated
ARK,EC 2.7.10.1,EC 2.7.10,Axl,JTK11,AXL oncogene,UFO,AI32364... |
Human | HEK293 Cells |
Axl, a member of the TAM (Tyro3, Axl, Mer) family, and its inhibitors can specifically break the kinase signaling nodes, allowing advanced patients to regain drug sensitivity with improved therapeutic efficacy. Overexpression and activation of Axl receptor tyrosine kinase have been widely accepted to promote cell proliferation, chemotherapy resistance, invasion, and metastasis in several human cancers, such as lung, breast, and pancreatic cancers. AXL Protein (Primary Amine Labeling), Human, Rec... | |||
TMPY-02442 |
ELK1 Protein, Human, Recombinant (His & GST)
ELK1, member of ETS oncogene family |
Human | Baculovirus Insect Cells |
E twenty-six (ETS)-like transcription factor 1, also known as Elk1 or Member of ETS oncogene family (ELK1), is a member of the ETS oncogene superfamily which is characterized by a common protein domain that regulates DNA binding to target sequences. Elk1 is expressed in the nuclei of non-neuronal cells and function as a transcription activator. It plays important roles in various contexts, including long-term memory formation, drug addiction, Alzheimer's disease, Down syndrome, breast cancer, an... | |||
TMPK-01158 |
Kallikrein 5/KLK5 Protein, Mouse, Recombinant (His)
SCTE,KLKL2,KLK5,KLK-L2,Klnc,Kallikrein c |
Mouse | HEK293 Cells |
The inhibition of kallikrein 5 (KLK5) has been identified as a potential strategy for treatment of the genetic skin disorder Netherton syndrome, in which loss-of-function mutations in the SPINK5 gene lead to down-regulation of the endogenous inhibitor LEKTI-1 and profound skin-barrier defects with severe allergic manifestations. To aid in the development of a medicine for this target, an X-ray crystallographic system was developed to facilitate fragment-guided chemistry and knowledge-based drug-... | |||
TMPK-00725 |
Hyaluronidase 2/HYAL2 Protein, Mouse, Recombinant (His)
Hyaluronidase-2,Hyal-2,Hyaluronidase 2,HYAL2 |
Mouse | HEK293 Cells |
Hyaluronidases, a family of enzymes that are able to degrade hyaluronic acid (HA), are employed in medicine to increase drug diffusion and reverse the effects of HA filler injections. Hyaluronidases are able to dissolve subcutaneous nodules or to correct excessive quantities of injected filler. Upregulation of hyaluronidase 2 (HYAL2), one of somatic hyaluronidase (HAase), was demonstrated in granulation tissue during the healing of equine superficial digital flexor tendon injuries. Hyaluronidase... | |||
TMPK-00408 |
AXL Protein, Human, Recombinant (His & Avi), Biotinylated
AXL oncogene,EC 2.7.10.1,AI323647,Axl,JTK11,ARK,EC 2.7.10,UF... |
Human | HEK293 Cells |
Axl, a member of the TAM (Tyro3, Axl, Mer) family, and its inhibitors can specifically break the kinase signaling nodes, allowing advanced patients to regain drug sensitivity with improved therapeutic efficacy. Overexpression and activation of Axl receptor tyrosine kinase have been widely accepted to promote cell proliferation, chemotherapy resistance, invasion, and metastasis in several human cancers, such as lung, breast, and pancreatic cancers. AXL Protein, Human, Recombinant (His & Avi), Bio... | |||
TMPK-00875 |
CD96 Protein, Human, Recombinant (His & Avi), Biotinylated
TACTILE,CD96,DKFZp667E2122,CD96 molecule |
Human | HEK293 Cells |
The receptors CD96 and TIGIT are expressed on the surface of T and natural killer (NK) cells, and recent studies suggest both play important inhibitory roles in immune function. CD96 has been shown to modulate immune cell activity in mice, with Cd96-/- mice displaying hypersensitive NK-cell responses to immune challenge and significant tumor resistance. The counterbalance between the putative inhibitory CD96 and TIGIT receptors and the activating receptor, CD226, offers unique strategies for imm... | |||
TMPY-03267 |
Sorcin/SRI Protein, Human, Recombinant (His & GST)
CP-22,CP22,sorcin,V19,SCN |
Human | Baculovirus Insect Cells |
Sorcin was originally identified in multidrug-resistant cells. It is a calcium-binding protein. Sorcin modulates excitation-contraction coupling in the heart, contributes to calcium homeostasis in the heart sarcoplasmic reticulum. Sorcin is overexpressed in the multi-drug resistant chinese hamster ovary cell line CHRC5 and a variety of multidrug-resistant tumor cell lines, but overexpression is not a sufficient or necessary condition for the acquisition of the multidrug-resistant phenotype. Sorc... | |||
TMPK-01352 |
SARS-CoV-2 PLpro/papain-like protease Protein (His & Avi)
Plpro,PL2-PRO,pp1a,nsp1,Replicase polyprotein 1a,Papain-like... |
SARS | E. coli |
The coronaviral proteases, papain-like protease (PLpro) and 3C-like protease (3CLpro), are attractive antiviral drug targets because they are essential for coronaviral replication. Although the primary function of PLpro and 3CLpro are to process the viral polyprotein in a coordinated manner, PLpro has the additional function of stripping ubiquitin and ISG15 from host-cell proteins to aid coronaviruses in their evasion of the host innate immune responses. SARS-CoV-2 PLpro/papain-like protease Pro... | |||
TMPY-06864 |
GLP1R Protein, Human, Recombinant (His & Avi)
glucagon-like peptide 1 receptor |
Human | HEK293 Cells |
Glucagon-like peptide (GLP)-1 receptor is encoded by GLP1R. GLP1R plays a critical role in mediating the biological actions of GLP1 in mammals and fish. The neuronal GLP1Rs mediate body weight and anorectic effects of liraglutide, but are not required for glucose-lowering effects. Glucagon-like peptide 1 receptor (GLP1R) signaling has been shown to have antipsychotic properties in animal models and to impact glucose-dependent insulin release, satiety, memory, and learning in man. Glucagon-like p... | |||
TMPJ-01145 |
ABCB5 Protein, Human, Recombinant (Trx)
ABCB5 P-gp,ATP-binding cassette sub-family B member 5,ABCB5,... |
Human | E. coli |
ATP-binding cassette sub-family B member 5(ABCB5) is a plasma membrane-spanning protein. ABCB5 is principally expressed in physiological skin and human malignant melanoma. ABCB5 has been suggested to regulate skin progenitor cell fusion and mediate chemotherapeutic drug resistance in stem-like tumor cell subpopulations in human malignant melanoma. It is commonly over-expressed on circulating melanoma tumour cells. Furthermore, the ABCB5+ melanoma- initiating cells were demonstrated to express FL... | |||
TMPY-03416 |
TNFAIP8 Protein, Human, Recombinant (His)
GG2-1,tumor necrosis factor, alpha-induced protein 8,SCCS2,S... |
Human | E. coli |
Tumor necrosis factor (TNF)-alpha-induced protein 8 (TNFAIP8) family is a newly identified protein with vital roles in maintaining immune homeostasis. Tumor necrosis factor-alpha-inducible protein 8 (TNFAIP8) is a TNF-alpha inducible anti-apoptotic protein with multiple roles in tumor growth and survival. by the creation of cellular autophagy events, TNFAIP8 promotes cell survival and drug resistance in prostate cancer cells. TNFAIP8 regulates Hippo pathway through interacting with LATS1 to prom... | |||
TMPJ-00295 |
NgR Protein, Mouse, Recombinant (hFc)
Nogo-66 Receptor,Nogo Receptor,NgR,RTN4R,NOGOR,Reticulon-4 R... |
Mouse | HEK293 Cells |
Nogo Receptor (NgR) is a glycosylphosphoinositol (GPI)-anchored protein that belongs to the Nogo recptor family. Human NgR is predominantly expressed in neurons and their axons in the central nervous systems. As a receptor for myelin-derived proteins Nogo, myelin-associated glycoprotein (MAG) and myelin oligodendrocyte glycoprotein (OMG), NgR mediates axonal growth inhibition and may play a role in regulating axonal regeneration and plasticity in the adult central nervous system. NgR may be prop... | |||
TMPJ-00922 |
DCK Protein, Human, Recombinant (His & T7)
DCK,Deoxycytidine Kinase |
Human | E. coli |
Deoxycytidine Kinase (DCK) is a member of the DCK/DGK family. DCK exists as a homodimer and is localized to the nucleus. DCK is required for the phosphorylation of the deoxyribonucleosides deoxycytidine (dC), deoxyguanosine (dG), and deoxyadenosine (dA). DCK has broad substrate specificity, and does not display selectivity based on the chirality of the substrate. In addition, DCK is also an essential enzyme for the phosphorylation of numerous nucleoside analogs widely employed as antiviral and c... | |||
TMPY-00648 |
UNC5A Protein, Human, Recombinant (hFc)
UNC5H1,unc-5 homolog A (C. elegans) |
Human | HEK293 Cells |
The netrin-1 receptor Uncoordinated Phenotype-5A, or UNC5A, plays an important role in predicting response to DNA damage induced by chemotherapeutic drug and regulating cell death in bladder cancer. Moreover, UNC5A is cumulatively downregulated by the unfolding protein response (UPR) at the transcriptional level in vitro and at the translational level both in vitro and in vivo. Also, UNC5A is a novel transcriptional target of p53 and plays a role in p53-dependent apoptosis. UNC5A Protein, Human,... | |||
TMPY-00999 |
UNC5A Protein, Human, Recombinant (His)
unc-5 homolog A (C. elegans),UNC5H1 |
Human | HEK293 Cells |
The netrin-1 receptor Uncoordinated Phenotype-5A, or UNC5A, plays an important role in predicting response to DNA damage induced by chemotherapeutic drug and regulating cell death in bladder cancer. Moreover, UNC5A is cumulatively downregulated by the unfolding protein response (UPR) at the transcriptional level in vitro and at the translational level both in vitro and in vivo. Also, UNC5A is a novel transcriptional target of p53 and plays a role in p53-dependent apoptosis. UNC5A Protein, Human,... | |||
TMPJ-01037 |
CXCR4 Protein, Human, Recombinant (hFc)
CXCR4,CD184,Fusin,D2S201E,FB22,HM89,HSY3RR,LAP3,LCR1,LESTR,N... |
Human | HEK293 Cells |
C-X-C chemokine receptor type 4 (CXCR4) is an alpha-chemokine receptor specific for stromal-derived-factor-1 (SDF-1 also called CXCL12), a molecule endowed with potent chemotactic activity for lymphocytes. This receptor is one of several chemokine receptors that HIV isolates can use to infect CD4+ T cells. CXCR4 stands out for its pleiotropic roles in both physiological and pathological conditions and it represents a crucial target in drug development. CXCL12 is the principal CXCR4 specific liga... | |||
TMPY-02394 |
IMPA1 Protein, Human, Recombinant (His)
IMPA,inositol(myo)-1(or 4)-monophosphatase 1,IMP |
Human | E. coli |
IMPA1 (Inositol Monophosphatase 1) is a Protein Coding gene. This gene encodes an enzyme that dephosphorylates Myo-inositol monophosphate to generate free Myo-inositol, a precursor of phosphatidylinositol, and is, therefore, an important modulator of intracellular signal transduction via the production of the second messenger's myoinositol 1,4,5-trisphosphate and diacylglycerol. Despite its many physiological functions, no clinical phenotype has been assigned to this gene dysfunction to date. Ad... | |||
TMPY-02909 |
ASGR2 Protein, Human, Recombinant (His)
HBXBP,ASGPR2,HL-2,asialoglycoprotein receptor 2,ASGP-R2,CLEC... |
Human | HEK293 Cells |
ASGR2 is a subunit of the asialoglycoprotein receptor. Asialoglycoprotein receptor, also known as the Ashwell receptor, which is specific for desialylated (galactosyl-terminal) glycoproteins and is expressed exclusively in hepatic parenchymal cells. This receptor is a transmembrane protein that plays a critical role in serum glycoprotein homeostasis by mediating the endocytosis and lysosomal degradation of glycoproteins with exposed terminal galactose or N-acetylgalactosamine residues. ASGR2 is ... | |||
TMPY-05693 |
SARS-CoV-2 Methyltransferase/ME Protein (His)
|
SARS-CoV-2 | E. coli |
Coronavirus encodes the 2’-O-MTase (2'O Methyltransferase) that is composed of the catalytic subunit nsp16 and the stimulatory subunit nsp10 and plays an important role in virus genome replication and evasion from innate immunity during viral infection. Nonstructural protein 16 (NSP16) / viral 2'O-methyltransferase (2'O-MTase) is highly conserved. The conserved 2'O-MTase activity is important for CoV pathogenesis and NSP16 is a conserved universal target for rapid live attenuated vaccine design ... | |||
TMPY-06836 |
NR3C1 Protein, Human, Recombinant (His)
GCCR,GRL,GR,nuclear receptor subfamily 3, group C, member 1 ... |
Human | E. coli |
NR3C1 (Nuclear Receptor Subfamily 3 Group C Member 1) is a Protein Coding gene. This gene encodes glucocorticoid receptor, which can function both as a transcription factor that binds to glucocorticoid response elements in the promoters of glucocorticoid responsive genes to activate their transcription, and as a regulator of other transcription factors. NR3C1 is a transcriptional regulator of many drug-metabolizing enzymes and anti-inflammatory molecules. NR3C1 polymorphisms associate with obesi... | |||
TMPJ-01028 |
Claudin-18.2 Protein, Human, Recombinant (Twin strep & Flag)
Claudin 18.2,CLDN18,Claudin-18,CLDN18.2,Claudin-18.2 |
Human | HEK293 Cells |
Claudin-18 (CLDN18) is a protein that in humans is encoded by the CLDN18 gene. It belongs to the group of claudins. CLDN18 belongs to the large claudin family of proteins, which form tight junction strands in epithelial cells. CLDN18 plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. CLDN18 has two isoform A1 and isoform A2. Human CLDN18.2 is highly expressed in a signifcant proportion of gastric and pancreat... | |||
TMPY-02081 |
PDE2A Protein, Human, Recombinant (aa 215-900, His)
phosphodiesterase 2A, cGMP-stimulated,cGSPDE,PED2A4,PDE2A1,C... |
Human | Baculovirus Insect Cells |
cGMP-dependent 3',5'-cyclic phosphodiesterase, also known as cyclic GMP-stimulated phosphodiesterase and PDE2A, is a peripheral membrane protein that belongs to the cyclic nucleotide phosphodiesterase family and PDE2 subfamily. Phosphodiesterases (PDEs) comprise a family of enzymes that regulate the levels of cyclic nucleotides, key second messengers that mediate a diverse array of functions. Phosphodiesterases (PDEs) modulate signaling by cyclic nucleotides in diverse processes such as cardiac ... | |||
TMPY-01099 |
GPT Protein, Rat, Recombinant (His)
Gpt1,ALAT,glutamic-pyruvate transaminase (alanine aminotrans... |
Rat | Baculovirus Insect Cells |
Alanine aminotransferase (ALT), also known as glutamate pyruvate transaminase (GPT), is a pyridoxal enzyme that belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family, Alanine aminotransferase subfamily. Gpt / Gpt1 / ALT catalyzes the reversible interconversion of L-alanine and 2-oxoglutalate to pyruvate and L-glutamate and plays a key role in the intermediary metabolism of glucose and amino acids. Gpt / Gpt1 / ALT is expressed in the liver, kidney, heart, and skeletal musc... | |||
TMPJ-00751 |
IgG4 hFc Protein, Human, Recombinant (aa 99-326)
IgG4 Fc,Ig γ-4 chain C region,Ig gamma-4 chain C region |
Human | HEK293 Cells |
As a monomeric immunoglobulin that is predominately involved in the secondary antibody response and the only isotype that can pass through the human placenta, Immunoglobulin G (IgG) is synthesized and secreted by plasma B cells, and constitutes 75% of serum immunoglobulins in humans. IgG antibodies protect the body against the pathogens by agglutination and immobilization, complement activation, toxin neutralization, as well as the antibody-dependent cell-mediated cytotoxicity (ADCC). IgG tetram... | |||
TMPY-01893 |
Serpin A12 Protein, Human, Recombinant (His)
OL-64,serpin peptidase inhibitor, clade A (α-1 antiproteinas... |
Human | HEK293 Cells |
Serpins are the largest and most diverse family of protease inhibitors. Most serpins control proteolytic cascades, certain serpins do not inhibit enzymes, but instead perform diverse functions such as storage (ovalbumin, in egg white), hormone carriage proteins (thyroxine-binding globulin, cortisol-binding globulin) and tumor suppressor genes (maspin). Most inhibitory serpins target chymotrypsin-like serine proteases. These enzymes are defined by the presence of a nucleophilic serine residue in ... | |||
TMPY-02072 |
HSF1 Protein, Human, Recombinant (His)
HSTF1,heat shock transcription factor 1 |
Human | E. coli |
Heat shock factor protein 1, also known as heat shock transcription factor 1, HSF1, and HSTF1, is a cytoplasm and nucleus protein that belongs to the HSF family. HSF1 is the major transcription factor of HSPs (heat shock proteins) in response to various stresses. Wild type HSF1 (heat shock transcriptional factor 1) is normally inactive. HSF1 / HSTF1 is a DNA-binding protein that specifically binds heat shock promoter elements (HSE) and activates transcription. In higher eukaryotes, HSF is unable... | |||
TMPY-01742 |
Acetylcholinesterase Protein, Mouse, Recombinant (His)
Acre,Chrne,acetylcholinesterase (Yt blood group) |
Mouse | HEK293 Cells |
Acetylcholinesterase, also known as ACHE, is an enzyme that degrades (through its hydrolytic activity) the neurotransmitter acetylcholine, producing choline and an acetate group. Acetylcholinesterase plays a crucial role in nerve impulse transmission at cholinergic synapses by rapid hydrolysis of the neurotransmitter acetylcholine (ACh). ACHE appears to be a potential therapeutic target at muscle injuries including organophosphate myopathy. It is an externally oriented membrane-bound enzyme and ... | |||
TMPY-02150 |
GADD45A Protein, Human, Recombinant (His & GST)
GADD45,growth arrest and DNA-damage-inducible, alpha,growth ... |
Human | Baculovirus Insect Cells |
GADD45A is a member of the GADD45 Family, and has been found to associate with several cytoplasmic and nuclear factors and has been implicated in several cellular functions, including MAPK signaling, cell cycle regulation, DNA repair and genomic stability, apoptosis, and immune responses. The GADD45 Family of genes is rapidly induced by different stressors, including differentiation-inducing cytokines, and there is a large body of evidence that their cognate proteins are key players in cellular ... | |||
TMPY-01576 |
Artemin Protein, Mouse, Recombinant (hFc)
artemin,neublastin |
Mouse | HEK293 Cells |
Artemin (ARTN) is a member of glial cell line-derived neurotrophic factor (GDNF) family of ligands, and its signaling is mediated via a multi-component receptor complex including the glycosylphosphatidylinositol-anchored GDNF family receptors a (GFRa1, GFRa3) and RET receptor tyrosine kinase. The major mechanism of ARTN action is via binding to a non-signaling co-receptor. The major function of ARTN is to drive the molecule to induce migration and axonal projection from sympathetic neurons. It a... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12411 |
Perphenazine D8 Dihydrochloride
|
Others | Others |
Perphenazine D8 Dihydrochloride is the deuterium labeled Perphenazine, which is an antipsychotic drug. | |||
T11891 |
Lumefantrine-d18
Benflumetol D18,苯芴醇 D18,Lumefantrine D18 |
Others | Others |
Lumefantrine D18 is an antimalarial drug, and is the deuterium labeled Lumefantrine. | |||
TMIJ-0449 |
Dimetridazole-d3
|
||
Dimetridazole-d3 是 Dimetridazole 的氘代化合物。Dimetridazole 的 CAS 号为 551-92-8。Dmetridazole 是一种对抗原生动物感染的硝基咪唑类药物。 | |||
T40915 |
L-Aspartic acid 13C
|
||
L-Aspartic acid 13C is a 13C labeled L-Aspartic acid. L-Aspartic acid is is an amino acid, shown to be a suitable prodrug for colon-specific drug deliverly. | |||
T31108 |
CTP-347
CTP347,CTP 347 |
||
CTP-347, a deuterated version of paroxetine, is potentially the best non-hormonal drug in its class for the treatment of hot flashes. | |||
T12336 |
Oxaprozin D4
Wy-21743 D4 |
Others | Others |
Oxaprozin D4 is the deuterium labeled Oxaprozin, is a non-steroidal anti-inflammatory drug (NSAID). | |||
T13155 |
Tiaprofenic acid D3
|
Others | Others |
Tiaprofenic acid D3 is a deuterium-labeled Tiaprofenic acid. Tiaprofenic acid is a nonsteroidal anti-inflammatory drug and treatment of rheumatic diseases. | |||
T19183 |
Albendazole-d3
Albendazole D3 |
Others | Others |
Albendazole D3 is the deuterium-labeled Albendazole. Albendazole is used as a drug indicated for the treatment of a variety of worm infestations. | |||
TMIJ-0207 |
(S)-Ketoprofen-d3
|
||
(S)-Ketoprofen-d3 是 (S)-Ketoprofen 的氘代化合物。(S)-Ketoprofen 的 CAS 号为 22161-81-5。S-(+)-Ketoprofen 抑制COX-1和COX-2的IC50值分别为 1.9 和 27 nM。 | |||
TMIJ-0037 |
Sarafloxacin-d8 Hydrochloride
|
||
Sarafloxacin-d8 Hydrochloride 是 Sarafloxacin Hydrochloride 的氘代化合物。Sarafloxacin Hydrochloride 的 CAS 号为 91296-87-6。Sarafloxacin hydrochloride是一种抗菌化合物。 | |||
TMIH-0496 |
Rifampicin-d8
|
||
Rifampicin-d8 是 Rifampicin 的氘代化合物。Rifampicin 的 CAS 号为 13292-46-1。Rifampicin是广谱抗生素,可抵抗细菌病原体以及具有抗流感病毒活性。 | |||
TMIH-0494 |
Rifampicin-d3
|
||
Rifampicin-d3 是 Rifampicin 的氘代化合物。Rifampicin 的 CAS 号为 13292-46-1。Rifampicin是广谱抗生素,可抵抗细菌病原体以及具有抗流感病毒活性。 | |||
TMIJ-0298 |
Flunixin-d3 (methyl-d3)
|
||
Flunixin-d3 (methyl-d3) 是 Flunixin 的氘代化合物。Flunixin 的 CAS 号为 38677-85-9。 | |||
TMID-0217 |
Norfluoxetine-d5 Hydrochloride
|
||
Norfluoxetine-d5 Hydrochloride 是 Norfluoxetine Hydrochloride 的氘代化合物。Norfluoxetine Hydrochloride 的 CAS 号为 57226-68-3。Norfluoxetine Hydrochloride 是氟西汀的活性代谢物。氟西汀是一种抗抑郁药。 | |||
TMIJ-0394 |
Hydroxy Ipronidazole-d3
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Hydroxy Ipronidazole-d3 是 Hydroxy Ipronidazole 的氘代化合物。Hydroxy Ipronidazole 的 CAS 号为 35175-14-5。 | |||
TMID-0199 |
Rifampicin-13C-d3
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Rifampicin-13C-d3 是 Rifampicin 的 13C 和氘代化合物。Rifampicin 的 CAS 号为 13292-46-1。Rifampicin是广谱抗生素,可抵抗细菌病原体以及具有抗流感病毒活性。 | |||
T38638 |
4-Trifluoromethylsalicylic acid-13C6
4-Trifluoromethylsalicylic acid-13C6,Desacetyl triflusal-13C6 |
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4-Trifluoromethylsalicylic acid-13C6 是 13C 标记的 4-Trifluoromethylsalicylic acid,主要用于药物开发过程中的定量示踪剂。4-Trifluoromethylsalicylic acid 也是一种血小板聚集抑制剂。 | |||
TMIH-0130 |
Butylphthalide-d7
NBP-d7 |
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Butylphthalide-d7 是 Butylphthalide 的氘代化合物。Butylphthalide 的 CAS 号为 6066-49-5。Butylphthalide 是一种抗脑缺血药物,最初分离自芹菜种中,对中风动物模型有效。 | |||
TMIJ-0096 |
Buspirone EP Impurity A-d8
Buspirone USP Related Compound A-d8 |
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Buspirone EP Impurity A-d8 是 Buspirone EP Impurity A 的氘代化合物。Buspirone EP Impurity A 的 CAS 号为 20980-22-7。2-(1-Piperazinyl)pyrimidine 用作抗焦虑药。 | |||
TMID-0015 |
Bendazac-d7
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Bendazac-d7 是 Bendazac 的氘代化合物。Bendazac 的 CAS 号为 20187-55-7。Bendazac 是一种氧乙酸,具有抗过敏、抗炎、利胆和抗血脂作用。它能够阻断蛋白质变性,延缓白内障的发生过程。 | |||
TMIJ-0105 |
3-Butylphthalide-d9
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3-Butylphthalide-d9 是 3-Butylphthalide 的氘代化合物。3-Butylphthalide 的 CAS 号为 6066-49-5。Butylphthalide 是一种抗脑缺血药物,最初分离自芹菜种中,对中风动物模型有效。 | |||
TMID-0198 |
Esmolol-d7 HCl
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Esmolol-d7 HCl 是 Esmolol HCl 的氘代化合物。Esmolol HCl 的 CAS 号为 81161-17-3。Esmolol hydrochloride 是一种心脏选择性β受体阻滞剂,用于治疗心律失常和严重高血压。 | |||
TMID-0241 |
Olmesartan-d6 Acid
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Olmesartan-d6 Acid 是 Olmesartan Acid 的氘代化合物。Olmesartan Acid 的 CAS 号为 144689-24-7。Olmesartan 是一种血管紧张素II受体 (AT1R) 拮抗剂,常用于研究高血压。 | |||
TMIJ-0102 |
Ropivacaine-d7
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Ropivacaine-d7 是 Ropivacaine 的氘代化合物。Ropivacaine 的 CAS 号为 84057-95-4。Ropivacaine 是有效的钠通道阻断剂,通过可逆地抑制钠离子内流从而引起神经纤维脉冲传导阻滞。Ropivacaine 也是一种 K2P(双孔钾通道)TREK-1的抑制剂,在 COS-7 细胞膜上的 IC50值为 402.7 μM。Ropivacaine 可以用于神经性疼痛的缓解的相关研究。 | |||
TMIJ-0059 |
Moxifloxacin-d4
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Moxifloxacin-d4 是 Moxifloxacin 的氘代化合物。Moxifloxacin 的 CAS 号为 151096-09-2。Moxifloxacin 是一种8-甲氧基喹诺酮类口服有效抗菌药物,用于急性细菌性鼻窦炎,慢性支气管炎的急性细菌性加重和感染性肺炎的研究。 | |||
TMID-0276 |
MAA-d3
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MAA-d3 是 MAA 的氘代化合物。MAA 的 CAS 号为 519-98-2。4-Methylamino antipyrine 是 Metamizole 的活性代谢产物,可用于疼痛和发烧的研究。Metamizole 是吡唑啉酮类非甾体抗炎药,可抑制COX。 | |||
TMIH-0290 |
Ketorolac-d5-P1
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Ketorolac-d5-P1 是 Ketorolac 的氘代化合物。Ketorolac 的 CAS 号为 74103-06-3。Ketorolac 是非甾体抗炎剂,是非选择性的COX抑制剂,对 COX-1 和 COX-2 的IC50值分别为 20 和 120 nM。 | |||
TMIH-0291 |
Ketorolac-d5-P2
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Ketorolac-d5-P2 是 Ketorolac 的氘代化合物。Ketorolac 的 CAS 号为 74103-06-3。Ketorolac 是非甾体抗炎剂,是非选择性的COX抑制剂,对 COX-1 和 COX-2 的IC50值分别为 20 和 120 nM。 | |||
TMIH-0024 |
10,11-Dihydro-10-hydroxycarbamazepine-d4
rac-Licarbazepine-d4 |
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10,11-Dihydro-10-hydroxycarbamazepine-d4 是 10,11-Dihydro-10-hydroxycarbamazepine 的氘代化合物。10,11-Dihydro-10-hydroxycarbamazepine 的 CAS 号为 29331-92-8。Licarbazepine 是一种有效的电压门控钠通道阻滞剂,具有抗惊厥和稳定情绪的功效。 | |||
TMIJ-0079 |
N-Carbobenzyloxyglycine-d2
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N-Carbobenzyloxyglycine-d2 是 N-Carbobenzyloxyglycine 的氘代化合物。N-Carbobenzyloxyglycine 的 CAS 号为 1138-80-3。Z-Glycine (Carbobenzoxyglycine) 是一种药物-脂质结合物,旨在促进脑渗透,基于其亲脂性和与生物膜中脂质的相似性。 | |||
TMIJ-0335 |
Dehydro aripiprazole-d8
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Dehydro aripiprazole-d8 是 Dehydro aripiprazole 的氘代化合物。Dehydro aripiprazole 的 CAS 号为 129722-25-4。Dehydroaripiprazole 是 Aripiprazole 的活性代谢产物,具有抗精神病活性。Aripiprazole 是也一种抗精神病药。 | |||
TMID-0185 |
(±)-Ropivacaine-d7
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(±)-Ropivacaine-d7 是 (±)-Ropivacaine 的氘代化合物。(±)-Ropivacaine 的 CAS 号为 84057-95-4。Ropivacaine 是有效的钠通道阻断剂,通过可逆地抑制钠离子内流从而引起神经纤维脉冲传导阻滞。Ropivacaine 也是一种 K2P(双孔钾通道)TREK-1的抑制剂,在 COS-7 细胞膜上的 IC50值为 402.7 μM。Ropivacaine 可以用于神经性疼痛的缓解的相关研究。 | |||
TMID-0281 |
Moxifloxacin-13C-d3
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Moxifloxacin-13C-d3 是 Moxifloxacin 的 13C 和氘代化合物。Moxifloxacin 的 CAS 号为 151096-09-2。Moxifloxacin 是一种8-甲氧基喹诺酮类口服有效抗菌药物,用于急性细菌性鼻窦炎,慢性支气管炎的急性细菌性加重和感染性肺炎的研究。 | |||
TMID-0184 |
Antipyrine-d3
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Antipyrine-d3 是 Antipyrine 的氘代化合物。Antipyrine 的 CAS 号为 60-80-0。Antipyrine 是一种退烧剂和止痛剂。它可用作氧化药物代谢的探针药物,常用于评估人类的肝氧化能力。 | |||
TMID-0082 |
Lopinavir-d8
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Lopinavir-d8 是 Lopinavir 的氘代化合物。Lopinavir 的 CAS 号为 192725-17-0。Lopinavir 是一种选择性肽模拟 HIV-1 蛋白酶的高效抑制剂。它通过阻止 HIV-1 的成熟而起作用,从而阻断其感染性。它也是SARS-CoV 3CLpro的抑制剂。 | |||
TMIJ-0215 |
Doxofylline-d4
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Doxofylline-d4 是 Doxofylline 的氘代化合物。Doxofylline 的 CAS 号为 69975-86-6。Doxofylline 是腺苷 A1 受体拮抗剂,且能抑制磷酸二酯酶 IV,用于治疗哮喘。 | |||
TMID-0118 |
Doxofylline-d6
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Doxofylline-d6 是 Doxofylline 的氘代化合物。Doxofylline 的 CAS 号为 69975-86-6。Doxofylline 是腺苷 A1 受体拮抗剂,且能抑制磷酸二酯酶 IV,用于治疗哮喘。 | |||
TMIJ-0305 |
10,11-Dihydro-10-hydroxy Carbamazepine-d4
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10,11-Dihydro-10-hydroxy Carbamazepine-d4 是 10,11-Dihydro-10-hydroxy Carbamazepine 的氘代化合物。10,11-Dihydro-10-hydroxy Carbamazepine 的 CAS 号为 29331-92-8。Licarbazepine 是一种有效的电压门控钠通道阻滞剂,具有抗惊厥和稳定情绪的功效。 | |||
TMIJ-0103 |
Suplatast Tosylate-d5
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Suplatast Tosylate-d5 是 Suplatast Tosylate 的氘代化合物。Suplatast Tosylate 的 CAS 号为 94055-76-2。Suplatast Tosilate 是一种口服有活性的 Th2 细胞因子抑制剂,能够阻碍 Th2 细胞产生 IL-4 和 IL-5 ,并对 IgE 的合成具有抑制作用。它是一种抗过敏剂,它具有抗纤维化、抗哮喘及抗炎特性。 | |||
T71288 |
Phenylbutazone-d9
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Phenylbutazone-d9 is intended for use as an internal standard for the quantification of phenylbutazone by GC- or LC-MS. Phenylbutazone is a non-steroidal anti-inflammatory drug and an inhibitor of the peroxidase activity of COX (IC50 = ~100 µM in the presence of hydrogen peroxide). It also inhibits prostaglandin I synthase (IC50 = ~25 µM in the presence of hydrogen peroxide). Phenylbutazone (2 mg/kg) reduces increases in type II collagen levels in the inflamed joints of an equine model of LPS-in... | |||
TMIH-0181 |
Demethoxy Curcumin-d4
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Demethoxy Curcumin-d4 是 Demethoxy Curcumin 的氘代化合物。Demethoxy Curcumin 的 CAS 号为 22608-11-3。Demethoxycurcumin是姜黄素的主要活性成分,有抗炎和抗癌作用。 | |||
TMID-0053 |
Amisulpride-d5
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Amisulpride-d5 是 Amisulpride 的氘代化合物。Amisulpride 的 CAS 号为 71675-85-9。Amisulpride 是多巴胺D2/D3受体拮抗剂,对于人多巴胺D2和D3的Ki分别为 2.8 和 3.2 nM。 | |||
TMID-0208 |
Hydroxychloroquine-d5
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Hydroxychloroquine-d5 是 Hydroxychloroquine 的氘代化合物。Hydroxychloroquine 的 CAS 号为 118-42-3。Hydroxychloroquine 是一种合成抗疟疾剂,有效抑制SARS-CoV-2感染,也抑制 Toll 样受体 7/9 信号传导。 | |||
TMID-0292 |
Tylosin-d3
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Tylosin-d3 是 Tylosin 的氘代化合物。Tylosin 的 CAS 号为 1401-69-0。Tylosin 是一种兽医用大环内酯类抗生素,是Streptomyces fradiae的产物。它对革兰氏阳性菌具有高抗菌活性。它是饲料添加剂用于促进动物生长。它被用于治疗家禽、猪和牛的细菌性痢疾和呼吸道疾病。 | |||
TMIJ-0139 |
Ticagrelor-d7
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Ticagrelor-d7 是 Ticagrelor 的氘代化合物。Ticagrelor 的 CAS 号为 274693-27-5。Ticagrelor (AZD6140) 是可逆的,可口服的P2Y12受体拮抗剂,可抑制血小板聚集。 | |||
T35915 |
Erlotinib-13C6
Erlotinib-13C6 |
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Erlotinib-13C6 (CP-358774-13C6) is a 13C-labeled Erlotinib. Erlotinib is a directly acting EGFR tyrosine kinase inhibitor, with an IC50 of 2 nM for human EGFR[1]. Erlotinib reduces EGFR autophosphorylation in intact tumor cells with an IC50 of 20 nM. Erlotinib is used for the treatment of non-small cell lung cancer[1].Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process[2]... | |||
TMIJ-0274 |
Sulindac-d3
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Sulindac-d3 是 Sulindac 的氘代化合物。Sulindac 的 CAS 号为 38194-50-2。Sulindac 是一种非甾体类抗炎剂,可抑制COX-2的活性,也可抑制 COX-2 的过表达。它是一种亚磺酰基茚衍生物前药,具有潜在的抗肿瘤活性。 | |||
TMID-0070 |
Amiodarone-d10 Hydrochloride
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Amiodarone-d10 Hydrochloride 是 Amiodarone Hydrochloride 的氘代化合物。Amiodarone Hydrochloride 的 CAS 号为 19774-82-4。Amiodarone hydrochloride是一种抗心绞痛和 III 类抗心律失常药物,通过抑制钾通道和电压门控钠通道来增加心室和心房肌肉作用的持续时间,可导致心率和血管阻力降低。它通过成纤维细胞中的ERK1/2和p38 MAPK信号传导诱导细胞增殖和肌成纤维细胞分化,可研究室上性和室性心律失常。 | |||
TMID-0069 |
Amiodarone-d4 HCl
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Amiodarone-d4 HCl 是 Amiodarone HCl 的氘代化合物。Amiodarone HCl 的 CAS 号为 19774-82-4。Amiodarone hydrochloride是一种抗心绞痛和 III 类抗心律失常药物,通过抑制钾通道和电压门控钠通道来增加心室和心房肌肉作用的持续时间,可导致心率和血管阻力降低。它通过成纤维细胞中的ERK1/2和p38 MAPK信号传导诱导细胞增殖和肌成纤维细胞分化,可研究室上性和室性心律失常。 | |||
T71212 |
Lornoxicam-d4
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Lornoxicam-d4 is intended for use as an internal standard for the quantification of lornoxicam by GC- or LC-MS. Lornoxicam is a COX inhibitor and non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory and analgesic properties. It inhibits production of thromboxane B2 from arachidonic acid in HEL human erythroleukemic cells, which endogenously express COX-1, as well as inhibits LPS-induced formation of prostaglandin F1α from arachidonic acid in Mono-Mac-6 cells, which endogenously e... | |||
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