618
158
23
76
52
Cat. No. | Product Name | ||
---|---|---|---|
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; | |||
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; | |||
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; | |||
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; | |||
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; | |||
L1120 | AMPK靶向分子库 | 80 compounds | |
80 个靶向AMPK 的分子集合,可用于高通量和高内涵筛选; | |||
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; | |||
L3300 | 组胺&褪黑色素化合物库 | 153 compounds | |
153 种生物活性小分子化合物,用于高通量、高内涵筛选; | |||
L7400 | 钠通道分子库 | 118 compounds | |
118 种钠通道相关化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L6120 | 黄酮类天然产物库 | 514 compounds | |
514 种黄酮类天然产物的独特集合,可用于高通量筛选和高内涵筛选; | |||
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; | |||
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; | |||
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; | |||
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; | |||
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; | |||
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; | |||
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; | |||
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; | |||
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; | |||
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; | |||
L6750 | 活血化瘀中药单体库 | 580 compounds | |
580种来源于常见活血化瘀中药的单体化合物,是药物开发、药理研究等领域的有效工具。 | |||
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 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T20766 |
Sulfisoxazole acetyl
Gantrisin,Acetylsulfisoxazole,Gantrisin Pediatric,Lipo Gantrisin,乙酰磺胺异噁唑 |
Antibacterial | Microbiology/Virology |
Sulfisoxazole acetyl (Gantrisin) 是 Sulfisoxazole 的一种衍生物,是口服有效的二氢蝶酸合酶抑制剂。Sulfisoxazole acetyl 显示出抗菌作用。 | |||
T7894 |
Tazarotenic acid
6-[2-(3,4-二氢-4,4-二甲基-2H-1-苯并噻喃-6-基)乙炔基]-3-吡啶甲酸,AGN-190299 |
Others | Others |
Tazarotenic acid (AGN-190299) 是 Tazarotene 的代谢物。它与视黄酸受体 (RAR) 的结合位点是类视黄醇作用的可能的分子靶点。它对疣状角化不良具有潜在的研究价值。 | |||
T1320 |
Disopyramide
Triombrin,Hypaque sodium,amidotrizoate sodium,达舒平 |
Potassium Channel; Sodium Channel; AChR | Membrane transporter/Ion channel; Neuroscience |
Disopyramide (Triombrin) 是用于研究房性和室性心律失常的 IA 类抗心律失常试剂。它阻断心肌快速内向钠电流,延长心肌动作电位持续时间。它抑制 HERG 编码的钾通道。它也表现出复杂的蛋白质结合,并具有强大的负性肌力作用。 | |||
T1676 |
Rosuvastatin
罗伐他汀,ZD 4522,瑞舒伐他汀 |
Potassium Channel; HMG-CoA Reductase; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Rosuvastatin (ZD 4522) 是一种抗血脂药,可竞争性抑制羟甲基戊二酰辅酶 A 还原酶,用于降低血浆胆固醇水平和预防心血管疾病。它降低低密度脂蛋白胆固醇、甘油三酯和 C-反应蛋白水平。它阻断人类醚-a-go-go 相关基因电流,IC50为 195 nM,延迟心脏复极化,延长动作电位持续时间和校正 QT 间期间隔。 | |||
T1510 |
Rosuvastatin calcium
ZD 4522 Calcium,ZD4522,Rosuvastatin hemicalcium,瑞舒伐他汀钙 |
Potassium Channel; HMG-CoA Reductase; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Rosuvastatin calcium (ZD4522) 是肝羟甲基戊二酰辅酶 A 还原酶的选择性和竞争性抑制剂,具有抗血脂活性。它降低成熟 hERG 的表达以及热休克蛋白 70 与 hERG 蛋白的相互作用,还降低低密度脂蛋白胆固醇、甘油三酯和 C-反应蛋白水平。它阻断人类醚-a-go-go 相关基因电流,延迟心脏复极化,来延长动作电位持续时间和校正 QT 间期间隔。 | |||
T9044 |
SORT-PGRN interaction inhibitor 1
|
Neurotensin Receptor | GPCR/G Protein |
SORT-PGRN interaction inhibitor 1 是一种 sortilin-progranulin 相互作用抑制剂,IC50为 2 μM。 | |||
T3189 |
B7/CD28 interaction inhibitor 1
CTLA-4 inhibitor |
Others | Others |
B7/CD28 interaction inhibitor 1 (CTLA-4 inhibitor) 是B7.1-CD28相互作用抑制剂(IC50:50 nM)。 | |||
T50083 |
Cell-cell interaction 1
|
Others | Others |
12-oxo-N-[1-(propan-2-yl)piperidin-4-yl]-6H,7H,8H,9H,10H,12H-azepino[2,1-b]quinazoline-3-carboxamide 可用作分子结构单元,用于多种化合物的合成。 | |||
T79106 |
SORT-PGRN interaction inhibitor 3
|
Neurotensin Receptor | GPCR/G Protein |
SORT-PGRN interaction inhibitor 3(Compound 13),一种IC50为0.17 μM的SORT-PGRN相互作用抑制剂,适用于神经退行性疾病研究。 | |||
T82245 |
HA-CD44 interaction inhibitor 1
|
Others | Others |
Antitumor agent-109(compound 6)是一款针对CD44的透明质酸抑制剂,具有抗肿瘤作用。它能够抑制MDA-MB-231细胞,EC50值仅为0.59 μM,显示出通过阻断透明质酸与CD44的相互作用,从而干预肿瘤的生长与侵袭的潜力。 | |||
T82902 |
Beclin1-Bcl-2 interaction inhibitor 1
|
Others | Others |
Beclin1-Bcl-2 interaction inhibitor 1,有效地抑制Beclin 1/Bcl-2的结合作用,适用于癌症和神经退行性疾病的研究领域。 | |||
T81126 |
SORT-PGRN interaction inhibitor 2
|
Others | Others |
SORT-PGRN interaction inhibitor 2为一种SORT-PGRN抑制剂,能降低哺乳动物细胞中SORT1蛋白水平并提升PGRN在细胞外的分泌,适于神经系统疾病研究之用。 | |||
T12350 |
p53 and MDM2 proteins-interaction-inhibitor dihydrochloride
|
Others | Others |
p53 and MDM2 proteins-interaction-inhibitor dihydrochloride is a interaction inhibitor between p53 and MDM2 proteins. | |||
T12351 |
p53 and MDM2 proteins-interaction-inhibitor (racemic)
p53-and-mdm2-proteins-interaction-inhibitor-racemic |
Others | Others |
p53 and MDM2 proteins-interaction-inhibitor (racemic) is an inhibitor of the interaction between p53 and MDM2 proteins. | |||
T28219 |
NusB-NusE interaction inhibitor-1
|
Others | Others |
NusB-NusE interaction inhibitor-1 is a modulator of the NusB-NusE interaction. | |||
T79756 |
Beclin1-ATG14L interaction inhibitor 1
|
Autophagy | Autophagy |
Beclin1-ATG14L interaction inhibitor 1 (com 19) 作为一种选择性抑制剂,特定抑制脂质激酶VPS34的复合物 I 中Beclin1与ATG14L的相互作用,而对Beclin 1-UVRAG作用重要的VPS34复合物 II 无影响。由此,其阻断VPS34复合物 I 形成,抑制自噬过程,但不干扰复合物 II 介导的囊泡运输。 | |||
T82244 |
HA-CD44 interaction inhibitor 2
|
Others | Others |
Antitumor agent-108作为一种Hyaluronic acid (HA)-CD44相互作用抑制剂,能够破坏癌症球体的完整性并显示出抗增殖活性。 | |||
T80381 |
SAAP Fraction 3
|
||
SAAP Fraction 3为具杀菌效能之抗菌肽,能在含锌盐的缓冲液中有效抑杀P. haemolytica。 | |||
T34905 |
Totrombopag
SB559448,SB 559448,SB-559448,LGD-4665,Synonym 2,LGD 4665,LGD4665 |
Others | Others |
Totrombopag (SB559448) 是对RSV 聚合酶有作用的候选化合物。 | |||
T5520L |
Cetrorelix diacetate
NS-75A,醋酸西曲瑞克,SB-075 acetate,SB-075 diacetate,Cetrorelix acetate,NS-75A diacetate |
GNRH Receptor | GPCR/G Protein |
Cetrorelix diacetate (NS-75A) 是GnRH 受体的强效拮抗剂(IC50:1.21 nM)。 | |||
T2599 |
Pirenperone
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Pirenperone 是5-HT2血清素受体拮抗剂,具有一定抗焦虑作用。 | |||
T24472 |
MIV-6R
MIV6R,VU05163101,VU0516310-1,VU0516310 1,MIV 6R |
Others | Others |
MIV-6R is an inhibitor of the menin- MLL interaction that acts by demonstrating strong and selective effects in MLL leukemia cells and validating specific mechanisms of action. | |||
T0990 |
Droperidol
氟派利多,NSC 169874,Dehydrobenzperidol,氟哌啶 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Droperidol (Dehydrobenzperidol) 是丁酰苯类多巴胺-2受体拮抗剂。 | |||
T2320 |
Indacaterol
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Indacaterol 是一种超长效β-肾上腺素受体激动剂。 | |||
T2552 |
Succimer
DMSA,Dimercaptosuccinic acid,二巯基丁二酸,meso-2,3-dimercaptosuccinic acid,内消旋-2,3-二巯基丁二酸 |
Others | Others |
Succimer (Dimercaptosuccinic acid) 是一种螯合剂,广泛用于铅中毒的研究。 | |||
T25832 |
Moveltipril
Moveltipril calcium,MC-838,Altiopril calcium |
RAAS | Endocrinology/Hormones |
Moveltipril (Moveltipril calcium) 是一种强效血管紧张素转换酶(ACE)抑制剂。 | |||
T1565 |
Deferiprone
去铁酮,Deferidone,CP20 |
Others; HCV Protease; Ferroptosis; UGT | Apoptosis; Metabolism; Microbiology/Virology; Others; Proteases/Proteasome |
Deferiprone (Deferidone) 是口服活性铁螯合剂,可研究地中海贫血中的输血性铁过载。 | |||
T24451 |
Mepyramine
NSC-13136,NSC13136,NSC 13136 |
Others | Others |
Mepyramine is a histamine H1 antagonist. It has mild hypnotic properties and some local anesthetic action and is used for allergies both parenterally and locally. | |||
T11007L |
Levofloxacin Hydrochloride Impurity A
Levofloxacin Hydrochloride Impurity A(117707-40-1 Free base),左氧氟沙星杂质A(盐酸盐) |
Antibacterial | Microbiology/Virology |
Levofloxacin Hydrochloride Impurity A 是一种喹诺酮类药物,具有广谱抗菌作用。 | |||
T9420 |
prifinium bromide
|
Others | Others |
Prifinium bromide 是抗胆碱能试剂,能够改善痉挛,具有止吐效果。 | |||
T1615 |
Irbesartan
厄贝沙坦,SR-47436,BMS-186295 |
Apoptosis; RAAS | Apoptosis; Endocrinology/Hormones |
Irbesartan (SR-47436) 是一种 1 型血管紧张素 II 受体拮抗剂,IC50为1.3 nM。 | |||
T16280 |
Nedocromil
FPL 59002,尼多克罗 |
Leukotriene Receptor; Prostaglandin Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Nedocromil (FPL 59002) 对多种介质的作用或形成有抑制作用,包括组胺,前列腺素 D2和白三烯 C4。 | |||
T79365 |
TIM-3-IN-2
|
Immunology/Inflammation related | Immunology/Inflammation |
TIM-3-IN-2 是 Tim3 抑制剂,可以抑制TIM-3与PtdSer、CEACAM1和Gal-9的结合,抑制TIM-3发挥作用。TIM-3-IN-2能够逆转TIM-3介导的促炎细胞因子的作用。 | |||
T0142 |
Brinzolamide
布林佐胺,AL-4862 |
Carbonic Anhydrase | Metabolism |
Brinzolamide (AL-4862) 是一种碳酸酐酶(carbonic anhydrase)II 抑制剂(IC50:3.19 nM)。 | |||
T2411 |
Luliconazole
NND 502,卢立康唑 |
Antibiotic; Antifungal | Microbiology/Virology |
Luliconazole (NND 502) 是一种咪唑类抗生素,具有广谱抗真菌活性。它可研究皮肤感染。 | |||
T60325 |
Viloxazine
Emovit,Viloxazin |
5-HT Receptor; Norepinephrine | GPCR/G Protein; Neuroscience |
Viloxazine (Viloxazin) (Viloxazin) is a dual-action compound that functions as a norepinephrine reuptake inhibitor and exhibits potent agonistic activity towards 5-HT 2C receptors while acting as an antagonist for 5-HT 2B receptors, with respective potency values of EC 50 = 32 μM and IC 50 = 27 μM. Its primary mechanism of action involves the modulation of serotonergic and noradrenergic pathways. Viloxazine is commonly employed in depression research [1] [2]. | |||
T0015 |
Mephenesin
Cresoxydiol,甲酚甘油醚,Memphenesin,Mephedan,Decontractyl |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Mephenesin (Cresoxydiol) 是 NMDA 受体拮抗剂,也是中枢性肌松弛剂。 | |||
T0462 |
Cilostazol
西洛他唑,OPC 21,OPC 13013 |
PDE; Autophagy | Autophagy; Metabolism |
Cilostazol (OPC 21) 是一种选择性的心血管系统中磷酸二酯酶 3 亚型PDE 3A 的抑制剂,IC50值为 0.2 μM。 | |||
T1269 |
Tripelennamine hydrochloride
Pyribenzamine hydrochloride,去敏灵,Tripelennamine HCl,Pyribenzamine HCl,盐酸曲吡那敏 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Tripelennamine hydrochloride (Pyribenzamine hydrochloride) 是一种组胺 H1 拮抗剂,具有低镇静作用,但经常刺激胃肠道。 | |||
T8468 |
CIL62
|
Caspase | Apoptosis; Proteases/Proteasome |
CIL62 是一种不依赖 caspase-3/7 的细胞死亡诱导剂。CIL62的作用机制是 Necrostatin-1 依赖性细胞死亡。 | |||
T2189 |
Sodium orthovanadate
Sodium vanadate,钒酸钠,Trisodium vanadate,Sodium pervanadate |
ATPase; Phosphatase | Membrane transporter/Ion channel; Metabolism |
Sodium orthovanadate 是一种蛋白酪氨酸磷酸酶,碱性磷酸酶和一些ATP 酶的抑制剂,有可能充当磷酸盐类似物。它具有胰岛素样作用、对心室肌的正性肌力作用和其他代谢作用。 | |||
T0692 |
Allopurinol
Zyloric,别嘌醇,Zyloprim,Lopurin,别嘌呤醇 |
ROS; Xanthine Oxidase | Immunology/Inflammation; Metabolism |
Allopurinol (Zyloric) 是一种黄嘌呤氧化酶(XO)抑制剂,IC50=7.82±0.12 μM。 | |||
TP1181 |
Bradykinin (2-9)
Des-Arg1-bradykinin |
Bradykinin Receptor | GPCR/G Protein |
Bradykinin (2-9) (Des-Arg1-bradykinin),是Bradykinin的一种氨基端截短肽类代谢物,通过Aminopeptidase P的切割作用形成。 | |||
T0002 |
Ethamsylate
Cyclonamine,Etamsylate,酚磺乙胺,Dicynene,Aglumin |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Ethamsylate (Dicynene) 通常用作止血药,增加毛细血管内皮阻力和血小板粘附,抑制前列腺素的生物合成和作用。 | |||
T0867 |
Bufexamac
Bufexamic acid,丁苯羟酸 |
COX; HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; Neuroscience |
Bufexamac (Bufexamic acid) 是 HDAC6 和 HDAC10 的抑制剂,也是一种COX 抑制剂,用于释放 IFN-α,具有抗炎、镇痛和解热作用。 | |||
T1570 |
Telmisartan
BIBR 277,替米沙坦 |
RAAS; Autophagy | Autophagy; Endocrinology/Hormones |
Telmisartan (BIBR 277) 是一种血管紧张素II 1型受体拮抗剂,能够抑制其活性,IC50值为 9.2 nM。 | |||
TP1785L |
Peptide T acetate(106362-32-7 free base)
|
Others; HIV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
Peptide T acetate(106362-32-7 free base) 是一种来自 HIV-1 gp120 V2 区域的八肽。它是一种合成八肽,其可能的作用机制是 gp120 对 CD4 受体的竞争性抑制以及与血管肠肽受体的结合和抑制细胞因子作用。 | |||
T7887 |
8-Hydroxyquinoline hemisulfate
8-羟基喹啉硫酸盐,Oxyquinoline sulfate |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
8-Hydroxyquinoline hemisulfate (Oxyquinoline sulfate) 是一种单质子双齿螯合剂,具有温和的抑菌、驱虫和杀螨作用。 | |||
T1096 |
Milrinone
Win 47203,米力农 |
PDE | Metabolism |
Milrinone (Win 47203) 是一种 PDE3抑制剂,也是一种强心药、血管舒张药。 | |||
T28829 |
Soquinolol
Soquinolol mucate |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Soquinolol (Soquinolol mucate) 是一种β肾上腺素能受体拮抗剂,具有较弱的局部麻醉活性。Soquinolol 具有良好的肠内疗效和较长的作用持续时间。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3S0081 |
Oxypeucedanin
(+-)-Oxypeucedanin,氧化前胡素,Oxypeucadanin |
Potassium Channel | Membrane transporter/Ion channel |
Oxypeucedanin ((+-)-Oxypeucedanin) 是呋喃香豆素衍生物,分离自Angelica dahurica。它是选择性开放通道阻滞剂,可抑制hKv1.5通道电流,IC50值为 76 nM。它延长心脏动作电位持续时间,是潜在的抗心律失常试剂。它通过抑制癌细胞迁移来诱导细胞凋亡。 | |||
T8118 |
Bekanamycin
Kanamycin B,卡那霉素,卡那霉素 B |
Antibacterial; Antibiotic | Microbiology/Virology |
Bekanamycin (Kanamycin B) 是一种提取自 Streptomyces kanamyceticus 的氨基糖苷类抗生素,抑制一系列革兰氏阳性和阴性细菌。 | |||
T3158 |
Harmane
Loturine,Harman,Aribine,哈尔满碱 |
Adrenergic Receptor; Monoamine Oxidase; Imidazoline Receptor | GPCR/G Protein; Neuroscience |
Harmane (Loturine) 是一种在咖啡和烟草烟雾中发现的 β-咔啉生物碱,是有效的神经毒素,可引起严重的动作震颤和精神病学表现。它还是选择性的单胺氧化酶抑制剂,具有致突变作用,对 MAO A/B 的 IC50值分别为 0.5 和 5 μM。 | |||
T3S1858 |
Lutein
Vegetable Lutein,叶黄素,Xanthophyll,Bo-Xan,Xantofyl |
Antibacterial | Microbiology/Virology |
Lutein (Xantofyl) 具有抗肿瘤作用。它具有抗诱变作用。 它具有广泛的抗菌作用。 它可能对治疗黄斑变性有用。 | |||
T5691 |
paulownin
泡桐素 |
Anti-infection | Microbiology/Virology |
Paulownin 是药用植物的成分,是泡桐木的成分。 | |||
T19603 |
Vitamin K
Kephton,维生素K,Vitamin K1(20) |
Endogenous Metabolite | Metabolism |
Vitamin K (Kephton) 具有凝血作用,对凝血因子、基质-Gla 蛋白和骨钙素很重要。 | |||
T1262 |
Tazobactam
Tazobactamum,Tazobactam acid,他唑巴坦酸,YTR-830H,CL-298741,他唑巴坦 |
Antibacterial; Antibiotic | Microbiology/Virology |
Tazobactam (YTR-830H) acid 是一种具有抗菌活性的β-内酰胺酶抑制剂。 | |||
T7521 |
Azaphen
Pipofezin hydrochloride,阿扎吩,Pipofezine hydrochloride,Azafen |
5-HT Receptor; Serotonin Transporter | GPCR/G Protein; Neuroscience |
Azaphen (Pipofezin hydrochloride) 是一种 5-羟色胺重吸收抑制剂。 | |||
T5S2204 |
Sibiricose A6
西伯利亚远志糖A6 |
Antioxidant | oxidation-reduction |
Sibiricose A6 是一种寡糖酯,分离自Polygalae Radix,具有抗氧化作用。 | |||
T6S1579 |
Monotropein
水晶兰苷,Monotropeine |
Others | Others |
Monotropein (Monotropeine) 是从Morinda officinalis 中获得,能够抑制硫酸葡聚糖硫酸钠诱导的结肠炎小鼠模型中炎性因子的表达。 | |||
T4755 |
2,3-Diaminopropanoic acid hydrochloride
DL-2,3-Diaminopropionic acid monohydroch,3-Amino-DL-alanine monohydrochloride,DL-2,3-二胺基丙酸盐酸盐 |
Others; Endogenous Metabolite | Metabolism; Others |
2,3-Diaminopropanoic acid hydrochloride (3-Amino-DL-alanine monohydrochloride) 是内源性代谢产物的一种。 | |||
T3741 |
(-)-borneol
L-Borneol,冰片 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
(-)-borneol (L-Borneol) 对 GABA 受体具有高效的正向调节作用,EC50 为 237 μM。 | |||
T4711 |
2,4-Dihydroxypyrimidine-5-carboxylic acid
脲嘧啶-5-羧酸,Isoorotic acid,Uracil-5-carboxylic acid |
Others; Endogenous Metabolite | Metabolism; Others |
2,4-Dihydroxypyrimidine-5-carboxylic acid (Isoorotic acid) 是内源性代谢产物的一种。 | |||
T4514 |
N-Acetyl-D-Glucosamine
N-乙酰-D-氨基葡萄糖,NAG,N-Acetyl-2-amino-2-deoxyglucose,Marine Sweet,N-Acetyl-2-amino-2-deoxy-D-glucose,N-乙酰氨基葡萄糖,GlcNAc |
Endogenous Metabolite | Metabolism |
N-Acetyl-D-Glucosamine (NAG) 是葡萄糖的单糖衍生物。 | |||
T6723 |
Voglibose
AO 128,伏格列波糖,Glustat,Basen |
Glucosidase | Metabolism |
Voglibose (Glustat) 是一种 valiolamine 的衍生物,可抑制α-葡萄糖苷酶活性,可作用于高血糖症等。 | |||
T5228 |
Nicotinuric acid
|
Others; Endogenous Metabolite | Metabolism; Others |
Nicotinuric acid 是一种酰基甘氨酸,通常是脂肪酸的次要代谢物。 酰基甘氨酸是通过甘氨酸 N-酰基转移酶的作用产生的。 | |||
T0759 |
Monobenzone
4-苄氧基苯酚,Benoquin |
Tyrosinase | Proteases/Proteasome |
Monobenzone (Benoquin) 是皮肤脱色剂。它可引起色素脱失和活跃的人白癜风,对白癜风具有潜在的研究价值。 | |||
T8294 |
Quercetagitrin
万寿菊苷,槲皮万寿菊素-7-O-Β-吡喃葡萄糖苷,Quercetagetin-7-O-glucoside |
Others | Others |
Quercetagitrin 是分离自非洲万寿菊花 (Tagetes erecta) 中,具有抗炎作用。 | |||
T1556 |
Ornidazole
Tiberal,Ornidazolum,NSC 95075,Ro 7-0207,奥硝唑 |
Antibacterial; Antibiotic; Parasite | Microbiology/Virology |
Ornidazole (Tiberal) 是一种5-硝基咪唑衍生物,能抗原生动物和厌氧菌。 | |||
T1080 |
2-Aminoethanethiol
2-Mercaptoethylamine,巯基乙胺,β-Mercaptoethylamine,β-MEA,Cysteamine |
Apoptosis; Others; Reactive Oxygen Species; Cysteine Protease; Somatostatin; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; GPCR/G Protein; Immunology/Inflammation; Metabolism; NF-κB; Others; Proteases/Proteasome |
2-Aminoethanethiol (Cysteamine) 是一种胱氨酸消耗剂。半胱胺的作用机制是胱氨酸二硫化物还原。 | |||
T1165 |
Ethionamide
Bayer 5312,乙硫异烟胺,2-ethylthioisonicotinamide,Ethinamide |
Dehydrogenase; CAT; Antibacterial; Antibiotic | Metabolism; Microbiology/Virology; oxidation-reduction |
Ethionamide (2-ethylthioisonicotinamide) 是一种抗结核抗生素。 | |||
T1431 |
Khellin
凯林,Amicardine,Methafrone,Visammin |
EGFR; Others | Angiogenesis; JAK/STAT signaling; Others; Tyrosine Kinase/Adaptors |
Khellin (Methafrone) 是从阿米芹中提取得到的一种呋喃并色酮,是EGFR 抑制剂,IC50为 0.15 µM。它体外具有抗增殖活性,还具有抗痉挛和冠状动脉舒张作用。 | |||
T4901 |
5'-Guanylic acid disodium salt
Guanosine 5'-monophosphate disodium salt,5'-鸟苷酸二钠,鸟苷钠5'-单磷酸,GMP-5 |
Others; Endogenous Metabolite | Metabolism; Others |
5'-Guanylic acid disodium salt (GMP-5) 由鸟嘌呤,核糖和磷酸组成,是信使 RNA 中的一种核苷酸单体。 鸟苷衍生物参与细胞内信号转导,并已鉴定存在于端粒,核糖体 DNA,免疫球蛋白重链转换区和原癌基因的控制区中的重复基因组序列中。 | |||
T3743 |
4-hydroxyphenylacetic acid
p-Hydroxyphenylacetic acid,4-羟基苯乙酸,对羟基苯乙酸,parahydroxy phenylacetate |
Antioxidant; Nrf2; Endogenous Metabolite | Immunology/Inflammation; Metabolism; oxidation-reduction |
4-hydroxyphenylacetic acid (parahydroxy phenylacetate) 是主要的微生物群衍生的多酚代谢物,能够诱导Nrf2表达,具有抗氧化作用。 | |||
T0739 |
Guaifenesin
Glycerol guaiacolate,Guaiacol glyceryl ether,愈创甘油醚,Guaiphenesin |
Others | Others |
Guaifenesin (Guaiphenesin) 是一种祛痰剂,来自于 Guajacum officinale Linné 木材中。它可以增加痰液体积和降低其粘度,缓解咳嗽不适,促进有效的咳嗽。 | |||
TWS1293 |
Angelic anhydride
2-Methylisocrotonic Anhydride,当归酸酐,(Z)-2-Methylbut-2-enoic anhydride |
Others | Others |
Angelic anhydride ((Z)-2-Methylbut-2-enoic anhydride) 是一种脂肪酸酐,来自于不饱和碳氢酸酐。 | |||
TN2247 |
Swertisin
|
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Swertisin 是从日本紫菜中分离出的 C-葡萄糖基黄酮,是腺苷 A1 受体拮抗剂,具有抗糖尿病、抗炎和抗氧化作用。 | |||
T41031 |
Protamine sulfate
|
Thrombin | Proteases/Proteasome |
Protamine sulfate是一种多阳离子肽类,作为一种抗肝素剂。该化合物能中和肝素的抗凝作用并增强脂质介导的基因转移。 | |||
TN1238 |
3,4-O-Isopropylidene-shikimic acid
3,4-O-异亚丙基莽草酸,3,4-O-Isopropylidene shikimic acid |
NOS; NO Synthase | Immunology/Inflammation |
3,4-O-Isopropylidene-shikimic acid (3,4-O-Isopropylidene shikimic acid) 是一种从Hypericum wightianum 中提取得到的天然产物。它具有抗炎症和抗氧化作用。 | |||
T5270 |
5-Methylcytosine
|
Others; DNA/RNA Synthesis; Endogenous Metabolite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Others |
5-Methylcytosine 是一种存在于真核 DNA 中的甲基化核苷酸碱基。它是由 DNA 甲基转移酶作用形成的表观遗传修饰。 | |||
T1590 |
Letrozole
CGS 20267,来曲唑 |
Aromatase; Autophagy | Autophagy; Endocrinology/Hormones |
Letrozole (CGS 20267) 是一种可口服的,选择性可逆的非甾体类芳香化酶抑制剂,IC50值为 11.5 nM。它选择性抑制雌激素的生物合成,可研究乳腺癌。 | |||
T40615 |
N,N'-Dimethylthiourea
N,N-二甲基硫脲,DMTU |
Antioxidant | oxidation-reduction |
N,N'-Dimethylthiourea (DMTU) 是一种分离自黑蒜的化合物。N,N'-Dimethylthiourea 具有口服活性的羟基自由基 (•OH) 的清除剂,通过活化的中性粒细胞在体外阻止 •OH 的产生。N,N'-Dimethylthiourea 通过发挥 •OH 清除和抗炎作用,防止水浸限制应激诱导的大鼠胃粘膜损伤。 | |||
T0122 |
Bergenin
Cuscutin,Bengenin,岩白菜素 |
Apoptosis; IL Receptor; Virus Protease; TNF; NF-κB; Antibacterial; NOD; Autophagy; Antifungal | Apoptosis; Autophagy; Immunology/Inflammation; Microbiology/Virology; NF-κB |
Bergenin (Bengenin) 是一种在许多药用植物中发现的多酚,有细胞保护和抗氧化作用。它还具有广泛的保肝、抗炎、抗肿瘤、抗病毒、抗真菌以及免疫调节作用。 | |||
T3892 |
Isoacteoside
异麦角甾苷,Isoverbascoside |
NF-κB | NF-κB |
Isoacteoside 具有抗炎作用,通过作用于 caspase-1、丝裂原活化蛋白激酶(c-Jun N-末端激酶、p38、细胞外信号调节蛋白激酶)和核因子-kappa B 途径介导。 | |||
T5707 |
3-O-Methylgalangin
3-Methylgalangin,GALANGIN-3-METHYLETHER,高良姜素 3-O-甲醚,高良姜素-3-甲醚 |
Antibacterial | Microbiology/Virology |
3-O-Methylgalangin (GALANGIN-3-METHYLETHER) 是一种来源于高良姜根茎的天然黄酮,具有抗菌活性,抑制胰腺脂肪酶。 | |||
T6S1371 |
Isovitexin
Homovitexin,Saponaretin,Apigenin-6-C-Glucoside,异牡荆黄素 |
NF-κB; JNK; Glucosidase | MAPK; Metabolism; NF-κB |
Isovitexin (Apigenin-6-C-Glucoside) 是从亚洲水稻种得到的一种黄酮,具有抗氧化和抗炎活性。它的作用与JNK1/2的抑制剂类似,抑制NF-κB 的活化。 | |||
TN1006 |
Tirucallol
|
NOS; NO Synthase; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Tirucallol 是一种四环三萜,分离自Euphorbia lacteal 乳胶。它能够抑制小鼠模型中的耳部水肿,并阻碍脂多糖刺激的巨噬细胞中亚硝酸盐的产生,具有局部消炎作用。 | |||
TN1691 |
Glabrol
光甘草酚,光甘草醇 |
P450; NF-κB; NO Synthase; Acyltransferase | Immunology/Inflammation; Metabolism; NF-κB |
Glabrol 是分离自甘草根的乙醇提取物中的一种异戊二烯类黄酮,是一种有效且非竞争性的酰基辅酶 A:胆固醇酰基转移酶(ACAT)抑制剂,抑制大鼠肝脏微粒体 ACAT 的IC50为 24.6 μM。 | |||
T2S0271 |
Voacamine
老刺木胺,Voacanginine |
Cannabinoid Receptor; P-gp | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Voacamine (Voacanginine) 是非洲马铃果中的一种吲哚生物碱,可抑制多药耐药肿瘤细胞中的 P-糖蛋白作用,具有强效的大麻素 CB1受体拮抗活性。 | |||
T5379 |
(Rac)-Antineoplaston A10
3-苯基乙酰氨基-2,6-哌啶二酮,Antineoplaston A10 |
Apoptosis; Ras | Apoptosis; GPCR/G Protein; MAPK |
(Rac)-Antineoplaston A10 (Antineoplaston A10) 是 Antineoplaston A10 的消旋体,是一种有抗肿瘤活性的天然产物。Antineoplaston A10 是一种Ras 抑制剂,可研究胶质瘤、淋巴瘤、星形细胞瘤和乳腺癌。 | |||
T8195 |
Lotusine
|
Others | Others |
Lotusine 是一种提取自Nelumbo nucifera Gaertn 的绿色种胚中的纯生物碱。它能够作用于心肌中动作电位及心脏浦肯野纤维缓慢内向电流。 | |||
T4S1876 |
3-Deoxyaconitine
|
Sodium Channel | Membrane transporter/Ion channel |
3-Deoxyaconitine 是一种二萜类生物碱,对钠离子通道有激活作用。 | |||
TN3831 |
(-)-Denudatin B
Denudatin B |
ATPase; Potassium Channel; Calcium Channel; PAFR | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism |
(-)-Denudatin B (Denudatin B) 源自 Magnolia fargesii。 (-)-Denudatin B 通过抑制胶原蛋白和凝血酶诱导的磷酸肌醇分解,在高浓度下具有非特异性抗血小板作用。 | |||
T0744 |
10-Undecenoic acid zinc salt
Zinc diundec-10-enoate,Zinc 10-undecenoate,Zinc undecylenate,十一烯酸锌 |
Antibiotic; Antifungal | Microbiology/Virology |
10-Undecenoic acid zinc salt (Zinc undecylenate) 是一种天然的或合成的抗真菌脂肪酸, 在乳膏中可局部用于治疗湿疹、真菌感染、癣和其他皮肤病。 锌具有收敛作用。 | |||
TN1413 |
Atranorin
荔枝素,巴美灵,荔枝素 |
Endogenous Metabolite; NO Synthase; Ras | GPCR/G Protein; Immunology/Inflammation; MAPK; Metabolism |
Atranorin 是地衣的次生代谢产物,具有显着的抗伤害、抗炎和氧化还原活性,对 H(2)O(2) 诱导的氧化应激下的细胞具有细胞保护作用。 | |||
T2965 |
Deoxycholic acid
Cholorebic,去氧胆酸,脱氧胆酸,Deoxycholate,Desoxycholic acid,Cholanoic Acid,Cholerebic |
Endogenous Metabolite; GPCR19 | GPCR/G Protein; Metabolism |
Deoxycholic acid (Cholanoic Acid) 是 G 蛋白偶联胆汁酸受体 TGR5的激活剂。 | |||
T3369 |
Nuciferine
(-)-Nuciferine,VLT 049,荷叶碱,Sanjoinine E |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Nuciferine ((-)-Nuciferine) 是一种在埃及蓝睡莲和水芙蓉中发现的生物碱,是5-HT2A、5-HT2B 和5-HT2C 拮抗剂,IC50分别为 478 nM、1 μM 和 131 nM。它也是5-HT7的反向激动剂,IC50为 150 nM。 | |||
T5S1708 |
Dendrobine
|
Others; Influenza Virus | Microbiology/Virology; Others |
Dendrobine 是从石斛中分离的一种生物碱,对甲型流感病毒具有抗病毒活性。 | |||
T5737 |
euphol
|
Others; Lipase; Endogenous Metabolite | Metabolism; Others |
Euphol 是从Euphorbia tirucalli 的汁液中分离出来的四环三萜醇,具有抗炎和免疫调节作用,口服具有活力。 它通过能够逆机制抑制单酰基甘油脂肪酶 (MGL) 的特性,IC50=315 nM。 外周 MGL 抑制能够调节内源性大麻素系统从而阻止炎症性疼痛的发展。 | |||
T5254 |
Glycodeoxycholate Sodium
Sodium glycyldeoxycholate,Sodium glycodeoxycholate,Glycodeoxycholic acid sodium salt,脱氧甘胆酸钠 |
Others; Endogenous Metabolite | Metabolism; Others |
Glycodeoxycholate Sodium 诱导肝细胞凋亡的机制与内切酶的DNA裂解有关。它是一种次级胆汁酸,由结肠环境中微生物菌群中存在的酶的作用产生。 | |||
------------------------ 更多 ------------------------ |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-04644 |
PDGFB Protein, Human, Recombinant (His)
platelet-derived growth factor beta polypeptide,SSV,c-sis,SI... |
Human | P. pastoris (Yeast) |
Platelet-derived growth factor-B (PDGFB) is necessary for normal cardiovascular development. The administration of PDGFB alone normalized tumor vasculature by increasing periendothelial coverage and vascular functionality. Interestingly, this effect exerted by PDGFB was also observed in the presence of DAPT. So PDGFB is able to improve tumor vascularity and allows the anticancer action of DAPT in the tumor. PDGFB Protein, Human, Recombinant (His) is expressed in yeast with His tag. The predicted... | |||
TMPH-02823 |
Peptide YY/PYY Protein, Mouse, Recombinant (GST)
Peptide tyrosine tyrosine,Pyy,Peptide YY |
Mouse | E. coli |
This gut peptide inhibits exocrine pancreatic secretion, has a vasoconstrictory action and inhibitis jejunal and colonic mobility. | |||
TMPH-02911 |
STC2 Protein, Mouse, Recombinant
Stc2,Stanniocalcin-2 |
Mouse | E. coli |
Has an anti-hypocalcemic action on calcium and phosphate homeostasis. STC2 Protein, Mouse, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 30.1 kDa and the accession number is O88452. | |||
TMPH-01294 |
EDNRA Protein, Human, Recombinant (His)
ET-A,Endothelin-1 receptor,hET-AR,ETA-R,ETRA,EDNRA,ETA |
Human | P. pastoris (Yeast) |
Receptor for endothelin-1. Mediates its action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system. The rank order of binding affinities for ET-A is: ET1 > ET2 >> ET3. | |||
TMPH-01770 |
Neurotrypsin Protein, Human, Recombinant (His & SUMO)
PRSS12,Motopsin,Serine protease 12,Leydin,Neurotrypsin |
Human | E. coli |
Plays a role in neuronal plasticity and the proteolytic action may subserve structural reorganizations associated with learning and memory operations. Neurotrypsin Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 43.4 kDa and the accession number is P56730. | |||
TMPH-03338 |
CHRM1 Protein, Rat, Recombinant (His)
Muscarinic acetylcholine receptor M1,CHRM1 |
Rat | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM1 Protein, Rat, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 21.1 kDa and the accession number is P08482. | |||
TMPH-01852 |
Peptide YY/PYY Protein, Human, Recombinant (GST)
Peptide tyrosine tyrosine,PYY-I,PYY,Peptide YY |
Human | E. coli |
This gut peptide inhibits exocrine pancreatic secretion, has a vasoconstrictory action and inhibitis jejunal and colonic mobility. Peptide YY/PYY Protein, Human, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 31.1 kDa and the accession number is P10082. | |||
TMPH-00716 |
RzoR Protein, E. coli, Recombinant (Flag & His)
Prophage outer membrane lipoprotein RzoR,Spanin from lambdoi... |
E. coli | E. coli |
Component of the spanin complex that disrupts the outer membrane and causes cell lysis during virus exit. The spanin complex conducts the final step in cell lysis by disrupting the outer membrane after holin and endolysin action have permeabilized the inner membrane and degraded the host peptidoglycans. | |||
TMPH-01717 |
CHRM5 Protein, Human, Recombinant (His)
CHRM5,Muscarinic acetylcholine receptor M5 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM5 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 31.5 kDa and the accession number is P08912. | |||
TMPH-03607 |
HOE-467A Protein, Streptomyces tendae, Recombinant (His & Myc & SUMO)
Tendamistat,Alpha-amylase inhibitor HOE-467A |
Streptomyces tendae | E. coli |
Inhibits mammalian alpha-amylases specifically but has no action on plant and microbial alpha-amylases. Forms a tight stoichiometric 1:1 complex with alpha-amylase. HOE-467A Protein, Streptomyces tendae, Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10xHis-SUMO and C-Myc tag. The predicted molecular weight is 28.0 kDa and the accession number is P01092. | |||
TMPH-01716 |
CHRM3 Protein, Human, Recombinant (B2M & His)
Muscarinic acetylcholine receptor M3,CHRM3 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM3 Protein, Human, Recombinant (B2M & His) is expressed in E. coli expression system with N-6xHis-B2M tag. The predicted molecular weight is 40.7 kDa and the accession number is P20309. | |||
TMPH-01714 |
CHRM1 Protein, Human, Recombinant (His)
Muscarinic acetylcholine receptor M1,CHRM1 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 20.8 kDa and the accession number is P11229. | |||
TMPH-02119 |
SLC5A2 Protein, Human, Recombinant (His & Myc)
Solute carrier family 5 member 2,Low affinity sodium-glucose... |
Human | E. coli |
Sodium-dependent glucose transporter. Has a Na(+) to glucose coupling ratio of 1:1.; Efficient substrate transport in mammalian kidney is provided by the concerted action of a low affinity high capacity and a high affinity low capacity Na(+)/glucose cotransporter arranged in series along kidney proximal tubules. | |||
TMPH-03210 |
TFPI Protein, Rabbit, Recombinant (E. coli, His)
Lipoprotein-associated coagulation inhibitor,Extrinsic pathw... |
Rabbit | E. coli |
Inhibits factor X (X(a)) directly and, in a Xa-dependent way, inhibits VIIa/tissue factor activity, presumably by forming a quaternary Xa/LACI/VIIa/TF complex. It possesses an antithrombotic action and also the ability to associate with lipoproteins in plasma. TFPI Protein, Rabbit, Recombinant (E. coli, His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 35.8 kDa and the accession number is P19761. | |||
TMPJ-00191 |
FSTL1 Protein, Human, Recombinant
FRP,Follistatin-Related Protein 1,Follistatin-Like Protein 1... |
Human | E. coli |
Follistatin-Related Protein 1 (FSTL1) is a secreted protein that contains two EF-hand domains, one follistatin-like domain, one Kazal-like domain, and one VWFC domain. Its functional significance in physiological and pathological processes is not completely understood. However, FSTL1 is thought to modulate the action of some growth factors on cell proliferation and differentiation. FSTL1 maybe an autoantigen associated with rheumatoid arthritis. | |||
TMPH-01672 |
Human metapneumovirus (strain CAN97-83) Matrix protein (His & Myc)
M,Matrix protein,M protein |
HMPV | E. coli |
Plays a crucial role in virus assembly into filaments and budding. Early in infection, localizes in the nucleus where it may inhibit host cell transcription. Later in infection, traffics to the cytoplasm through the action of host CRM1 to associate with inclusion bodies, the site of viral transcription and replication. During virus assembly and budding, acts as a bridge between the nucleocapsid and the lipid bilayer. | |||
TMPK-00861 |
A2AR Protein-VLP, Human, Recombinant
RDC8,Adenosine A2a R,ADORA2,ADORA 2,ADORA2A,A2aR |
Human | HEK293 Cells |
Adenosine is a neuromodulator in the adult central nervous system. Membrane-bound receptors for adenosine have been identified and cDNAs for A1, A2a, A2b, and A3 adenosine receptor subtypes have been cloned recently.Expression of A2a adenosine receptor mRNA in cranial ganglia, carotid body, and intermediate lobe of the pituitary gland similarly suggests novel sites of adenosine action during development and in the adult. | |||
TMPH-01673 |
Human metapneumovirus (strain CAN97-83) Matrix protein (His)
M,Matrix protein,M protein |
HMPV | P. pastoris (Yeast) |
Plays a crucial role in virus assembly into filaments and budding. Early in infection, localizes in the nucleus where it may inhibit host cell transcription. Later in infection, traffics to the cytoplasm through the action of host CRM1 to associate with inclusion bodies, the site of viral transcription and replication. During virus assembly and budding, acts as a bridge between the nucleocapsid and the lipid bilayer. | |||
TMPH-02203 |
THRA Protein, Human, Recombinant (His)
c-erbA-1,c-erbA-alpha,THRA,Thyroid hormone receptor alpha,V-... |
Human | E. coli |
Nuclear hormone receptor that can act as a repressor or activator of transcription. High affinity receptor for thyroid hormones, including triiodothyronine and thyroxine.; Does not bind thyroid hormone and functions as a weak dominant negative inhibitor of thyroid hormone action. THRA Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 58.9 kDa and the accession number is P10827. | |||
TMPH-03260 |
Carboxypeptidase A1 Protein, Rat, Recombinant (His & Myc)
Cpa1,Carboxypeptidase A1,Cpa |
Rat | E. coli |
Carboxypeptidase that catalyzes the release of a C-terminal amino acid, but has little or no action with -Asp, -Glu, -Arg, -Lys or -Pro. Catalyzes the conversion of leukotriene C4 to leukotriene F4 via the hydrolysis of an amide bond. Carboxypeptidase A1 Protein, Rat, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 39.6 kDa and the accession number is P00731. | |||
TMPH-03211 |
TFPI Protein, Rabbit, Recombinant (His)
TFPI,Lipoprotein-associated coagulation inhibitor,Extrinsic ... |
Rabbit | HEK293 Cells |
Inhibits factor X (X(a)) directly and, in a Xa-dependent way, inhibits VIIa/tissue factor activity, presumably by forming a quaternary Xa/LACI/VIIa/TF complex. It possesses an antithrombotic action and also the ability to associate with lipoproteins in plasma. TFPI Protein, Rabbit, Recombinant (His) is expressed in HEK293 mammalian cells with N-10xHis tag. The predicted molecular weight is 35.4 kDa and the accession number is P19761. | |||
TMPY-02395 |
PDGFB Protein, Cynomolgus, Recombinant (mFc)
血小板源生长因子,platelet-derived growth factor beta polypeptide,pla... |
Cynomolgus | HEK293 Cells |
Platelet-derived growth factor-B (PDGFB) is necessary for normal cardiovascular development. The administration of PDGFB alone normalized tumor vasculature by increasing periendothelial coverage and vascular functionality. Interestingly, this effect exerted by PDGFB was also observed in the presence of DAPT. So PDGFB is able to improve tumor vascularity and allows the anticancer action of DAPT in the tumor. PDGFB Protein, Cynomolgus, Recombinant (mFc) is expressed in HEK293 mammalian cells with ... | |||
TMPH-00120 |
Ribonuclease clavin Protein, Aspergillus clavatus, Recombinant (His & Myc)
cla,Ribonuclease clavin |
Aspergillus clavatus | E. coli |
Clavin has the same substrate specificity as alpha-sarcin. It is specific for purines in both single- and double-stranded RNA. Its toxic action on eukaryotic cells is the result of cleavage of a single phosphodiester bond in the 60S subunit of ribosomes. Ribonuclease clavin Protein, Aspergillus clavatus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 24.5 kDa and the accession number is P0CL71. | |||
TMPH-00890 |
DBI Protein, Human, Recombinant (aa 2-104, His)
Acyl-CoA-binding protein,Diazepam-binding inhibitor,DBI,Endo... |
Human | E. coli |
Binds medium- and long-chain acyl-CoA esters with very high affinity and may function as an intracellular carrier of acyl-CoA esters. It is also able to displace diazepam from the benzodiazepine (BZD) recognition site located on the GABA type A receptor. It is therefore possible that this protein also acts as a neuropeptide to modulate the action of the GABA receptor. DBI Protein, Human, Recombinant (aa 2-104, His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecul... | |||
TMPY-05076 |
PDGFB Protein, Canine, Recombinant (His)
platelet-derived growth factor beta polypeptide,platelet-der... |
Canine | P. pastoris (Yeast) |
Platelet-derived growth factor-B (PDGFB) is necessary for normal cardiovascular development. The administration of PDGFB alone normalized tumor vasculature by increasing periendothelial coverage and vascular functionality. Interestingly, this effect exerted by PDGFB was also observed in the presence of DAPT. So PDGFB is able to improve tumor vascularity and allows the anticancer action of DAPT in the tumor. PDGFB Protein, Canine, Recombinant (His) is expressed in yeast with His tag. The predicte... | |||
TMPH-01715 |
CHRM2 Protein, Human, Recombinant (His)
CHRM2,Muscarinic acetylcholine receptor M2 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is adenylate cyclase inhibition. Signaling promotes phospholipase C activity, leading to the release of inositol trisphosphate (IP3); this then triggers calcium ion release into the cytosol. CHRM2 Protein, Human, Recombinant (His) is expressed in E. col... | |||
TMPH-00589 |
SpoT Protein, E. coli, Recombinant (His & Myc)
Bifunctional (p)ppGpp synthase/hydrolase SpoT,spoT |
E. coli | E. coli |
In eubacteria ppGpp (guanosine 3'-diphosphate 5'-diphosphate) is a mediator of the stringent response which coordinates a variety of cellular activities in response to changes in nutritional abundance. This enzyme catalyzes both the synthesis and degradation of ppGpp. The second messengers ppGpp and c-di-GMP together control biofilm formation in response to translational stress; ppGpp represses biofilm formation while c-di-GMP induces it. ppGpp activates transcription of CsrA-antagonistic small ... | |||
TMPY-03182 |
PLRP2 Protein, Human, Recombinant (His)
PLRP2,pancreatic lipase-related protein 2 |
Human | Baculovirus Insect Cells |
Galactolipase, also known as PNLIPRP2, is a lipase with broad substrate specificity. It can hydrolyze both phospholipids and galactolipids. Galactolipase acts preferentially on monoglycerides, phospholipids and galactolipids. It also hydrolyses milk fat with a lower catalytic efficiency. The expressed galactolipase shows a lipolytic activity that is, however, only marginally dependent on the presence of colipase. The lipolytic activity of pancreatic extracts and human pancreatic juice on Labraso... | |||
TMPY-00554 |
CHRNB3 Protein, Human, Recombinant (His)
cholinergic receptor, nicotinic, beta 3 (neuronal),cholinerg... |
Human | HEK293 Cells |
Cholinergic nicotinic receptor (CHRN) gene family has been known to mediate the highly additive effects of nicotine in the body, and implicated nicotine dependence (ND) and related phenotypes. Cigarette smoking is protective in Parkinson's disease (PD), possibly because of nicotine action on brain nicotinic-acetylcholine receptors. The beta3 nicotinic-acetylcholine receptor subunit (encoded by CHRNB3) is depleted in the striatum of PD patients and associated with nicotine dependence. CHRNB3 Prot... | |||
TMPK-01285 |
FSHB Protein, Cynomolgus, Recombinant (His)
Follitropin,FSH-B,FSH-beta,FSH-β,FSHB |
Cynomolgus | HEK293 Cells |
Fertility is dependent on follicle-stimulating hormone (FSH), a product of gonadotrope cells of the anterior pituitary gland. Hypothalamic gonadotropin-releasing hormone (GnRH) and intra-pituitary activins are regarded as the primary drivers of FSH synthesis and secretion. Both stimulate expression of the FSH beta subunit gene (Fshb), although the underlying mechanisms of GnRH action are poorly described relative to those of the activins. FSHB Protein, Cynomolgus, Recombinant (His) is expressed ... | |||
TMPH-03235 |
DBI Protein, Rat, Recombinant (His & Myc)
Endozepine (EP),ACBP,DBI,Acyl-CoA-binding protein,Diazepam-b... |
Rat | E. coli |
Binds medium- and long-chain acyl-CoA esters with very high affinity and may function as an intracellular carrier of acyl-CoA esters. It is also able to displace diazepam from the benzodiazepine (BZD) recognition site located on the GABA type A receptor. It is therefore possible that this protein also acts as a neuropeptide to modulate the action of the GABA receptor. DBI Protein, Rat, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted mo... | |||
TMPY-05077 |
PDGFB Protein, Rhesus, Recombinant (His)
platelet-derived growth factor β polypeptide,platelet-derive... |
Rhesus | P. pastoris (Yeast) |
Platelet-derived growth factor-B (PDGFB) is necessary for normal cardiovascular development. The administration of PDGFB alone normalized tumor vasculature by increasing periendothelial coverage and vascular functionality. Interestingly, this effect exerted by PDGFB was also observed in the presence of DAPT. So PDGFB is able to improve tumor vascularity and allows the anticancer action of DAPT in the tumor. PDGFB Protein, Rhesus, Recombinant (His) is expressed in yeast with His tag. The predicte... | |||
TMPK-01020 |
FSHB Protein, Mouse, Recombinant (hFc)
FSH-beta,FSH-B,FSHB,FSH-β,Follitropin |
Mouse | HEK293 Cells |
Fertility is dependent on follicle-stimulating hormone (FSH), a product of gonadotrope cells of the anterior pituitary gland. Hypothalamic gonadotropin-releasing hormone (GnRH) and intra-pituitary activins are regarded as the primary drivers of FSH synthesis and secretion. Both stimulate expression of the FSH beta subunit gene (Fshb), although the underlying mechanisms of GnRH action are poorly described relative to those of the activins. FSHB Protein, Mouse, Recombinant (hFc) is expressed in HE... | |||
TMPH-02492 |
DBI Protein, Mouse, Recombinant (His & Myc)
Endozepine (EP),Diazepam-binding inhibitor,DBI,Acyl-CoA-bind... |
Mouse | E. coli |
Binds medium- and long-chain acyl-CoA esters with very high affinity and may function as an intracellular carrier of acyl-CoA esters. It is also able to displace diazepam from the benzodiazepine (BZD) recognition site located on the GABA type A receptor. It is therefore possible that this protein also acts as a neuropeptide to modulate the action of the GABA receptor. DBI Protein, Mouse, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted ... | |||
TMPJ-01192 |
ELAPOR1 Protein, Human, Recombinant (His)
ELAPOR1,Endosome-Lysosome Associated Apoptosis And Autophagy... |
Human | HEK293 Cells |
Endosome/lysosome-associated apoptosis and autophagy regulator (ELAPOR1), also known as EIG121 protein, is a type I transmembrane protein induced by estrogen. The estrogen-induced gene 121 (EIG121) has been associated with breast and endometrial cancers,but its mechanism of action remains unknown.May protect cells from cell death by inducing cytosolic vacuolization and upregulating the autophagy pathway. That EIG121 is a good endometrial biomarker associated with a hyperestrogenic state and estr... | |||
TMPK-00109 |
Artemin Protein, Human, Recombinant (hFc)
ARTNE,ARTN,Neublastin,Enovin,Artemin,NBN,EVN |
Human | 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. | |||
TMPY-04877 |
PDGFB Protein, Mouse, Recombinant (His)
platelet-derived growth factor β polypeptide,血小板源生长因子,Sis,pl... |
Mouse | P. pastoris (Yeast) |
Platelet-derived growth factor-B (PDGFB) is necessary for normal cardiovascular development. The administration of PDGFB alone normalized tumor vasculature by increasing periendothelial coverage and vascular functionality. Interestingly, this effect exerted by PDGFB was also observed in the presence of DAPT. So PDGFB is able to improve tumor vascularity and allows the anticancer action of DAPT in the tumor. PDGFB Protein, Mouse, Recombinant (His) is expressed in yeast with His tag. The predicted... | |||
TMPJ-00650 |
FIBP Protein, Human, Recombinant
FIBP,aFGF Intracellular-Binding Protein,FGF-1 Intracellular-... |
Human | E. coli |
Acidic Fibroblast Growth Factor Intracellular-Binding Protein (FIBP) is highly expressed in the heart, skeletal muscle, and pancreas. Acidic Fibroblast Growth Factor is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. FIBP is an intracellular protein that binds ... | |||
TMPJ-01050 |
GRB2 Protein, Human, Recombinant (His)
Growth Factor Receptor-Bound Protein 2,SH2/SH3 Adapter GRB2,... |
Human | E. coli |
As an adaptor protein, Growth Factor Receptor-Bound Protein 2 (GRB2) is involved in siganl transduction and consists of a central SH2 domain flanked by two SH3 domains. GRB2 associates with activated Tyr-phosphorylated EGF receptor/EGFR and PDGF receptors via its SH2 domain, stimulating GTP binding to Ras, which in turn activates MAPK and other signaling pathway.It also associates to other cellular Tyr-phosphorylated proteins such as SIT1, IRS1, IRS4, SHC and LNK. probably via the concerted acti... | |||
TMPY-04195 |
CHRNB3 Protein, Human, Recombinant (hFc)
cholinergic receptor, nicotinic, β 3 (neuronal),cholinergic ... |
Human | HEK293 Cells |
Cholinergic nicotinic receptor (CHRN) gene family has been known to mediate the highly additive effects of nicotine in the body, and implicated nicotine dependence (ND) and related phenotypes. Cigarette smoking is protective in Parkinson's disease (PD), possibly because of nicotine action on brain nicotinic-acetylcholine receptors. The beta3 nicotinic-acetylcholine receptor subunit (encoded by CHRNB3) is depleted in the striatum of PD patients and associated with nicotine dependence. CHRNB3 Prot... | |||
TMPJ-01310 |
TRIM5 Protein, Human, Recombinant (His)
RNF88,Tripartite motif-containing protein 5,RING finger prot... |
Human | E. coli |
Tripartite motif-containing Motif 5 is a protein that in humans is encoded by the TRIM5 gene.It is a 493 amino acids protein that belongs to the TRIM/RBCC family.It contains 1 B box-type zinc finger, 1 B30.2/SPRY domain and 1 RING-type zinc finger. TRIM5 present in the cytoplasm recognizes motifs within the capsid proteins and interferes with the uncoating process, therefore preventing successful reverse transcription and transport to the nucleus of the viral genome. The exact mechanism of actio... | |||
TMPY-03990 |
Profilin 4 Protein, Human, Recombinant (His)
profilin family, member 4 |
Human | E. coli |
PFN4, also known as profilin 4, is a member of the profilin family. Profilin can be detected in all eukaryotic organisms. It plays an important role in the spatially and temporally controlled growth of actin microfilaments. Profilin is one of the most abundant actin monomer binders, but proteins such as CAP and (in mammals) thymosin β4 have some functional overlaps with profilin. In contrast, ADF/cofilin has some properties that antagonize profilin action. PFN4 also functions in the dynamic turn... | |||
TMPJ-00553 |
Lp-PLA2/PLA2G7 Protein, Human, Recombinant (aa 22-441, His)
PAF Acetylhydrolase,LDL-Associated Phospholipase A2,LDL-PLA(... |
Human | HEK293 Cells |
Platelet-Activating Factor Acetylhydrolase (PAFAH) is a secreted enzyme which belongs to the AB hydrolase superfamily and Lipase family and catalyzes the degradation of platelet-activating factor to biologically inactive products. PAFAH is produced by inflammatory cells and hydrolyzes oxidised phospholipids in LDL. PAFAH has been implicated in the development of atherosclerosis and has also been identified as a marker for cardiac disease. PAFAH might have a major physiologic effect in the presen... | |||
TMPJ-00891 |
Kallikrein 2/KLK2 Protein, Human, Recombinant (His)
hGK-1,Kallikrein-2,Tissue Kallikrein-2,KLK2,Glandular Kallik... |
Human | HEK293 Cells |
Kallikrein-2 (KLK2) is a secreted serine protease that belongs to the peptidase S1 family of Kallikrein subfamily. KLK2 contains 1 peptidase S1 domain. It is highly expressed in the human prostate gland. KLK2 can cleave Met-Lys and Arg-Ser bonds in kininogen to release Lys-bradykinin, but Preferential cleavages of Arg-|-Xaa bonds in small molecule substrates. It also highly selective action to release kallidin (lysyl-bradykinin) from kininogen involves hydrolysis of Met-|-Xaa or Leu-|-Xaa. KLK2 ... | |||
TMPJ-00660 |
IMPase2 Protein, Human, Recombinant (His)
Inositol-1(or 4)-Monophosphatase 2,IMPA2,IMP 2,IMPase 2,Inos... |
Human | E. coli |
Inositol monophosphatase 2, also known as Inositol-1(or 4)-monophosphatase 2, Myo-inositol monophosphatase A2 and IMPA2, is an enzyme which belongs to the inositol monophosphatase family. IMPA2 catalyzes the dephosphoylration of inositol monophosphate with cofactor Magnesium and Inhibited by high Li+ and restricted Mg2+ concentrations. IMPA2 plays an important role in phosphatidylinositol signaling. IMPA2 can use the myo-inositol monophosphates, scylloinositol 1,4-diphosphate, glucose-1-phosphat... | |||
TMPJ-01374 |
UPB1 Protein, Human, Recombinant (His)
β-Ureidopropionase,Beta-Alanine Synthase,β-Alanine Synthase,... |
Human | E. coli |
β-Ureidopropionase is a cytoplasmic protein which belongs to the CN hydrolase family of BUP subfamily. β-Ureidopropionase binds one zinc ion per subunit, catalyzes the last step in the pyrimidine degradation pathway. β-Ureidopropionase can convert N-carbamyl-beta-aminoisobutyric acid and N-carbamyl-beta-alanine to beta-aminoisobutyric acid and beta-alanine, ammonia and carbon dioxide, respectively. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidi... | |||
TMPJ-01427 |
SARS-CoV-2 NSP7 Protein (His)
SARS-CoV 2 nsp7 |
SARS-CoV-2 | E. coli |
The ∼30kb positive-stranded RNA genome of coronaviruses encodes a replication/transcription machinery that is unusually complex and composed of 16 nonstructural proteins (nsps). The four proteins nsp7 to nsp10, which are conserved among all CoVs but have no functional homologs outside of the Coronaviridae, are translated as part of the viral polyproteins pp1a and pp1ab, and the mature proteins are released by the action of the SARS-CoV protease nsp5. Hexadecamer of nsp7 and nsp8 may possess dsRN... | |||
TMPY-03616 |
NAPG Protein, Human, Recombinant (His)
γSNAP,GAMMASNAP,N-ethylmaleimide-sensitive factor attachment... |
Human | E. coli |
NAPG (NSF Attachment Protein Gamma, also known as gamma SNAP) is a Protein Coding gene. This gene encodes soluble NSF attachment protein gamma. The encoded protein mediates platelet exocytosis and controls the membrane fusion events of this process. NAPG is required for vesicular transport between the endoplasmic reticulum and the Golgi apparatus. NAPG belongs to the SNAP family. It is widely expressed in the brain, thyroid, and other tissues. SNAPs enable N-ethyl-maleimide-sensitive fusion prot... | |||
TMPY-03269 |
Prolyl Endopeptidase Protein, Mouse, Recombinant (His)
PEP,AI450383,AI047692,D10Wsu136e,prolyl endopeptidase,Pop |
Mouse | Baculovirus Insect Cells |
Prolyl endopeptidase, also known as PREP, belongs to a distinct class of serine peptidases. It is a large cytosolic enzyme which was first described in the cytosol of rabbit brain as an oligopeptidase. Prolyl endopeptidase degrades the nonapeptide bradykinin at the Pro-Phe bond. It is involved in the maturation and degradation of peptide hormones and neuropeptides such as alpha-melanocyte-stimulating hormone, luteinizing hormone-releasing hormone (LH-RH), thyrotropin-releasing hormone, angiotens... | |||
TMPJ-00914 |
YY1 Protein, Human, Recombinant (His)
NF-E1,Transcriptional repressor protein YY1,Yin and yang 1,I... |
Human | E. coli |
Transcriptional repressor protein YY1(YY1)contains 4 C2H2-type zinc fingers and belongs to the YY transcription factor family. Multifunctional transcription factor exhibits positive and negative control on a large number of cellular and viral genes by binding to sites overlapping the transcription start site. The effect on transcription regulation of the protein is depending upon the context in which it binds and diverse mechanisms of action include direct activation or repression, indirect acti... | |||
------------------------ 更多 ------------------------ |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIH-0486 |
Ramelteon-d5
|
||
Ramelteon-d5 是 Ramelteon 的氘代化合物。Ramelteon 的 CAS 号为 196597-26-9。Ramelteon 是强效高选择性和可口服的MT1/MT2激动剂,Ki值分别为 14 和 112 pM,有用于失眠症的研究潜力。 | |||
TMIJ-0172 |
Mifepristone-d6
|
||
Mifepristone-d6 是 Mifepristone 的氘代化合物。Mifepristone 的 CAS 号为 84371-65-3。Mifepristone 是一种黄体酮受体和糖皮质激素受体拮抗剂,在体外实验中的IC50值分别为 0.2 nM 和 2.6 nM。 | |||
TMID-0146 |
Methylprednisolone-d7
|
||
Methylprednisolone-d7 是 Methylprednisolone 的氘代化合物。Methylprednisolone 的 CAS 号为 83-43-2。Methylprednisolone 是一种具有类似抗炎作用的强的松龙衍生物。它是皮质类固醇,可作用于糖皮质激素受体。它通过激活ACE2并降低 IL-6 水平来改善严重的COVID-19。 | |||
TMID-0196 |
Allopurinol-d2
|
||
Allopurinol-d2 是 Allopurinol 的氘代化合物。Allopurinol 的 CAS 号为 315-30-0。Allopurinol 是一种黄嘌呤氧化酶(XO)抑制剂,IC50=7.82±0.12 μM。 | |||
TMIH-0297 |
Ledipasvir-d6
|
||
Ledipasvir-d6 是 Ledipasvir 的氘代化合物。Ledipasvir 的 CAS 号为 1256388-51-8。Ledipasvir 是一种丙型肝炎病毒 NS5A 抑制剂。它也是 P-糖蛋白抑制剂和乳腺癌抗性蛋白抑制剂。 | |||
TMID-0299 |
Zonisamide-d4
|
||
Zonisamide-d4 是 Zonisamide 的氘代化合物。Zonisamide 的 CAS 号为 68291-97-4。Zonisamide 是锌酶碳酸酐酶 (carbonic anhydrase) 的有效抑制剂,对人类线粒体同工酶 hCA II 和 hCA V 作用的Ki值分别为 35.2 nM 和 20.6 nM。Zonisamide 具有抗癫痫活性,在癫痫、癫痫发作和帕金森病的研究中具有价值。 | |||
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-0133 |
Empagliflozin-d4
|
||
Empagliflozin-d4 是 Empagliflozin 的氘代化合物。Empagliflozin 的 CAS 号为 864070-44-0。Empagliflozin 是有效的、选择性的钠葡萄糖协同转运蛋白-2 (SGLT-2) 抑制剂,对人 SGLT-2 的IC50为 3.1 nM。 | |||
TMIJ-0028 |
17β-Estradiol-2,4-d2
|
||
17β-Estradiol-2,4-d2 是 17β-Estradiol 的氘代化合物。17β-Estradiol 的 CAS 号为 50-28-2。Estradiol 是一种类固醇性激素,对于女性生育能力和第二性征的维持至关重要。它通过雌激素受体 β 途径上调 IL-6 表达。 | |||
TMIJ-0260 |
Bilastine-d4
|
||
Bilastine-d4 是 Bilastine 的氘代化合物。Bilastine 的 CAS 号为 202189-78-4。Bilastine是新型抗组胺药,对H1组胺受体具有高度选择性,起效快,作用时间长的特性,可用于变应性鼻结膜炎和荨麻疹。 | |||
TMIJ-0259 |
Bilastine-d6
|
||
Bilastine-d6 是 Bilastine 的氘代化合物。Bilastine 的 CAS 号为 202189-78-4。Bilastine是新型抗组胺药,对H1组胺受体具有高度选择性,起效快,作用时间长的特性,可用于变应性鼻结膜炎和荨麻疹。 | |||
TMIH-0485 |
Ramelteon-d3
|
||
Ramelteon-d3 是 Ramelteon 的氘代化合物。Ramelteon 的 CAS 号为 196597-26-9。Ramelteon 是强效高选择性和可口服的MT1/MT2激动剂,Ki值分别为 14 和 112 pM,有用于失眠症的研究潜力。 | |||
TMIJ-0185 |
Telmisartan-13C-d3
|
||
Telmisartan-13C-d3 是 Telmisartan 的 13C 和氘代化合物。Telmisartan 的 CAS 号为 144701-48-4。Telmisartan 是一种血管紧张素II 1型受体拮抗剂,能够抑制其活性,IC50值为 9.2 nM。 | |||
TMID-0145 |
Methylprednisolone-d2
|
||
Methylprednisolone-d2 是 Methylprednisolone 的氘代化合物。Methylprednisolone 的 CAS 号为 83-43-2。Methylprednisolone 是一种具有类似抗炎作用的强的松龙衍生物。它是皮质类固醇,可作用于糖皮质激素受体。它通过激活ACE2并降低 IL-6 水平来改善严重的COVID-19。 | |||
TMIJ-0196 |
17β-Estradiol-16,16,17-d3
|
||
17β-Estradiol-16,16,17-d3 是 17β-Estradiol 的氘代化合物。17β-Estradiol 的 CAS 号为 50-28-2。Estradiol 是一种类固醇性激素,对于女性生育能力和第二性征的维持至关重要。它通过雌激素受体 β 途径上调 IL-6 表达。 | |||
TMIJ-0032 |
17beta-Estradiol-13C2
|
||
17beta-Estradiol-13C2 是 17beta-Estradiol 的 13C 的标记化合物。17beta-Estradiol 的 CAS 号为 50-28-2。Estradiol 是一种类固醇性激素,对于女性生育能力和第二性征的维持至关重要。它通过雌激素受体 β 途径上调 IL-6 表达。 | |||
TMIH-0183 |
Dequalinium Chloride-d4
|
||
Dequalinium Chloride-d4 是 Dequalinium Chloride 的氘代化合物。Dequalinium Chloride 的 CAS 号为 522-51-0。Dequalinium chloride 是一种apamin敏感型的钾离子通道选择性阻断剂。 | |||
TMID-0211 |
4-Hydroxyphenylacetic Acid-d6
|
||
4-Hydroxyphenylacetic Acid-d6 是 4-Hydroxyphenylacetic Acid 的氘代化合物。4-Hydroxyphenylacetic Acid 的 CAS 号为 156-38-7。4-Hydroxyphenylacetic acid 是主要的微生物群衍生的多酚代谢物,能够诱导Nrf2表达,具有抗氧化作用。 | |||
TMID-0108 |
17β-Estradiol-2,4,16,16,17-d5
|
||
17β-Estradiol-2,4,16,16,17-d5 是 17β-Estradiol 的氘代化合物。17β-Estradiol 的 CAS 号为 50-28-2。Estradiol 是一种类固醇性激素,对于女性生育能力和第二性征的维持至关重要。它通过雌激素受体 β 途径上调 IL-6 表达。 | |||
TMIH-0013 |
(S)-Empagliflozin-d4
|
||
(S)-Empagliflozin-d4 是 (S)-Empagliflozin 的氘代化合物。(S)-Empagliflozin 的 CAS 号为 864070-44-0。Empagliflozin 是有效的、选择性的钠葡萄糖协同转运蛋白-2 (SGLT-2) 抑制剂,对人 SGLT-2 的IC50为 3.1 nM。 | |||
TMIJ-0031 |
Sulfamethoxazole-13C6
|
||
Sulfamethoxazole-13C6 是 Sulfamethoxazole 的 13C 的标记化合物。Sulfamethoxazole 的 CAS 号为 723-46-6。Sulfamethoxazole是磺胺类抗菌素,用于细菌感染。Sulfonamides是对氨基苯甲酸的竞争性拮抗剂。 | |||
TMID-0022 |
Spironolactone-d3
|
||
Spironolactone-d3 是 Spironolactone 的氘代化合物。Spironolactone 的 CAS 号为 52-01-7。Abbolactone 是一种可口服的醛固酮盐皮质激素受体拮抗剂,IC50值为 24 nM。它也是雄激素受体拮抗剂,促进足细胞自噬,IC50值为 77 nM。 | |||
TMID-0148 |
Nandrolone 17-propionate-d3
|
||
Nandrolone 17-propionate-d3 是 Nandrolone 17-propionate 的氘代化合物。Nandrolone 17-propionate 的 CAS 号为 7207-92-3。Nandrolone propionate 是合成代谢类固醇,主要由雄激素和保氮剂组成,具有作用时间相对较长的特点。 | |||
TMIH-0555 |
Telbivudine-d3
|
||
Telbivudine-d3 是 Telbivudine 的氘代化合物。Telbivudine 的 CAS 号为 3424-98-4。Telbivudine 是一种乙型肝炎病毒复制的抗病毒抑制剂,是一种具有口服活性的胸腺嘧啶核苷类似物。 | |||
TMIJ-0222 |
Exemestane-d3
|
||
Exemestane-d3 是 Exemestane 的氘代化合物。Exemestane 的 CAS 号为 107868-30-4。Exemestane 是一种选择性的、具有口服活性的、不可逆的甾体芳香酶抑制剂,能够作用于人胎盘芳香酶 (IC50:30 nM) 和大鼠卵巢芳香酶 (IC50:40 nM),可用于研究激素依赖性乳腺癌。 | |||
TMID-0055 |
17β-estradiol-d4
|
||
17β-estradiol-d4 是 17β-estradiol 的氘代化合物。17β-estradiol 的 CAS 号为 50-28-2。Estradiol 是一种类固醇性激素,对于女性生育能力和第二性征的维持至关重要。它通过雌激素受体 β 途径上调 IL-6 表达。 | |||
TMIJ-0497 |
Lacidipine-d10
|
||
Lacidipine-d10 是 Lacidipine 的氘代化合物。Lacidipine 的 CAS 号为 103890-78-4。Lacidipine 是一种L型钙离子通道阻断剂。 | |||
TMIJ-0154 |
Lenvatinib-d4
|
||
Lenvatinib-d4 是 Lenvatinib 的氘代化合物。Lenvatinib 的 CAS 号为 417716-92-8。Lenvatinib 是一种口服具有活性的,多靶点酪氨酸激酶抑制剂,能够抑制血管内皮生长因子受体(VEGFR1-3),成纤维细胞生长因子受体(FGFR1-4),干细胞因子受体(KIT),血小板衍生生长因子受体(PDGFR),转染期间重排(RET),具有效抗癌的作用。 | |||
TMID-0048 |
Dinotefuran-d3
|
||
Dinotefuran-d3 是 Dinotefuran 的氘代化合物。Dinotefuran 的 CAS 号为 165252-70-0。Dinotefuran是一种新型烟碱类杀虫剂, 通过抑制烟碱乙酰胆碱受体而破坏昆虫的神经系统起作用。 | |||
TMIJ-0223 |
Exemestane-13C-d3
|
||
Exemestane-13C-d3 是 Exemestane 的 13C 和氘代化合物。Exemestane 的 CAS 号为 107868-30-4。Exemestane 是一种选择性的、具有口服活性的、不可逆的甾体芳香酶抑制剂,能够作用于人胎盘芳香酶 (IC50:30 nM) 和大鼠卵巢芳香酶 (IC50:40 nM),可用于研究激素依赖性乳腺癌。 | |||
TMIJ-0074 |
Retigabine-d4
|
||
Retigabine-d4 是 Retigabine 的氘代化合物。Retigabine 的 CAS 号为 150812-12-7。Retigabine dihydrochloride 是一种抗惊厥药,用作有治疗经验的成年患者部分性癫痫的辅助治疗。作用机制涉及神经元 K(V)7.2-7.5(以前的 KCNQ2-5)电压激活 K(+) 通道的开放。 | |||
TMIH-0086 |
Amifampridine-d3 2HCl
|
||
Amifampridine-d3 2HCl 是 Amifampridine 2HCl 的氘代化合物。Amifampridine 2HCl 的 CAS 号为 54-96-6。Amifampridine 可用于罕见肌肉疾病的研究。 | |||
TMIJ-0110 |
Clarithromycin-13C-d3
|
||
Clarithromycin-13C-d3 是 Clarithromycin 的 13C 和氘代化合物。Clarithromycin 的 CAS 号为 81103-11-9。Clarithromycin 具有广谱的抗菌活性。它抑制CYP3A4催化的三唑仑 α-羟基化,IC50(Ki) 值为 56 (43) μM。它抑制 HERG 钾电流。它可削弱连接 hERG1 和 PI3K 的信号通路影响自噬流 。 | |||
TMIJ-0326 |
Cyclosporin A-d4 (Major)
|
||
Cyclosporin A-d4 (Major) 是 Cyclosporin A 的氘代化合物。Cyclosporin A 的 CAS 号为 59865-13-3。Cyclosporine A 是一种能与亲环素结合的抑制剂。 根据它的作用机制可作为钙调神经磷酸酶抑制剂、细胞色素 P450 3A4 抑制剂和 P-糖蛋白抑制剂。 | |||
TMID-0248 |
Triamcinolone acetonide-d6
|
||
Triamcinolone acetonide-d6 是 Triamcinolone acetonide 的氘代化合物。Triamcinolone acetonide 的 CAS 号为 76-25-5。Triamcinolone acetonide 是皮质类固醇。 它是皮质类固醇激素受体激动剂。 它是抗炎糖皮质激素,局部用于治疗各种皮肤疾病。它的有效性是 prednisone 的八倍。 | |||
TMIJ-0304 |
Lithocholic Acid-d4
|
||
Lithocholic Acid-d4 是 Lithocholic Acid 的氘代化合物。Lithocholic Acid 的 CAS 号为 434-13-9。Lithocholic acid是由鹅去氧胆酸盐通过细菌作用形成的胆汁酸,通常与甘氨酸或牛磺酸结合,被用作利胆剂。 它作为清洁剂溶解脂肪以供吸收,并且本身被吸收。 | |||
TMID-0076 |
Busulfan-d8
|
||
Busulfan-d8 是 Busulfan 的氘代化合物。Busulfan 的 CAS 号为 55-98-1。Busulfan 是二甲磺酸盐的合成衍生物,具有抗肿瘤和细胞毒特性。是一种烷化剂,对骨髓具有选择性免疫抑制作用。 | |||
TMIJ-0228 |
Lidocaine-d6 HCl
|
||
Lidocaine-d6 HCl 是 Lidocaine HCl 的氘代化合物。Lidocaine HCl 的 CAS 号为 73-78-9。Lidocaine hydrochloride 抑制涉及复杂电压和依赖性的钠通道。它通过调节 miR-145 表达和进一步抑制MEK/ERK和NF-κB信号通路来减少胃癌细胞的生长,迁移和侵袭。Lidocaine 是一种酰胺衍生物,是一种研究室性心律失常的药物和有效的肿瘤抑制剂。 | |||
TMID-0263 |
Lidocaine-d10 Hydrochloride
|
||
Lidocaine-d10 Hydrochloride 是 Lidocaine Hydrochloride 的氘代化合物。Lidocaine Hydrochloride 的 CAS 号为 73-78-9。Lidocaine hydrochloride 抑制涉及复杂电压和依赖性的钠通道。它通过调节 miR-145 表达和进一步抑制MEK/ERK和NF-κB信号通路来减少胃癌细胞的生长,迁移和侵袭。Lidocaine 是一种酰胺衍生物,是一种研究室性心律失常的药物和有效的肿瘤抑制剂。 | |||
TMID-0006 |
Budesonide-d8
mixture of diastereomers-d8 |
||
Budesonide-d8 是 Budesonide 的氘代化合物。Budesonide 的 CAS 号为 51333-22-3。Budesonide 是吸入型糖皮质类固醇,是一种口服具有活性的糖皮质激素受体激动剂。它能够减小肺部肿瘤的体积,逆转 DNA 低度甲基化,调节基因的 mRNA 表达。它是能够用于哮喘的抗炎药。 | |||
TMID-0070 |
Amiodarone-d10 Hydrochloride
|
||
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
|
||
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。 | |||
TMID-0115 |
Dehydroepiandrosterone-2,2,3,4,4,6-d6
DHEA-d6 |
||
Dehydroepiandrosterone-2,2,3,4,4,6-d6 是 Dehydroepiandrosterone 的氘代化合物。Dehydroepiandrosterone 的 CAS 号为 53-43-0。Dehydroepiandrosterone 是一种类固醇激素。它通过多种信号传导途径介导其作用,并通过转化成雄激素和雌激素衍生物(例如,雄激素,雌激素,7α和7β DHEA (Prasterone),以及7α和7β表雄甾酮衍生物)在特异性受体上起作用。 | |||
TMIH-0257 |
Glycoursodeoxycholic Acid-d4
|
||
Glycoursodeoxycholic Acid-d4 是 Glycoursodeoxycholic Acid 的氘代化合物。Glycoursodeoxycholic Acid 的 CAS 号为 64480-66-6。Glycoursodeoxycholic acid 是一种酰基甘氨酸和胆汁酸-甘氨酸缀合物,是熊去氧胆酸的代谢物。 | |||
TMIJ-0189 |
Ranitidine-d6 HCl
|
||
Ranitidine-d6 HCl 是 Ranitidine HCl 的氘代化合物。Ranitidine HCl 的 CAS 号为 66357-59-3。Ranitidine hydrochloride 是一种具有口服活性的组胺 H2 受体选择性拮抗剂,IC50为 3.3 μM。它还是一种CYP2C19和CYP2C9的弱抑制剂,可抑制胃液分泌。 | |||
TMID-0120 |
Valproic Acid-d15
|
||
Valproic Acid-d15 是 Valproic Acid 的氘代化合物。Valproic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 | |||
TMIJ-0163 |
Valproic Acid-d4
|
||
Valproic Acid-d4 是 Valproic Acid 的氘代化合物。Valproic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 | |||
TMIJ-0431 |
2-(Propyl-3,3,3-d3)pentanoic-5,5,5-d3 Acid
|
||
2-(Propyl-3,3,3-d3)pentanoic-5,5,5-d3 Acid 是 2-pentanoic Acid 的氘代化合物。2-pentanoic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 | |||
T36537 |
Nitrofurantoin-13C3
Nitrofurantoin-13C3 |
||
Nitrofurantoin-13C3is intended for use as an internal standard for the quantification of nitrofurantoin by GC- or LC-MS. Nitrofurantoin is a nitrofuran antibiotic.1In vivo, nitrofurantoin (25-100 mg/kg) reducesE. colireplication and abscess formation in the renal medulla of infected rats in a dose-dependent manner. It prevents kidney and bladder infection in rats following bladder inoculation with clinical isolates ofP. mirabilis. Nitrofurantoin also prevents alkalization of urine, as well as ca... | |||
T36021 |
Flumequine-13C3
Flumequine-13C3 |
||
Flumequine-13C3is intended for use as an internal standard for the quantification of flumequine by GC- or LC-MS. Flumequine is a fluoroquinolone antibiotic.1It is active againstS. aureus, S. pyogenes, B. subtilis, E. coli, P. aeruginosa, S. faecalis, andK. pneumoniae(MICs = 1-100 μg/ml). Flumequine is also active against field isolates of B. hyodysenteriae (MICs = 6.25-200 μg/ml).2It inhibits DNA gyrase, disrupting supercoiling of bacterial DNA to block transcription and replication.3In vivo, fl... | |||
------------------------ 更多 ------------------------ |