3952
376
27
233
103
Cat. No. | Product Name | ||
---|---|---|---|
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; | |||
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 | |||
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; | |||
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 | |||
L4150 | 新颖已知活性精选库 | 989 compounds | |
989 种百里挑一的活性化合物; | |||
L7000 | 活性脂质化合物库 | 385 compounds | |
385 种生物活性小分子化合物,用于高通量、高内涵筛选; | |||
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; | |||
D7800 | 新颖已知活性库 | 8118 compounds | |
提高成功率:新增8118种已知活性化合物,提高实验成功率。 | |||
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; | |||
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; | |||
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; | |||
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; | |||
L1580 | GPCR库Plus | 338 compounds | |
338 种GPCR 靶向、结构新颖的化合物; | |||
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。 | |||
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 | |||
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。 | |||
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; | |||
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; | |||
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; | |||
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; | |||
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; | |||
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; | |||
L8720 | 细胞焦亡化合物库 | 1066 compounds | |
1066 种细胞焦亡相关的化合物,可以用于细胞焦亡相关研究。 | |||
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; | |||
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; | |||
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 |
---|---|---|---|
TP1555L1 |
Fibronectin Active Fragment Control acetate
Fibronectin Active Fragment Control acetate(97461-84-2 Free base) |
||
Fibronectin Active Fragment Control acetate 是纤连蛋白的活性片段,这是一种糖蛋白。 | |||
T5401 |
GSK2983559 active metabolite
GSK2983559,RIPK2 inhibitor 1,RIPK2-IN-1 |
RIP kinase | Apoptosis; NF-κB |
GSK2983559 active metabolite (RIPK2-IN-1) 是一种受体相互作用蛋白-2 激酶抑制剂。 | |||
TP1555 |
Fibronectin Active Fragment Control
|
||
Fibronectin is a high-molecular weight (~440kDa) extracellular matrix glycoprotein that binds to membrane-spanning receptor proteins called integrins.In addition to integrins, fibronectin also binds extracellular matrix components such as collagen, fibrin | |||
T14122 |
Active-mono-sulfone-PEG8-acid
|
Others | Others |
Active-mono-sulfone-PEG8-acid is a polyethylene glycol (PEG) derivative serving as a linker for PROTAC synthesis[1]. | |||
T10480 | Bay 41-4109 (less active enantiomer) | HBV | Microbiology/Virology |
Bay 41-4109 less active enantiomer shows less activity than Bay 41-4109. BAY 41-4109 is a potent HBV inhibitor (IC50: 53 nM). | |||
T19667 |
R-138727
Prasugrel active metabolite |
Others | Others |
R-138727 is a novel P2Y12 receptor inhibitor. | |||
T29705 |
AG-2000 Free Base
Lansoprazole sulfenamide active metabolite |
Others | Others |
AG-2000 Free Base is a bio-active chemical. Detailed information has not been published. | |||
T13646 |
Desisobutyryl-ciclesonide
CIC-AP,Ciclesonide active principle |
Others | Others |
Desisobutyryl-ciclesonide has an affinity for glucocorticoid receptors. Desisobutyryl-ciclesonide is the active metabolite of Ciclesonide. | |||
T29704 |
AG-1812 free base
UNII-6RI44GB0V9,HE078804,AC1MIZB6,Lansoprazole disulfide active metabolite |
Others | Others |
ABT-1812 is a bio-active chemical. | |||
T9966 |
GSK-1520489A
|
Wee1 | Cell Cycle/Checkpoint |
GSK-1520489 A 是一种活性 PKMYT1 抑制剂。 | |||
T8580 |
Bupranolol
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Bupranolol 是竞争性的、口服活性的、非选择性的β-adrenoceptor 拮抗剂,无固有的拟交感神经活性。 | |||
T1292 |
Tiapride hydrochloride
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Tiapride 是一种大脑中 D2/3 多巴胺受体的选择性阻滞剂。 它用于治疗各种精神和神经系统疾病,包括运动障碍、酒精戒断综合征、精神病的阴性症状以及老年人的攻击和激动。 | |||
T8348 |
Phentolamine
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Phentolamine 是一种 alpha-1 和 alpha-2 选择性肾上腺素能受体拮抗剂。 | |||
T9732 |
VY-3-135
|
Fatty Acid Synthase | Metabolism |
VY-3-135 是口服有效的乙酰辅酶 A 合成酶 2 (ACSS2)选择性 抑制剂,IC50为 44 nM,对重组人 ACSS1 或 ACSS3 没有抑制活性。它有效抑制 ACSS2 依赖性脂肪酸代谢,但对肿瘤中的基因表达没有影响。 | |||
T8734 |
Choline
|
Others | Others |
Choline hydroxide 是一种普遍存在的水溶性营养素,通常与 B 族维生素有关。 | |||
T9565 |
OSBPL7-IN-1
|
Others | Others |
OSBPL7-IN-1 是口服有效的氧甾醇结合蛋白样 7 (OSBPL7)抑制剂。它促进质膜上ABCA1的增加,但不影响 mRNA 表达。 | |||
T34896 |
Tofisopam
Emandaxin,托非索洋,Grandaxin |
Others | Others |
Tofisopam (Grandaxin) 是2,3-苯二氮卓类化合物,具有抗焦虑活性,可口服。 | |||
T20525 |
Chloramphenicol palmitate
|
Antibacterial; Antibiotic | Microbiology/Virology |
Chloramphenicol palmitate 是一种广谱抗生素,对革兰氏阳性和革兰氏阴性细菌具有活性。 Chloramphenicol palmitate 可用于在含有氯霉素抗性基因的转化细胞中作为细菌选择剂的研究。 | |||
T9805 |
BAY 2666605
|
PDE | Metabolism |
BAY 2666605 是一种具有口服活性的 PDE3A 和 PDE3B 抑制剂,IC50 分别为 87 nM 和 50 nM。 BAY 2666605 具有抗癌作用。 | |||
T9590 |
T-1095
|
SGLT; transporter | GPCR/G Protein; Metabolism |
T-1095 是一种口服有活性的Na+-葡萄糖协同转运蛋白选择性抑制剂,能够抑制 SGLT1 (IC50:22.8 µm) 及 SGLT2 (IC50:2.3 µm) 。它可用于研究糖尿病。 | |||
T11689 |
ITI-214
ITI214 |
PDE | Metabolism |
ITI-214 是一种中枢神经系统活性抑制剂,具有口服生物活性的PDE1抑制剂 (Kiof 58 pM),对其他 PDE 家族成员和一系列酶、受体、转运体和离子通道具有良好的选择性,在各种运动和认知功能的动物模型中显示出有效性。 | |||
T40732 |
TMPD dihydrochloride
|
Others | Others |
TMPD dihydrochloride 是酶促转化氧化还原的活性底物和用于还原血红素过氧化物酶的电子供体。 | |||
T9164 |
BMS-986242
BMS986242 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
BMS-986242 是具有口服具有活力、强效的、选择性的 indoleamine-2,3-dioxygenase 1 抑制剂,可用于研究癌症。 | |||
T2629 |
UNC2881
|
TAM Receptor | Tyrosine Kinase/Adaptors |
UNC2881 是一种特异性Mer 激酶抑制剂,可抑制稳态的Mer 激酶磷酸化,其IC50=22 nM。 | |||
T2678 |
LB42708
|
Transferase | Metabolism |
LB42708 是一种口服有活力的特异性法尼基转移酶抑制剂。它对H-Ras、N-Ras 和K-Ras4B 的法尼基化均有抑制作用,其IC50分别为 0.8 nM、1.2 nM 和 2.0 nM。 | |||
T7686 |
Ramiprilat
|
RAAS | Endocrinology/Hormones |
Ramiprilat 是 Ramipril 的活性代谢物,是一种口服有活力的血管紧张素转换酶 (ACE) 抑制剂,其 Ki=7 pM。它可用于研究心力衰竭以及高血压。 | |||
T17158 |
trans-AUCB
t-AUCB |
Epoxide Hydrolase | Metabolism |
trans-AUCB (t-AUCB) 是口服具有活力的、选择性的可溶性环氧水解酶 (sEH) 抑制剂,对人,小鼠和大鼠的 sEH 的IC50分别为 1.3 nM,8 nM,8 nM。它具有抗神经胶质瘤特性。 | |||
T9303 |
MRTX1133
|
Ras | GPCR/G Protein; MAPK |
MRTX1133 是一种 KRAS G12D 抑制剂 (KD=0.2 pM),具有强效性、选择性和非共价性。MRTX1133 对 KRAS G12D 突变的肿瘤具有抑制活性,而对 KRAS 野生型肿瘤无抑制活性。 | |||
T8581 |
Flecainide hydrochloride
|
Others | Others |
Flecainide hydrochloride 是一种用于预防和治疗异常快速心率的药物。这包括室性和室上性心动过速。 | |||
T9977 |
SGK1-IN-4
|
SGK | Metabolism |
SGK1-IN-4 是 SGK1 的特异性抑制剂,可用于骨关节炎研究。 | |||
T7503 |
Upadacitinib
乌帕替尼,ABT-494 |
JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
Upadacitinib (ABT-494) 是高效选择性的,具有口服活性的 JAK1抑制剂,IC50为43 nM,可用于多种自身免疫性疾病的研究。它对 JAK1 的选择性约为 JAK2 的 74 倍。 | |||
T36670 |
JNJ-67856633
|
MALT | Immunology/Inflammation |
JNJ-67856633 是口服有效的、选择性的、变构性的 MALT1 protease 抑制剂。在某些情况下,JNJ-67856633可以导致肿瘤停滞。 | |||
T21593 |
AAL-993
|
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
AAL-993 是口服有效的VEGFR 选择性抑制剂,抑制 VEGFR1、VEGFR2 和 VEGFR3 的IC50分别为 130 nM、23 nM 和 18 nM,对其他酪氨酸激酶的抑制作用较弱。AAL-993 具有抗血管生成和抗肿瘤的活性。 | |||
T4628 |
Seladelpar
MBX 8025 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Seladelpar (MBX 8025) 是一种有效的,具有口服活性的, 特异性PPAR-δ激动剂,EC50为 2 nM。 | |||
T22304 |
Desciclovir
BW A515U,地昔洛韦,6-Deoxyacyclovir,DCV |
Antifection | Microbiology/Virology |
Desciclovir (DCV) 是抗疱疹药物阿昔洛韦的前药,口服有活性,在体内被黄嘌呤氧化酶转化成为阿昔洛韦。 | |||
T60024 |
CFT7455
Cemsidomide |
Ligand for E3 Ligase | PROTAC |
CFT7455 (Cemsidomide) 是一种抗癌剂,对 cereblon E3 连接酶具有高亲和力,Kd 为 0.9 nM。 CFT7455 是锌指转录因子 Ikaros (IKZF1) 和 Aiolos (IKZF3) 的口服活性降解剂。 | |||
T9786 |
Lu AF27139
|
P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
Lu AF27139 是一种有效的选择性 P2X7 受体拮抗剂(人和大鼠的 IC50 分别为 12 和 2.4 nM,小鼠、人和大鼠的 Ki 分别为 22、54 和 13 nM)。 Lu AF27139 可用于中枢神经系统疾病研究。 | |||
T28167 |
NGB 2904
NGB2904 HCl,NGB-2904,NGB2904 |
Others; Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience; Others |
NGB 2904 是一种具有口服活性的、选择性的多巴胺(DA) D3受体拮抗剂,可用于具可卡因成瘾。 | |||
T21976 |
ONO-8130
|
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
ONO-8130 是前列腺素 EP1 受体选择性拮抗剂,口服有活力,能够阻断 L6 脊髓中ERK 的磷酸化。它可缓解环磷酰胺致膀胱炎小鼠的膀胱疼痛,可用于研究间质性膀胱炎。 | |||
T9627 |
PHD-1-IN-1
|
HIF/HIF Prolyl-Hydroxylase | Chromatin/Epigenetic; Metabolism |
PHD-1-IN-1 是口服有效的缺氧诱导因子脯氨酰羟化酶结构域 1抑制剂,IC50为 0.034 μM。它与活性位 Fe2+具有独特的单齿结合相互作用,并诱导形成一个 “Arg367-out” 口袋。 | |||
T0600 |
10,11-Dihydrocarbamazepine
双氢卡马西平,10,11-二氢卡马西平,Dihydrocarbamazepine |
Others | Others |
10,11-Dihydrocarbamazepine (Dihydrocarbamazepine) 是一种 Oxcarbazepine 的活性代谢物,也是一种有机中间体。Oxcarbazepine 能够几乎完全的、迅速的转化为 10,11-Dihydrocarbamazepine,可能具有抗惊厥效果。 | |||
T10826 |
CK-666
|
HIV Protease; Microtubule Associated | Cytoskeletal Signaling; Microbiology/Virology; Proteases/Proteasome |
CK-666 是一种肌动蛋白相关蛋白 Arp2/3 复合物的细胞渗透性抑制剂。 它与 Arp2/3 复合物结合,稳定复合物的非活性状态,阻止 Arp2 和 Arp3 亚基进入活化的丝状短节距构象。 | |||
T2578 |
Didanosine
ddI,去羟肌苷,2',3'-Dideoxyinosine |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Didanosine (ddI) 是一种逆转录酶抑制剂,IC50为490nM。 | |||
T21793 |
CGP 35348
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
CGP 35348 是 GABAB 受体的选择性拮抗剂 (EC50 = 34 μM)。 CGP 35348 可用于研究白化新生小鼠脑损伤后的神经肌肉协调和空间学习。 | |||
T22675 |
Co 102862
V 102862 |
Others; Sodium Channel | Membrane transporter/Ion channel; Others |
Co 102862 是一种电压门控钠通道阻滞剂。 Co 102862 可用于抗惊厥的研究。 | |||
T1448 |
Dasatinib
BMS-354825,达沙替尼 |
Apoptosis; Bcr-Abl; Src; c-Kit; Autophagy | Angiogenesis; Apoptosis; Autophagy; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
Dasatinib (BMS-354825) 是一种酪氨酸激酶抑制剂,抑制 Src 和 Bcr-Abl (Ki=16/30 pM),具有口服活性和 ATP 竞争性。Dasatinib 具有抗肿瘤活性,用于治疗白血病和淋巴瘤等。 | |||
T22436 |
Takeda-6d
|
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Takeda-6d 是一种新型、有效的 DFG-out RAF/血管内皮生长因子受体 2 (VEGFR2) 抑制剂,IC50 分别为 7.0 nM 和 2.2 nM。 | |||
T1072 |
Loxeen
Pridinol methanesulfonate,Α,Α-二苯基-1-哌啶丙醇(普立地诺 甲磺酸盐 ) |
AChR | Neuroscience |
Loxeen (Pridinol methanesulfonate) 用作抗胆碱能药物和抗帕金森病药物。 | |||
T2316 |
Omarigliptin
MK-3102,奥格列汀 |
Proteasome; DPP-4 | Proteases/Proteasome; Ubiquitination |
Omarigliptin (MK-3102) 是高效选择性 DPP4抑制剂,IC50=为1.6nM。 | |||
T1613 |
Hydralazine hydrochloride
Hydralazine HCl,Apresoline,盐酸肼屈嗪 |
MAO; HIF/HIF Prolyl-Hydroxylase | Chromatin/Epigenetic; Metabolism; Neuroscience |
Hydralazine hydrochloride (Apresoline) 是一种直接作用的血管舒张剂,可抗高血压。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11351 |
Galanthamine N-Oxide
|
AChE | Neuroscience |
Galanthamine N-Oxide 是分离于Zephyranthes concolor 的球茎中的一种生物碱。它抑制电鳗乙酰胆碱酯酶,EC50=26.2 μM。它是TcAChE,hAChE 和 hBChE 酶活性位点中底物调节的显著抑制剂。 | |||
T4S1114 |
Dryocrassin ABBA
东北贯众素,Dryocrassin |
Influenza Virus; Antibacterial | Microbiology/Virology |
Dryocrassin ABBA (Dryocrassin) 是一种从苦参中提取的黄酮类天然产物,具有抗病毒和抗菌活性。它抑制树突状细胞的免疫刺激功能,延长同种异体皮肤移植成活率。 | |||
T3858 |
macranthoidin A
灰毡毛忍冬皂苷甲,金银花 |
Others | Others |
Macranthoidin A 是一种具有口服活性的、提取于金银花中的皂苷。它对四氯化碳,对乙酰氨基酚和镉所致的肝损伤具有保护作用,对耳巴豆油的溶胀具有明显的抑制作用。 | |||
T1560 |
Prednisolone
氢化泼尼松,Predonine,Hydroretrocortine,泼尼松龙,Metacortandralone |
Glucocorticoid Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Prednisolone (Hydroretrocortine) 是有口服活性的皮质类固醇和糖皮质激素。它的抗炎特性约为氢化可的松的四倍,同时减少了水和盐的保留。它能够用于眼部抗炎研究。 | |||
T5784 |
Topotecan
NSC 609669,拓扑替康,SKF 104864A |
Topoisomerase; Autophagy | Autophagy; DNA Damage/DNA Repair |
Topotecan (NSC-609669) 是一种拓扑异构酶 I 抑制剂,通过抑制 DNA 拓扑异构酶起抗肿瘤作用,可用于治疗卵巢癌。 | |||
T1611 |
Isotretinoin
13-cis-Retinoic acid,异维A酸 |
Retinoid Receptor; Endogenous Metabolite; Autophagy | Autophagy; Metabolism |
Isotretinoin (13-cis-Retinoic acid) 是一种天然存在的维甲酸,具有潜在的抗肿瘤活性。 它结合并激活核视黄酸受体 (RAR), 活化的 RARs 作为促进细胞分化和凋亡的转录因子。它是一种类维生素A 和维生素A 衍生物,用于治疗严重的痤疮和某些形式的皮肤、头颈癌。 | |||
T1326 |
Gentamicin sulfate
SCH9724,Gentamycin sulfate,NSC-82261,硫酸庆大霉素 |
ribosome; DHFR; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Gentamicin sulfate (SCH9724) 是一种广谱的氨基糖苷类抗生素,具有口服活性。Gentamicin sulfate 可以用于抑制敏感生物体中的蛋白质合成。 | |||
T0974 |
Novobiocin Sodium
Albamycinsodium,新生霉素钠,Cathomycin,Albamycin |
Potassium Channel; DNA gyrase; Topoisomerase; Antibacterial; Antibiotic; ABC; Autophagy | Autophagy; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology |
Novobiocin Sodium (Albamycinsodium) 是源自 Streptomyces niveus 的抗生素。 它的化学结构类似于香豆素。Novobiocin 与 DNA 促旋酶结合并阻断三磷酸腺苷活性。 | |||
T5283 |
NADH disodium salt
Disodium NADH,NADH, disodium salt hydrate,beta-烟酰胺腺嘌呤二核苷二钠 |
Others; Endogenous Metabolite | Metabolism; Others |
NADH disodium salt hydrate是氧化还原酶的辅酶。 NADH在分解代谢过程中起到再生电子供体的作用,包括糖酵解,柠檬酸循环和β-氧化。 | |||
TN6774 |
Emodin 6-O-β-D-glucoside
大黄素-6-O-β-D-葡萄糖苷,Glucoemodin |
Others | Others |
Emodin 6-O-β-D-glucoside (Glucoemodin) 是一种从 Reynoutria japonica 中提取的活性化合物。它具有显著的抗炎和屏障保护活性,可用于研究动脉粥样硬化及糖尿病并发症。 | |||
T2881 |
Crustecdysone
Commisterone,B-ecdysone,Commisterone,20-Hydroxyecdysone,Ecdysterone,B-ecdysone,β-蜕皮甾酮,Hydroxyecdysone,羟基蜕皮激素 |
Others; Caspase; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Metabolism; Others; Proteases/Proteasome |
Crustecdysone (Hydroxyecdysone) 是来源于露水草的一种蜕皮激素,可调节昆虫的蜕皮或蜕皮过程。它是 Ecdysone 的活性代谢物,通过 20E 核受体复合物 EcR-USP 抑制半胱天冬酶活性并诱导自噬,在心血管系统中具有调节或保护作用。 | |||
T6194 |
Fidaxomicin
非达米星,Tiacumicin B,OPT-80,Clostomicin B1,PAR-101 |
Apoptosis; DNA/RNA Synthesis; Antibacterial; Antibiotic | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Fidaxomicin (Tiacumicin B) 是一种大环RNA 聚合酶抑制剂,具有窄谱活性。它选择性地根除致病性艰难梭菌,对构成正常健康肠道菌群的多种细菌影响很小。 | |||
T2719 |
Succinic acid
Asuccin,Amber acid,琥珀酸,1,2-Ethanedicarboxylic acid,Wormwood acid,Butanedioic acid,1,4-Butandioic Acid |
Endogenous Metabolite | Metabolism |
Succinic acid (1,2-Ethanedicarboxylic acid) 是无氧代谢的发酵产物,也是三羧酸循环的中间产物。 | |||
T3417 |
Amentoflavone
Didemethyl-ginkgetin,穗花杉双黄酮,Amenthoflavone,3',8''-Biapigenin |
Apoptosis; P450; Phospholipase; Reactive Oxygen Species; Opioid Receptor; COX; Antibacterial; RSV; Antifungal | Apoptosis; Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; NF-κB |
Amentoflavone (3',8''-Biapigenin) 是一种具有很多生物活性的双黄酮类天然产物,有抗炎、抗氧化和神经保护等作用。 | |||
T2755 |
Rhoifolin
野漆树苷,Apigenin-7-O-rhamnoglucoside,Apigenin 7-O-neohesperidoside,Rhoifoloside |
Others; p38 MAPK; NF-κB; transporter; IGF-1R; Autophagy | Autophagy; MAPK; Metabolism; NF-κB; Others; Tyrosine Kinase/Adaptors |
Rhoifolin (Apigenin 7-O-neohesperidoside) 是从琯溪蜜柚叶子分离的一种黄酮糖苷。它通过 RANKL 诱导的NF-κB 和MAPK 途径改善钛颗粒刺激的骨溶解并减少破骨细胞生成。它通过增强脂联素分泌,胰岛素受体-β的酪氨酸磷酸化和GLUT4易位有助于治疗糖尿病并发症。 | |||
T3055 |
Liensinine Perchlorate
|
Apoptosis; Others | Apoptosis; Others |
Liensinine Perchlorate 是元莲的成分,可诱导结直肠癌细胞凋亡,具有抗高血压和抗癌活性。 | |||
T3912 |
Saikosaponin B1
柴胡皂苷B1,柴胡皂苷 B1 |
Others | Others |
Saikosaponin B1 是柴胡的生物活性成分,具有抗癌作用。它能够靶向SMO 抑制 Hedgehog 通路,显著抑制髓母细胞瘤模型中的肿瘤生长。 | |||
T0646 |
5-Aminosalicylic Acid
Mesalazine,5-ASA,5-氨基水杨酸,Mesalamine |
NF-κB; Lipoxygenase; COX; Glutathione Peroxidase; Endogenous Metabolite; PAK; PPAR | Cytoskeletal Signaling; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Neuroscience; NF-κB |
5-Aminosalicylic Acid (5-ASA) 是一种特异性的PPARγ激动剂,还抑制 p21-激活激酶1(PAK1) 和NF-κB,具有抗炎活性。 | |||
T3367 |
Macranthoidin B
灰毡毛忍冬皂苷乙,金银花,Macranthoiside I |
Others | Others |
Macranthoidin B 是一种活性天然皂苷。 | |||
T3742 |
3-Methylcatechol
3-甲基苯邻二酚,3-Methylpyrocatechol,2,3-Toluenediol,3-甲基邻苯二酚,2,3-dihydroxytoluene |
Others | Others |
3-Methylcatechol (2,3-Toluenediol) 是由 Pseudomonas putidaMC2 产生,能够用作化学合成中的分子砌块。 | |||
T20191 |
(-)-Camphoric acid
(-)-樟脑酸,L-Camphoric acid,Camphoric acid, (-)- |
GluR | Neuroscience |
(-)-Camphoric acid (L-Camphoric acid) 是一种活性较低的樟脑酸对映异构体,樟脑酸可诱导 GluR 表达。 | |||
T4082 |
Astragaloside
|
MMP; ERK; JNK | MAPK; Proteases/Proteasome |
Astragaloside 是黄芪中的主要活性成分之一。 | |||
T5556 |
5a-Pregnane-3,20-dione
|
Endogenous Metabolite | Metabolism |
5a-Pregnane-3,20-dione 是内源性的孕酮代谢物。 | |||
T3848 |
(Iso)-Isomucronulatol 7-O-glucoside
Isomucronulatol 7-O-glucoside,7,2'-dihydroxy-3',4'-dimethoxyisoflavane-7-O-glucoside,黄芪异黄烷苷,7,2′-Dihydroxy-3′,4′-dimethoxyisoflavan 7-O-β-D-glucoside |
Others | Others |
Isomucronulatol 7-O-glucoside 是一种具有生物活性的异黄酮,分离自黄芪中。 | |||
T3760 |
2'-Hydroxy-5'-methoxyacetophenone
2'-羟基-5'-甲氧基苯乙酮,5-Methoxy-2-hydroxyacetophenone |
Others | Others |
2'-Hydroxy-5'-methoxyacetophenone (5-Methoxy-2-hydroxyacetophenone) 是一种活性生化剂。 | |||
T8263 |
3,4'-Dihydroxyflavone
|
Influenza Virus | Microbiology/Virology |
3,4'-Dihydroxyflavone 是一种口服活性黄酮类化合物,具有抗甲型流感病毒的抗病毒活性。 | |||
T19554 |
L-Aspartic aicd sodium
L-Aspartic acid sodium,Sodium L-aspartate |
Others; Sodium Channel; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Others |
L-Aspartic aicd sodium (Sodium L-aspartate) 是一种氨基酸,是一种结肠特异性活性分子输送的前体活性分子,可促进大鼠前脑膜囊泡的 Na+外排。 | |||
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。 | |||
TN6736 |
Dihydrolanosterol
24,25-Dihydrolanosterol,Lanostenol,二氢羊毛甾醇 |
Others | Others |
Dihydrolanosterol 是一种 CYP51 的底物,能够阻碍胆固醇的合成。 | |||
TN1927 |
Methyl Kakuol
1-(6-methoxy-1,3-benzodioxol-5-yl)propan-1-one |
TRP/TRPV Channel | Membrane transporter/Ion channel |
Methyl Kakuol 是 TRPA1 的激动剂,EC50 为 0.27 µM,可用于作为 MBST 成分 Asiasari Radix 的活性成分的研究。 | |||
T4S1173 |
Agrimol B
仙鹤草酚B,仙鹤草酚 B |
Sirtuin; PPAR | Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism |
Agrimol B 是从仙鹤草中分离得到的一种多酚衍生物,可抑制脂肪形成,降低PPARγ的表达,诱导SIRT1易位和表达。 | |||
T19398 |
L-Octanoylcarnitine
|
Endogenous Metabolite | Metabolism |
L-Octanoylcarnitine 是存在于血浆中的活性辛酰肉碱,是一种乳腺癌的潜在生物标志物。 | |||
T6S1652 |
Benzoylpaeoniflorin
|
COX | Immunology/Inflammation; Neuroscience |
Benzoylpaeoniflorin 是一种从白芍中提取的天然化合物,可以降低细胞凋亡,对冠心病具有潜在的研究价值。 | |||
T3764 |
1-Triacontanol
Myricyl alcohol,1-Triacontanol,三十烷醇,Melissyl alcohol,Well-Bloom,Miraculan,Lithospermoside,triacontan-1-ol |
Others | Others |
1-Triacontanol (Melissyl alcohol) 是天然存在的植物生长调节剂。它是饱和长链醇,能够促进许多植物的生长。 | |||
T13669 |
(E)-Cinnamamide
trans-Cinnamamide,肉桂酰胺 |
Others | Others |
(E)-Cinnamamide (trans-Cinnamamide) 是 Cinnamamide 的活性较低的异构体,Cinnamamide 是一种有效的非致命化学驱虫剂,适用于减少鸟类害虫的损害。 | |||
T6S1884 |
Benzoylhypaconine
苯甲酰次乌头碱,Benzoylhypacoitine,苯甲酰次乌头原碱 |
Others | Others |
Benzoylhypaconine (Benzoylhypacoitine) 是来自 Aconitum 中的一种单酯生物碱,也是Aconitum 的主要药理和毒性成分。 | |||
TL0002 |
Liquiritin apioside
|
Others | Others |
Liquiritin apioside 是一种从甘草中获得的黄酮,具有镇咳活性。 | |||
T3S2197 |
Polygalic acid
Senegenic acid,远志皂甙 |
Others | Others |
Polygalic acid (Senegenic acid) 是一种三萜皂苷,是远志 (Polygala tenuifolia) 的一种主要活性成分。 | |||
T3014 |
(±)-Abscisic acid
Abscisic acid,Dormin,脱落酸,Abscisinsaeure |
Others | Others |
(±)-Abscisic acid 是一种口服具有活性的植物激素,也存在与动物中。它可以调节哺乳动物的血糖。 | |||
T3227 |
Danshensu
Salvianic acid A,Dan shen suan A,丹参素 |
Apoptosis; Nrf2; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation |
Danshensu (Dan shen suan A) 是丹参的有效成分,能够激活 Nrf2信号通路,具有保护心血管作用。 | |||
TMO2787 |
Anthraquinone
dioxoanthracene,Anthradione,anthracenedione,蒽醌 |
Virus Protease | Microbiology/Virology |
Anthraquinone (Anthradione) 是常用于缓解便秘的草药中的主要活性成分,可用作染料形成前体。 | |||
TQ0070 |
Luteolin-3-O-beta-D-glucuronide
|
Others | Others |
Luteolin-3-O-beta-D-glucuronide 是木犀草素葡萄糖醛酸,木犀草素的 3’ 端位置有 β-d-葡萄糖苷酸残基。 | |||
T4587 |
Mirificin
BCP10902,Puerarin Apioside,葛根素芹菜糖苷,芹糖葛根素苷 |
Tyrosinase | Proteases/Proteasome |
Mirificin (BCP10902) 是一种葛根中的异黄酮。它能够抑制酪氨酸酶(Tyrosinase),IC50=12.66 μM。 | |||
T6S0630 |
Hypaconitine
|
P450; TNF | Apoptosis; Metabolism |
Hypaconitine 是从乌头属种分离的一种高毒性成分,可研究风湿病。 | |||
T21495 |
Spinosyn A
|
Others | Others |
Spinosyn A 是聚酮化合物衍生的大环内酯,来自多刺甘蔗多孢菌。Spinosyn A 是有效的杀虫剂。 | |||
T4911 |
α-Arbutin
4-hydroxyphenyl-D-lucopyranoside,alpha-Arbutoside,α-熊果苷,alpha-Arbutin |
Tyrosinase | Proteases/Proteasome |
α-Arbutin (4-hydroxyphenyl-D-lucopyranoside) 是一种流行的、有效的皮肤增白剂,也是一种酪氨酸酶 (tyrosinase) 抑制剂。 | |||
TN1499 |
Cimiracemoside C
千层纸素A-7-0-Β-D-葡萄糖醛酸苷,Cimicifugoside M |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Cimiracemoside C (Cimicifugoside M) 是在升麻中发现的一种天然产物,可激活 AMPK 并具有抗糖尿病的潜在活性。 | |||
TQ0288 |
Hexahydrocurcumin
|
Reactive Oxygen Species; ROS; COX | Immunology/Inflammation; Metabolism; Neuroscience; NF-κB |
Hexahydrocurcumin 是一种选择性口服活性COX-2抑制剂,对 COX-1 无活性,是姜黄素的主要代谢产物之一,。它具有抗氧化,抗癌和抗炎作用。 | |||
T2S1181 |
Aloenin
Aloenin A,Aloearbonaside,芦荟宁 |
Beta-Secretase; AChR | Neuroscience |
Aloenin (Aloenin A) A 是一种具有清除过氧自由基作用的天然产物,对 β-分泌酶 (BACE) 具有中等抑制活性。 | |||
TN3176L |
(2R)-6-Methoxynaringenin
|
||
(2R)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one 是 黄芩中的潜在活性成分之一。 | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPK-00539 |
PLAU/uPA Protein (active form), Cynomolgus, Recombinant (His)
URK,ATF,UPA,u-PA,Urokinase,QPD,PLAU,BDPLT5 |
Cynomolgus | HEK293 Cells |
Plasminogen activator, urokinase (uPA) is a secreted serine protease whose Dysregulation is often accompanied by various cancers. PLAU inhibition could suppress tumor growth. Collectively, PLAU is necessary for tumor progression and can be a diagnostic and prognostic biomarker in HNSCC. PLAU/uPA Protein (active form), Cynomolgus, Recombinant (His) is expressed in HEK293 mammalian cells with C-His tag. The predicted molecular weight is 47.23 kDa and the accession number is A0A2K5WND1. | |||
TMPK-00274 |
PLAU/uPA Protein (active form), Human, Recombinant (His & Avi), Biotinylated
QPD,Urokinase,BDPLT5,UPA,ATF,URK,u-PA,PLAU |
Human | HEK293 Cells |
Plasminogen activator, urokinase (uPA) is a secreted serine protease whose Dysregulation is often accompanied by various cancers. PLAU inhibition could suppress tumor growth. Collectively, PLAU is necessary for tumor progression and can be a diagnostic and prognostic biomarker in HNSCC. PLAU/uPA Protein (active form), Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian cells with C-His-Avi tag. The predicted molecular weight is 49.3 kDa and the accession number is P0074... | |||
TMPK-00114 |
C-Reactive Protein /CRP Protein, Human, Recombinant (His)
C-reactive protein,MGC88244,PTX1MGC149895,CRP,pentr... |
Human | HEK293 Cells |
C-reactive protein (CRP) is a polypeptide molecule belonging to the family of pentraxins. CRP is synthesized primarily by the liver in response to certain pro-inflammatory cytokines. It plays an important role in innate immunity, opsonization by its properties, complement activation and immunoglobulins receptor binding. CRP is a protein of the acute systemic inflammation and is, therefore, a prime marker of inflammation.The CRP is quantified by immunonephelometry or immunoturbidimetry. C-Reactiv... | |||
TMPY-02047 |
C-Reactive Protein Protein, Rat, Recombinant (His)
C-reactive protein, pentraxin-related |
Rat | HEK293 Cells |
C-Reactive Protein Protein, Rat, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 24.6 kDa and the accession number is H6X2V1. | |||
TMPY-03363 |
C-Reactive Protein Protein, Human, Recombinant
C-Reactive Protein,C-reactive protein, pen... |
Human | HEK293 Cells |
C-Reactive Protein Protein, Human, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 23 kDa and the accession number is P02741-1. | |||
TMPY-05336 |
C-Reactive Protein Protein, Human, Recombinant, Biotinylated
C-Reactive Protein,PTX1,C-reactive protein... |
Human | HEK293 Cells |
C-Reactive Protein Protein, Human, Recombinant, Biotinylated is expressed in HEK293 mammalian cells. The predicted molecular weight is 23 kDa and the accession number is P02741-1. | |||
TMPY-05249 |
ITK Protein, Human, Recombinant (Actived By LCK, GST)
LYK,PSCTK2,LPFS1,IL2-inducible T-cell kinase,EMT |
Human | Baculovirus Insect Cells |
ITK Protein, Human, Recombinant (Actived By LCK, GST) is expressed in Baculovirus insect cells with GST tag. The predicted molecular weight is 57.7 kDa and the accession number is Q08881. | |||
TMPY-01581 |
C-Reactive Protein Protein, Mouse, Recombinant (His)
C-reactive protein, pentraxin-related,AI255847 |
Mouse | HEK293 Cells |
C-Reactive Protein Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 24.4 kDa and the accession number is P14847. | |||
TMPY-06937 |
C-Reactive Protein Protein, Human, Recombinant (His & Avi), Biotinylated
C-Reactive Protein,PTX1,C-reactive protein... |
Human | HEK293 Cells |
C-Reactive Protein Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian cells with His and Avi tag. The predicted molecular weight is 26.3 kDa and the accession number is P02741-1. | |||
TMPK-01333 |
C-Reactive Protein /CRP Protein, Cynomolgus, Recombinant (His)
C-reactive protein,pentraxin 1,PTX1,PTX1MGC149895,M... |
Cynomolgus | HEK293 Cells |
C-reactive protein (CRP) is a polypeptide molecule belonging to the family of pentraxins. CRP is synthesized primarily by the liver in response to certain pro-inflammatory cytokines. It plays an important role in innate immunity, opsonization by its properties, complement activation and immunoglobulins receptor binding. CRP is a protein of the acute systemic inflammation and is, therefore, a prime marker of inflammation.The CRP is quantified by immunonephelometry or immunoturbidimetry. C-Reactiv... | |||
TMPJ-00254 |
TGF beta 3 Protein, Human/Mouse/Rat, Recombinant
Latency-associated peptide,TGF-beta-3,Transforming growth fa... |
Human,Mouse,Rat | HEK293 Cells |
Transforming growth factor beta 3(TGFB3) is a member of a TGF -β superfamily which is defined by theirstructural and functional similarities. TGFB3 is secreted as a complex with LAP. This latent form of TGFB3becomes active upon cleavage by plasmin, matrix metalloproteases, thrombospondin -1, and a subset ofintegrins. It binds with high affinity to TGF- β RII, a type II serine/threonine kinase receptor. TGFB3 is involved incell differentiation, embryogenesis and development.It is believed to regu... | |||
TMPY-05717 |
Integrin alpha V beta 8 Protein, Human, Recombinant (His)
Integrin alpha V β8,Integrin α V β 8 |
Human | HEK293 Cells |
Integrin alpha V beta 8 is a receptor for fibronectin. It recognizes the sequence R-G-D in its ligands. ITGAVB8 does not appear to assume different activation states; and the cytoplasmic tail does not connect to the cytoskeleton. It binds ligands containing an RGD motif; including vitronectin; fibrin and the latency associated peptide (LAP) of the latent TGF-beta complex. High affinity binding of alpha V beta 8 to LAP allows proteolytic cleavage by MT1-MMP; which releases active TGF-beta. This m... | |||
TMPY-00672 |
Azurocidin/CAP37 Protein, Human, Recombinant (His)
AZU,NAZC,azurocidin 1,hHBP,AZAMP,HUMAZUR,CAP37,HBP,AZU1 |
Human | HEK293 Cells |
Azurocidin (AZU1), also known as heparin-binding protein (HBP) or cationic antimicrobial protein 37 (CAP37), is an azurophil granule antibiotic protein, with monocyte chemotactic and antibacterial activity. The Azurophil granules, specialized lysosomes of the neutrophil, contain at least 10 proteins implicated in the killing of microorganisms. Azurocidin is a member of the serine protease family that includes Cathepsin G, neutrophil elastase (NE), and proteinase 3 (PR3), however, Azurocidin is n... | |||
TMPY-02585 |
Acid sphingomyelinase/SMPD1 Protein, Mouse, Recombinant (His)
aSMase,ASM,Zn-SMase,A-SMase,sphingomyelin phosphodiesterase ... |
Mouse | Baculovirus Insect Cells |
Sphingomyelin phosphodiesterase 1 (SMPD1) , also known as ASM ( acid sphingomyelinase ), is a member of the acid sphingomyelinase family of enzymes. Three isoforms have been identified, isoform 1 is 631 amino acids (aa) in length as the pro form, while Isoform 2 and isoform 3 have lost catalytic activity. The active SMPD1 isoform 1 contains one saposin B-type domain that likely interacts with sphingomyelin, and a catalytic region. Human SMPD1 is 86% aa identical to mouse SMPD1. SMPD1 is a monome... | |||
TMPJ-00137 |
APRIL/TNFSF13 Protein, Human, Recombinant (Flag & His)
TRDL-1,TNF- and APOL-related leukocyte expressed ligand 2,Tu... |
Human | HEK293 Cells |
APRIL (a proliferation-inducing ligand), also known as TNFSF13, TALL2, TRDL1, and CD256, is a member of the TNF ligand superfamily. It is synthesized as a 32 kDa proprotein which is cleaved by furin in the Golgi to release the active 17 kDa soluble molecule. Secreted human APRIL, which consists almost entirely of a single TNF homology domain, shares 85% amino acid sequence identity with mouse and rat APRIL. Both APRIL and its close relative BAFF bind and signal through the TNF superfamily recept... | |||
TMPY-02185 |
Coagulation factor XIII B/F13B Protein, Human, Recombinant (His)
Coagulation factor 13,coagulation factor XIII, B polypeptide... |
Human | HEK293 Cells |
Coagulation factor XIII B chain, also known as Fibrin-stabilizing factor B subunit, Protein-glutamine gamma-glutamyltransferase B chain, Transglutaminase B chain and F13B, is a secreted protein which contains 1 Sushi ( CCP / SCR ) domains. Coagulation factor XIII is the last zymogen to become activated in the blood coagulation cascade. Plasma factor XIII is a heterotetramer composed of 2 A subunits and 2 B subunits. The A subunits have catalytic function, and the B subunits do not have en... | |||
TMPY-01104 |
Coagulation factor XI/F11 Protein, Human, Recombinant (His)
coagulation factor 11,coagulation factor XI,FXI |
Human | HEK293 Cells |
Factor XI (plasma thromboplastin antecedent) is a plasma glycoprotein, and a zymogen acting as a serine protease which participates in blood coagulation as a catalyst in the conversion of factor IX to factor IXa in the presence of calcium ions. It is an unusual dimeric protease, with structural features that distinguish it from vitamin K-dependent coagulation proteases. The factor XI is synthesized in the liver as a single polypeptide chain with a molecular weight estimated between 125 ~160 kDa ... | |||
TMPJ-00897 |
TPSB2 Protein, Mouse, Recombinant (His)
Tryptase-2,Mast cell protease 6,Tryptase beta-2,Tryptase β-2... |
Mouse | HEK293 Cells |
Tryptase beta-2(Tpsb2), also known as Mast cell protease 6(mMCP-6), belongs to the peptidase S1 family and Tryptase subfamily. Tryptase is the major neutral protease present in mast cells and is secreted upon the coupled activation-degranulation response of this cell type. It plays a role in innate immunity. Tpsb2 can be detected primarily in skin during embryogenesis. Tpsb2 can not be detected at early embryonic stages but is abundantly expressed in later stages with a peak at E17.5-E18.5. Tryp... | |||
TMPH-03429 |
DOG1 Protein, S. cerevisiae, Recombinant (His)
DOG1,2-DOG-6-P 1,2-deoxyglucose-6-phosphatase 1,2-deoxygluco... |
Saccharomyces cerevisiae | P. pastoris (Yeast) |
Active on 2-DOG-6P, also very active on fructose-1P. DOG1 Protein, S. cerevisiae, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 29.1 kDa and the accession number is P38774. | |||
TMPH-01629 |
LOXL1 Protein, Human, Recombinant (His)
Lysyl oxidase-like protein 1,LOXL1,Lysyl oxidase homolog 1 |
Human | E. coli |
Active on elastin and collagen substrates. | |||
TMPH-02825 |
ACOX1 Protein, Mouse, Recombinant (Myc)
AOX,Peroxisomal fatty acyl-CoA oxidase,EC:1.3.3.6,Peroxisoma... |
Mouse | E. coli |
Catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. First enzyme of the fatty acid beta-oxidation pathway.; Shows highest activity against medium-chain fatty acyl-CoAs and activity decreases with increasing chain length.; Is active against a much broader range of substrates and shows activity towards very long-chain acyl-CoAs. Is twice as active as isoform 1 against 16-hydroxy-palmitoyl-CoA and is 25% more active against 1,16-hexadecanodioyl-CoA. | |||
TMPH-02474 |
HAOX1 Protein, Mouse, Recombinant (His)
Hao1,Glyoxylate oxidase,Glycolate oxidase,2-Hydroxyacid oxid... |
Mouse | E. coli |
Has 2-hydroxyacid oxidase activity. Most active on the 2-carbon substrate glycolate, but is also active on 2-hydroxy fatty acids, with high activity towards 2-hydroxy palmitate and 2-hydroxy octanoate. HAOX1 Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 45.0 kDa and the accession number is Q9WU19. | |||
TMPH-00660 |
NikR Protein, E. coli, Recombinant (His)
nikR,Nickel-responsive regulator |
E. coli | E. coli |
Transcriptional repressor of the nikABCDE operon. Is active in the presence of excessive concentrations of intracellular nickel. | |||
TMPH-01628 |
LOXL1 Protein, Human, Recombinant
Lysyl oxidase-like protein 1,Lysyl oxidase homolog 1,LOXL1 |
Human | E. coli |
Active on elastin and collagen substrates. LOXL1 Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 53.0 kDa and the accession number is Q08397. | |||
TMPH-00655 |
McjB Protein, E. coli, Recombinant (His & Myc)
Microcin J25-processing protein McjB,mcjB |
E. coli | E. coli |
Along with McjC, necessary and sufficient to process the inactive microcin J25 (McjA) precursor into the active peptide. | |||
TMPK-01092 |
OSCAR Protein, Human, Recombinant (hFc)
Poly-Ig receptor 3,PIGR3,OSCAR,PIgR-3,MGC33613,mOSCAR |
Human | HEK293 Cells |
Osteoclast-associated receptor (OSCAR) is a co-stimulatory receptor in osteoclastogenesis. Synovial tissues from active rheumatoid arthritis (RA) patients express higher levels of OSCAR compared with osteoarthritic and normal patients. OSCAR and tartrate-resistant acid phosphatase (TRAP) expression levels did not differ between the cartilage pannus junction (CPJ) and non-CPJ regions in active RA. OSCAR Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with C-hFc tag. The p... | |||
TMPK-01117 |
OSCAR Protein, Mouse, Recombinant (hFc)
PIgR-3,Poly-Ig receptor 3,OSCAR,MGC33613,mOSCAR,PIGR3 |
Mouse | HEK293 Cells |
Osteoclast-associated receptor (OSCAR) is a co-stimulatory receptor in osteoclastogenesis. Synovial tissues from active rheumatoid arthritis (RA) patients express higher levels of OSCAR compared with osteoarthritic and normal patients. OSCAR and tartrate-resistant acid phosphatase (TRAP) expression levels did not differ between the cartilage pannus junction (CPJ) and non-CPJ regions in active RA. OSCAR Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with C-hFc tag. The p... | |||
TMPJ-00542 |
TPSB2 Protein, Human, Recombinant (His)
Tryptase-2,Tryptase Beta-2,TPS2,TPSB2,Tryptase II,Tryptase β... |
Human | HEK293 Cells |
Tryptases are Trypsin-like Serine Proteases. β-Tryptases are the main isoenzymes in mast cells. Βtryptases form active tetramers with heparin proteoglycan. In the tetramer, the unique arrangement of the active sites facing a narrow central pore, β-Tryptases are resistant to macromolecule protease inhibitors . When mast cells are activated, β-Tryptases are released and participate in provoking inflammatory conditions . β-Tryptases have been implicated as mediators in the pathogenesis of asthma an... | |||
TMPJ-01326 |
HDHD2 Protein, Human, Recombinant (His)
HDHD2,Haloacid Dehalogenase-Like Hydrolase Domain-Containing... |
Human | E. coli |
Haloacid Dehalogenase-Like Hydrolase Domain-Containing Protein 22 (HDHD2) is a member of the HAD-like hydrolase superfamily. HDHD2 includes L-2-Haloacid Dehalogenase, Epoxide Hydrolases and Phosphatases. There are two active sites in HDHD2 - an L-2-Haloacid Dehalogenase and a Carboxylate group. The L-2-Haloacid Dehalogenase active site catalyzes the hydrolytic dehalogenation of D- and L-2-Haloalkanoic Acids, producing L- and D-2-Hydroxyalkanoic Acids. | |||
TMPY-02522 |
OTUB2 Protein, Human, Recombinant (His)
OTU deubiquitinase, ubiquitin aldehyde binding 2,OTU2,OTB2,C... |
Human | E. coli |
Otubain 2 (OTUB2) is a member of DUBs that belong to the ovarian tumour (OTU) superfamily of proteins which consists of a five-stranded β-sheet sandwiched in between a small helical amino-terminal region consisting of α1 and α2, and a large helical region comprised of α3-α10. Like other DUBs, otubain 2 (OTUB2) cleaves proteins precisely at the ubiquitin-protein bond so that ubiquitylation process can be reversed and regulated. Otubain 2 (OTUB2)'s active-site cleft is sterically occluded by a nov... | |||
TMPH-00596 |
Colicin-E1 Protein, E. coli, Recombinant (Cell-Free, His & Myc)
Colicin-E1,cea |
E. coli | E. coli |
This colicin is a channel-forming colicin. This class of transmembrane toxins depolarize the cytoplasmic membrane, leading to dissipation of cellular energy.; Colicins are polypeptide toxins produced by and active against E.coli and closely related bacteria. | |||
TMPH-00597 |
Colicin-E1 Protein, E. coli, Recombinant (His & Myc)
cea,Colicin-E1 |
E. coli | E. coli |
This colicin is a channel-forming colicin. This class of transmembrane toxins depolarize the cytoplasmic membrane, leading to dissipation of cellular energy.; Colicins are polypeptide toxins produced by and active against E.coli and closely related bacteria. | |||
TMPH-00229 |
Cathelicidin-4 Protein, Bovine, Recombinant (His & SUMO)
Cathelicidin-4,Indolicidin,CATHL4 |
Bovine | E. coli |
Potent microbicidal activity; active against S.aureus and E.coli. Cathelicidin-4 Protein, Bovine, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 17.9 kDa and the accession number is P33046. | |||
TMPH-01736 |
PGLYRP2 Protein, Human, Recombinant (His)
PGLYRP2,Peptidoglycan recognition protein long,Peptidoglycan... |
Human | P. pastoris (Yeast) |
May play a scavenger role by digesting biologically active peptidoglycan (PGN) into biologically inactive fragments. Has no direct bacteriolytic activity. PGLYRP2 Protein, Human, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 62.0 kDa and the accession number is Q96PD5. | |||
TMPH-01737 |
PGLYRP2 Protein, Human, Recombinant (His & SUMO)
N-acetylmuramoyl-L-alanine amidase,Peptidoglycan recognition... |
Human | E. coli |
May play a scavenger role by digesting biologically active peptidoglycan (PGN) into biologically inactive fragments. Has no direct bacteriolytic activity. PGLYRP2 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 76.0 kDa and the accession number is Q96PD5. | |||
TMPK-00478 |
Carbonic Anhydrase 12 Protein, Cynomolgus, Recombinant (His)
CA12,CAXII,Carbonic anhydrase,CA-XII,Tumor antigen HOM-RCC-3... |
Cynomolgus | HEK293 Cells |
Carbonic anhydrases (CAs) are a family of enzymes involved in the pH regulation of metabolically active cells/tissues. Carbonic anhydrase XII (CA XII) is a key mediator of several signaling pathways that are involved in cancer development. | |||
TMPH-00598 |
Colicin-E5 Protein, E. coli, Recombinant (His & SUMO)
Colicin-E5,col |
E. coli | E. coli |
Colicins are polypeptide toxins produced by and active against E.coli and closely related bacteria. This colicin is an endonuclease. Colicin-E5 Protein, E. coli, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 24.8 kDa and the accession number is P18000. | |||
TMPH-03475 |
MglB Protein, Salmonella typhimurium, Recombinant (His)
D-galactose/D-glucose-binding protein,D-galactose-binding pe... |
Salmonella typhimurium | P. pastoris (Yeast) |
This protein is involved in the active transport of galactose and glucose. It plays a role in the chemotaxis towards the two sugars by interacting with the trg chemoreceptor. MglB Protein, Salmonella typhimurium, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 35.4 kDa and the accession number is P23905. | |||
TMPH-00739 |
Thioredoxin-1 Protein, E. coli, Recombinant (His)
Thioredoxin 1,trxA |
E. coli | E. coli |
Participates in various redox reactions through the reversible oxidation of its active center dithiol to a disulfide and catalyzes dithiol-disulfide exchange reactions. Thioredoxin-1 Protein, E. coli, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 15.7 kDa and the accession number is P0AA25. | |||
TMPY-00821 |
HGFA Protein (pro form), Human, Recombinant (His)
MGC138397,HGFA,RP11-529E1.2,肝细胞生长因子,MGC138395 |
Human | HEK293 Cells |
HGF activator (HGFA) is a serum-derived serine protease and belongs to the peptidase family S1.HGFA is responsible for the conversion of hepatocyte growth factor (HGF), from the inactive single-chain precursor to the active heterodimeric form, which is a potent mitogen, motogen, and morphogen for liver cells, epithelial cells, and endothelial cells. HGFA is synthesized and secreted by the liver and circulates in the plasma as an inactive single-chain zymogen in normal states. The zymogen is clea... | |||
TMPY-01580 |
PRSS2 Protein, Mouse, Recombinant (His)
Tesp4,protease, serine 2,Try2,Ta,TRY8,TRYP,Prss2 |
Mouse | HEK293 Cells |
Trypsin-2, also known as Trypsin II, Anionic trypsinogen, Serine protease 2, PRSS2 and TRY2, is a secreted protein that belongs to the trypsin serine protease family including Trypsin, PRSS1, PRSS2 and PRSS3. It consists of a signal peptide (residues 1-15), a pro region (residues 16-23), and a proteolytically active mature chain (residues 24-247). PRSS2 contains one peptidase S1 domain. It is secreted into the duodenum, hydrolysing peptides into their smaller building blocks, which is necessary ... | |||
TMPH-03261 |
Cathepsin D Protein, Rat, Recombinant (His & Myc)
Ctsd,Cathepsin D |
Rat | E. coli |
Acid protease active in intracellular protein breakdown. Plays a role in APP processing following cleavage and activation by ADAM30 which leads to APP degradation. Cathepsin D Protein, Rat, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 45.2 kDa and the accession number is P24268. | |||
TMPH-01240 |
MCM2 Protein, Human, Recombinant (His)
DNA replication licensing factor MCM2,Nuclear protein BM28,M... |
Human | E. coli |
Acts as component of the MCM2-7 complex (MCM complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the MCM2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active ... | |||
TMPH-02254 |
Trypsin-1 Protein, Human, Recombinant (His & Myc)
Trypsin-1,PRSS1,Serine protease 1,Beta-trypsin,Trypsin I,Ani... |
Human | E. coli |
Has activity against the synthetic substrates Boc-Phe-Ser-Arg-Mec, Boc-Leu-Thr-Arg-Mec, Boc-Gln-Ala-Arg-Mec and Boc-Val-Pro-Arg-Mec. The single-chain form is more active than the two-chain form against all of these substrates. | |||
TMPH-00516 |
StxA2 Protein, Enterobacteria phage 933W, Recombinant (E189K, His & Myc)
Verotoxin 2 subunit A,Verocytotoxin 2 subunit A,Shiga-like t... |
Enterobacteria phage 933W | E. coli |
The A subunit is responsible for inhibiting protein synthesis through the catalytic inactivation of 60S ribosomal subunits. After endocytosis, the A subunit is cleaved by furin in two fragments, A1 and A2: A1 is the catalytically active fragment, and A2 is essential for holotoxin assembly with the B subunits. | |||
TMPH-02408 |
SPI Protein, Lentinula edodes, Recombinant (His)
Serine protease inhibitor |
Lentinula edodes | E. coli |
Serine protease inhibitor. Active against beta-trypsin and alpha-chymotrypsin with dissociation constants of 0.35 nM and 40 nM respectively. Inhibits factor XIa, but not other enzymes involved in coagulation and fibrinolysis. Does not inhibit subtilisin, lysyl endopeptidase, arginyl endopeptidase or papain. | |||
TMPH-02195 |
TXNDC17 Protein, Human, Recombinant (GST)
Thioredoxin-like protein 5,Protein 42-9-9,Thioredoxin domain... |
Human | E. coli |
Disulfide reductase. May participate in various redox reactions through the reversible oxidation of its active center dithiol to a disulfide and catalyze dithiol-disulfide exchange reactions. Modulates TNF-alpha signaling and NF-kappa-B activation. Has peroxidase activity and may contribute to the elimination of cellular hydrogen peroxide. | |||
TMPH-01246 |
POLR3A Protein, Human, Recombinant (His)
RNA polymerase III subunit C160,RNA polymerase III 155 kDa s... |
Human | E. coli |
DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates. Largest and catalytic core component of RNA polymerase III which synthesizes small RNAs, such as 5S rRNA and tRNAs. Forms the polymerase active center together with the second largest subunit. A single-stranded DNA template strand of the promoter is positioned within the central active site cleft of Pol III. A bridging helix emanates from RPC1 and crosses the cleft ... | |||
TMPH-00181 |
Cry1Ia Protein, Bacillus thuringiensis subsp., Recombinant (His & KSI)
cryV1,cry1Ia,cryV,81 kDa crystal protein,Insecticidal delta-... |
Bacillus thuringiensis subsp. Kurstaki | E. coli |
Promotes colloidosmotic lysis by binding to the midgut epithelial cells of certain coleopteran and lepidopteran species. Active on Plutella xylostella and Bombyx mori. Cry1Ia Protein, Bacillus thuringiensis subsp., Recombinant (His & KSI) is expressed in E. coli expression system with N-6xHis-KSI tag. The predicted molecular weight is 24.9 kDa and the accession number is Q45752. | |||
TMPH-00361 |
Beta-mammal toxin Cn2 Protein, Centruroides noxius, Recombinant (His)
Toxin 2,Beta-mammal toxin Cn2,Toxin II.9.2.2 |
Centruroides noxius | P. pastoris (Yeast) |
Mammal beta-toxins bind voltage-independently at site-4 of sodium channels (Nav) and shift the activation voltage to more negative potentials. This toxin is active against mammals. Beta-mammal toxin Cn2 Protein, Centruroides noxius, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 9.6 kDa and the accession number is P01495. | |||
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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIH-0519 |
Selexipag Active Metabolite-d7
|
||
Selexipag Active Metabolite-d7 是 Selexipag Active Metabolite 的氘代化合物。Selexipag Active Metabolite 的 CAS 号为 475085-57-5。MRE269 是一种口服的长效前列环素受体激动剂前药,是 Selexipag 的活性代谢物,用于治疗肺动脉高压。 | |||
TMIH-0315 |
Lurasidone Inactive Metabolite 14283-d8
5α/6α-Hydroxy Lurasidone-d8 Hydrochloride (Mixture of Diastereomers) |
||
Lurasidone Inactive Metabolite 14283-d8 是 Lurasidone Inactive Metabolite 14283 的氘代化合物。Lurasidone Inactive Metabolite 14283 的 CAS 号为 186204-31-9。 | |||
TMIH-0316 |
Lurasidone Inactive Metabolite 14326-d8
5β/6β-Hydroxy Lurasidone-d8 Hydrochloride (Mixture of Diastereomers) |
||
Lurasidone Inactive Metabolite 14326-d8 是 Lurasidone Inactive Metabolite 14326 的氘代化合物。Lurasidone Inactive Metabolite 14326 的 CAS 号为 186204-33-1。 | |||
T60016 |
VV116
GS-621763-d1,JT001 |
SARS-CoV; RSV | Microbiology/Virology |
VV116 (JT001) 是一种针对呼吸道合胞病毒和 SARS-CoV-2 感染的选择性和口服活性核苷抗病毒剂。 | |||
T24046 |
WNK-IN-11-d3
WNK inhibitor-12,WNKIN12,WNK IN 12,WNK inhibitor 12,WNK-IN-12 |
||
WNK-IN-12 is an effective, selective, and orally active WNK1 kinase inhibitor. | |||
T19305 |
Eldecalcitol-d6
|
Others | Others |
Eldecalcitol is an orally active analogue of active vitamin D used in the treatment of osteoporosis. Eldecalcitol-d6 is the deuterium labeled Eldecalcitol. | |||
T10663 |
Calcitriol-d6
Calcitriol D6,骨化三醇 D6 |
Others | Others |
Calcitriol D6 is the deuterated form of Calcitriol, which is the hormonally active form of vitamin D. Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor. | |||
T12329 |
Ospemifene D4
FC-1271a D4 |
Estrogen/progestogen Receptor | Endocrinology/Hormones |
Ospemifene D4 is a deuterium labeled Ospemifene. Ospemifene is a selective and orally active modulator of estrogen receptor. | |||
T11817 |
Lansoprazole Sulfide D4
|
Proton pump | Membrane transporter/Ion channel |
Lansoprazole Sulfide D4 is a deuterium labeled Lansoprazole Sulfide. Lansoprazole Sulfide is an orally active anti-TB (Mycobacterium tuberculosis) agent with IC50 values of 0.59 μM intracellularly and 0.46 μM in broth.Lansoprazole Sulfide is an active metabolite of the proton pump inhibitor Lansoprazole. | |||
T13181 |
Tolcapone D7
Ro 40-7592 D7 |
Transferase | Metabolism |
Tolcapone D7 is a deuterium-labeled Tolcapone. Tolcapone is a selective and orally active inhibitor of COMT. | |||
T12638 |
(R)-Praziquantel-d11
(R)-吡喹酮 D11,(R)-Praziquantel D11 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
(R)-Praziquantel D11 is the deuterium labeled (R)-Praziquantel. (R)-Praziquantel is the active enantiomer of Praziquantel, is a partial the human 5-HT2B receptor agonist | |||
T12144 |
N-Desethyl Oxybutynin-d5 hydrochloride
N-Desethyl Oxybutynin D5 hydrochloride |
Others | Others |
N-Desethyl Oxybutynin D5 hydrochloride is the the active metabolite Oxybutynin, is deuterium labeled N-Desethyl Oxybutynin hydrochloride. | |||
T19489 |
O-Desmethyl gefitinib D8
|
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
O-Desmethyl gefitinib D8 is a deuterium labeled O-Desmethyl gefitinib that is an active metabolite of Gefitinib in human plasma. | |||
TMIJ-0229 |
Mesalamine-d3
|
||
Mesalamine-d3 是 Mesalamine 的氘代化合物。Mesalamine 的 CAS 号为 89-57-6。5-Aminosalicylic Acid 是一种特异性的PPARγ激动剂,还抑制 p21-激活激酶1 (PAK1) 和NF-κB,具有抗炎活性。 | |||
T12355 |
Palbociclib-d8
PD 0332991 D8,Palbociclib D8 |
CDK | Cell Cycle/Checkpoint |
Palbociclib D8 is a deuterium labeled Palbociclib. Palbociclib is a selective and orally active inhibitor of CDK4 and CDK6 (IC50s of 11 and 16 nM, respectively). | |||
T13137 |
TGFβRI-IN-1
|
TGF-beta/Smad | Stem Cells |
TGFβRI-IN-1 is an oral active and selective inhibitor of TGFβ receptor type I (TGFβRI) kinase(IC50 values of 2 nM and 7.6 μM for TGFβRI and TGFβRII, respectively ). | |||
T10282 |
Aliskiren D6 Hydrochloride
SPP 100 D6 Hydrochloride,CGP60536B D6 Hydrochloride,CGP 60536 D6 Hydrochloride |
Others | Others |
Aliskiren (CGP 60536) D6 Hydrochloride is a deuterium-labeled Aliskiren. Aliskiren hemifumarate is a direct and orally active renin inhibitor (IC50: 1.5 nM). | |||
T12210 |
Netupitant D6
CID-6451149 D6 |
Others | Others |
Netupitant D6 is the deuterium labeled Netupitant, which is a selective and orally active antagonist of neurokinin-1 receptor. | |||
T13195 |
Trandolapril D5
RU44570 D5 |
Others | Others |
Trandolapril D5 is a deuterium labeled Trandolapril. Trandolapril is an orally active inhibitor of angiotensin converting enzyme (ACE) for hypertension and congestive heart failure (CHF). | |||
T19187 |
Aliskiren D6 hemifumarate
CGP 60536 D6 hemifumarate,SPP 100 D6 hemifumarate,CGP60536B D6 hemifumarate |
RAAS | Endocrinology/Hormones |
Aliskiren (CGP 60536) D6 hemifumarate is a deuterium-labeled Aliskiren hemifumarate. Aliskiren hemifumarate is a direct and orally active renin inhibitor (IC50: 1.5 nM). | |||
T19273 |
Debutyldronedarone D7
SR-35021 D7 |
Others | Others |
Debutyldronedarone D7 is deuterium-labeled Debutyldronedarone, which is the main circulating active metabolite of dronedarone in the body. | |||
TMID-0301 |
Vitamin-d4-d3
|
||
Vitamin-d4-d3 是 Vitamin 的氘代化合物。Vitamin 的 CAS 号为 511-28-4。 | |||
T11585 |
Hydroxy Itraconazole D8
R-63373 D8 |
Others | Others |
Hydroxy Itraconazole D8 is the deuterium-labeled Hydroxy Itraconazole. Hydroxy Itraconazole is an active metabolite of Itraconazole, which is a triazole antifungal agent. | |||
TMIJ-0093 |
Keto Pioglitazone-d4
|
||
Keto Pioglitazone-d4 是 Keto Pioglitazone 的氘代化合物。Keto Pioglitazone 的 CAS 号为 146062-45-5。 | |||
T31813 |
Fludalanine
MK641,D-Alanine-2-d, 3-fluoro-,3-Fluoro-D-(2-2H)alanine |
||
Fludalanine (MK641), an analogue of D-alanine, irreversiably inactivates racemase and also inhibits synthase. When used in combination with cycloserine, it has been found to be more active against a variety of non-mycobacterium organisms than fludalanine | |||
T71984 |
Enrofloxacin-d5
|
||
Enrofloxacin-d5 is intended for use as an internal standard for the quantification of enrofloxacin by GC- or LC-MS. Enrofloxacin is a fluoroquinolone antibiotic. It is active against panels of Campylobacter, E. coli, and Salmonella isolates (mean MIC50s = 0.06, 0.5, and 0.03 µg/ml, respectively). It is also active against equine isolates of L. intracellularis (MICs = 0.125-0.5 µg/ml). Enrofloxacin inhibits bacterial DNA gyrase. In vivo, enrofloxacin (10 mg/kg) increases survival in a mouse model... | |||
TMID-0300 |
Vitamin-d4-d5
|
||
Vitamin-d4-d5 是 Vitamin 的氘代化合物。Vitamin 的 CAS 号为 511-28-4。 | |||
T10144 |
4-Hydroxyatomoxetine D3
|
Others | Others |
4-Hydroxyatomoxetine D3 is a deuterium labeled 4-Hydroxyatomoxetine. 4-Hydroxyatomoxetine is an active metabolite of Atomoxetine. 4-Hydroxyatomoxetine is metabolized by CYP2D6. Atomoxetine is a noradrenaline reuptake inhibitor. | |||
T10149 |
4-Hydroxypropranolol-d7 hydrochloride
(±)-4-hydroxy Propranolol D7 hydrochloride,4-Hydroxypropranolol D7 hydrochloride |
Others | Others |
4-Hydroxypropranolol D7 hydrochloride is deuterium-labeled 4-Hydroxypropranolol hydrochloride. 4-Hydroxypropranolol hydrochloride is an active metabolite of Propranolol, with a potency comparable to Propranolol. It inhibits β1- and β2-adrenergic receptors | |||
T12955 |
Sofosbuvir D6
PSI-7977 D6,GS-7977 D6 |
Others | Others |
Sofosbuvir D6 is the deuterium labeled Sofosbuvir. Sofosbuvir is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity. | |||
TMID-0271 |
Miloxacin-d3
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Miloxacin-d3 是 Miloxacin 的氘代化合物。Miloxacin 的 CAS 号为 37065-29-5。 | |||
T10351 |
Aprocitentan D4
ACT-132577 D4 |
Others | Others |
Aprocitentan D4 (ACT-132577 D4) is a deuterium-labeled Aprocitentan. Aprocitentan is a major and pharmacologically active metabolite of Macitentan. Aprocitentan is a dual ETA/ETB antagonist (IC50s: 3.4 nM and 987 nM; pA2s: 6.7 and 5.5). | |||
TMIH-0295 |
LBQ657-d4
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LBQ657-d4 是 LBQ657 的氘代化合物。LBQ657 的 CAS 号为 149709-44-4。Sacubitrilat 是活性的脑啡肽酶 (NEP) 抑制剂。 | |||
TMIJ-0174 |
Eszopiclone-d8
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Eszopiclone-d8 是 Eszopiclone 的氘代化合物。Eszopiclone 的 CAS 号为 138729-47-2。 | |||
T11088 |
Doxepin D3 Hydrochloride
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Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Doxepin D3 Hydrochloride is a deuterium-labeled doxepin hydrochloride.Doxepin hydrochloride is an oral active tricyclic antidepressant used as a sedative.Doxepin hydrochloride is also an effective CYP450 inhibitor, significantly inhibiting CYP450 2C19 and | |||
T36021 |
Flumequine-13C3
Flumequine-13C3 |
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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... | |||
TMIJ-0141 |
(S)-Amlodipine-d4
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(S)-Amlodipine-d4 是 (S)-Amlodipine 的氘代化合物。(S)-Amlodipine 的 CAS 号为 103129-82-4。Levamlodipine 是一种二氢吡啶钙通道阻滞剂,具有舒张血管的作用,可用于高血压和心绞痛的研究。 | |||
T12521 |
Ponatinib-d8
AP24534 D8 |
Others | Others |
Ponatinib D8 is a deuterium labeled Ponatinib. Ponatinib is an orally active inhibitor of multi-targeted kinase(Abl, PDGFRα, VEGFR2, FGFR1, and Src with IC50s of 0.37 nM, 1.1 nM, 1.5 nM, 2.2 nM, and 5.4 nM, respectively). | |||
T11246 |
Etoricoxib-d4
MK-0663 D4,依托考昔 D4,L-791456 D4,Etoricoxib D4 |
Others | Others |
Etoricoxib D4 is a non steroidal anti-inflammatory agent, acting as a selective and orally active COX-2 inhibitor, with IC50s of 1.1 μM and 116 μM for COX-2 and COX-1 in human whole blood.Etoricoxib D4 is a deuterium labeled Etoricoxib. | |||
TMID-0079 |
Norfloxacin-d8
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Norfloxacin-d8 是 Norfloxacin 的氘代化合物。Norfloxacin 的 CAS 号为 70458-96-7。Norfloxacin是广谱抗生素,能通过结合DNA旋转酶抑制革兰氏阳性和阴性菌。 | |||
T11197 |
Enclomiphene D4 hydrochloride
(E)-Clomiphene D4 hydrochloride,Enclomifene D4 hydrochloride,trans-Clomiphene D4 hydrochloride |
Others | Others |
Enclomiphene D4 hydrochloride ((E)-Clomiphene D4 hydrochloride; trans-Clomiphene D4 hydrochloride; Enclomifene D4 hydrochloride) is a potent and orally active oestrogen receptor antagonist, with antioestrogenic property.Enclomiphene D4 hydrochloride ((E)-Clomiphene D4 hydrochloride; trans-Clomiphene D4 hydrochloride; Enclomifene D4 hydrochloride) is a deuterium labeled Enclomiphene. | |||
TMIJ-0230 |
Oseltamivir EP Impurity C-d3 HCl
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Oseltamivir EP Impurity C-d3 HCl 是 Oseltamivir EP Impurity C HCl 的氘代化合物。Oseltamivir EP Impurity C HCl 的 CAS 号为 1415963-60-8。 | |||
TMID-0217 |
Norfluoxetine-d5 Hydrochloride
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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。 | |||
TMIH-0154 |
Ciprofloxacin-d8
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Ciprofloxacin-d8 是 Ciprofloxacin 的氘代化合物。Ciprofloxacin 的 CAS 号为 85721-33-1。Ciprofloxacin是一种有高抗菌活性的氟喹诺酮类抗生素。 | |||
TMIJ-0252 |
Benazeprilat-d5
Benazepril EP Impurity C-d5 |
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Benazeprilat-d5 是 Benazeprilat 的氘代化合物。Benazeprilat 的 CAS 号为 86541-78-8。Benazeprilat(CGS 14831) 是一种具有口服活性的贝那普利活性代谢物。Benazeprilat 具有高效的抗血压活性,可与其他其他类别的化合物(包括噻嗪类利尿剂和钙通道阻滞剂)联合使用来减少与心血管风险和继发性终末器官损伤相关的疾病的发生。Benazeprilat 可能用于研究急性左心室衰竭。 | |||
TMIH-0394 |
Nirmatrelvir-d9
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Nirmatrelvir-d9 是 Nirmatrelvir 的氘代化合物。Nirmatrelvir 的 CAS 号为 2628280-40-8。PF-07321332 是一种有效的口服活性SARS-CoV 3CLPRO抑制剂,对 SARS-CoV-2 病毒有针对性,可研究 COVID-19。它是一种胰蛋白酶样蛋白酶抑制剂,可抑制气道上皮钠通道功能。 | |||
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-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。 | |||
TMIJ-0271 |
N-Desethyl Amodiaquine-d5 DiHCl
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N-Desethyl Amodiaquine-d5 DiHCl 是 N-Desethyl Amodiaquine DiHCl 的氘代化合物。N-Desethyl Amodiaquine DiHCl 的 CAS 号为 79352-78-6。N-Desethyl amodiaquine 是一种抗寄生虫剂,是主要的生物活性阿莫地喹代谢物。它对菌株 V1/S 和 3D7 的 IC50值分别为 97 nM 和 25 nM。 | |||
TMID-0302 |
Vitamin K3-d3
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Vitamin K3-d3 是 Vitamin K3 的氘代化合物。Vitamin K3 的 CAS 号为 58-27-5。Menadione是合成的萘醌,能够在体内转化成活性维生素K2。 | |||
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