Metabolism
Metabolism(代谢)
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Metabolism 相关产品(3072)
- GC11610PemetrexedCAS: 150399-23-8纯度: >99.50% / >98.00% / >99.00%
An antifolate with anticancer activity
- GC11638SulfaphenazoleCAS: 526-08-9纯度: >99.50% / >98.00% / >98.50%
Sulfaphenazole是一种磺胺类抗菌药物。它竞争性地抑制细菌二氢叶酸合酶,阻断细菌叶酸合成,从而抑制细菌生长和繁殖。
- GC1172017-AAG (KOS953)CAS: 75747-14-7纯度: >99.00% / >98.00%
17-AAG(格尔德霉素)是一种天然的苯醌安沙霉素抗生素,是第一个确定的 Hsp90 抑制剂。
- GC11806β-Glycerophosphate (sodium salt hydrate)CAS: 13408-09-8纯度: >98.00%
An inhibitor of alkaline phosphatase
- GC118704-Methylumbelliferyl-β-D-GlucopyranosideCAS: 18997-57-4纯度: >99.00% / >98.00%
4-Methylumbelliferyl-β-D-Glucopyranoside是一种β-D-葡萄糖苷,可作为β-葡萄糖苷酶的荧光底物,用于检测该酶的活性。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC11610 | Pemetrexed | 150399-23-8 | >99.50% / >98.00% / >99.00% | |
An antifolate with anticancer activity | ||||
| GC11631 | Melittin | 20449-79-0 | >98.00% | |
蜂毒肽是一种 PLA2 活化剂,可刺激低分子量 PLA2 的活性,而不会增加高分子量 PLA2 的活性。 | ||||
| GC11638 | Sulfaphenazole | 526-08-9 | >99.50% / >98.00% / >98.50% | |
Sulfaphenazole是一种磺胺类抗菌药物。它竞争性地抑制细菌二氢叶酸合酶,阻断细菌叶酸合成,从而抑制细菌生长和繁殖。 | ||||
| GC11644 | Edoxaban | 480449-70-5 | >98.00% | |
Edoxaban (DU-176b) 是一种具有口服活性、高效、选择性和直接的因子 Xa (FXa) 抑制剂,对游离人 FXa 和凝血酶原酶的 Ki 值分别为 0.561 和 2.98 nM。 | ||||
| GC11669 | Tamoxifen Citrate | 54965-24-1 | >99.50% | |
A selective estrogen receptor modulator | ||||
| GC11675 | Amidepsine A | 169181-28-6 | - | |
A diacylglycerol acyltransferase inhibitor | ||||
| GC11720 | 17-AAG (KOS953) | 75747-14-7 | >99.00% / >98.00% | |
17-AAG(格尔德霉素)是一种天然的苯醌安沙霉素抗生素,是第一个确定的 Hsp90 抑制剂。 | ||||
| GC11731 | 4-phenyl-1,2,3-Thiadiazole | 25445-77-6 | - | |
Selective inhibitor of CYP2B4 and CYP2E1 | ||||
| GC11732 | GW 590735 | 622402-22-6;343321-96-0 | - | |
A potent and selective agonist of PPARα | ||||
| GC11741 | ML-265 | 1221186-53-3 | >98.00% | |
ML-265 被广泛用作公认的 PKM2(丙酮酸激酶肌肉亚型 2)激活剂 ML-265 激活 PKM2 在生物化学(AC50 = 92 nM)和基于细胞的测定中对 PKM1(丙酮酸激酶肌肉亚型 1)、PKL 和 PKR 具有高选择性。 | ||||
| GC11758 | 4-phenyl-5-methyl-1,2,3-Thiadiazole | 64273-28-5 | - | |
CYP2B4 and CYP2E1 inhibitor | ||||
| GC11780 | Bestatin | 58970-76-6 | >99.50% / >98.00% | |
Bestatin是氨基肽酶N(APN/CD13)抑制剂,其IC 50 值为14.9±3.4μM。 | ||||
| GC11782 | Ophiobolin A | 4611-05-6 | >95.00% | |
A calmodulin antagonist | ||||
| GC11786 | Acetylcysteine | 616-91-1 | >99.00% | |
乙酰半胱氨酸是半胱氨酸的 N-乙酰基衍生物。 | ||||
| GC11806 | β-Glycerophosphate (sodium salt hydrate) | 13408-09-8 | >98.00% | |
An inhibitor of alkaline phosphatase | ||||
| GC11816 | Posaconazole hydrate | 1198769-38-8 | - | |
An antifungal agent | ||||
| GC11835 | Deferasirox | 201530-41-8 | >99.50% | |
Deferasirox是一种具口服活性的铁螯合剂,用于治疗铁过载疾病。 | ||||
| GC11864 | 6,7-dihydroxy Bergamottin | 145414-76-2 | >98.00% | |
A potent CYP3A4 inhibitor | ||||
| GC11870 | 4-Methylumbelliferyl-β-D-Glucopyranoside | 18997-57-4 | >99.00% / >98.00% | |
4-Methylumbelliferyl-β-D-Glucopyranoside是一种β-D-葡萄糖苷,可作为β-葡萄糖苷酶的荧光底物,用于检测该酶的活性。 | ||||
| GC11882 | GKT137831 | 1218942-37-0 | >99.00% | |
GKT137831是一种口服有效的双重NADPH氧化酶1/4(NOX1/NOX4)抑制剂,活性处于亚微摩尔范围,可预防高糖诱导的人主动脉内皮细胞氧化应激,并减轻糖尿病小鼠的动脉粥样硬化进展。 | ||||
| GC11884 | GPP 78 hydrochloride | - | - | |
Inhibitor of Nampt | ||||
| GC11908 | Cisplatin | 15663-27-1 | >98.00% / >99.00% / >99.50% | |
顺铂是最好的、最早的基于金属的化疗药物之一,用于治疗广泛的实体癌症,如睾丸癌、卵巢癌、膀胱癌、肺癌、宫颈癌、头颈部肿瘤和胃癌等。 | ||||
| GC11916 | GQ-16 | 870554-67-9 | - | |
A PPARγ partial agonist | ||||
| GC11930 | KNK437 | 218924-25-5 | >98.00% | |
Prevents the synthesis of inducible heat shock proteins | ||||
