Metabolism
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Metabolism 相关产品(3072)
- GC13079VoriconazoleCAS: 137234-62-9纯度: >99.50%
Voriconazole是一种强效竞争性抑制剂,可抑制CYP2B6(IC 50 =1.71μM)、CYP2C9(IC 50 =3.62μM)、CYP2C19(IC 50 =5.25μM)和CYP3A(IC 50 =2.90μM)。
- GC13139FG-4592 (ASP1517)CAS: 808118-40-3纯度: >99.50%
FG-4592 作为一种口服生物可利用的缺氧诱导因子 (HIF) 脯氨酰羟化酶抑制剂,可通过 HIF 介导的转录促进协调性红细胞生成。
- GC13464GSK 2837808ACAS: 1445879-21-9纯度: >99.00%
GSK2837808A 是一种选择性的 LDHA (lactate dehydrogenase A) 的抑制剂,对hLDHA和hLDHB的IC50分别为2.6 nM和43 nM.GSK2837808A(10 µM;24-72h)通过促进有氧糖酵解、增殖、细胞周期和细胞凋亡抵抗,阻断了着丝粒蛋白N (CENP-N)过表达对鼻咽癌细胞的影响。
- GC13470RhapontigeninCAS: 500-65-2纯度: >98.00% / >99.50%
Rhapontigenin(丹叶大黄素)是一种有效的细胞色素P4501A1选择性灭活剂,IC 50 为0.4μM,对P4501A1的选择性分别是P4501A2和P4501B1的400倍和23倍。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC12962 | Isatin | 91-56-5 | >98.00% | |
Isatin (Indoline-2,3-dione) 是一种有效的单胺氧化酶 (MAO) 抑制剂,IC50 为 3 μM。 | ||||
| GC12981 | OU749 | 519170-13-9 | - | |
Inhibitor of γ-glutamyl transferase | ||||
| GC12992 | Fluorometholone Acetate | 3801-06-7 | >98.00% | |
A synthetic glucocorticoid | ||||
| GC13063 | N-Benzylpalmitamide | 74058-71-2 | >98.00% | |
A long-chain fatty acid amide | ||||
| GC13079 | Voriconazole | 137234-62-9 | >99.50% | |
Voriconazole是一种强效竞争性抑制剂,可抑制CYP2B6(IC 50 =1.71μM)、CYP2C9(IC 50 =3.62μM)、CYP2C19(IC 50 =5.25μM)和CYP3A(IC 50 =2.90μM)。 | ||||
| GC13083 | Siramesine | 147817-50-3 | - | |
A selective σ 2 receptor agonist | ||||
| GC13124 | LY2608204 | 1234703-40-2 | >98.00% | |
An activator of glucokinase | ||||
| GC13130 | Apixaban | 503612-47-3 | >99.50% | |
An inhibitor of Factor Xa | ||||
| GC13139 | FG-4592 (ASP1517) | 808118-40-3 | >99.50% | |
FG-4592 作为一种口服生物可利用的缺氧诱导因子 (HIF) 脯氨酰羟化酶抑制剂,可通过 HIF 介导的转录促进协调性红细胞生成。 | ||||
| GC13147 | AG-221 (Enasidenib) | 1446502-11-9 | >99.50% | |
An inhibitor of mutant IDH2 | ||||
| GC13262 | A-771726 | 163451-81-8 | >98.00% | |
An active metabolite of leflunomide | ||||
| GC13275 | Ibudilast | 50847-11-5 | >99.50% | |
An inhibitor of PDE4 | ||||
| GC13276 | Oleyloxyethyl Phosphorylcholine | 84601-19-4 | - | |
A PLA 2 inhibitor | ||||
| GC13293 | LP533401 hcl | 1040526-12-2 | >98.50% | |
An inhibitor of gut-derived serotonin biosynthesis | ||||
| GC13307 | PU-WS13 | 1454619-14-7 | >98.00% | |
PU-WS13是一种嘌呤支架类Grp94特异性热休克蛋白90(Hsp90)抑制剂。 | ||||
| GC13319 | 5,8,11-Eicosatriynoic Acid | 13488-22-7 | - | |
A nonselective inhibitor of lipoxygenases | ||||
| GC13336 | CBR-5884 | 681159-27-3 | >99.00% | |
A selective PHGDH inhibitor | ||||
| GC13351 | VU0359595 | 1246303-14-9 | >95.00% | |
A selective PLD 1 inhibitor | ||||
| GC13362 | TOK-001 | 851983-85-2 | >99.50% | |
A CYP17 inhibitor | ||||
| GC13379 | 1-Naphthyl 3,5-dinitrobenzoate | 93261-39-3 | - | |
A dual inhibitor of 5-LO and mPGES-1 | ||||
| GC13444 | Doxofylline | 69975-86-6 | >99.00% | |
A bronchodilator | ||||
| GC13464 | GSK 2837808A | 1445879-21-9 | >99.00% | |
GSK2837808A 是一种选择性的 LDHA (lactate dehydrogenase A) 的抑制剂,对hLDHA和hLDHB的IC50分别为2.6 nM和43 nM.GSK2837808A(10 µM;24-72h)通过促进有氧糖酵解、增殖、细胞周期和细胞凋亡抵抗,阻断了着丝粒蛋白N (CENP-N)过表达对鼻咽癌细胞的影响。 | ||||
| GC13470 | Rhapontigenin | 500-65-2 | >98.00% / >99.50% | |
Rhapontigenin(丹叶大黄素)是一种有效的细胞色素P4501A1选择性灭活剂,IC 50 为0.4μM,对P4501A1的选择性分别是P4501A2和P4501B1的400倍和23倍。 | ||||
| GC13516 | AS 1949490 | 1203680-76-5 | >98.00% | |
A selective SHIP2 inhibitor | ||||
