Dehydrogenase
Dehydrogenase(脱氢酶)
Dehydrogenases, belonging to the class of oxidoreductases which catalyze donor-acceptor reactions to transfer electron molecules from the oxidant to the reluctant, are a diverse group of enzymes that are able to transfer one or more hydrides (H-) from a substrate to an electron acceptor, such as nicotinamide adenine dinucleotide (NAD+), nicotinamide adenine dinucleotide phosphate (NADP+) or Riboflavin, through oxidation and reduction. Three commonly studied dehydrogenase enzymes include alcohol dehydrogenase (ADH) which catalyzes the reduction of acetylaldehyde to ethanol in plant cells, succinate dehydrogenase which oxidizes succinate to fumarate, and lactate dehydrogenase which catalyzes the reversible oxidation of lactate to pyruvate.
Dehydrogenase 相关产品(39)
- GC17107PluriSIn #1 (NSC 14613)CAS: 91396-88-2纯度: >99.50%
A selective inhibitor of stearoyl-CoA desaturase
- GC104626-AminonicotinamideCAS: 329-89-5纯度: >98.00% / >98.50% / >99.50%
6-Aminonicotinamide是一种有效的烟酰胺抗代谢物,是竞争性 NADP+ 依赖性酶葡萄糖-6-磷酸脱氢酶 (G6PD) 的抑制剂(K i =0.46μM)。
- 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。
- GC13670MethylmalonateCAS: 516-05-2纯度: >98.00%
A dicarboxylic acid and byproduct of propionate catabolism
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC10531 | AGI-5198 | 1355326-35-0 | >98.00% | |
A potent, selective inhibitor of IDH1 mutations | ||||
| GC13614 | Mycophenolate Mofetil | 128794-94-5 | >99.50% | |
A prodrug form of mycophenolic acid | ||||
| GC14783 | Trilostane | 13647-35-3 | >99.50% | |
A 3β-hydroxysteroid dehydrogenase inhibitor | ||||
| GC17107 | PluriSIn #1 (NSC 14613) | 91396-88-2 | >99.50% | |
A selective inhibitor of stearoyl-CoA desaturase | ||||
| GC17467 | Gimeracil | 103766-25-2 | >99.50% | |
A DYPD inhibitor | ||||
| GC10438 | WIN 18446 | 1477-57-2 | >98.00% / >97.00% | |
WIN 18446 (Fertilysin)是乙醛脱氢酶1A2(ALDH1A2)的有效抑制剂,IC 50 值为0.3μM。 | ||||
| GC10462 | 6-Aminonicotinamide | 329-89-5 | >98.00% / >98.50% / >99.50% | |
6-Aminonicotinamide是一种有效的烟酰胺抗代谢物,是竞争性 NADP+ 依赖性酶葡萄糖-6-磷酸脱氢酶 (G6PD) 的抑制剂(K i =0.46μM)。 | ||||
| GC10902 | CVT 10216 | 1005334-57-5 | >99.00% | |
A selective, reversible ALDH2 inhibitor | ||||
| GC11149 | L-a-Hydroxyglutaric acid disodium salt | 63512-50-5 | - | |
An α-hydroxy acid | ||||
| GC12204 | STK393606 | 355827-05-3 | - | |
A selective inhibitor of 15-PGDH | ||||
| 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 | ||||
| GC13336 | CBR-5884 | 681159-27-3 | >99.00% | |
A selective PHGDH inhibitor | ||||
| 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。 | ||||
| GC13611 | CGP 3466B maleate | 200189-97-5 | >98.00% | |
A GAPDH ligand | ||||
| GC13670 | Methylmalonate | 516-05-2 | >98.00% | |
A dicarboxylic acid and byproduct of propionate catabolism | ||||
| GC13760 | TC HSD 21 | 330203-01-5 | - | |
An inhibitor of 17β-HSD3 | ||||
| GC13776 | Piericidin A | 2738-64-9 | >95.00% | |
Piericidin A是一种天然的线粒体NADH-泛醌氧化还原酶(复合物I)抑制剂。 | ||||
| GC14757 | AGI-6780 | 1432660-47-3 | >98.00% | |
A potent, selective inhibitor of mutant IDH2 | ||||
| GC14851 | Vidofludimus | 717824-30-1 | >98.50% | |
An immunosuppressive drug that inhibits DHODH | ||||
| GC14921 | CPI-613 (Devimistat) | 95809-78-2 | >98.00% | |
An inhibitor of α-ketoglutarate dehydrogenase | ||||
| GC15266 | Qc 1 | 403718-45-6 | >98.00% | |
Qc 1 是一种可逆的非竞争性苏氨酸脱氢酶 (TDH) 抑制剂。 | ||||
| GC15547 | Inosine-5'-monophosphate (sodium salt hydrate) | 20813-76-7 | - | |
A 5’-ribonucleoside | ||||
| GC15601 | AG-120 | 1448347-49-6 | >99.50% / >98.00% | |
AG-120 (Ivosidenib)是一种突变型异柠檬酸脱氢酶1(mIDH1)抑制剂。 | ||||
