Dehydrogenase
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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.
Products Related to Dehydrogenase(36)
- GC16816GalloflavinCAS: 568-80-9Purity: >98.00%
La galloflavine est un puissant inhibiteur de la lactate déshydrogénase (LDH). Les Kis calculés pour le pyruvate sont de 5,46 μM (LDH-A) et 15,06 μM (LDH-B). La galloflavine entrave la prolifération des cellules cancéreuses en bloquant la glycolyse et la production d'ATP.
- GC16860NCT-502CAS: 1542213-00-2Purity: >99.00%
Le NCT-502 est un inhibiteur de la phosphoglycérate déshydrogénase humaine (PHGDH), cytotoxique pour les cellules cancéreuses dépendantes de la PHGDH, et réduit la production de sérine dérivée du glucose, avec une IC50 de 3,7 μM contre la PHGDH.
- GC16951StiripentolCAS: 49763-96-4Purity: >99.50%
Stiripentol (STP) est un agent anticonvulsivant, qui peut inhiber la N-déméthylation du CLB en NCLB médiée par le CYP3A4 (de manière non compétitive) et le CYP2C19 (de manière compétitive) avec Ki de 1,59 ± 0,07 et 0,516 ± 0,065 μM et IC50 de 1,58 et 3,29 μM, respectivement .
- GC17107PluriSIn #1 (NSC 14613)CAS: 91396-88-2Purity: >99.50%
A selective inhibitor of stearoyl-CoA desaturase
- GC17293PHGDH-inactiveCAS: 1914971-16-6Purity: >99.50%
La PHGDH-inactive n'a aucune activité contre la PHGDH et sert de contrÔle négatif de NCT-502 et NCT-503.
- GC17914FomepizoleCAS: 7554-65-6Purity: >99.50%
Le fomépizole (4-méthylpyrazole) est un puissant inhibiteur du cytochrome P450 (CYP2E1).
- GC25039AG-120 (racemic)CAS: 1448346-63-1Purity: >98%
AG-120 (racemic), the racemic mixture of AG-120, is an orally available inhibitor of isocitrate dehydrogenase type 1 (IDH1) with potential antineoplastic activity.
- GC25389Ethyl potassium malonateCAS: 6148-64-7Purity: >98%
Ethyl potassium malonate (Potassium 3-ethoxy-3-oxopropanoate) is used as a competitive inhibitor of the enzyme succinate dehydrogenase. It acts as a precursor to produce (trimethylsilyl)ethyl malonate, which is utilized to prepare beta-ketoesters by acylation and serves as an intermediate for the preparation of ethyl tert-butyl malonate.
- GC50508PKUMDL WQ 2101CAS: 304481-72-9Purity: >98%
Negative allosteric modulator of 3-phosphoglycerate dehydrogenase (PHGDH)
- GC50509PKUMDL WQ 2201CAS: 592474-91-4Purity: >98%
Negative allosteric modulator of 3-Phosphoglycerate dehydrogenase (PHGDH)
- GC81900CP61 acetatePurity: >98.50%
CP61 acetate is a CtBP1 and CtBP2 inhibitor that binds to dimeric CtBP1 and allosterically inhibits NADH binding, disrupting the NADH -dependent dimerization of CtBP1 and CtBP2, inducing aberrant mitosis and micronucleus formation, thereby inhibiting cell proliferation and colony formation.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC16816 | Galloflavin | 568-80-9 | >98.00% | |
La galloflavine est un puissant inhibiteur de la lactate déshydrogénase (LDH). Les Kis calculés pour le pyruvate sont de 5,46 μM (LDH-A) et 15,06 μM (LDH-B). La galloflavine entrave la prolifération des cellules cancéreuses en bloquant la glycolyse et la production d'ATP. | ||||
| GC16860 | NCT-502 | 1542213-00-2 | >99.00% | |
Le NCT-502 est un inhibiteur de la phosphoglycérate déshydrogénase humaine (PHGDH), cytotoxique pour les cellules cancéreuses dépendantes de la PHGDH, et réduit la production de sérine dérivée du glucose, avec une IC50 de 3,7 μM contre la PHGDH. | ||||
| GC16951 | Stiripentol | 49763-96-4 | >99.50% | |
Stiripentol (STP) est un agent anticonvulsivant, qui peut inhiber la N-déméthylation du CLB en NCLB médiée par le CYP3A4 (de manière non compétitive) et le CYP2C19 (de manière compétitive) avec Ki de 1,59 ± 0,07 et 0,516 ± 0,065 μM et IC50 de 1,58 et 3,29 μM, respectivement . | ||||
| GC17107 | PluriSIn #1 (NSC 14613) | 91396-88-2 | >99.50% | |
A selective inhibitor of stearoyl-CoA desaturase | ||||
| GC17293 | PHGDH-inactive | 1914971-16-6 | >99.50% | |
La PHGDH-inactive n'a aucune activité contre la PHGDH et sert de contrÔle négatif de NCT-502 et NCT-503. | ||||
| GC17467 | Gimeracil | 103766-25-2 | >99.50% | |
A DYPD inhibitor | ||||
| GC17914 | Fomepizole | 7554-65-6 | >99.50% | |
Le fomépizole (4-méthylpyrazole) est un puissant inhibiteur du cytochrome P450 (CYP2E1). | ||||
| GC25039 | AG-120 (racemic) | 1448346-63-1 | >98% | |
AG-120 (racemic), the racemic mixture of AG-120, is an orally available inhibitor of isocitrate dehydrogenase type 1 (IDH1) with potential antineoplastic activity. | ||||
| GC25389 | Ethyl potassium malonate | 6148-64-7 | >98% | |
Ethyl potassium malonate (Potassium 3-ethoxy-3-oxopropanoate) is used as a competitive inhibitor of the enzyme succinate dehydrogenase. It acts as a precursor to produce (trimethylsilyl)ethyl malonate, which is utilized to prepare beta-ketoesters by acylation and serves as an intermediate for the preparation of ethyl tert-butyl malonate. | ||||
| GC50508 | PKUMDL WQ 2101 | 304481-72-9 | >98% | |
Negative allosteric modulator of 3-phosphoglycerate dehydrogenase (PHGDH) | ||||
| GC50509 | PKUMDL WQ 2201 | 592474-91-4 | >98% | |
Negative allosteric modulator of 3-Phosphoglycerate dehydrogenase (PHGDH) | ||||
| GC81900 | CP61 acetate | - | >98.50% | |
CP61 acetate is a CtBP1 and CtBP2 inhibitor that binds to dimeric CtBP1 and allosterically inhibits NADH binding, disrupting the NADH -dependent dimerization of CtBP1 and CtBP2, inducing aberrant mitosis and micronucleus formation, thereby inhibiting cell proliferation and colony formation. | ||||
