- Signaling Pathways
- Metabolic Enzyme/Protease
- NADH Dehydrogenase
NADH Dehydrogenase
NADH Dehydrogenase
- [1]. Heikal A, et al. Activation of type II NADH dehydrogenase by quinolinequinones mediates antitubercular cell death. J Antimicrob Chemother. 2016 Oct;71(10):2840-7. [Content Brief]
- [2]. Herrmann JM, et al. Apoptosis inducing factor and mitochondrial NADH dehydrogenases: redox-controlled gear boxes to switch between mitochondrial biogenesis and cell death. Biol Chem. 2020 Aug 25;402(3):289-297. [Content Brief]
- [3]. Weiss H, et al. The respiratory-chain NADH dehydrogenase (complex I) of mitochondria. Eur J Biochem. 1991 May 8;197(3):563-76. [Content Brief]
- [4]. Shapiro B L, et al. Mitrochondrial NADH dehydrogenase in cystic fibrosis. Proceedings of the National Academy of Sciences, 1979, 76(6): 2979-2983.
- [5]. Yagi T, et al. NADH dehydrogenases: from basic science to biomedicine. J Bioenerg Biomembr. 2001 Jun;33(3):233-42. [Content Brief]
- [6]. Miller JL, et al. The type I NADH dehydrogenase of Mycobacterium tuberculosis counters phagosomal NOX2 activity to inhibit TNF-alpha-mediated host cell apoptosis. PLoS Pathog. 2010 Apr 22;6(4):e1000864. [Content Brief]
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NADH Dehydrogenase Related Products (6)
Related Products (6)
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LCC-12 formate
0 ImagesCat. No.: HY-W722277APurity: 99.9%LCC-12 formate is a mitochondria-targeted Copper2+ -selective binder and metabolic/epigenetic reprogramming agent. LCC-12 formate inhibits NAD (H) redox cycling and reduces the NAD (H) pool. LCC-12 formate downregulates the expression of inflammatory genes and improves outcomes in mouse models of bacterial sepsis, endotoxemia, and SARS-CoV-2 infection. LCC-12 formate can be used in research related to acute inflammation, endotoxemia, sepsis, and SARS-CoV-2 infection. -
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Glutamate Dehydrogenase, Bovine Liver
0 ImagesCat. No.: HY-E70003AGlutamate Dehydrogenase, Bovine Liver (EC 1.4.1.4) catalyzes the reversible oxidative deamination of glutamate to alpha-ketoglutarate and ammonia. -
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Pleurocidin
0 ImagesPleurocidin is an Antimicrobial peptide. Pleurocidin is derived from the skin mucosa or intestinal secretions of Pseudopleuronectes americanus. Pleurocidin inhibits the expression of key proteins in the MAPK and NF-κB inflammatory signaling pathways. Pleurocidin alters serum inflammatory and immune cytokine levels, regulates the down-regulation of tight junction proteins, and modulates the intestinal flora. Pleurocidin exerts antibacterial activity by inducing bacterial membrane damage, hydroxyl radical formation, and NADH depletion, and also produces a synergistic effect with Antibiotics. Pleurocidin alleviates DSS-induced ulcerative colitis. Pleurocidin can be used for research on ulcerative colitis, bacterial infections, and bacterial biofilm-related infections. -
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3-(2',5'-Disulfophenylimino)-3H-phenothiazine sodium
0 ImagesCat. No.: HY-W906543ACAS No.: 1419158-69-23-(2',5'-Disulfophenylimino)-3H-phenothiazine sodium (Compound M2) is a lectron-transfer mediator. 3-(2',5'-Disulfophenylimino)-3H-phenothiazine sodium offers good enzyme reactivity and interference-free electrocatalysis of NADH. 3-(2',5'-Disulfophenylimino)-3H-phenothiazine (sodium) can be used for the research of type 2 diabetes. -
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- 2'-Deoxy-NAD+
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2'-Deoxy-NAD+ sodium
0 ImagesCat. No.: HY-137673ACAS No.: 1514900-83-42'-Deoxy-NAD+ sodium is a noncompetitive NAD+ inhibitor with a Ki of 32 μM. 2'-Deoxy-NAD+ sodium can be utilized as a substrate to study the ADP-ribosyl transfer reaction. -
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