Target type: molecularfunction
Catalysis of the reaction: 3-deoxyglucosone + H2O + NAD+ = 2-dehydro-3-deoxy-D-gluconate + 2 H+ + NADH. [PMID:17175089, RHEA:67244]
3-Deoxyglucosone dehydrogenase activity is a catalytic activity that oxidizes 3-deoxyglucosone to 3-deoxy-D-erythro-hexosulose. This enzyme plays a significant role in the detoxification of 3-deoxyglucosone, a highly reactive dicarbonyl compound that forms during the Maillard reaction and is implicated in several chronic diseases, including diabetes and neurodegenerative disorders. The reaction catalyzed by 3-deoxyglucosone dehydrogenase typically involves the transfer of electrons from 3-deoxyglucosone to a suitable electron acceptor, such as NAD+ or NADP+. This oxidation process converts 3-deoxyglucosone into a less reactive form, thereby preventing its accumulation and potential damage to cellular components. 3-Deoxyglucosone dehydrogenase activity is found in a variety of organisms, including bacteria, fungi, and mammals. In humans, this activity is primarily associated with the enzyme aldose reductase, which is also involved in the reduction of glucose to sorbitol. The precise mechanism of 3-deoxyglucosone dehydrogenase activity is still under investigation, but it is believed to involve the formation of an enzyme-substrate complex that facilitates the transfer of electrons. Understanding the molecular function of 3-deoxyglucosone dehydrogenase activity is crucial for developing therapeutic strategies to target 3-deoxyglucosone-mediated oxidative stress and associated pathologies.'
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Protein | Definition | Taxonomy |
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Retinal dehydrogenase 1 | An aldehyde dehydrogenase 1A1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P00352] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
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disulfiram | organic disulfide; organosulfur acaricide | angiogenesis inhibitor; antineoplastic agent; apoptosis inducer; EC 1.2.1.3 [aldehyde dehydrogenase (NAD(+))] inhibitor; EC 3.1.1.1 (carboxylesterase) inhibitor; EC 3.1.1.8 (cholinesterase) inhibitor; EC 5.99.1.2 (DNA topoisomerase) inhibitor; ferroptosis inducer; fungicide; NF-kappaB inhibitor | |
perphenazine | perphenazine : A phenothiazine derivative in which the phenothiazine tricycle carries a chloro substituent at the 2-position and a 3-[4-(2-hydroxyethyl)piperazin-1-yl]propyl group at N-10. Perphenazine: An antipsychotic phenothiazine derivative with actions and uses similar to those of CHLORPROMAZINE. | N-(2-hydroxyethyl)piperazine; N-alkylpiperazine; organochlorine compound; phenothiazines | antiemetic; dopaminergic antagonist; phenothiazine antipsychotic drug |
thiram | thiram : An organic disulfide that results from the formal oxidative dimerisation of N,N-dimethyldithiocarbamic acid. It is widely used as a fungicidal seed treatment. Thiram: A dithiocarbamate chemical, used commercially in the rubber processing industry and as a fungicide. In vivo studies indicate that it inactivates the enzyme GLUTATHIONE REDUCTASE. It has mutagenic activity and may induce chromosomal aberrations. | organic disulfide | antibacterial drug; antifungal agrochemical; antiseptic drug |
cystamine dihydrochloride | |||
uvitex swn | Uvitex SWN: optical brightner from Ciba; structure | 7-aminocoumarins | fluorochrome |
bis(1-piperidylthiocarbonyl)disulfide | bis(1-piperidylthiocarbonyl)disulfide: indicator for analysis of copper; structure | ||
win 18446 | WIN 18446 : A carboxamide that is 1,8-diaminooctane in which a hydrogen attached to each of the amino groups has been replaced by a dichloroacetyl group. Inhibitor of aldehyde dehydrogenase 1a2 (ALDH1a2). Inhibits the biosynthesis of retinoic acid from retinol in neonatal and adult murine testis. It down-regulates sex related genes in zebrafish. | organochlorine compound; secondary carboxamide | EC 1.2.1.3 [aldehyde dehydrogenase (NAD(+))] inhibitor |
4-(diethylamino)benzaldehyde | 4-(diethylamino)benzaldehyde : A member of the class of benzaldehydes carrying a diethylamino substituent at position 4. | aromatic amine; benzaldehydes; tertiary amino compound | EC 1.2.1.3 [aldehyde dehydrogenase (NAD(+))] inhibitor |
daidzin | daidzein 7-O-beta-D-glucoside : A glycosyloxyisoflavone that is daidzein attached to a beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage. It is used in the treatment of alcohol dependency (antidipsotropic). daidzin: a potent, selective, and reversible inhibitor of human mitochondrial aldehyde dehydrogenase | 7-hydroxyisoflavones 7-O-beta-D-glucoside; hydroxyisoflavone; monosaccharide derivative | plant metabolite |
7-butyl-8-[[4-(3-chlorophenyl)-1-piperazinyl]methyl]-1,3-dimethylpurine-2,6-dione | piperazines | ||
2-acetylfuranonaphthoquinone | 2-acetylfuranonaphthoquinone: has antineoplastic activity; structure in first source | ||
nct-501 | NCT-501: inhibits aldehyde dehydrogenase 1A1; structure in first source |