Reaction Details |
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Target | Glutathione reductase, mitochondrial |
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Ligand | BDBM50300754 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_589949 (CHEMBL1050857) |
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IC50 | >50000±n/a nM |
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Citation | Rai, G; Sayed, AA; Lea, WA; Luecke, HF; Chakrapani, H; Prast-Nielsen, S; Jadhav, A; Leister, W; Shen, M; Inglese, J; Austin, CP; Keefer, L; Arnér, ES; Simeonov, A; Maloney, DJ; Williams, DL; Thomas, CJ Structure mechanism insights and the role of nitric oxide donation guide the development of oxadiazole-2-oxides as therapeutic agents against schistosomiasis. J Med Chem52:6474-83 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Glutathione reductase, mitochondrial |
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Name: | Glutathione reductase, mitochondrial |
Synonyms: | GLUR | GRD1 | GSHR_HUMAN | GSR | Glutathione reductase | Glutathione reductase (GR) |
Type: | Enzyme |
Mol. Mass.: | 56271.52 |
Organism: | Homo sapiens (Human) |
Description: | P00390 |
Residue: | 522 |
Sequence: | MALLPRALSAGAGPSWRRAARAFRGFLLLLPEPAALTRALSRAMACRQEPQPQGPPPAAG
AVASYDYLVIGGGSGGLASARRAAELGARAAVVESHKLGGTCVNVGCVPKKVMWNTAVHS
EFMHDHADYGFPSCEGKFNWRVIKEKRDAYVSRLNAIYQNNLTKSHIEIIRGHAAFTSDP
KPTIEVSGKKYTAPHILIATGGMPSTPHESQIPGASLGITSDGFFQLEELPGRSVIVGAG
YIAVEMAGILSALGSKTSLMIRHDKVLRSFDSMISTNCTEELENAGVEVLKFSQVKEVKK
TLSGLEVSMVTAVPGRLPVMTMIPDVDCLLWAIGRVPNTKDLSLNKLGIQTDDKGHIIVD
EFQNTNVKGIYAVGDVCGKALLTPVAIAAGRKLAHRLFEYKEDSKLDYNNIPTVVFSHPP
IGTVGLTEDEAIHKYGIENVKTYSTSFTPMYHAVTKRKTKCVMKMVCANKEEKVVGIHMQ
GLGCDEMLQGFAVAVKMGATKADFDNTVAIHPTSSEELVTLR
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BDBM50300754 |
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n/a |
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Name | BDBM50300754 |
Synonyms: | 2-Oxy-4-phenyl-furazan-3-carboxylic acid amide | 3-carbamoyl-4-phenyl-1,2,5-oxadiazole 2-oxide | CHEMBL500868 |
Type | Small organic molecule |
Emp. Form. | C9H7N3O3 |
Mol. Mass. | 205.1702 |
SMILES | NC(=O)c1c(no[n+]1[O-])-c1ccccc1 |
Structure |
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