Reaction Details |
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Target | L-lactate dehydrogenase B chain |
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Ligand | BDBM50594014 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2210642 (CHEMBL5123591) |
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IC50 | 1100±n/a nM |
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Citation | Moya-Garzon, MD; Rodriguez-Rodriguez, B; Martin-Higueras, C; Franco-Montalban, F; Fernandes, MX; Gomez-Vidal, JA; Pey, AL; Salido, E; Diaz-Gavilan, M New salicylic acid derivatives, double inhibitors of glycolate oxidase and lactate dehydrogenase, as effective agents decreasing oxalate production. Eur J Med Chem237:0 (2022) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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L-lactate dehydrogenase B chain |
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Name: | L-lactate dehydrogenase B chain |
Synonyms: | L-lactate dehydrogenase B | L-lactate dehydrogenase B chain | LDH heart subunit | LDH-B | LDH-H | LDHB | LDHB_HUMAN | Lactate dehydrogenase B (LDHB) | Renal carcinoma antigen NY-REN-46 |
Type: | Oxidoreductase; homotetramer |
Mol. Mass.: | 36635.55 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 334 |
Sequence: | MATLKEKLIAPVAEEEATVPNNKITVVGVGQVGMACAISILGKSLADELALVDVLEDKLK
GEMMDLQHGSLFLQTPKIVADKDYSVTANSKIVVVTAGVRQQEGESRLNLVQRNVNVFKF
IIPQIVKYSPDCIIIVVSNPVDILTYVTWKLSGLPKHRVIGSGCNLDSARFRYLMAEKLG
IHPSSCHGWILGEHGDSSVAVWSGVNVAGVSLQELNPEMGTDNDSENWKEVHKMVVESAY
EVIKLKGYTNWAIGLSVADLIESMLKNLSRIHPVSTMVKGMYGIENEVFLSLPCILNARG
LTSVINQKLKDDEVAQLKKSADTLWDIQKDLKDL
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BDBM50594014 |
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n/a |
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Name | BDBM50594014 |
Synonyms: | CHEMBL5182027 |
Type | Small organic molecule |
Emp. Form. | C18H17BrN2O4 |
Mol. Mass. | 405.243 |
SMILES | N.OC(=O)c1cc(ccc1O)-c1ccc(CNc2ccc(Br)cc2)o1 |
Structure |
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