Reaction Details |
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Target | L-lactate dehydrogenase B chain |
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Ligand | BDBM23251 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Enzyme Assay |
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pH | 7.5±0 |
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Temperature | 294.15±0 K |
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IC50 | 7.8e+3±n/a nM |
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Citation | Ward, RA; Brassington, C; Breeze, AL; Caputo, A; Critchlow, S; Davies, G; Goodwin, L; Hassall, G; Greenwood, R; Holdgate, GA; Mrosek, M; Norman, RA; Pearson, S; Tart, J; Tucker, JA; Vogtherr, M; Whittaker, D; Wingfield, J; Winter, J; Hudson, K Design and synthesis of novel lactate dehydrogenase a inhibitors by fragment-based lead generation. J Med Chem55:3285-306 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, 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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BDBM23251 |
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n/a |
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Name | BDBM23251 |
Synonyms: | 1,2,5-Thiadiazole, TDA1 | 4-hydroxy-1,2,5-thiadiazole-3-carboxylic acid | LDHA Inhibitor, 1 |
Type | Small organic molecule |
Emp. Form. | C3H2N2O3S |
Mol. Mass. | 146.125 |
SMILES | OC(=O)c1ns[nH]c1=O |
Structure |
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