Reaction Details |
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Target | ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 |
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Ligand | BDBM50178769 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_325283 (CHEMBL859694) |
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IC50 | >100000±n/a nM |
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Citation | Napper, AD; Hixon, J; McDonagh, T; Keavey, K; Pons, JF; Barker, J; Yau, WT; Amouzegh, P; Flegg, A; Hamelin, E; Thomas, RJ; Kates, M; Jones, S; Navia, MA; Saunders, JO; DiStefano, PS; Curtis, R Discovery of indoles as potent and selective inhibitors of the deacetylase SIRT1. J Med Chem48:8045-54 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 |
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Name: | ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 |
Synonyms: | CD38 | CD38_HUMAN | Lymphocyte differentiation antigen CD38 |
Type: | PROTEIN |
Mol. Mass.: | 34333.62 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1509931 |
Residue: | 300 |
Sequence: | MANCEFSPVSGDKPCCRLSRRAQLCLGVSILVLILVVVLAVVVPRWRQQWSGPGTTKRFP
ETVLARCVKYTEIHPEMRHVDCQSVWDAFKGAFISKHPCNITEEDYQPLMKLGTQTVPCN
KILLWSRIKDLAHQFTQVQRDMFTLEDTLLGYLADDLTWCGEFNTSKINYQSCPDWRKDC
SNNPVSVFWKTVSRRFAEAACDVVHVMLNGSRSKIFDKNSTFGSVEVHNLQPEKVQTLEA
WVIHGGREDSRDLCQDPTIKELESIISKRNIQFSCKNIYRPDKFLQCVKNPEDSSCTSEI
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BDBM50178769 |
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n/a |
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Name | BDBM50178769 |
Synonyms: | (+/-)-6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide | 6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide | CHEMBL420311 |
Type | Small organic molecule |
Emp. Form. | C13H13ClN2O |
Mol. Mass. | 248.708 |
SMILES | NC(=O)C1CCCc2c1[nH]c1ccc(Cl)cc21 |
Structure |
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