Reaction Details |
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Target | Histone deacetylase 3 |
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Ligand | BDBM50249583 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_1680080 |
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IC50 | >30000±n/a nM |
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Citation | Piizzi, G; Parker, DT; Peng, Y; Dobler, M; Patnaik, A; Wattanasin, S; Liu, E; Lenoir, F; Nunez, J; Kerrigan, J; McKenney, D; Osborne, C; Yu, D; Lanieri, L; Bojkovic, J; Dzink-Fox, J; Lilly, MD; Sprague, ER; Lu, Y; Wang, H; Ranjitkar, S; Xie, L; Wang, B; Glick, M; Hamann, LG; Tommasi, R; Yang, X; Dean, CR Design, Synthesis, and Properties of a Potent Inhibitor of Pseudomonas aeruginosa Deacetylase LpxC. J Med Chem60:5002-5014 (2017) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Histone deacetylase 3 |
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Name: | Histone deacetylase 3 |
Synonyms: | HD3 | HDAC3 | HDAC3_HUMAN | Histone deacetylase 3 (HDAC3) | Human HDAC3 | RPD3-2 | SMAP45 |
Type: | Enzyme |
Mol. Mass.: | 48829.55 |
Organism: | Homo sapiens (Human) |
Description: | O15379 |
Residue: | 428 |
Sequence: | MAKTVAYFYDPDVGNFHYGAGHPMKPHRLALTHSLVLHYGLYKKMIVFKPYQASQHDMCR
FHSEDYIDFLQRVSPTNMQGFTKSLNAFNVGDDCPVFPGLFEFCSRYTGASLQGATQLNN
KICDIAINWAGGLHHAKKFEASGFCYVNDIVIGILELLKYHPRVLYIDIDIHHGDGVQEA
FYLTDRVMTVSFHKYGNYFFPGTGDMYEVGAESGRYYCLNVPLRDGIDDQSYKHLFQPVI
NQVVDFYQPTCIVLQCGADSLGCDRLGCFNLSIRGHGECVEYVKSFNIPLLVLGGGGYTV
RNVARCWTYETSLLVEEAISEELPYSEYFEYFAPDFTLHPDVSTRIENQNSRQYLDQIRQ
TIFENLKMLNHAPSVQIHDVPADLLTYDRTDEADAEERGPEENYSRPEAPNEFYDGDHDN
DKESDVEI
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BDBM50249583 |
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n/a |
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Name | BDBM50249583 |
Synonyms: | CHEMBL4097399 |
Type | Small organic molecule |
Emp. Form. | C16H21N3O4 |
Mol. Mass. | 319.3556 |
SMILES | CC#CCOc1ccc(cc1)C(=O)N[C@H](C(=O)NO)C(C)(C)N |r| |
Structure |
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