Reaction Details |
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Target | Histone deacetylase 3 |
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Ligand | BDBM50027591 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1443002 (CHEMBL3379480) |
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IC50 | 98±n/a nM |
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Citation | Giannini, G; Vesci, L; Battistuzzi, G; Vignola, D; Milazzo, FM; Guglielmi, MB; Barbarino, M; Santaniello, M; Fantò, N; Mor, M; Rivara, S; Pala, D; Taddei, M; Pisano, C; Cabri, W ST7612AA1, a thioacetate-¿(¿-lactam carboxamide) derivative selected from a novel generation of oral HDAC inhibitors. J Med Chem57:8358-77 (2014) [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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BDBM50027591 |
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n/a |
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Name | BDBM50027591 |
Synonyms: | CHEMBL3356931 |
Type | Small organic molecule |
Emp. Form. | C18H31N3O3S |
Mol. Mass. | 369.522 |
SMILES | SCCCCC[C@H](NC(=O)[C@@H]1CCCC(=O)N1)C(=O)NC1CCCC1 |r| |
Structure |
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