Reaction Details |
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Target | Histone deacetylase 3 |
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Ligand | BDBM50435604 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1552953 (CHEMBL3760237) |
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IC50 | 92±n/a nM |
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Citation | Thaler, F; Moretti, L; Amici, R; Abate, A; Colombo, A; Carenzi, G; Fulco, MC; Boggio, R; Dondio, G; Gagliardi, S; Minucci, S; Sartori, L; Varasi, M; Mercurio, C Synthesis, biological characterization and molecular modeling insights of spirochromanes as potent HDAC inhibitors. Eur J Med Chem108:53-67 (2016) [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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BDBM50435604 |
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n/a |
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Name | BDBM50435604 |
Synonyms: | CHEMBL2390995 |
Type | Small organic molecule |
Emp. Form. | C23H23FN2O4 |
Mol. Mass. | 410.4381 |
SMILES | ONC(=O)C=Cc1ccc2OC3(CCN(Cc4ccc(F)cc4)CC3)CC(=O)c2c1 |w:5.5| |
Structure |
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