Reaction Details |
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Target | Histone acetyltransferase KAT2B |
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Ligand | BDBM50247913 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_495684 (CHEMBL1006963) |
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IC50 | 6500±n/a nM |
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Citation | Gorsuch, S; Bavetsias, V; Rowlands, MG; Aherne, GW; Workman, P; Jarman, M; McDonald, E Synthesis of isothiazol-3-one derivatives as inhibitors of histone acetyltransferases (HATs). Bioorg Med Chem17:467-74 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Histone acetyltransferase KAT2B |
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Name: | Histone acetyltransferase KAT2B |
Synonyms: | Histone acetyltransferase KAT2A/KAT2B | Histone acetyltransferase PCAF | KAT2B | KAT2B_HUMAN | PCAF |
Type: | PROTEIN |
Mol. Mass.: | 93045.76 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1502838 |
Residue: | 832 |
Sequence: | MSEAGGAGPGGCGAGAGAGAGPGALPPQPAALPPAPPQGSPCAAAAGGSGACGPATAVAA
AGTAEGPGGGGSARIAVKKAQLRSAPRAKKLEKLGVYSACKAEESCKCNGWKNPNPSPTP
PRADLQQIIVSLTESCRSCSHALAAHVSHLENVSEEEMNRLLGIVLDVEYLFTCVHKEED
ADTKQVYFYLFKLLRKSILQRGKPVVEGSLEKKPPFEKPSIEQGVNNFVQYKFSHLPAKE
RQTIVELAKMFLNRINYWHLEAPSQRRLRSPNDDISGYKENYTRWLCYCNVPQFCDSLPR
YETTQVFGRTLLRSVFTVMRRQLLEQARQEKDKLPLEKRTLILTHFPKFLSMLEEEVYSQ
NSPIWDQDFLSASSRTSQLGIQTVINPPPVAGTISYNSTSSSLEQPNAGSSSPACKASSG
LEANPGEKRKMTDSHVLEEAKKPRVMGDIPMELINEVMSTITDPAAMLGPETNFLSAHSA
RDEAARLEERRGVIEFHVVGNSLNQKPNKKILMWLVGLQNVFSHQLPRMPKEYITRLVFD
PKHKTLALIKDGRVIGGICFRMFPSQGFTEIVFCAVTSNEQVKGYGTHLMNHLKEYHIKH
DILNFLTYADEYAIGYFKKQGFSKEIKIPKTKYVGYIKDYEGATLMGCELNPRIPYTEFS
VIIKKQKEIIKKLIERKQAQIRKVYPGLSCFKDGVRQIPIESIPGIRETGWKPSGKEKSK
EPRDPDQLYSTLKSILQQVKSHQSAWPFMEPVKRTEAPGYYEVIRFPMDLKTMSERLKNR
YYVSKKLFMADLQRVFTNCKEYNPPESEYYKCANILEKFFFSKIKEAGLIDK
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BDBM50247913 |
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n/a |
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Name | BDBM50247913 |
Synonyms: | 2-(3-Pyridyl)-isothiazol-3(2H)-one | CHEMBL487498 |
Type | Small organic molecule |
Emp. Form. | C8H6N2OS |
Mol. Mass. | 178.211 |
SMILES | O=c1ccsn1-c1cccnc1 |
Structure |
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