Reaction Details Report a problem with these data
Target
Histone deacetylase 3
Ligand
BDBM197350
Substrate
n/a
Meas. Tech.
Enzyme Assay
IC50
10±n/a nM
Citation
 Nan, F; Chen, F; Zhang, Y; Li, J; Zhou, Y; Su, M; Ding, J; Meng, L; Xie, X; Wang, S Thiazole compounds, methods for preparation and use thereof US Patent  US9216962 Publication Date 12/22/2015 
Target
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:
MAKTVAYFYDPDVGNFHYGAGHPMKPHRLALTHSLVLHYGLYKKMIVFKPYQASQHDMCRFHSEDYIDFLQRVSPTNMQGFTKSLNAFNVGDDCPVFPGLFEFCSRYTGASLQGATQLNNKICDIAINWAGGLHHAKKFEASGFCYVNDIVIGILELLKYHPRVLYIDIDIHHGDGVQEAFYLTDRVMTVSFHKYGNYFFPGTGDMYEVGAESGRYYCLNVPLRDGIDDQSYKHLFQPVINQVVDFYQPTCIVLQCGADSLGCDRLGCFNLSIRGHGECVEYVKSFNIPLLVLGGGGYTVRNVARCWTYETSLLVEEAISEELPYSEYFEYFAPDFTLHPDVSTRIENQNSRQYLDQIRQTIFENLKMLNHAPSVQIHDVPADLLTYDRTDEADAEERGPEENYSRPEAPNEFYDGDHDNDKESDVEI
  
Inhibitor
Name:
BDBM197350
Synonyms:
US9216962, CFH395-C
Type:
Small organic molecule
Emp. Form.:
C17H22N4O3S2
Mol. Mass.:
394.512
SMILES:
ONC(=O)CCCCCCNC(=O)c1nc(sc1C1CC1)-c1nccs1
Structure:
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