Reaction Details |
![](/images/Email.png) | Report a problem with these data |
Target | Histone deacetylase 3 |
---|
Ligand | BDBM50519457 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_2053167 (CHEMBL4708168) |
---|
IC50 | 187±n/a nM |
---|
Citation | Gawel, JM; Shouksmith, AE; Raouf, YS; Nawar, N; Toutah, K; Bukhari, S; Manaswiyoungkul, P; Olaoye, OO; Israelian, J; Radu, TB; Cabral, AD; Sina, D; Sedighi, A; de Araujo, ED; Gunning, PT PTG-0861: A novel HDAC6-selective inhibitor as a therapeutic strategy in acute myeloid leukaemia. Eur J Med Chem201:0 (2020) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Histone deacetylase 3 |
---|
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
|
|
|
BDBM50519457 |
---|
n/a |
---|
Name | BDBM50519457 |
Synonyms: | CHEMBL4452620 |
Type | Small organic molecule |
Emp. Form. | C18H20N2O3 |
Mol. Mass. | 312.363 |
SMILES | CC(C)(C)c1ccc(cc1)C(=O)Nc1ccc(cc1)C(=O)NO |
Structure |
|