Reaction Details |
| Report a problem with these data |
Target | Histone deacetylase 8 |
---|
Ligand | BDBM50239822 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_1667235 (CHEMBL4017031) |
---|
IC50 | 6760±n/a nM |
---|
Citation | Krieger, V; Hamacher, A; Gertzen, CGW; Senger, J; Zwinderman, MRH; Marek, M; Romier, C; Dekker, FJ; Kurz, T; Jung, M; Gohlke, H; Kassack, MU; Hansen, FK Design, Multicomponent Synthesis, and Anticancer Activity of a Focused Histone Deacetylase (HDAC) Inhibitor Library with Peptoid-Based Cap Groups. J Med Chem60:5493-5506 (2017) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Histone deacetylase 8 |
---|
Name: | Histone deacetylase 8 |
Synonyms: | HD8 | HDAC8 | HDAC8_HUMAN | HDACL1 | Histone deacetylase 8 (HDAC-8) | Human HDAC8 |
Type: | Enzyme |
Mol. Mass.: | 41749.60 |
Organism: | Homo sapiens (Human) |
Description: | Q9BY41 |
Residue: | 377 |
Sequence: | MEEPEEPADSGQSLVPVYIYSPEYVSMCDSLAKIPKRASMVHSLIEAYALHKQMRIVKPK
VASMEEMATFHTDAYLQHLQKVSQEGDDDHPDSIEYGLGYDCPATEGIFDYAAAIGGATI
TAAQCLIDGMCKVAINWSGGWHHAKKDEASGFCYLNDAVLGILRLRRKFERILYVDLDLH
HGDGVEDAFSFTSKVMTVSLHKFSPGFFPGTGDVSDVGLGKGRYYSVNVPIQDGIQDEKY
YQICESVLKEVYQAFNPKAVVLQLGADTIAGDPMCSFNMTPVGIGKCLKYILQWQLATLI
LGGGGYNLANTARCWTYLTGVILGKTLSSEIPDHEFFTAYGPDYVLEITPSCRPDRNEPH
RIQQILNYIKGNLKHVV
|
|
|
BDBM50239822 |
---|
n/a |
---|
Name | BDBM50239822 |
Synonyms: | CHEMBL4080343 |
Type | Small organic molecule |
Emp. Form. | C24H32N4O4 |
Mol. Mass. | 440.5353 |
SMILES | CN(C)c1ccc(cc1)C(=O)N(CCCCCC(=O)NO)CC(=O)Nc1ccc(C)cc1 |
Structure |
|