Reaction Details |
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Target | Histone deacetylase 8 |
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Ligand | BDBM50350235 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_761697 (CHEMBL1816689) |
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IC50 | 200±n/a nM |
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Citation | Whitehead, L; Dobler, MR; Radetich, B; Zhu, Y; Atadja, PW; Claiborne, T; Grob, JE; McRiner, A; Pancost, MR; Patnaik, A; Shao, W; Shultz, M; Tichkule, R; Tommasi, RA; Vash, B; Wang, P; Stams, T Human HDAC isoform selectivity achieved via exploitation of the acetate release channel with structurally unique small molecule inhibitors. Bioorg Med Chem19:4626-34 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Histone deacetylase 8 |
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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
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BDBM50350235 |
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n/a |
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Name | BDBM50350235 |
Synonyms: | CHEMBL1812334 |
Type | Small organic molecule |
Emp. Form. | C20H20ClF2N3O2 |
Mol. Mass. | 407.842 |
SMILES | N[C@H](Cc1cccc(Cl)c1)C(=O)N1CCN(CC1)C(=O)c1cc(F)ccc1F |r| |
Structure |
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