Target
Histone deacetylase 6
Ligand
BDBM50396042
Substrate
n/a
Meas. Tech.
ChEMBL_861418 (CHEMBL2174032)
IC50
>10000±n/a nM
Citation
 Olsen, CAMontero, ALeman, LJGhadiri, MR Macrocyclic peptoid-Peptide hybrids as inhibitors of class I histone deacetylases. ACS Med Chem Lett 3:749-753 (2012) [PubMed]  Article 
Target
Name:
Histone deacetylase 6
Synonyms:
Cereblon/Histone deacetylase 6 | HD6 | HDAC6 | HDAC6_HUMAN | Histone deacetylase 6 (HDAC6) | Human HDAC6 | KIAA0901 | ORF Names:JM21
Type:
Chromatin regulator; hydrolase; repressor
Mol. Mass.:
131381.51
Organism:
Homo sapiens (Human)
Description:
Q9UBN7
Residue:
1215
Sequence:
MTSTGQDSTTTRQRRSRQNPQSPPQDSSVTSKRNIKKGAVPRSIPNLAEVKKKGKMKKLGQAMEEDLIVGLQGMDLNLEAEALAGTGLVLDEQLNEFHCLWDDSFPEGPERLHAIKEQLIQEGLLDRCVSFQARFAEKEELMLVHSLEYIDLMETTQYMNEGELRVLADTYDSVYLHPNSYSCACLASGSVLRLVDAVLGAEIRNGMAIIRPPGHHAQHSLMDGYCMFNHVAVAARYAQQKHRIRRVLIVDWDVHHGQGTQFTFDQDPSVLYFSIHRYEQGRFWPHLKASNWSTTGFGQGQGYTINVPWNQVGMRDADYIAAFLHVLLPVALEFQPQLVLVAAGFDALQGDPKGEMAATPAGFAQLTHLLMGLAGGKLILSLEGGYNLRALAEGVSASLHTLLGDPCPMLESPGAPCRSAQASVSCALEALEPFWEVLVRSTETVERDNMEEDNVEESEEEGPWEPPVLPILTWPVLQSRTGLVYDQNMMNHCNLWDSHHPEVPQRILRIMCRLEELGLAGRCLTLTPRPATEAELLTCHSAEYVGHLRATEKMKTRELHRESSNFDSIYICPSTFACAQLATGAACRLVEAVLSGEVLNGAAVVRPPGHHAEQDAACGFCFFNSVAVAARHAQTISGHALRILIVDWDVHHGNGTQHMFEDDPSVLYVSLHRYDHGTFFPMGDEGASSQIGRAAGTGFTVNVAWNGPRMGDADYLAAWHRLVLPIAYEFNPELVLVSAGFDAARGDPLGGCQVSPEGYAHLTHLLMGLASGRIILILEGGYNLTSISESMAACTRSLLGDPPPLLTLPRPPLSGALASITETIQVHRRYWRSLRVMKVEDREGPSSSKLVTKKAPQPAKPRLAERMTTREKKVLEAGMGKVTSASFGEESTPGQTNSETAVVALTQDQPSEAATGGATLAQTISEAAIGGAMLGQTTSEEAVGGATPDQTTSEETVGGAILDQTTSEDAVGGATLGQTTSEEAVGGATLAQTTSEAAMEGATLDQTTSEEAPGGTELIQTPLASSTDHQTPPTSPVQGTTPQISPSTLIGSLRTLELGSESQGASESQAPGEENLLGEAAGGQDMADSMLMQGSRGLTDQAIFYAVTPLPWCPHLVAVCPIPAAGLDVTQPCGDCGTIQENWVCLSCYQVYCGRYINGHMLQHHGNSGHPLVLSYIDLSAWCYYCQAYVHHQALLDVKNIAHQNKFGEDMPHPH
  
Inhibitor
Name:
BDBM50396042
Synonyms:
CHEMBL2170017
Type:
Small organic molecule
Emp. Form.:
C36H54N8O5
Mol. Mass.:
678.8646
SMILES:
CCC(=O)CCCCC[C@@H]1NC(=O)[C@H](CCCN=C(N)N)NC(=O)CCN(CC=C(C)C)C(=O)CN(CCc2c[nH]c3ccccc23)C1=O |r,wU:13.13,9.8,(56.09,-30.64,;54.73,-29.9,;53.42,-30.71,;53.46,-32.24,;52.07,-29.97,;50.75,-30.77,;49.4,-30.04,;48.09,-30.84,;46.73,-30.11,;45.52,-31.06,;44.06,-30.63,;43.65,-29.12,;44.6,-27.91,;41.81,-29.09,;40.95,-27.82,;39.42,-27.75,;38.63,-26.44,;37.11,-26.47,;36.31,-25.15,;37.06,-23.76,;34.83,-25.16,;41.35,-30.56,;39.92,-31.09,;38.65,-30.21,;39.92,-32.61,;41.35,-33.06,;41.36,-34.54,;40.03,-35.31,;38.69,-34.53,;37.36,-35.3,;36.03,-34.53,;37.36,-36.84,;42.79,-35.04,;42.82,-36.58,;44,-34.54,;43.97,-33.06,;44.73,-34.39,;44.72,-35.93,;46.05,-36.7,;47.45,-36.09,;48.48,-37.24,;47.7,-38.57,;48.16,-40.02,;47.14,-41.16,;45.63,-40.83,;45.17,-39.37,;46.2,-38.24,;45.59,-32.74,;46.92,-33.78,)|
Structure:
Search PDB for entries with ligand similarity: