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TargetNuclear receptor ROR-gamma [238-497]
LigandBDBM175913
Substrate/Competitorn/a
Meas. Tech.TR-FRET Assay
pH6.8±n/a
IC50 500±n/a nM
Commentsextracted
Citation Finsinger, DWucherer-Plietker, MBlume, B Substituted tetrazolo[1,5-a]pyrazines as ROR-gamma inhibitors US Patent US9688684 Publication Date 6/27/2017
More Info.:Get all data from this article,  Assay Method
 
Nuclear receptor ROR-gamma [238-497]
Name:Nuclear receptor ROR-gamma [238-497]
Synonyms:NR1F3 | RORC | RORG | RORG_HUMAN | RZRG | Retinoid-related orphan receptor gamma (RORgamma-LBD)
Type:Protein
Mol. Mass.:29835.99
Organism:Homo sapiens (Human)
Description:Human RORgamma ligand-binding domain.
Residue:260
Sequence:
HPGLGELGQGPDSYGSPSFRSTPEAPYASLTEIEHLVQSVCKSYRETCQLRLEDLLRQRS
NIFSREEVTGYQRKSMWEMWERCAHHLTEAIQYVVEFAKRLSGFMELCQNDQIVLLKAGA
MEVVLVRMCRAYNADNRTVFFEGKYGGMELFRALGCSELISSIFDFSHSLSALHFSEDEI
ALYTALVLINAHRPGLQEKRKVEQLQYNLELAFHHHLCKTHRQSILAKLPPKGKLRSLCS
QHVERLQIFQHLHPIVVQAA
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  Blast E-value cutoff:
BDBM175913
n/a
NameBDBM175913
Synonyms:US9688684, Compound 110: 7-(3-Bromo-benzyl)-8-(4-isopropoxy-phenyl)-5,6,7,8-tetrahydro-tetrazolo[1,5-a]pyrazine
TypeSmall organic molecule
Emp. Form.C20H22BrN5O
Mol. Mass.428.326
SMILESCC(C)Oc1ccc(cc1)C1N(Cc2cccc(Br)c2)CCn2nnnc12
Structure
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