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TargetNuclear receptor ROR-gamma [238-497]
LigandBDBM175864
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:
BDBM175864
n/a
NameBDBM175864
Synonyms:US9688684, Compound 61: 8-(3-Isopropyl-1-phenyl-1H-pyrazol-4-yl)-7-thiophen-2-ylmethyl-5,6,7,8-tetrahydro-tetrazolo[1,5-a]pyrazine
TypeSmall organic molecule
Emp. Form.C21H23N7S
Mol. Mass.405.519
SMILESCC(C)c1nn(cc1C1N(Cc2cccs2)CCn2nnnc12)-c1ccccc1
Structure
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