Reaction Details |
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Target | Nuclear receptor ROR-gamma [238-497] |
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Ligand | BDBM175893 |
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Substrate/Competitor | n/a |
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Meas. Tech. | M1H Assay |
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IC50 | 5445±n/a nM |
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Citation | Finsinger, D; Wucherer-Plietker, M; Blume, B Substituted tetrazolo[1,5-a]pyrazines as ROR-gamma inhibitors US Patent US9688684 Publication Date 6/27/2017 |
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More Info.: | Get all data from this article, Assay Method |
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Nuclear receptor ROR-gamma [238-497] |
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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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BDBM175893 |
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n/a |
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Name | BDBM175893 |
Synonyms: | US9688684, Compound 90: 7-Benzyl-8-(4-ethyl-phenyl)-5,6,7,8-tetrahydro-tetrazolo[1,5-a]pyrazine |
Type | Small organic molecule |
Emp. Form. | C19H21N5 |
Mol. Mass. | 319.4035 |
SMILES | CCc1ccc(cc1)C1N(Cc2ccccc2)CCn2nnnc12 |
Structure |
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