Reaction Details |
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Target | Nuclear receptor ROR-gamma |
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Ligand | BDBM50445878 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1513553 (CHEMBL3610010) |
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IC50 | 1000±n/a nM |
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Citation | Wang, Y; Cai, W; Cheng, Y; Yang, T; Liu, Q; Zhang, G; Meng, Q; Han, F; Huang, Y; Zhou, L; Xiang, Z; Zhao, YG; Xu, Y; Cheng, Z; Lu, S; Wu, Q; Xiang, JN; Elliott, JD; Leung, S; Ren, F; Lin, X Discovery of Biaryl Amides as Potent, Orally Bioavailable, and CNS Penetrant ROR¿t Inhibitors. ACS Med Chem Lett6:787-92 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Nuclear receptor ROR-gamma |
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Name: | Nuclear receptor ROR-gamma |
Synonyms: | NR1F3 | Nuclear receptor ROR-gamma | Nuclear receptor ROR-gamma (RORC) | Nuclear receptor subfamily 1 group F member 3 | RAR-related orphan receptor C (RORc) | RORC | RORG | RORG_HUMAN | RZRG | Retinoid-related orphan receptor-gamma | Retinoid-related orphan receptor-gamma (RORc) |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 58218.40 |
Organism: | Homo sapiens (Human) |
Description: | P51449 |
Residue: | 518 |
Sequence: | MDRAPQRQHRASRELLAAKKTHTSQIEVIPCKICGDKSSGIHYGVITCEGCKGFFRRSQR
CNAAYSCTRQQNCPIDRTSRNRCQHCRLQKCLALGMSRDAVKFGRMSKKQRDSLHAEVQK
QLQQRQQQQQEPVVKTPPAGAQGADTLTYTLGLPDGQLPLGSSPDLPEASACPPGLLKAS
GSGPSYSNNLAKAGLNGASCHLEYSPERGKAEGRESFYSTGSQLTPDRCGLRFEEHRHPG
LGELGQGPDSYGSPSFRSTPEAPYASLTEIEHLVQSVCKSYRETCQLRLEDLLRQRSNIF
SREEVTGYQRKSMWEMWERCAHHLTEAIQYVVEFAKRLSGFMELCQNDQIVLLKAGAMEV
VLVRMCRAYNADNRTVFFEGKYGGMELFRALGCSELISSIFDFSHSLSALHFSEDEIALY
TALVLINAHRPGLQEKRKVEQLQYNLELAFHHHLCKTHRQSILAKLPPKGKLRSLCSQHV
ERLQIFQHLHPIVVQAAFPPLYKELFSTETESPVGLSK
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BDBM50445878 |
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n/a |
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Name | BDBM50445878 |
Synonyms: | CHEMBL3105815 |
Type | Small organic molecule |
Emp. Form. | C19H16Cl2N2O3S2 |
Mol. Mass. | 455.378 |
SMILES | CCS(=O)(=O)c1ccc(CC(=O)Nc2nc(cs2)-c2cc(Cl)ccc2Cl)cc1 |
Structure |
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