Reaction Details | |||
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Target | Isoform 2 of Nuclear receptor ROR-gamma (RORgT) | ||
Ligand | BDBM256386 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | TR-FRET Assay | ||
pH | 7±n/a | ||
Temperature | 277.15±n/a K | ||
IC50 | 50±n/a nM | ||
Comments | extracted | ||
Citation | Barr, KJ; Maclean, JK; Zhang, H; Beresis, RT; Zhang, D; Andresen, BM; Anthony, NJ; Lapointe, BT; Sciammetta, N 3-cyclohexenyl and cyclohexyl substituted indole and indazole compounds as RORgammaT inhibitors and uses thereof US Patent US9487490 Publication Date 11/8/2016 | ||
More Info.: | Get all data from this article, Assay Method | ||
Isoform 2 of Nuclear receptor ROR-gamma (RORgT) | |||
Name: | Isoform 2 of Nuclear receptor ROR-gamma (RORgT) | ||
Synonyms: | Isoform 2 of Nuclear receptor ROR-gamma | NR1F3 | Nuclear receptor ROR-gamma (RORgT) | Nuclear receptor ROR-gammaT | RORC | RORG | RORG_HUMAN | RZRG | Retinoid-related orphan receptor-gamma (RORgT) | Retinoid-related orphan receptor-gamma (RORĪ³T) | ||
Type: | Protein | ||
Mol. Mass.: | 55831.73 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P51449-2 | ||
Residue: | 497 | ||
Sequence: |
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BDBM256386 | |||
n/a | |||
Name | BDBM256386 | ||
Synonyms: | US9487490, 9A | ||
Type | Small organic molecule | ||
Emp. Form. | C23H19ClF4N2O3 | ||
Mol. Mass. | 482.855 | ||
SMILES | C[C@@]1(CC[C@@H](CC1)c1nn(C(=O)c2c(Cl)cccc2C(F)(F)F)c2cccc(F)c12)C(O)=O |r,wU:4.7,1.0,wD:1.33,(-2.14,8.14,;-2.41,6.62,;-3.44,5.48,;-2.96,4.01,;-1.45,3.69,;-.42,4.84,;-.9,6.3,;-.98,2.23,;-1.88,.98,;-.98,-.27,;-1.45,-1.73,;-.42,-2.87,;-2.96,-2.05,;-3.99,-.91,;-3.51,.56,;-5.5,-1.23,;-5.97,-2.69,;-4.94,-3.84,;-3.44,-3.51,;-2.41,-4.66,;-2.8,-6.15,;-1.32,-5.75,;-.87,-4.66,;.49,.21,;1.82,-.56,;3.15,.21,;3.15,1.75,;1.82,2.52,;1.82,4.06,;.49,1.75,;-3.51,7.69,;-4.99,7.27,;-3.14,9.18,)| | ||
Structure |