Reaction Details | |||
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Target | Isoform 2 of Nuclear receptor ROR-gamma (RORgT) | ||
Ligand | BDBM256385 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | TR-FRET Assay | ||
pH | 7±n/a | ||
Temperature | 277.15±n/a K | ||
IC50 | 16±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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BDBM256385 | |||
n/a | |||
Name | BDBM256385 | ||
Synonyms: | US9487490, 8A | ||
Type | Small organic molecule | ||
Emp. Form. | C22H17ClF4N2O3 | ||
Mol. Mass. | 468.829 | ||
SMILES | OC(=O)[C@H]1CC[C@@H](CC1)c1nn(C(=O)c2c(Cl)cccc2C(F)(F)F)c2cccc(F)c12 |r,wU:6.9,wD:3.2,(-2.81,9.19,;-1.72,8.1,;-.23,8.5,;-2.12,6.61,;-3.62,6.16,;-4.02,4.67,;-2.93,3.59,;-1.44,3.98,;-1.04,5.47,;-3.33,2.1,;-2.42,.85,;-3.33,-.39,;-2.93,-1.88,;-4.02,-2.97,;-1.44,-2.28,;-.35,-1.19,;-.75,.3,;1.13,-1.59,;1.53,-3.08,;.44,-4.17,;-1.04,-3.77,;-2.13,-4.86,;-3.67,-4.86,;-3.22,-5.95,;-1.74,-6.34,;-4.79,.08,;-6.13,-.69,;-7.46,.08,;-7.46,1.62,;-6.13,2.39,;-6.13,3.93,;-4.79,1.62,)| | ||
Structure |