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Assay Detail

CHEMBL2188274

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Functional
Antagonist activity at human TRPV1 expressed in CHOK1 cells assessed as inhibition of pH-induced activity by FLIPR assay
76
Total Activities
76
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type CHO-K1
Confidence 9 — Direct single protein target
Curated By Autocuration

Publication

2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent transient receptor potential vanilloid 1 (TRPV1) antagonists: structure-activity relationships of 2-amino derivatives in the N-(6-trifluoromethylpyridin-3-ylmethyl) C-region.
Kim MS, Ryu H, Kang DW, Cho SH, Seo S, Park YS, Kim MY, Kwak EJ, Kim YS, Bhondwe RS, Kim HS, Park SG, Son K, Choi S, DeAndrea-Lazarus IA, Pearce LV, Blumberg PM, Frank R, Bahrenberg G, Stockhausen H, Kögel BY, Schiene K, Christoph T, Lee J.
J Med Chem (2012) 55 : 8392 -8408
PubMed 22957803 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 76 6.97 8.20

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2177429 1 8.20
CHEMBL2177432 1 8.10
CHEMBL2177428 1 8.08
CHEMBL2178064 1 7.98
CHEMBL2177425 1 7.92
CHEMBL2178063 1 7.83
CHEMBL2177441 1 7.77
CHEMBL2177435 1 7.76
CHEMBL2177404 1 7.70
CHEMBL2178065 1 7.67
CHEMBL2179150 1 7.64
CHEMBL2177402 1 7.62
CHEMBL2177418 1 7.60
CHEMBL2177434 1 7.60
CHEMBL2177433 1 7.59
CHEMBL2177419 1 7.56
CHEMBL2177411 1 7.55
CHEMBL2178059 1 7.52
CHEMBL2177410 1 7.51
CHEMBL2177405 1 7.51
CHEMBL2179146 1 7.51
CHEMBL2179149 1 7.47
CHEMBL2179148 1 7.42
CHEMBL2179147 1 7.41
CHEMBL2177440 1 7.40
CHEMBL2177437 1 7.37
CHEMBL2179152 1 7.35
CHEMBL2177414 1 7.34
CHEMBL2177424 1 7.33
CHEMBL2178072 1 7.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2177429 IC50 = 6.3 nM 8.20
CHEMBL2177432 IC50 = 8.0 nM 8.10
CHEMBL2177428 IC50 = 8.4 nM 8.08
CHEMBL2178064 IC50 = 10.5 nM 7.98
CHEMBL2177425 IC50 = 12.1 nM 7.92
CHEMBL2178063 IC50 = 14.7 nM 7.83
CHEMBL2177441 IC50 = 17.0 nM 7.77
CHEMBL2177435 IC50 = 17.4 nM 7.76
CHEMBL2177404 IC50 = 19.8 nM 7.70
CHEMBL2178065 IC50 = 21.3 nM 7.67
CHEMBL2179150 IC50 = 23.1 nM 7.64
CHEMBL2177402 IC50 = 24.0 nM 7.62
CHEMBL2177418 IC50 = 25.1 nM 7.60
CHEMBL2177434 IC50 = 25.0 nM 7.60
CHEMBL2177433 IC50 = 25.6 nM 7.59
CHEMBL2177419 IC50 = 27.8 nM 7.56
CHEMBL2177411 IC50 = 28.2 nM 7.55
CHEMBL2178059 IC50 = 30.0 nM 7.52
CHEMBL2177410 IC50 = 31.0 nM 7.51
CHEMBL2177405 IC50 = 31.0 nM 7.51
CHEMBL2179146 IC50 = 30.7 nM 7.51
CHEMBL2179149 IC50 = 34.0 nM 7.47
CHEMBL2179148 IC50 = 38.3 nM 7.42
CHEMBL2179147 IC50 = 39.2 nM 7.41
CHEMBL2177440 IC50 = 40.0 nM 7.40
CHEMBL2177437 IC50 = 43.0 nM 7.37
CHEMBL2179152 IC50 = 44.5 nM 7.35
CHEMBL2177414 IC50 = 45.2 nM 7.34
CHEMBL2177424 IC50 = 46.7 nM 7.33
CHEMBL2178072 IC50 = 50.0 nM 7.30
CHEMBL2178066 IC50 = 57.4 nM 7.24
CHEMBL2177438 IC50 = 81.0 nM 7.09
CHEMBL2177431 IC50 = 97.3 nM 7.01
CHEMBL2179153 IC50 = 108.0 nM 6.97
CHEMBL191247 IC50 = 116.0 nM 6.94
CHEMBL2179151 IC50 = 117.0 nM 6.93
CHEMBL2179154 IC50 = 117.0 nM 6.93
CHEMBL2177413 IC50 = 139.0 nM 6.86
CHEMBL2178083 IC50 = 140.0 nM 6.85
CHEMBL2178062 IC50 = 148.0 nM 6.83
CHEMBL2177439 IC50 = 159.0 nM 6.80
CHEMBL2177400 IC50 = 169.0 nM 6.77
CHEMBL2177422 IC50 = 192.0 nM 6.72
CHEMBL2178084 IC50 = 203.0 nM 6.69
CHEMBL2178071 IC50 = 209.0 nM 6.68
CHEMBL2178067 IC50 = 211.0 nM 6.68
CHEMBL2177423 IC50 = 218.0 nM 6.66
CHEMBL2177430 IC50 = 254.0 nM 6.59
CHEMBL2178077 IC50 = 260.0 nM 6.58
CHEMBL2177408 IC50 = 280.0 nM 6.55