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Assay Detail

CHEMBL1839320

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of SCD1 in human HepG2 cells
19
Total Activities
19
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HepG2
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Stearoyl-CoA desaturase (CHEMBL5555)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Bicyclic heteroaryl inhibitors of stearoyl-CoA desaturase: from systemic to liver-targeting inhibitors.
Ramtohul YK, Powell D, Leclerc JP, Leger S, Oballa R, Black C, Isabel E, Li CS, Crane S, Robichaud J, Guay J, Guiral S, Zhang L, Huang Z.
Bioorg Med Chem Lett (2011) 21 : 5692 -5696
PubMed 21871798 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 19 6.73 7.80

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1834443 1 7.80
CHEMBL1834453 1 7.77
CHEMBL1834262 1 7.54
CHEMBL1834452 1 7.33
CHEMBL1834454 1 7.32
CHEMBL1834456 1 7.28
CHEMBL1834442 1 7.23
CHEMBL1834447 1 6.79
CHEMBL1834457 1 6.78
CHEMBL1834446 1 6.74
CHEMBL1834451 1 6.59
CHEMBL1834441 1 6.57
CHEMBL1834449 1 6.50
CHEMBL1834448 1 6.42
CHEMBL1834445 1 6.12
CHEMBL1834450 1 4.97
CHEMBL1833979 1 4.61
CHEMBL1834455 1 -
CHEMBL1834444 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1834443 IC50 = 16.0 nM 7.80
CHEMBL1834453 IC50 = 17.0 nM 7.77
CHEMBL1834262 IC50 = 29.0 nM 7.54
CHEMBL1834452 IC50 = 47.0 nM 7.33
CHEMBL1834454 IC50 = 48.0 nM 7.32
CHEMBL1834456 IC50 = 53.0 nM 7.28
CHEMBL1834442 IC50 = 59.0 nM 7.23
CHEMBL1834447 IC50 = 162.0 nM 6.79
CHEMBL1834457 IC50 = 168.0 nM 6.78
CHEMBL1834446 IC50 = 182.0 nM 6.74
CHEMBL1834451 IC50 = 257.0 nM 6.59
CHEMBL1834441 IC50 = 268.0 nM 6.57
CHEMBL1834449 IC50 = 319.0 nM 6.50
CHEMBL1834448 IC50 = 378.0 nM 6.42
CHEMBL1834445 IC50 = 755.0 nM 6.12
CHEMBL1834450 IC50 = 10639.0 nM 4.97
CHEMBL1833979 IC50 = 24345.0 nM 4.61
CHEMBL1834455 IC50 < 39.0 nM -
CHEMBL1834444 IC50 - -