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Assay Detail

CHEMBL2166382

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

Binding
Displacement of [I125]ET1 from recombinant ETA receptor expressed in CHO cells after 2 hrs by TopCount analysis
60
Total Activities
60
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Cell Type CHO
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Endothelin-1 receptor (CHEMBL252)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

The discovery of N-[5-(4-bromophenyl)-6-[2-[(5-bromo-2-pyrimidinyl)oxy]ethoxy]-4-pyrimidinyl]-N'-propylsulfamide (Macitentan), an orally active, potent dual endothelin receptor antagonist.
Bolli MH, Boss C, Binkert C, Buchmann S, Bur D, Hess P, Iglarz M, Meyer S, Rein J, Rey M, Treiber A, Clozel M, Fischli W, Weller T.
J Med Chem (2012) 55 : 7849 -7861
PubMed 22862294 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 60 8.26 9.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2165339 1 9.52
CHEMBL112624 1 9.40
CHEMBL2163692 1 9.40
CHEMBL2103873 MACITENTAN 4.0 1 9.30
CHEMBL2165332 1 9.15
CHEMBL2165338 1 9.10
CHEMBL2165329 1 9.00
CHEMBL2163704 1 8.96
CHEMBL2163694 1 8.96
CHEMBL2163690 1 8.92
CHEMBL2165333 1 8.85
CHEMBL2165330 1 8.85
CHEMBL2163725 1 8.85
CHEMBL2163708 1 8.82
CHEMBL2165334 1 8.80
CHEMBL2163720 1 8.77
CHEMBL2165337 1 8.77
CHEMBL2163691 1 8.72
CHEMBL2163716 1 8.72
CHEMBL2163723 1 8.68
CHEMBL2163693 1 8.66
CHEMBL2163702 1 8.66
CHEMBL2165335 1 8.64
CHEMBL2163689 1 8.55
CHEMBL2163701 1 8.55
CHEMBL2163705 1 8.52
CHEMBL2163703 1 8.49
CHEMBL2163724 1 8.47
CHEMBL2165326 APROCITENTAN 4.0 1 8.47
CHEMBL2165336 1 8.44

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2165339 IC50 = 0.3 nM 9.52
CHEMBL112624 IC50 = 0.4 nM 9.40
CHEMBL2163692 IC50 = 0.4 nM 9.40
CHEMBL2103873 MACITENTAN IC50 = 0.5 nM 9.30
CHEMBL2165332 IC50 = 0.7 nM 9.15
CHEMBL2165338 IC50 = 0.8 nM 9.10
CHEMBL2165329 IC50 = 1.0 nM 9.00
CHEMBL2163704 IC50 = 1.1 nM 8.96
CHEMBL2163694 IC50 = 1.1 nM 8.96
CHEMBL2163690 IC50 = 1.2 nM 8.92
CHEMBL2165333 IC50 = 1.4 nM 8.85
CHEMBL2165330 IC50 = 1.4 nM 8.85
CHEMBL2163725 IC50 = 1.4 nM 8.85
CHEMBL2163708 IC50 = 1.5 nM 8.82
CHEMBL2165334 IC50 = 1.6 nM 8.80
CHEMBL2163720 IC50 = 1.7 nM 8.77
CHEMBL2165337 IC50 = 1.7 nM 8.77
CHEMBL2163691 IC50 = 1.9 nM 8.72
CHEMBL2163716 IC50 = 1.9 nM 8.72
CHEMBL2163723 IC50 = 2.1 nM 8.68
CHEMBL2163693 IC50 = 2.2 nM 8.66
CHEMBL2163702 IC50 = 2.2 nM 8.66
CHEMBL2165335 IC50 = 2.3 nM 8.64
CHEMBL2163689 IC50 = 2.8 nM 8.55
CHEMBL2163701 IC50 = 2.8 nM 8.55
CHEMBL2163705 IC50 = 3.0 nM 8.52
CHEMBL2163703 IC50 = 3.2 nM 8.49
CHEMBL2163724 IC50 = 3.4 nM 8.47
CHEMBL2165326 APROCITENTAN IC50 = 3.4 nM 8.47
CHEMBL2165336 IC50 = 3.6 nM 8.44
CHEMBL2163719 IC50 = 3.8 nM 8.42
CHEMBL2163697 IC50 = 4.3 nM 8.37
CHEMBL2163688 IC50 = 4.3 nM 8.37
CHEMBL2163715 IC50 = 4.3 nM 8.37
CHEMBL2165340 IC50 = 4.4 nM 8.36
CHEMBL2163711 IC50 = 6.7 nM 8.17
CHEMBL2165331 IC50 = 6.8 nM 8.17
CHEMBL2165328 IC50 = 6.9 nM 8.16
CHEMBL2163728 IC50 = 6.9 nM 8.16
CHEMBL2163721 IC50 = 7.0 nM 8.15
CHEMBL2163706 IC50 = 7.7 nM 8.11
CHEMBL2163717 IC50 = 7.9 nM 8.10
CHEMBL2163698 IC50 = 8.0 nM 8.10
CHEMBL2163714 IC50 = 9.4 nM 8.03
CHEMBL2163718 IC50 = 9.9 nM 8.00
CHEMBL2163709 IC50 = 10.4 nM 7.98
CHEMBL2163713 IC50 = 14.0 nM 7.85
CHEMBL2163726 IC50 = 14.0 nM 7.85
CHEMBL2163700 IC50 = 17.8 nM 7.75
CHEMBL314691 BQ-123 IC50 = 20.5 nM 7.69