Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL644415

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

Binding
In vitro inhibitory activity against rabbit lung Angiotensin I converting enzyme at pH 8.3
69
Total Activities
68
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Oryctolagus cuniculus
Confidence 9 — Direct single protein target
Curated By Intermediate

Target

Angiotensin-converting enzyme (CHEMBL4074)
Type SINGLE PROTEIN
Organism Oryctolagus cuniculus

Publication

Angiotensin-converting enzyme inhibitors. New orally active antihypertensive (mercaptoalkanoyl)- and [(acylthio)alkanoyl]glycine derivatives.
Suh JT, Skiles JW, Williams BE, Youssefyeh RD, Jones H, Loev B, Neiss ES, Schwab A, Mann WS, Khandwala A.
J Med Chem (1985) 28 : 57 -66
PubMed 2981324 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 69 6.82 8.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL160361 1 8.30
CHEMBL1907938 1 7.80
CHEMBL1560 CAPTOPRIL 4.0 1 7.77
CHEMBL348040 1 7.75
CHEMBL23523 1 7.75
CHEMBL346255 1 7.72
CHEMBL346561 2 7.70
CHEMBL23727 1 7.64
CHEMBL158962 1 7.52
CHEMBL23841 1 7.51
CHEMBL278348 1 7.51
CHEMBL345858 1 7.50
CHEMBL23641 1 7.48
CHEMBL23518 1 7.46
CHEMBL422013 1 7.36
CHEMBL350484 1 7.36
CHEMBL406430 1 7.35
CHEMBL347259 1 7.32
CHEMBL159075 1 7.29
CHEMBL422535 1 7.26
CHEMBL346588 1 7.26
CHEMBL350258 1 7.22
CHEMBL347447 1 7.19
CHEMBL346495 1 7.14
CHEMBL348043 1 7.12
CHEMBL345619 1 7.12
CHEMBL160689 1 7.12
CHEMBL158972 1 7.10
CHEMBL160770 1 7.09
CHEMBL158673 1 7.07

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL160361 IC50 = 5.0 nM 8.30
CHEMBL1907938 IC50 = 16.0 nM 7.80
CHEMBL1560 CAPTOPRIL IC50 = 17.0 nM 7.77
CHEMBL23523 IC50 = 18.0 nM 7.75
CHEMBL348040 IC50 = 18.0 nM 7.75
CHEMBL346255 IC50 = 19.0 nM 7.72
CHEMBL346561 IC50 = 20.0 nM 7.70
CHEMBL23727 IC50 = 23.0 nM 7.64
CHEMBL158962 IC50 = 30.0 nM 7.52
CHEMBL278348 IC50 = 31.0 nM 7.51
CHEMBL23841 IC50 = 31.0 nM 7.51
CHEMBL345858 IC50 = 32.0 nM 7.50
CHEMBL23641 IC50 = 33.0 nM 7.48
CHEMBL23518 IC50 = 35.0 nM 7.46
CHEMBL422013 IC50 = 44.0 nM 7.36
CHEMBL350484 IC50 = 44.0 nM 7.36
CHEMBL406430 IC50 = 45.0 nM 7.35
CHEMBL347259 IC50 = 48.0 nM 7.32
CHEMBL159075 IC50 = 51.0 nM 7.29
CHEMBL346561 IC50 = 52.0 nM 7.28
CHEMBL346588 IC50 = 55.0 nM 7.26
CHEMBL422535 IC50 = 55.0 nM 7.26
CHEMBL350258 IC50 = 60.0 nM 7.22
CHEMBL347447 IC50 = 64.0 nM 7.19
CHEMBL346495 IC50 = 72.0 nM 7.14
CHEMBL160689 IC50 = 75.0 nM 7.12
CHEMBL345619 IC50 = 75.0 nM 7.12
CHEMBL348043 IC50 = 75.0 nM 7.12
CHEMBL158972 IC50 = 79.0 nM 7.10
CHEMBL160770 IC50 = 82.0 nM 7.09
CHEMBL158673 IC50 = 85.0 nM 7.07
CHEMBL350718 IC50 = 88.0 nM 7.06
CHEMBL347635 IC50 = 95.0 nM 7.02
CHEMBL158994 IC50 = 110.0 nM 6.96
CHEMBL346535 IC50 = 120.0 nM 6.92
CHEMBL347633 IC50 = 130.0 nM 6.89
CHEMBL160927 IC50 = 130.0 nM 6.89
CHEMBL159000 IC50 = 130.0 nM 6.89
CHEMBL347853 IC50 = 140.0 nM 6.85
CHEMBL160567 IC50 = 160.0 nM 6.80
CHEMBL158617 IC50 = 170.0 nM 6.77
CHEMBL284139 IC50 = 190.0 nM 6.72
CHEMBL157543 IC50 = 210.0 nM 6.68
CHEMBL160473 IC50 = 220.0 nM 6.66
CHEMBL160985 IC50 = 220.0 nM 6.66
CHEMBL159151 IC50 = 270.0 nM 6.57
CHEMBL346254 IC50 = 270.0 nM 6.57
CHEMBL345692 IC50 = 280.0 nM 6.55
CHEMBL554712 IC50 = 280.0 nM 6.55
CHEMBL26338 IC50 = 300.0 nM 6.52