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Assay Detail

CHEMBL648337

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Functional
Inhibitory activity against angiotensin converting enzyme (ACE)
133
Total Activities
126
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Confidence 8 — Homologous single protein target
Curated By Expert

Target

Angiotensin-converting enzyme (CHEMBL1808)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Three-dimensional quantitative structure-activity relationship of angiotesin-converting enzyme and thermolysin inhibitors. II. A comparison of CoMFA models incorporating molecular orbital fields and desolvation free energies based on active-analog and complementary-receptor-field alignment rules.
Waller CL, Marshall GR.
J Med Chem (1993) 36 : 2390 -2403
PubMed 8360884 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 133 7.20 9.94

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL35561 1 9.94
CHEMBL35309 1 9.88
CHEMBL80665 1 9.64
CHEMBL78629 1 9.60
CHEMBL35682 1 9.54
CHEMBL284734 1 9.53
CHEMBL285935 1 9.53
CHEMBL286339 1 9.31
CHEMBL34832 1 9.28
CHEMBL289022 1 9.28
CHEMBL312224 1 9.22
CHEMBL34650 1 9.20
CHEMBL431707 1 9.11
CHEMBL33025 1 9.06
CHEMBL284843 1 9.05
CHEMBL310750 1 9.00
CHEMBL284345 1 8.97
CHEMBL80779 1 8.96
CHEMBL1237 LISINOPRIL ANHYDROUS 4.0 1 8.92
CHEMBL39538 1 8.92
CHEMBL80906 1 8.77
CHEMBL433442 1 8.72
CHEMBL78346 1 8.66
CHEMBL309308 1 8.66
CHEMBL445561 1 8.59
CHEMBL78340 1 8.59
CHEMBL78726 1 8.55
CHEMBL312431 1 8.54
CHEMBL311268 1 8.54
CHEMBL311363 1 8.52

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL35561 IC50 = 0.1148 nM 9.94
CHEMBL35309 IC50 = 0.1318 nM 9.88
CHEMBL80665 IC50 = 0.2291 nM 9.64
CHEMBL78629 IC50 = 0.2512 nM 9.60
CHEMBL35682 IC50 = 0.2884 nM 9.54
CHEMBL285935 IC50 = 0.2951 nM 9.53
CHEMBL284734 IC50 = 0.2951 nM 9.53
CHEMBL286339 IC50 = 0.4898 nM 9.31
CHEMBL34832 IC50 = 0.5248 nM 9.28
CHEMBL289022 IC50 = 0.5248 nM 9.28
CHEMBL312224 IC50 = 0.6026 nM 9.22
CHEMBL34650 IC50 = 0.631 nM 9.20
CHEMBL431707 IC50 = 0.7762 nM 9.11
CHEMBL33025 IC50 = 0.871 nM 9.06
CHEMBL284843 IC50 = 0.8913 nM 9.05
CHEMBL310750 IC50 = 1.0 nM 9.00
CHEMBL284345 IC50 = 1.072 nM 8.97
CHEMBL80779 IC50 = 1.096 nM 8.96
CHEMBL39538 IC50 = 1.202 nM 8.92
CHEMBL1237 LISINOPRIL ANHYDROUS IC50 = 1.202 nM 8.92
CHEMBL80906 IC50 = 1.698 nM 8.77
CHEMBL433442 IC50 = 1.905 nM 8.72
CHEMBL309308 IC50 = 2.188 nM 8.66
CHEMBL78346 IC50 = 2.188 nM 8.66
CHEMBL78340 IC50 = 2.57 nM 8.59
CHEMBL445561 IC50 = 2.57 nM 8.59
CHEMBL78726 IC50 = 2.818 nM 8.55
CHEMBL311268 IC50 = 2.884 nM 8.54
CHEMBL312431 IC50 = 2.884 nM 8.54
CHEMBL309941 IC50 = 3.02 nM 8.52
CHEMBL311363 IC50 = 3.02 nM 8.52
CHEMBL287518 IC50 = 3.236 nM 8.49
CHEMBL311757 IC50 = 3.467 nM 8.46
CHEMBL309962 RENTIAPRIL IC50 = 3.715 nM 8.43
CHEMBL277270 IC50 = 3.981 nM 8.40
CHEMBL419649 IC50 = 4.786 nM 8.32
CHEMBL78731 IC50 = 5.248 nM 8.28
CHEMBL611148 IC50 = 6.026 nM 8.22
CHEMBL311471 IC50 = 6.457 nM 8.19
CHEMBL309601 IC50 = 7.079 nM 8.15
CHEMBL311525 IC50 = 8.913 nM 8.05
CHEMBL310841 IC50 = 10.0 nM 8.00
CHEMBL420391 IC50 = 12.02 nM 7.92
CHEMBL430630 IC50 = 12.02 nM 7.92
CHEMBL435360 IC50 = 12.02 nM 7.92
CHEMBL78353 IC50 = 15.14 nM 7.82
CHEMBL35419 IC50 = 15.85 nM 7.80
CHEMBL79189 IC50 = 19.95 nM 7.70
CHEMBL1560 CAPTOPRIL IC50 = 22.91 nM 7.64
CHEMBL78489 IC50 = 34.67 nM 7.46