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

CHEMBL659792

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

Binding
Compound was evaluated for inhibitory activity against human heart chymase (HHC)
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Chymase (CHEMBL4068)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Peptidyl human heart chymase inhibitors. 2. Discovery of highly selective difluoromethylene ketone derivatives with Glu at P3 site.
Eda M, Ashimori A, Akahoshi F, Yoshimura T, Inoue Y, Fukaya C, Nakajima M, Fukuyama H, Imada T, Takai S, Shiota N, Miyazaki M, Nakamura N.
Bioorg Med Chem Lett (1998) 8 : 919 -924
PubMed 9871512 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 10 7.97 8.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL355430 1 8.52
CHEMBL436061 1 8.41
CHEMBL169707 1 8.25
CHEMBL355132 1 8.22
CHEMBL170697 1 8.17
CHEMBL170152 1 7.85
CHEMBL366721 1 7.68
CHEMBL433799 1 7.64
CHEMBL171769 1 7.56
CHEMBL367094 1 7.44

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL355430 Ki = 3.0 nM 8.52
CHEMBL436061 Ki = 3.9 nM 8.41
CHEMBL169707 Ki = 5.6 nM 8.25
CHEMBL355132 Ki = 6.0 nM 8.22
CHEMBL170697 Ki = 6.7 nM 8.17
CHEMBL170152 Ki = 14.2 nM 7.85
CHEMBL366721 Ki = 21.1 nM 7.68
CHEMBL433799 Ki = 22.8 nM 7.64
CHEMBL171769 Ki = 27.5 nM 7.56
CHEMBL367094 Ki = 36.6 nM 7.44