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Assay Detail

CHEMBL884359

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Binding
Compound was tested in vitro for inhibition of Dipeptidylpeptidase II
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Dipeptidyl peptidase 2 (CHEMBL3976)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-activity relationships of boronic acid inhibitors of dipeptidyl peptidase IV. 1. Variation of the P2 position of Xaa-boroPro dipeptides.
Coutts SJ, Kelly TA, Snow RJ, Kennedy CA, Barton RW, Adams J, Krolikowski DA, Freeman DM, Campbell SJ, Ksiazek JF, Bachovchin WW.
J Med Chem (1996) 39 : 2087 -2094
PubMed 8642568 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 6.62 7.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL67279 TALABOSTAT 3.0 1 7.82
CHEMBL305170 1 7.68
CHEMBL63860 1 7.22
CHEMBL1790478 1 6.14
CHEMBL63895 1 6.11
CHEMBL65406 1 4.75

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL67279 TALABOSTAT IC50 = 15.0 nM 7.82
CHEMBL305170 IC50 = 21.0 nM 7.68
CHEMBL63860 IC50 = 60.0 nM 7.22
CHEMBL1790478 IC50 = 730.0 nM 6.14
CHEMBL63895 IC50 = 770.0 nM 6.11
CHEMBL65406 IC50 = 18000.0 nM 4.75