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Assay Detail

CHEMBL3738916

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

Binding
Inhibition of human uPA for 15 mins using pyro-Glu-Gly-Arg-p-nitroanilide as substrate
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Urokinase-type plasminogen activator (CHEMBL3286)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design of Specific Serine Protease Inhibitors Based on a Versatile Peptide Scaffold: Conversion of a Urokinase Inhibitor to a Plasma Kallikrein Inhibitor.
Xu P, Xu M, Jiang L, Yang Q, Luo Z, Dauter Z, Huang M, Andreasen PA.
J Med Chem (2015) 58 : 8868 -8876
PubMed 26536069 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 6 4.03 4.03

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3735080 1 4.03
CHEMBL3734777 1 -
CHEMBL3736473 1 -
CHEMBL3735263 1 -
CHEMBL3735513 1 -
CHEMBL3735217 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3735080 Ki = 93000.0 nM 4.03
CHEMBL3734777 Ki > 1000000.0 nM -
CHEMBL3736473 Ki > 1000000.0 nM -
CHEMBL3735263 Ki > 1000000.0 nM -
CHEMBL3735513 Ki > 1000000.0 nM -
CHEMBL3735217 Ki > 1000000.0 nM -