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Assay Detail

CHEMBL3385908

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

Binding
Inhibition of human factor10a assessed as reduction in hydrolysis of chromogenic substrate S-2765 by Cheng-Prusoff equation analysis
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

Coagulation factor X (CHEMBL244)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

How a β-D-glucoside side chain enhances binding affinity to thrombin of inhibitors bearing 2-chlorothiophene as P1 moiety: crystallography, fragment deconstruction study, and evaluation of antithrombotic properties.
Belviso BD, Caliandro R, de Candia M, Zaetta G, Lopopolo G, Incampo F, Colucci M, Altomare CD.
J Med Chem (2014) 57 : 8563 -8575
PubMed 25268757 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 6 7.29 10.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3343301 1 10.05
CHEMBL3343300 1 9.60
CHEMBL3343299 1 9.22
CHEMBL3343304 1 5.16
CHEMBL3343302 1 4.94
CHEMBL3343303 1 4.74

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3343301 Ki = 0.09 nM 10.05
CHEMBL3343300 Ki = 0.25 nM 9.60
CHEMBL3343299 Ki = 0.6 nM 9.22
CHEMBL3343304 Ki = 6900.0 nM 5.16
CHEMBL3343302 Ki = 11600.0 nM 4.94
CHEMBL3343303 Ki = 18300.0 nM 4.74