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

CHEMBL700876

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

Functional
The compound was tested for the inhibition of platelet aggregation
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Confidence 1 — Organism
Curated By Intermediate

Target

Homo sapiens (CHEMBL372)
Type ORGANISM
Organism Homo sapiens

Publication

Nonpeptide GPIIB/IIIA inhibitors. 16. Thieno[2,3-b]thiophene -sulfonamides are potent inhibitors of platelet aggregation
Prugh JD, Gould RJ, Lynch RJ, Zhang G, Cook JJ, Holahan MA, Stranieri MT, Sitko GR, Lee Gaul S, Bednar RA, Bednar B, Hartman GD
Bioorg Med Chem Lett (1997) 7 : 865 -870
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 7.59 8.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL293601 1 8.10
CHEMBL78760 1 8.10
CHEMBL78570 1 8.10
CHEMBL78503 1 8.05
CHEMBL312113 1 8.00
CHEMBL80432 1 7.96
CHEMBL78517 1 7.89
CHEMBL310964 1 7.68
CHEMBL169796 1 7.64
CHEMBL80381 1 7.50
CHEMBL352847 1 7.44
CHEMBL355050 1 7.12
CHEMBL312330 1 6.39
CHEMBL80307 1 6.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL293601 IC50 = 8.0 nM 8.10
CHEMBL78760 IC50 = 8.0 nM 8.10
CHEMBL78570 IC50 = 8.0 nM 8.10
CHEMBL78503 IC50 = 9.0 nM 8.05
CHEMBL312113 IC50 = 10.0 nM 8.00
CHEMBL80432 IC50 = 11.0 nM 7.96
CHEMBL78517 IC50 = 13.0 nM 7.89
CHEMBL310964 IC50 = 21.0 nM 7.68
CHEMBL169796 IC50 = 23.0 nM 7.64
CHEMBL80381 IC50 = 32.0 nM 7.50
CHEMBL352847 IC50 = 36.0 nM 7.44
CHEMBL355050 IC50 = 76.0 nM 7.12
CHEMBL312330 IC50 = 410.0 nM 6.39
CHEMBL80307 IC50 = 500.0 nM 6.30