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Assay Detail

CHEMBL702339

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

Functional
In vitro inhibition of platelet aggregation by measuring its effect on the ADP-stimulated aggregation of human platelets
12
Total Activities
12
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 glycoprotein IIb/IIIa inhibitors: substituted quinazolinediones and quinazolinones as potent fibrinogen receptor antagonists.
Liverton NJ, Armstrong DJ, Claremon DA, Remy DC, Baldwin JJ, Lynch RJ, Zhang G, Gould RJ.
Bioorg Med Chem Lett (1998) 8 : 483 -486
PubMed 9871603 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 7.19 8.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL315065 1 8.05
CHEMBL1704 1 7.82
CHEMBL118749 1 7.43
CHEMBL117985 1 7.37
CHEMBL145645 1 7.21
CHEMBL144573 1 7.17
CHEMBL144596 1 7.13
CHEMBL344594 1 7.00
CHEMBL142152 1 6.85
CHEMBL435486 1 6.80
CHEMBL142797 1 6.80
CHEMBL143889 1 6.68

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL315065 IC50 = 9.0 nM 8.05
CHEMBL1704 IC50 = 15.0 nM 7.82
CHEMBL118749 IC50 = 37.0 nM 7.43
CHEMBL117985 IC50 = 43.0 nM 7.37
CHEMBL145645 IC50 = 61.0 nM 7.21
CHEMBL144573 IC50 = 67.0 nM 7.17
CHEMBL144596 IC50 = 74.0 nM 7.13
CHEMBL344594 IC50 = 100.0 nM 7.00
CHEMBL142152 IC50 = 140.0 nM 6.85
CHEMBL435486 IC50 = 160.0 nM 6.80
CHEMBL142797 IC50 = 160.0 nM 6.80
CHEMBL143889 IC50 = 210.0 nM 6.68