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

CHEMBL700679

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

Functional
Evaluated in vitro for the inhibition of Adenosine (ADO) phosphorylation in intact IMR-32 human neuroblastoma cells.
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type IMR-32
Confidence 1 — Organism
Curated By Expert

Target

IMR-32 (CHEMBL614585)
Type CELL-LINE
Organism Homo sapiens

Publication

Design, synthesis, and structure-activity relationship of 6-alkynylpyrimidines as potent adenosine kinase inhibitors.
Gomtsyan A, Didomenico S, Lee CH, Matulenko MA, Kim K, Kowaluk EA, Wismer CT, Mikusa J, Yu H, Kohlhaas K, Jarvis MF, Bhagwat SS.
J Med Chem (2002) 45 : 3639 -3648
PubMed 12166937 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 6.79 8.15

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL338508 1 8.15
CHEMBL121182 1 7.34
CHEMBL434792 1 7.03
CHEMBL121415 1 7.03
CHEMBL121361 1 7.00
CHEMBL121623 1 6.93
CHEMBL120976 1 6.91
CHEMBL120984 1 6.84
CHEMBL120953 1 6.70
CHEMBL331778 1 6.55
CHEMBL121475 1 6.41
CHEMBL420879 1 6.16
CHEMBL332689 1 6.00
CHEMBL120650 1 6.00
CHEMBL119839 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL338508 IC50 = 7.0 nM 8.15
CHEMBL121182 IC50 = 46.0 nM 7.34
CHEMBL434792 IC50 = 94.0 nM 7.03
CHEMBL121415 IC50 = 94.0 nM 7.03
CHEMBL121361 IC50 = 100.0 nM 7.00
CHEMBL121623 IC50 = 118.0 nM 6.93
CHEMBL120976 IC50 = 124.0 nM 6.91
CHEMBL120984 IC50 = 146.0 nM 6.84
CHEMBL120953 IC50 = 198.0 nM 6.70
CHEMBL331778 IC50 = 280.0 nM 6.55
CHEMBL121475 IC50 = 388.0 nM 6.41
CHEMBL420879 IC50 = 700.0 nM 6.16
CHEMBL332689 IC50 = 1000.0 nM 6.00
CHEMBL120650 IC50 = 1000.0 nM 6.00
CHEMBL119839 IC50 > 1000.0 nM -