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

CHEMBL645374

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

Binding
Compound was evaluated for inhibition of adenylate cyclase from rat brain
10
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Tissue Brain
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Adenylate cyclase type 5 (CHEMBL2880)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Synthesis of 2',5'-dideoxy-2-fluoroadenosine and 2',5'-dideoxy-2,5'-difluoroadenosine: potent P-site inhibitors of adenylyl cyclase.
Ye S, Rezende MM, Deng WP, Herbert B, Daly JW, Johnson RA, Kirk KL.
J Med Chem (2004) 47 : 1207 -1213
PubMed 14971900 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 5.20 6.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2079578 2 6.05
CHEMBL2079579 2 6.01
CHEMBL2448167 1 5.55
CHEMBL1229920 2 5.34
CHEMBL449329 DEOXYADENOSINE 1 4.82
CHEMBL1090 VIDARABINE 4.0 1 4.09
CHEMBL477 ADENOSINE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2079578 IC50 = 890.0 nM 6.05
CHEMBL2079579 IC50 = 980.0 nM 6.01
CHEMBL2448167 IC50 = 2800.0 nM 5.55
CHEMBL1229920 IC50 = 4600.0 nM 5.34
CHEMBL449329 DEOXYADENOSINE IC50 = 15000.0 nM 4.82
CHEMBL2079579 IC50 = 29000.0 nM 4.54
CHEMBL1090 VIDARABINE IC50 = 82000.0 nM 4.09
CHEMBL2079578 IC50 > 100000.0 nM -
CHEMBL477 ADENOSINE IC50 > 300000.0 nM -
CHEMBL1229920 IC50 > 100000.0 nM -