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Assay Detail

CHEMBL873052

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

Binding
Compound was evaluated for the inhibition of adenosine deaminase
7
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Adenosine deaminase (CHEMBL1910)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Adenosine deaminase inhibitors. Conversion of a single chiral synthon into erythro- and threo-9-(2-hydroxy-3-nonyl)adenines.
Bastian G, Bessodes M, Panzica RP, Abushanab E, Chen SF, Stoeckler JD, Parks RE.
J Med Chem (1981) 24 : 1383 -1385
PubMed 7310814 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 7 8.34 10.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1580 PENTOSTATIN 4.0 1 10.00
CHEMBL284483 COFORMYCIN 2.0 1 10.00
CHEMBL50378 EHNA 2 9.40
CHEMBL296435 (+)-EHNA 1 8.70
CHEMBL1555103 1 7.10
CHEMBL2114367 1 6.91

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1580 PENTOSTATIN Ki = 0.1 nM 10.00
CHEMBL284483 COFORMYCIN Ki = 0.1 nM 10.00
CHEMBL50378 EHNA Ki = 0.4 nM 9.40
CHEMBL296435 (+)-EHNA Ki = 2.0 nM 8.70
CHEMBL1555103 Ki = 80.0 nM 7.10
CHEMBL2114367 Ki = 122.0 nM 6.91
CHEMBL50378 EHNA Ki = 500.0 nM 6.30