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Assay Detail

CHEMBL4394895

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

ADMET
Inhibition of purified human adenosine kinase using varying levels of [3H]Ado as substrate in presence of adenosine deaminase inhibitor deoxycoformycin by Line-weaver burk plot analysis
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type ADMET
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Adenosine kinase (CHEMBL3589)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-Guided Drug Design of 6-Substituted Adenosine Analogues as Potent Inhibitors of Mycobacterium tuberculosis Adenosine Kinase.
Crespo RA, Dang Q, Zhou NE, Guthrie LM, Snavely TC, Dong W, Loesch KA, Suzuki T, You L, Wang W, O'Malley T, Parish T, Olsen DB, Sacchettini JC.
J Med Chem (2019) 62 : 4483 -4499
PubMed 31002508 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 1 7.52 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL99203 IODOTUBERCIDIN 1 7.52

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL99203 IODOTUBERCIDIN Ki = 30.0 nM 7.52