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Assay Detail

CHEMBL646137

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

Binding
In vitro binding affinity towards human adenosine deaminase (ADA)
7
Total Activities
7
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

Structure-based design and synthesis of non-nucleoside, potent, and orally bioavailable adenosine deaminase inhibitors.
Terasaka T, Okumura H, Tsuji K, Kato T, Nakanishi I, Kinoshita T, Kato Y, Kuno M, Seki N, Naoe Y, Inoue T, Tanaka K, Nakamura K.
J Med Chem (2004) 47 : 2728 -2731
PubMed 15139750 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 7 7.04 8.11

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL93280 1 8.11
CHEMBL92404 1 8.01
CHEMBL93560 1 7.96
CHEMBL328139 1 7.89
CHEMBL327830 1 6.17
CHEMBL93647 1 5.92
CHEMBL329433 1 5.23

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL93280 Ki = 7.7 nM 8.11
CHEMBL92404 Ki = 9.8 nM 8.01
CHEMBL93560 Ki = 11.0 nM 7.96
CHEMBL328139 Ki = 13.0 nM 7.89
CHEMBL327830 Ki = 680.0 nM 6.17
CHEMBL93647 Ki = 1200.0 nM 5.92
CHEMBL329433 Ki = 5900.0 nM 5.23