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Assay Detail

CHEMBL990750

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

Binding
Inhibition of active form of human liver glycogen phosphorylase
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Glycogen phosphorylase, liver form (CHEMBL2568)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis, and pharmacological evaluation of N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives as potent glycogen phosphorylase inhibitors.
Onda K, Shiraki R, Ogiyama T, Yokoyama K, Momose K, Katayama N, Orita M, Yamaguchi T, Furutani M, Hamada N, Takeuchi M, Okada M, Ohta M, Tsukamoto S.
Bioorg Med Chem (2008) 16 : 10001 -10012
PubMed 18952447 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 6.49 7.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL458289 1 7.70
CHEMBL457860 1 7.44
CHEMBL457650 1 7.32
CHEMBL457643 1 7.20
CHEMBL444029 1 7.17
CHEMBL457861 1 6.80
CHEMBL457877 1 6.50
CHEMBL458092 1 6.36
CHEMBL505339 1 6.23
CHEMBL457029 1 6.10
CHEMBL455988 1 6.09
CHEMBL458091 1 6.05
CHEMBL99889 1 6.04
CHEMBL457878 1 5.92
CHEMBL496723 1 5.80
CHEMBL513263 1 5.07
CHEMBL459139 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL458289 IC50 = 20.0 nM 7.70
CHEMBL457860 IC50 = 36.0 nM 7.44
CHEMBL457650 IC50 = 48.0 nM 7.32
CHEMBL457643 IC50 = 63.0 nM 7.20
CHEMBL444029 IC50 = 68.0 nM 7.17
CHEMBL457861 IC50 = 160.0 nM 6.80
CHEMBL457877 IC50 = 320.0 nM 6.50
CHEMBL458092 IC50 = 440.0 nM 6.36
CHEMBL505339 IC50 = 590.0 nM 6.23
CHEMBL457029 IC50 = 800.0 nM 6.10
CHEMBL455988 IC50 = 810.0 nM 6.09
CHEMBL458091 IC50 = 900.0 nM 6.05
CHEMBL99889 IC50 = 920.0 nM 6.04
CHEMBL457878 IC50 = 1200.0 nM 5.92
CHEMBL496723 IC50 = 1600.0 nM 5.80
CHEMBL513263 IC50 = 8500.0 nM 5.07
CHEMBL459139 IC50 > 10000.0 nM -