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Assay Detail

CHEMBL4668629

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

Binding
Inhibition of C-terminal His6-tagged human CypD K133I mutant expressed in Escherichia coli BL21(DE3) using Suc-Ala-Ala-Cis-Pro-Phe-pNA as substrate by spectrophotometric analysis
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Fragment Linking Strategies for Structure-Based Drug Design.
Bancet A,Raingeval C,Lomberget T,Le Borgne M,Guichou JF,Krimm I
J Med Chem (2020) 63 : 11420 -11435
PubMed 32539387 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 5.96 6.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4092230 1 6.70
CHEMBL3647424 1 5.21
CHEMBL3408644 1 -
CHEMBL4745604 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4092230 IC50 = 200.0 nM 6.70
CHEMBL3647424 IC50 = 6200.0 nM 5.21
CHEMBL3408644 IC50 > 5000000.0 nM -
CHEMBL4745604 IC50 > 5000000.0 nM -