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Assay Detail

CHEMBL5385457

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

Binding
Inhibition of mouse recombinant N-terminal IgG tagged and C-terminal His tagged C1S (22 to 694 aa residues) expressed in Expi293 cells using Z-Lys-SBzl peptide as substrate pretreated with compound followed by substrate addition incubated for 60 mins
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Mus musculus
Cell Type Expi293
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Discovery of a Novel Series of Potent, Selective, Orally Available, and Brain-Penetrable C1s Inhibitors for Modulation of the Complement Pathway.
Ikeda Z, Kamei T, Sasaki Y, Reynolds M, Sakai N, Yoshikawa M, Tawada M, Morishita N, Dougan DR, Chen CH, Levin I, Zou H, Kuno M, Arimura N, Kikukawa Y, Kondo M, Tohyama K, Sato K.
J Med Chem (2023) 66 : 6354 -6371
PubMed 37120845 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.21 7.21

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5417464 1 7.21

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5417464 IC50 = 61.0 nM 7.21