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Assay Detail

CHEMBL2438909

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

Binding
Inhibition of SARS coronavirus 3CL-protease R188I mutant using H-TSAVLQSGFRK-NH2 as substrate after 60 mins by HPLC analysis
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Severe acute respiratory syndrome-related coronavirus
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Development of potent dipeptide-type SARS-CoV 3CL protease inhibitors with novel P3 scaffolds: design, synthesis, biological evaluation, and docking studies.
Thanigaimalai P, Konno S, Yamamoto T, Koiwai Y, Taguchi A, Takayama K, Yakushiji F, Akaji K, Chen SE, Naser-Tavakolian A, Schön A, Freire E, Hayashi Y.
Eur J Med Chem (2013) 68 : 372 -384
PubMed 23994330 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 5.67 6.13

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2435614 1 6.13
CHEMBL2435605 1 5.89
CHEMBL2435617 1 5.89
CHEMBL2435622 1 5.82
CHEMBL2435610 1 5.34
CHEMBL2435612 1 5.32
CHEMBL2435616 1 5.28

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2435614 IC50 = 740.0 nM 6.13
CHEMBL2435605 IC50 = 1300.0 nM 5.89
CHEMBL2435617 IC50 = 1300.0 nM 5.89
CHEMBL2435622 IC50 = 1500.0 nM 5.82
CHEMBL2435610 IC50 = 4600.0 nM 5.34
CHEMBL2435612 IC50 = 4800.0 nM 5.32
CHEMBL2435616 IC50 = 5200.0 nM 5.28