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Compound Detail

CHEMBL2316745

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Cc1nc(C(=O)[C@H](C[C@@H]2CCNC2=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)OCc2ccccc2)C(C)C)sc1C

Basic Information

ChEMBL ID CHEMBL2316745
Phase Preclinical
Structure Type BOTH
InChI Key ZWHYRYQLLXZDJK-QORCZRPOSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

613.8
MW (Da)
3.44
ALogP
8
HBA
4
HBD
155.6
PSA (Ų)
0.24
QED
1
Ro5 Violations
14
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C31H43N5O6S
MW 613.78
Aromatic Rings 2
Heavy Atoms 43
NP-Likeness -0.22

Activity Summary

IC50 1 meas. best 4.66

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.66 4.66 22000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 22000.0 nM 4.66 Inhibition of SARS coronavirus 3C-like protease R188I mutant using H-TSAVLQSGFRK... 23245752

Literature References

PubMed DOI Target Context # Activities
23245752 10.1016/j.bmc.2012.11.017 Unchecked 2

Data from ChEMBL 36 via Core Engine