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Compound Detail

CHEMBL5532074

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CN1C(=O)[C@H](Cc2ccccc2)N(C(=O)[C@@H](NC(=O)c2cccs2)C(C)(C)C)CCCOc2ccc(Cl)c(F)c2CN1C#N

Basic Information

ChEMBL ID CHEMBL5532074
Phase Preclinical
Structure Type MOL
InChI Key OLMYDHXKXWAHIK-RBJSKKJNSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

640.2
MW (Da)
5.26
ALogP
7
HBA
1
HBD
106.0
PSA (Ų)
0.38
QED
2
Ro5 Violations
5
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H35ClFN5O4S
MW 640.18
Aromatic Rings 3
Heavy Atoms 44
NP-Likeness -0.79

Activity Summary

Ki 1 meas. best 5.52

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cathepsin S
CHEMBL2954
Ki 5.52 5.52 3020.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Cathepsin S Ki = 3020.0 nM 5.52 Inhibition of recombinant human cathepsin S using Z-Phe-Arg-AMC as substrate inc... 38753594

Literature References

PubMed DOI Target Context # Activities
38753594 10.1021/acs.jmedchem.4c00053 Replicase polyprotein 1ab 3
38753594 10.1021/acs.jmedchem.4c00053 Procathepsin L 2
38753594 10.1021/acs.jmedchem.4c00053 Cathepsin B 2
38753594 10.1021/acs.jmedchem.4c00053 Cathepsin S 2

Data from ChEMBL 36 via Core Engine