Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL60512

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
CC[C@@H](C)[C@@H](NC(C)=O)C(=O)N[C@@H](CC1CCCCC1)C(=O)N[C@H](CS)C(=O)O

Basic Information

ChEMBL ID CHEMBL60512
Phase Preclinical
Structure Type BOTH
InChI Key PJPNMQZIQFHKBJ-VJUNAUMWSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

429.6
MW (Da)
1.49
ALogP
5
HBA
5
HBD
124.6
PSA (Ų)
0.32
QED
0
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H35N3O5S
MW 429.58
Aromatic Rings 0
Heavy Atoms 29
NP-Likeness 0.20

Activity Summary

Ki 1 meas. best 4.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
NS3
CHEMBL1293269
Ki 4.6 4.6 25000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
NS3 Ki = 25000.0 nM 4.6 Inhibitory activity against hepatitis C virus (HCV) NS3 protease (full-length) 11206459

Literature References

PubMed DOI Target Context # Activities
11206459 10.1016/s0960-894x(00)00625-9 NS3 1

Data from ChEMBL 36 via Core Engine