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Compound Detail

CHEMBL179084

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CC[C@@H](C)[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(=O)O)NC(C)=O)C(=O)N[C@@H](CC1CCCCC1)C(=O)N[C@@H](CS)C(=O)O

Basic Information

ChEMBL ID CHEMBL179084
Phase Preclinical
Structure Type BOTH
InChI Key CSWPZICAVWHBCE-ZZOXDLJQSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

787.0
MW (Da)
0.33
ALogP
10
HBA
10
HBD
286.5
PSA (Ų)
0.06
QED
2
Ro5 Violations
24
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C35H58N6O12S
MW 786.95
Aromatic Rings 0
Heavy Atoms 54
NP-Likeness 0.30

Activity Summary

Ki 1 meas. best 9.12

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
NS3
CHEMBL1293269
Ki 9.12 9.12 0.8 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
NS3 Ki = 0.75 nM 9.12 Inhibitory constant against hepatitis C virus NS3 protease 15633995

Literature References

PubMed DOI Target Context # Activities
15633995 10.1021/jm0400101 NS3 1

Data from ChEMBL 36 via Core Engine