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Compound Detail

CHEMBL360983

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CC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC1CCCCC1)C(=O)N[C@H](C(=O)N1C[C@@H](OCc2ccccc2)C[C@H]1C(=O)NC1(C(=O)O)CC1)C(C)C

Basic Information

ChEMBL ID CHEMBL360983
Phase Preclinical
Structure Type BOTH
InChI Key DDYNDQYNGBVAAZ-HWKKFYSMSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

842.9
MW (Da)
0.83
ALogP
10
HBA
8
HBD
286.9
PSA (Ų)
0.08
QED
2
Ro5 Violations
22
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C41H58N6O13
MW 842.94
Aromatic Rings 1
Heavy Atoms 60
NP-Likeness 0.10

Activity Summary

IC50 1 meas. best 7.29

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
NS3
CHEMBL1293269
IC50 7.29 7.29 51.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
NS3 IC50 = 51.0 nM 7.29 Inhibitory concentration 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