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Compound Detail

CHEMBL1093972

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CC(C)(C)[C@H](NC(=O)NC1(CS(=O)(=O)c2ccccn2)CCCCC1)C(=O)N1C[C@H]2[C@@H]([C@H]1C(=O)NC(CC1CCC1)C(=O)C(N)=O)C2(C)C

Basic Information

ChEMBL ID CHEMBL1093972
Phase Preclinical
Structure Type MOL
InChI Key DOXWDHUPMOIGSO-LIFJXQIBSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

700.9
MW (Da)
2.48
ALogP
8
HBA
4
HBD
197.7
PSA (Ų)
0.24
QED
1
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C35H52N6O7S
MW 700.90
Aromatic Rings 1
Heavy Atoms 49
NP-Likeness -0.04

Activity Summary

Ki 1 meas. best 8.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 8.0 8.0 10.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 10.0 nM 8.0 Inhibition of HCV NS4A tagged recombinant single chain NS3 protease after 15 min... 20303756

Literature References

PubMed DOI Target Context # Activities
20303756 10.1016/j.bmcl.2010.02.063 Unchecked 2
20303756 10.1016/j.bmcl.2010.02.063 Hepatitis C virus 1

Data from ChEMBL 36 via Core Engine