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Compound Detail

CHEMBL388332

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C=C[C@@H]1C[C@]1(NC(=O)[C@@H]1C[C@@H](Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)CN1C(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)C(=O)NNC(=O)c1ccccc1

Basic Information

ChEMBL ID CHEMBL388332
Phase Preclinical
Structure Type MOL
InChI Key CDOWCVMWIGMULL-FLGZPZLISA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

805.0
MW (Da)
5.72
ALogP
9
HBA
4
HBD
177.3
PSA (Ų)
0.11
QED
2
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C45H52N6O8
MW 804.95
Aromatic Rings 4
Heavy Atoms 59
NP-Likeness -0.30

Activity Summary

Ki 1 meas. best 5.8

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 5.8 5.8 1600.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 1600.0 nM 5.8 Inhibition of HCV NS3 protease in presence of pH 7.5 HEPES buffer 17449253

Literature References

PubMed DOI Target Context # Activities
17449253 10.1016/j.bmc.2007.03.089 Unchecked 1
17449253 10.1016/j.bmc.2007.03.089 Hepatitis C virus 1

Data from ChEMBL 36 via Core Engine