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Compound Detail

CHEMBL395065

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COC(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN(CC(C)C)NC(=O)[C@@H]1CN(c2ccccc2)C(=O)O1)C(C)(C)C

Basic Information

ChEMBL ID CHEMBL395065
Phase Preclinical
Structure Type MOL
InChI Key KLUPNGHJEAUIGT-YIPNQBBMSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

611.7
MW (Da)
2.86
ALogP
8
HBA
4
HBD
149.5
PSA (Ų)
0.25
QED
1
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H45N5O7
MW 611.74
Aromatic Rings 2
Heavy Atoms 44
NP-Likeness -0.09

Activity Summary

Ki 1 meas. best 7.97

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 7.97 7.97 10.6 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 10.6 nM 7.97 Inhibition of Wild type HIV1 Protease by FRET based assay 17696512

Literature References

PubMed DOI Target Context # Activities
17696512 10.1021/jm070284z Protease 1

Data from ChEMBL 36 via Core Engine