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Compound Detail

CHEMBL243868

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O=C(N[C@@H](Cc1ccccc1)[C@@H](O)CN(Cc1ccc(-c2ccccn2)cc1)NC(=O)[C@@H]1CN(c2ccccc2)C(=O)O1)[C@@H]1CN(c2ccccc2)C(=O)O1

Basic Information

ChEMBL ID CHEMBL243868
Phase Preclinical
Structure Type MOL
InChI Key GQKWNYLKLDCKEF-ZQWQDMLBSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

740.8
MW (Da)
4.72
ALogP
9
HBA
3
HBD
153.6
PSA (Ų)
0.14
QED
1
Ro5 Violations
14
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C42H40N6O7
MW 740.82
Aromatic Rings 5
Heavy Atoms 55
NP-Likeness -0.49

Activity Summary

Ki 1 meas. best 6.52

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 6.52 6.52 300.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 300.0 nM 6.52 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