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Compound Detail

CHEMBL569236

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CC(C)[C@H](NC(=O)OCc1cccnc1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)OCc1cccnc1)C(C)C

Basic Information

ChEMBL ID CHEMBL569236
Phase Preclinical
Structure Type MOL
InChI Key ACUNRNHXDMKZIB-AEKIIXOMSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

768.9
MW (Da)
3.86
ALogP
10
HBA
6
HBD
201.1
PSA (Ų)
0.08
QED
2
Ro5 Violations
19
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C42H52N6O8
MW 768.91
Aromatic Rings 4
Heavy Atoms 56
NP-Likeness -0.10

Activity Summary

IC50 1 meas. best 8.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
IC50 8.89 8.89 1.3 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease IC50 = 1.288 nM 8.89 Inhibition of HIV1 protease expressed in Escherichia coli K12 assessed as inhibi... 19616874

Literature References

PubMed DOI Target Context # Activities
19616874 10.1016/j.ejmech.2009.05.016 Protease 1

Data from ChEMBL 36 via Core Engine