Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL4288541

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
COc1ccc(S(=O)(=O)N(CC(C)C)C[C@@H](O)[C@H](Cc2ccccc2)NC(=O)O[C@@H]2C[C@@H]3OC(=O)N[C@@H]3C2)cc1

Basic Information

ChEMBL ID CHEMBL4288541
Phase Preclinical
Structure Type MOL
InChI Key SUKOCHXFOBSBBB-CVCYMHMSSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

575.7
MW (Da)
2.68
ALogP
8
HBA
3
HBD
143.5
PSA (Ų)
0.35
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 C28H37N3O8S
MW 575.68
Aromatic Rings 2
Heavy Atoms 40
NP-Likeness 0.13

Activity Summary

Ki 1 meas. best 8.88

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 8.88 8.88 1.3 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 1.33 nM 8.88 Inhibition of HIV1 wild type NL4-3 protease expressed in Escherichia coli Rosett... 30354121

Literature References

PubMed DOI Target Context # Activities
30354121 10.1021/acs.jmedchem.8b01227 Human immunodeficiency virus 1 1
30354121 10.1021/acs.jmedchem.8b01227 Protease 1

Data from ChEMBL 36 via Core Engine