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

CHEMBL4096186

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
COc1ccc2c(c1)OCCCCCCOCCN(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)O[C@H]1CO[C@H]3OCC[C@H]31)S2(=O)=O

Basic Information

ChEMBL ID CHEMBL4096186
Phase Preclinical
Structure Type MOL
InChI Key NNLNIEOWTPFSEM-VOFGOOHBSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

648.8
MW (Da)
3.12
ALogP
10
HBA
2
HBD
142.1
PSA (Ų)
0.44
QED
1
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H44N2O10S
MW 648.78
Aromatic Rings 2
Heavy Atoms 45
NP-Likeness 0.12

Activity Summary

Ki 1 meas. best 8.01

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 8.01 8.01 9.8 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 9.85 nM 8.01 Inhibition of HIV-1 protease using fluorogenic substrate by fluorescence assay 28958624

Literature References

PubMed DOI Target Context # Activities
28958624 10.1016/j.bmcl.2017.09.003 Human immunodeficiency virus 1 1
28958624 10.1016/j.bmcl.2017.09.003 Unchecked 1

Data from ChEMBL 36 via Core Engine