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

CHEMBL3605645

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
CCN(C(=O)OC(C)(C)C)[C@H]1CO[C@@H]2OC[C@H](OC(=O)N[C@@H](Cc3ccccc3)[C@H](O)CN(CC(C)C)S(=O)(=O)c3ccc(OC)cc3)[C@@H]21

Basic Information

ChEMBL ID CHEMBL3605645
Phase Preclinical
Structure Type MOL
InChI Key CWBMLTUGPJYFNV-FZCPHSFBSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

705.9
MW (Da)
4.04
ALogP
10
HBA
2
HBD
153.2
PSA (Ų)
0.29
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 C35H51N3O10S
MW 705.87
Aromatic Rings 2
Heavy Atoms 49
NP-Likeness -0.37

Activity Summary

Ki 1 meas. best 10.32

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 10.32 10.32 0.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 0.048 nM 10.32 Inhibition of HIV1 protease 26306007

Literature References

PubMed DOI Target Context # Activities
26306007 10.1021/acs.jmedchem.5b00900 Protease 1
26306007 10.1021/acs.jmedchem.5b00900 Human immunodeficiency virus 1 1

Data from ChEMBL 36 via Core Engine