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Compound Detail

CHEMBL4095267

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COc1ccc2c(c1)OCCCCCN(S(C)(=O)=O)CCN(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 CHEMBL4095267
Phase Preclinical
Structure Type MOL
InChI Key NNSYWKKEKVRMGS-VOFGOOHBSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

711.9
MW (Da)
1.97
ALogP
11
HBA
2
HBD
170.2
PSA (Ų)
0.39
QED
2
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H45N3O11S2
MW 711.86
Aromatic Rings 2
Heavy Atoms 48
NP-Likeness -0.20

Activity Summary

Ki 1 meas. best 7.48

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 7.48 7.48 33.3 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 33.3 nM 7.48 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