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Compound Detail

CHEMBL4449179

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CC(C)CN(C[C@@H](O)[C@H](Cc1cccc(F)c1)NC(=O)OC1C[C@@H]2CO[C@@H]3OC1C[C@H]23)S(=O)(=O)c1ccc2nc(NC3CC3)sc2c1

Basic Information

ChEMBL ID CHEMBL4449179
Phase Preclinical
Structure Type MOL
InChI Key CVVGZOFYLPKPDP-CVWHRZPGSA-N
1
Targets
2
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

688.8
MW (Da)
4.50
ALogP
10
HBA
3
HBD
139.3
PSA (Ų)
0.24
QED
1
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H41FN4O7S2
MW 688.84
Aromatic Rings 3
Heavy Atoms 47
NP-Likeness -0.61

Activity Summary

IC50 1 meas. best 8.89
Ki 1 meas.

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus 1
CHEMBL378
IC50 8.89 8.89 1.3 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Human immunodeficiency virus 1 IC50 = 1.28 nM 8.89 Antiviral activity against HIV1 LAI infected in human MT2 cells 32348139

Literature References

PubMed DOI Target Context # Activities
32348139 10.1021/acs.jmedchem.0c00202 Protease 1
32348139 10.1021/acs.jmedchem.0c00202 Human immunodeficiency virus 1 1

Data from ChEMBL 36 via Core Engine