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Compound Detail

CHEMBL359093

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CC(C)OC(=O)c1cccn1S(=O)(=O)c1cc(Cl)ccc1[N+](=O)[O-]

Basic Information

ChEMBL ID CHEMBL359093
Phase Preclinical
Structure Type MOL
InChI Key DZPAUCCVTKZCTH-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

372.8
MW (Da)
2.85
ALogP
7
HBA
0
HBD
108.5
PSA (Ų)
0.45
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C14H13ClN2O6S
MW 372.79
Aromatic Rings 2
Heavy Atoms 24
NP-Likeness -1.66

Activity Summary

EC50 1 meas. best 4.52

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
MT4
CHEMBL388
EC50 4.52 4.52 30000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
MT4 EC50 = 30000.0 nM 4.52 Effective concentration against HIV-1 induced cytopathogenicity in MT-4 cells 8558522

Literature References

PubMed DOI Target Context # Activities
8558522 10.1021/jm950568w MT4 3

Data from ChEMBL 36 via Core Engine