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Compound Detail

CHEMBL253534

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CN(c1ccc2c(c1)S(=O)(=O)N=C(c1c(O)c(-c3cccs3)nn(CCC(C)(C)C)c1=O)N2)S(C)(=O)=O

Basic Information

ChEMBL ID CHEMBL253534
Phase Preclinical
Structure Type MOL
InChI Key XISZSFJEMVMFNT-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
3
PK Parameters
6
Publications
0
Known Names

Molecular Properties

565.7
MW (Da)
3.07
ALogP
10
HBA
2
HBD
151.0
PSA (Ų)
0.46
QED
1
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H27N5O6S3
MW 565.70
Aromatic Rings 3
Heavy Atoms 37
NP-Likeness -1.58

Activity Summary

EC50 1 meas. best 6.46

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatitis C virus
CHEMBL379
EC50 6.46 6.46 350.0 1

Pharmacokinetic Data

Parameter Value Units Species
F 3.0 % Macaca fascicularis
T1/2 0.4333 hr Homo sapiens
T1/2 0.1117 hr Macaca mulatta

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Hepatitis C virus EC50 = 350.0 nM 6.46 Antiviral activity against HCV 1b replicon in human Huh7/C24 cells after 72 hrs 18442904

Literature References

PubMed DOI Target Context # Activities
18442904 10.1016/j.bmcl.2008.04.005 Caco-2 2
18442904 10.1016/j.bmcl.2008.04.005 Cynomolgus monkey 2
18442904 10.1016/j.bmcl.2008.04.005 Hepatitis C virus 1
18442904 10.1016/j.bmcl.2008.04.005 Liver microsomes 1
18442904 10.1016/j.bmcl.2008.04.005 ADMET 1
18442904 10.1016/j.bmcl.2008.04.005 No relevant target 1

Data from ChEMBL 36 via Core Engine