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

CHEMBL43369

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
O=S(=O)([O-])c1cc(/N=N/c2ccc3cccnc3c2O)ccc1/C=C/c1ccc(/N=N/c2ccc3cccnc3c2O)cc1S(=O)(=O)[O-].[Na+].[Na+]

Basic Information

ChEMBL ID CHEMBL43369
Phase Preclinical
Structure Type MOL
InChI Key LWYQQBCVBJBWJP-KTAQGKCLSA-L
Parent Compound CHEMBL1615435
Active Moiety CHEMBL1615435
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

682.7
MW (Da)
7.69
ALogP
12
HBA
4
HBD
224.4
PSA (Ų)
0.07
QED
3
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H20N6Na2O8S2
MW 726.66
Aromatic Rings 6
Heavy Atoms 48
NP-Likeness -0.35

Activity Summary

EC50 1 meas. best 5.19

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
AIK-T4
CHEMBL614024
EC50 5.19 5.19 6400.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
AIK-T4 EC50 = 6400.0 nM 5.19 Ability to prevent HIV-1 induced T4 cell killing and HIV-1 replication. 7752188

Literature References

PubMed DOI Target Context # Activities
7752188 10.1021/jm00010a007 AIK-T4 1
7752188 10.1021/jm00010a007 Unchecked 1

Data from ChEMBL 36 via Core Engine