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Compound Detail

CHEMBL289345

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O=S(=O)([O-])c1cc(/N=N/c2cc(S(=O)(=O)[O-])c3cccnc3c2O)ccc1/C=C/c1ccc(/N=N/c2cc(S(=O)(=O)[O-])c3cccnc3c2O)cc1S(=O)(=O)[O-].[Na+].[Na+].[Na+].[Na+]

Basic Information

ChEMBL ID CHEMBL289345
Phase Preclinical
Structure Type MOL
InChI Key JBISMGFDJQAWEF-ULVSVMGDSA-J
Parent Compound CHEMBL1615820
Active Moiety CHEMBL1615820
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

842.8
MW (Da)
6.18
ALogP
16
HBA
6
HBD
333.2
PSA (Ų)
0.05
QED
4
Ro5 Violations
10
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H18N6Na4O14S4
MW 930.75
Aromatic Rings 6
Heavy Atoms 56
NP-Likeness -0.25

Activity Summary

EC50 1 meas. best 5.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
AIK-T4
CHEMBL614024
EC50 5.89 5.89 1300.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
AIK-T4 EC50 = 1300.0 nM 5.89 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