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Compound Detail

CHEMBL1788182

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O=S(=O)([O-])c1cc(S(=O)(=O)[O-])c2cc(NS(=O)(=O)c3cccc4c(S(=O)(=O)Nc5ccc6cc(S(=O)(=O)[O-])cc(S(=O)(=O)[O-])c6c5)cccc34)ccc2c1.[Na+].[Na+].[Na+].[Na+]

Basic Information

ChEMBL ID CHEMBL1788182
Phase Preclinical
Structure Type MOL
InChI Key RAKQRQZGXUQTFB-UHFFFAOYSA-J
Parent Compound CHEMBL292533
Active Moiety CHEMBL292533
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

858.9
MW (Da)
3.73
ALogP
12
HBA
6
HBD
309.8
PSA (Ų)
0.11
QED
3
Ro5 Violations
10
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H18N2Na4O16S6
MW 946.83
Aromatic Rings 6
Heavy Atoms 54
NP-Likeness -0.58

Activity Summary

EC50 1 meas. best 4.85

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus 1
CHEMBL378
EC50 4.85 4.85 14000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Human immunodeficiency virus 1 EC50 = 14000.0 nM 4.85 Antiviral activity against HIV-1 (HTLV-IIIB) in MT-4 cells 8336338

Literature References

PubMed DOI Target Context # Activities
8336338 10.1021/jm00066a008 Human immunodeficiency virus 1 2

Data from ChEMBL 36 via Core Engine