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Compound Detail

CHEMBL1807132

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CC(=O)OCC(=O)N(/N=N/c1ccc([N+](=O)[O-])cc1Br)c1ccc([N+](=O)[O-])cc1Br

Basic Information

ChEMBL ID CHEMBL1807132
Phase Preclinical
Structure Type MOL
InChI Key PWKNTGLFTMPBQS-FMQUCBEESA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

545.1
MW (Da)
4.62
ALogP
9
HBA
0
HBD
157.6
PSA (Ų)
0.21
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C16H11Br2N5O7
MW 545.10
Aromatic Rings 2
Heavy Atoms 30
NP-Likeness -0.79

Activity Summary

IC50 1 meas. best 6.31

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
HeLa
CHEMBL399
IC50 6.31 6.31 490.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
HeLa IC50 = 490.0 nM 6.31 Cytotoxicity against human HeLa cells after 72 hrs by MTT assay 21550697

Literature References

PubMed DOI Target Context # Activities
28063354 10.1016/j.ejmech.2016.12.060 Staphylococcus aureus 2
28063354 10.1016/j.ejmech.2016.12.060 Escherichia coli 2
21550697 10.1016/j.ejmech.2011.04.024 HeLa 1
28063354 10.1016/j.ejmech.2016.12.060 Mycolicibacterium smegmatis 1
28063354 10.1016/j.ejmech.2016.12.060 Saccharomyces cerevisiae 1

Data from ChEMBL 36 via Core Engine