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Compound Detail

CHEMBL1806680

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O=C(c1ccccc1C(F)(F)F)N(/N=N/c1ccc([N+](=O)[O-])cc1C(F)(F)F)c1ccc([N+](=O)[O-])cc1C(F)(F)F

Basic Information

ChEMBL ID CHEMBL1806680
Phase Preclinical
Structure Type MOL
InChI Key VDWMYGOXHPACGP-ULIFNZDWSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

595.3
MW (Da)
7.91
ALogP
7
HBA
0
HBD
131.3
PSA (Ų)
0.12
QED
2
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H10F9N5O5
MW 595.33
Aromatic Rings 3
Heavy Atoms 41
NP-Likeness -0.92

Activity Summary

IC50 1 meas. best 5.27

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
HeLa
CHEMBL399
IC50 5.27 5.27 5350.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
HeLa IC50 = 5350.0 nM 5.27 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 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 Staphylococcus aureus 1
28063354 10.1016/j.ejmech.2016.12.060 Saccharomyces cerevisiae 1

Data from ChEMBL 36 via Core Engine