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Compound Detail

CHEMBL1806685

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

Basic Information

ChEMBL ID CHEMBL1806685
Phase Preclinical
Structure Type MOL
InChI Key HLBAFZYYUJKPQF-OCOZRVBESA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
12
Publications
0
Known Names

Molecular Properties

499.7
MW (Da)
5.81
ALogP
7
HBA
0
HBD
131.3
PSA (Ų)
0.16
QED
1
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C16H8ClF6N5O5
MW 499.71
Aromatic Rings 2
Heavy Atoms 33
NP-Likeness -0.98

Activity Summary

IC50 1 meas. best 6.1

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
HeLa
CHEMBL399
IC50 6.1 6.1 800.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
HeLa IC50 = 800.0 nM 6.1 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 5
28063354 10.1016/j.ejmech.2016.12.060 Escherichia coli 5
28063354 10.1016/j.ejmech.2016.12.060 No relevant target 4
28063354 10.1016/j.ejmech.2016.12.060 Mycolicibacterium smegmatis 2
28063354 10.1016/j.ejmech.2016.12.060 Streptococcus pneumoniae 2
28063354 10.1016/j.ejmech.2016.12.060 Bacillus subtilis 2
28063354 10.1016/j.ejmech.2016.12.060 Enterococcus faecalis 2
28063354 10.1016/j.ejmech.2016.12.060 Pseudomonas aeruginosa 2
28063354 10.1016/j.ejmech.2016.12.060 Klebsiella pneumoniae 2
28063354 10.1016/j.ejmech.2016.12.060 Acinetobacter baumannii 2
21550697 10.1016/j.ejmech.2011.04.024 HeLa 1
28063354 10.1016/j.ejmech.2016.12.060 Saccharomyces cerevisiae 1

Data from ChEMBL 36 via Core Engine