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Compound Detail

CHEMBL233549

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O=C(CCNc1cccc(F)c1)c1cccc([N+](=O)[O-])c1

Basic Information

ChEMBL ID CHEMBL233549
Phase Preclinical
Structure Type MOL
InChI Key ZNWIIHBNDHFYOY-UHFFFAOYSA-N
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

288.3
MW (Da)
3.42
ALogP
4
HBA
1
HBD
72.2
PSA (Ų)
0.50
QED
0
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C15H13FN2O3
MW 288.28
Aromatic Rings 2
Heavy Atoms 21
NP-Likeness -1.85

Activity Summary

EC50 1 meas. best 6.09
IC50 1 meas. best 5.48

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Trypanosoma brucei
CHEMBL612849
EC50 6.09 6.09 820.0 1
Trypanothione reductase
CHEMBL1837
IC50 5.48 5.48 3300.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Trypanosoma brucei EC50 = 820.0 nM 6.09 Antiproliferative activity against Trypanosoma brucei 17197182
Trypanothione reductase IC50 = 3300.0 nM 5.48 Inhibition of TR by DTNB-coupled assay 17197182

Literature References

PubMed DOI Target Context # Activities
17197182 10.1016/j.bmcl.2006.12.016 Trypanothione reductase 1
17197182 10.1016/j.bmcl.2006.12.016 Glutathione reductase, mitochondrial 1
17197182 10.1016/j.bmcl.2006.12.016 Unchecked 1
17197182 10.1016/j.bmcl.2006.12.016 Trypanosoma brucei 1

Data from ChEMBL 36 via Core Engine