Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL4060724

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
COc1ccc2ncc(F)c([C@@H](O)CC[C@@H]3CCN(C4CC(c5ccccn5)C4)C[C@@H]3C(=O)O)c2c1

Basic Information

ChEMBL ID CHEMBL4060724
Phase Preclinical
Structure Type MOL
InChI Key GDDPWCZEXJNABU-NROMVHIPSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

493.6
MW (Da)
4.56
ALogP
6
HBA
2
HBD
95.8
PSA (Ų)
0.47
QED
0
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H32FN3O4
MW 493.58
Aromatic Rings 3
Heavy Atoms 36
NP-Likeness -0.20

Activity Summary

IC50 2 meas. best 5.5

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 5.5 4.9 3130.0 2

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 3130.0 nM 5.5 Inhibition of Staphylococcus aureus DNA gyrase 28610977
Unchecked IC50 = 50000.0 nM 4.3 Inhibition of Staphylococcus aureus DNA topoisomerase 4 28610977

Literature References

PubMed DOI Target Context # Activities
28610977 10.1016/j.bmcl.2017.06.009 Staphylococcus aureus 4
28610977 10.1016/j.bmcl.2017.06.009 Unchecked 2

Data from ChEMBL 36 via Core Engine