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Compound Detail

CHEMBL519397

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CCNC(=O)Nc1nc2cc(-n3cnc(C(=O)NC4CC4)c3)cc(-c3ccccn3)c2[nH]1

Basic Information

ChEMBL ID CHEMBL519397
Phase Preclinical
Structure Type MOL
InChI Key XTMGTPTXHXWURI-UHFFFAOYSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

430.5
MW (Da)
2.84
ALogP
6
HBA
4
HBD
129.6
PSA (Ų)
0.37
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 C22H22N8O2
MW 430.47
Aromatic Rings 4
Heavy Atoms 32
NP-Likeness -1.62

Activity Summary

Ki 2 meas. best 8.15

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 8.15 8.15 7.0 1
DNA gyrase
CHEMBL3038482
Ki 7.92 7.92 12.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 7.0 nM 8.15 Inhibition of Escherichia coli topoisomerase 4 18690678
DNA gyrase Ki = 12.0 nM 7.92 Inhibition of Staphylococcus aureus DNA gyrase 18690678

Literature References

PubMed DOI Target Context # Activities
18690678 10.1021/jm800318d Staphylococcus aureus 2
18690678 10.1021/jm800318d Unchecked 2
18690678 10.1021/jm800318d Haemophilus influenzae 1
18690678 10.1021/jm800318d Streptococcus pneumoniae 1
18690678 10.1021/jm800318d DNA gyrase 1

Data from ChEMBL 36 via Core Engine