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Compound Detail

CHEMBL3741453

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CCCn1c(=O)ccc2c(-c3cnc(-c4ccc(C(=O)O)nc4)s3)n[nH]c21

Basic Information

ChEMBL ID CHEMBL3741453
Phase Preclinical
Structure Type MOL
InChI Key ILUNDOXROOQFGD-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

381.4
MW (Da)
3.02
ALogP
7
HBA
2
HBD
113.8
PSA (Ų)
0.55
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C18H15N5O3S
MW 381.42
Aromatic Rings 4
Heavy Atoms 27
NP-Likeness -1.18

Activity Summary

IC50 1 meas. best 7.25

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 7.25 7.25 56.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 56.0 nM 7.25 Inhibition of Staphylococcus aureus topoisomerase 4 by fluorescence analysis 26487916

Literature References

PubMed DOI Target Context # Activities
26487916 10.1021/acsmedchemlett.5b00266 DNA gyrase subunit B 1
26487916 10.1021/acsmedchemlett.5b00266 Unchecked 1
26487916 10.1021/acsmedchemlett.5b00266 Staphylococcus aureus 1
26487916 10.1021/acsmedchemlett.5b00266 Streptococcus pneumoniae 1
26487916 10.1021/acsmedchemlett.5b00266 No relevant target 1

Data from ChEMBL 36 via Core Engine