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Compound Detail

CHEMBL156813

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COC(=O)c1c(Br)c(OC)cc(O)c1CSC[C@H](Nc1nc(-c2ccc([N+](=O)[O-])cc2)cs1)C(=O)OC

Basic Information

ChEMBL ID CHEMBL156813
Phase Preclinical
Structure Type MOL
InChI Key MULKVQPCLGZOFQ-INIZCTEOSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
15
Publications
0
Known Names

Molecular Properties

612.5
MW (Da)
4.87
ALogP
12
HBA
2
HBD
150.1
PSA (Ų)
0.17
QED
2
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H22BrN3O8S2
MW 612.48
Aromatic Rings 3
Heavy Atoms 37
NP-Likeness -0.81

Activity Summary

IC50 1 meas. best 6.31

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.31 6.31 490.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 490.0 nM 6.31 Inhibition of Escherichia coli DNA gyrase B ATPase activity 20045642

Literature References

PubMed DOI Target Context # Activities
11170652 10.1021/jm0010623 Staphylococcus aureus 6
11170652 10.1021/jm0010623 Streptococcus pyogenes 4
11170652 10.1021/jm0010623 DNA topoisomerase 1 3
11170652 10.1021/jm0010623 DNA topoisomerase 2-beta 2
11170652 10.1021/jm0010623 Enterococcus faecium 2
11170652 10.1021/jm0010623 Enterococcus faecalis 2
11170652 10.1021/jm0010623 Klebsiella pneumoniae 2
11170652 10.1021/jm0010623 DNA topoisomerase II 1
11170652 10.1021/jm0010623 Staphylococcus epidermidis 1
11170652 10.1021/jm0010623 Staphylococcus haemolyticus 1
11170652 10.1021/jm0010623 Staphylococcus saprophyticus 1
11170652 10.1021/jm0010623 Proteus vulgaris 1
11170652 10.1021/jm0010623 Proteus mirabilis 1
11170652 10.1021/jm0010623 Escherichia coli 1
20045642 10.1016/j.bmcl.2009.12.060 Unchecked 1

Data from ChEMBL 36 via Core Engine