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Compound Detail

CHEMBL157831

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COC(=O)c1c(Br)c(OC)cc(O)c1CSC[C@H](Nc1nc(-c2ccc([N+](=O)[O-])cc2)cs1)c1nc(C)no1

Basic Information

ChEMBL ID CHEMBL157831
Phase Preclinical
Structure Type MOL
InChI Key RIXLZRBJGRFRFF-KRWDZBQOSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
15
Publications
0
Known Names

Molecular Properties

636.5
MW (Da)
5.76
ALogP
13
HBA
2
HBD
162.7
PSA (Ų)
0.12
QED
3
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C24H22BrN5O7S2
MW 636.51
Aromatic Rings 4
Heavy Atoms 39
NP-Likeness -1.20

Activity Summary

IC50 1 meas. best 6.8

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.8 6.8 160.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 160.0 nM 6.8 Inhibition of Escherichia coli DNA gyrase B ATPase activity 20045642

Literature References

PubMed DOI Target Context # Activities
11170652 10.1021/jm0010623 Staphylococcus aureus 8
11170652 10.1021/jm0010623 Streptococcus pyogenes 5
11170652 10.1021/jm0010623 DNA topoisomerase 1 3
11170652 10.1021/jm0010623 Enterococcus faecalis 3
11170652 10.1021/jm0010623 DNA topoisomerase 2-beta 2
11170652 10.1021/jm0010623 Staphylococcus epidermidis 2
11170652 10.1021/jm0010623 Enterococcus faecium 2
11170652 10.1021/jm0010623 Klebsiella pneumoniae 2
11170652 10.1021/jm0010623 DNA topoisomerase II 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