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Compound Detail

CHEMBL5082238

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O=C(O)COc1ccc(/C=C2/SC(=O)N(Cc3ccc(F)cc3)C2=O)cc1Br

Basic Information

ChEMBL ID CHEMBL5082238
Phase Preclinical
Structure Type MOL
InChI Key FHFIEFIJJDWDCA-LZYBPNLTSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

466.3
MW (Da)
4.29
ALogP
5
HBA
1
HBD
83.9
PSA (Ų)
0.64
QED
0
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C19H13BrFNO5S
MW 466.28
Aromatic Rings 2
Heavy Atoms 28
NP-Likeness -1.62

Activity Summary

IC50 1 meas. best 4.56

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.56 4.56 27400.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 27400.0 nM 4.56 Inhibition of Enterococcus faecalis OG1RF YycG autophosphorylation by Kinase-Glo... 34657423

Literature References

PubMed DOI Target Context # Activities
34657423 10.1021/acs.jmedchem.1c00939 Enterococcus faecalis 10
34657423 10.1021/acs.jmedchem.1c00939 Unchecked 4
34657423 10.1021/acs.jmedchem.1c00939 Staphylococcus epidermidis 2
34657423 10.1021/acs.jmedchem.1c00939 Staphylococcus aureus 2
34657423 10.1021/acs.jmedchem.1c00939 Vero 1
34657423 10.1021/acs.jmedchem.1c00939 Enterococcus faecium 1
34657423 10.1021/acs.jmedchem.1c00939 Streptococcus agalactiae 1
34657423 10.1021/acs.jmedchem.1c00939 Escherichia coli 1

Data from ChEMBL 36 via Core Engine