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Compound Detail

CHEMBL231230

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Cc1ccc(S(=O)(=O)N(Cc2ccccc2)c2ccc(Nc3nc(N4CCCC(O)C4)nc(N4C[C@H](N)C[C@H](N)C4)n3)cc2O)cc1

Basic Information

ChEMBL ID CHEMBL231230
Phase Preclinical
Structure Type MOL
InChI Key FYMSLIHDWCELIQ-YHQISMHQSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

659.8
MW (Da)
2.85
ALogP
12
HBA
5
HBD
187.1
PSA (Ų)
0.18
QED
2
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H41N9O4S
MW 659.82
Aromatic Rings 4
Heavy Atoms 47
NP-Likeness -1.19

Activity Summary

IC50 1 meas. best 4.36

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Escherichia coli
CHEMBL354
IC50 4.36 4.36 44000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Escherichia coli IC50 = 44000.0 nM 4.36 Inhibition of protein synthesis in Escherichia coli by coupled transcription-tra... 17188860

Literature References

PubMed DOI Target Context # Activities
17188860 10.1016/j.bmcl.2006.12.024 Escherichia coli 1
17188860 10.1016/j.bmcl.2006.12.024 Staphylococcus aureus 1

Data from ChEMBL 36 via Core Engine