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Compound Detail

CHEMBL231332

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Cc1ccc(S(=O)(=O)N(Cc2ccccc2)c2ccc(Nc3nc(N4CC(N)C4)nc(N4C[C@H](N)C[C@H](N)C4)n3)cc2O)cc1

Basic Information

ChEMBL ID CHEMBL231332
Phase Preclinical
Structure Type MOL
InChI Key WEIHEAUKCFFZJQ-ZRZAMGCNSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

630.8
MW (Da)
2.04
ALogP
12
HBA
5
HBD
192.8
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 C31H38N10O3S
MW 630.78
Aromatic Rings 4
Heavy Atoms 45
NP-Likeness -1.21

Activity Summary

IC50 1 meas. best 4.96

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Escherichia coli
CHEMBL354
IC50 4.96 4.96 11000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Escherichia coli IC50 = 11000.0 nM 4.96 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