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Compound Detail

CHEMBL398200

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NC[C@@H]1C[C@H](CN)CN(c2nc(Nc3ccc(NC(=O)c4ccc(Cl)cc4)c(O)c3)nc(N3C[C@H](N)C[C@H](N)C3)n2)C1

Basic Information

ChEMBL ID CHEMBL398200
Phase Preclinical
Structure Type MOL
InChI Key DFZBHYLMJLPXHM-ALFLXDJESA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

596.1
MW (Da)
1.45
ALogP
12
HBA
7
HBD
210.6
PSA (Ų)
0.18
QED
3
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H38ClN11O2
MW 596.14
Aromatic Rings 3
Heavy Atoms 42
NP-Likeness -1.08

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