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Compound Detail

CHEMBL4083503

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NC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H](NC(=O)CCCc3cn(Cc4ccc(CN5CCN(c6cc7c(cc6F)c(=O)c(C(=O)O)cn7C6CC6)CC5)cc4)nn3)C[C@@H]2N)[C@H](O)[C@@H](O)[C@@H]1O

Basic Information

ChEMBL ID CHEMBL4083503
Phase Preclinical
Structure Type MOL
InChI Key MYENMPCBZOWLRJ-RCHLUYSYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

1055.1
MW (Da)

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C49H67FN10O15
MW 1055.13

Activity Summary

IC50 1 meas. best 5.66

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Escherichia coli
CHEMBL354
IC50 5.66 5.66 2190.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Escherichia coli IC50 = 2190.0 nM 5.66 Inhibition of protein translation in Escherichia coli S30 cell extract using cir... 28343755

Literature References

PubMed DOI Target Context # Activities
28343755 10.1016/j.bmc.2017.02.068 Escherichia coli 13
28343755 10.1016/j.bmc.2017.02.068 Bacillus subtilis 1
28343755 10.1016/j.bmc.2017.02.068 Staphylococcus epidermidis 1

Data from ChEMBL 36 via Core Engine