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Compound Detail

CHEMBL4472809

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CC(=O)N[C@H]1CNC(=O)[C@H](Cc2ccccc2)N(C)C(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC1=O

Basic Information

ChEMBL ID CHEMBL4472809
Phase Preclinical
Structure Type MOL
InChI Key CATQLTPYJAXNNQ-YFNVTMOMSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

576.6
MW (Da)
-2.82
ALogP
8
HBA
7
HBD
206.3
PSA (Ų)
0.18
QED
2
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H40N6O8
MW 576.65
Aromatic Rings 1
Heavy Atoms 41
NP-Likeness 0.97

Activity Summary

IC50 2 meas. best 5.86

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 5.86 5.86 1390.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 1390.0 nM 5.86 Inhibition of AgrC-1 in Staphylococcus aureus RN9222 incubated for 1 hr in prese... 31658413

Literature References

PubMed DOI Target Context # Activities
31658413 10.1021/acs.jmedchem.9b00798 Unchecked 2

Data from ChEMBL 36 via Core Engine