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Compound Detail

CHEMBL5287601

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O=C(/C=C/c1ccc(O)c(O)c1CCc1ccc(O)c(O)c1)O[C@@H](Cc1ccc(O)c(O)c1)C(=O)O

Basic Information

ChEMBL ID CHEMBL5287601
Phase Preclinical
Structure Type MOL
InChI Key HSDCJXAKGZDZKN-CRAXIPPQSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

496.5
MW (Da)
2.96
ALogP
9
HBA
7
HBD
185.0
PSA (Ų)
0.13
QED
1
Ro5 Violations
9
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H24O10
MW 496.47
Aromatic Rings 3
Heavy Atoms 36
NP-Likeness 1.15

Activity Summary

IC50 1 meas. best 4.94

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Sortase A
CHEMBL5362
IC50 4.94 4.94 11600.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Sortase A IC50 = 11600.0 nM 4.94 Inhibition of Staphylococcus aureus SrtA using EDANS-Dabcyl as substrate by FRET... 34516107

Literature References

PubMed DOI Target Context # Activities
34516107 10.1021/acs.jmedchem.1c00386 Staphylococcus aureus 2
34516107 10.1021/acs.jmedchem.1c00386 Sortase A 1

Data from ChEMBL 36 via Core Engine