Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL1269421

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
O=C(c1cc(O)c(O)c(Br)c1)c1cc(O)c(O)c(Br)c1

Basic Information

ChEMBL ID CHEMBL1269421
Phase Preclinical
Structure Type MOL
InChI Key QWGGKBRLOGNRAY-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
10
Publications
0
Known Names

Molecular Properties

404.0
MW (Da)
3.27
ALogP
5
HBA
4
HBD
98.0
PSA (Ų)
0.46
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C13H8Br2O5
MW 404.01
Aromatic Rings 2
Heavy Atoms 20
NP-Likeness 0.35

Activity Summary

IC50 1 meas. best 5.05

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Isocitrate lyase
CHEMBL5359
IC50 5.05 5.05 8890.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Isocitrate lyase IC50 = 8890.0 nM 5.05 Inhibition of Candida albicans ATCC 10231 isocitrate lyase 20888765

Literature References

PubMed DOI Target Context # Activities
20888765 10.1016/j.bmcl.2010.09.015 Isocitrate lyase 1
20888765 10.1016/j.bmcl.2010.09.015 Staphylococcus aureus 1
20888765 10.1016/j.bmcl.2010.09.015 Bacillus subtilis 1
20888765 10.1016/j.bmcl.2010.09.015 Micrococcus luteus 1
20888765 10.1016/j.bmcl.2010.09.015 Proteus vulgaris 1
20888765 10.1016/j.bmcl.2010.09.015 Salmonella typhimurium 1
20888765 10.1016/j.bmcl.2010.09.015 Candida albicans 1
20888765 10.1016/j.bmcl.2010.09.015 Aspergillus fumigatus 1
20888765 10.1016/j.bmcl.2010.09.015 Trichophyton rubrum 1
20888765 10.1016/j.bmcl.2010.09.015 Trichophyton mentagrophytes 1

Data from ChEMBL 36 via Core Engine