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Compound Detail

CHEMBL1270044

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Oc1cc(Br)c(COCc2cc(O)c(O)c(Br)c2Br)cc1O

Basic Information

ChEMBL ID CHEMBL1270044
Phase Preclinical
Structure Type MOL
InChI Key CFWIAMPRQNGELY-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
10
Publications
0
Known Names

Molecular Properties

498.9
MW (Da)
4.51
ALogP
5
HBA
4
HBD
90.2
PSA (Ų)
0.47
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C14H11Br3O5
MW 498.95
Aromatic Rings 2
Heavy Atoms 22
NP-Likeness 0.79

Activity Summary

IC50 1 meas. best 4.81

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Isocitrate lyase
CHEMBL5359
IC50 4.81 4.81 15610.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Isocitrate lyase IC50 = 15610.0 nM 4.81 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