Synonyms
Source Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...

Structure

InChI Key KNURQRIPZJJYQO-PJIMMEPBSA-N
Smiles O[C@@H]1CO[C@@H](Oc2cc3C(=O)Oc4c(O)c(O)cc5C(=O)Oc(c2O)c3c45)[C@H](O)[C@H]1O
InChI
InChI=1S/C19H14O12/c20-6-1-4-9-10-5(18(27)30-15(9)12(6)23)2-8(13(24)16(10)31-17(4)26)29-19-14(25)11(22)7(21)3-28-19/h1-2,7,11,14,19-25H,3H2/t7-,11+,14-,19+/m1/s1

Physicochemical Descriptors

Property Name Value
Molecular Formula C19H14O12
Molecular Weight 434.31
AlogP 0.17
Hydrogen Bond Acceptor 12.0
Hydrogen Bond Donor 6.0
Number of Rotational Bond 2.0
Polar Surface Area 192.43
Molecular species ACID
Aromatic Rings 2.0
Heavy Atoms 31.0
Assay Description Organism Bioactivity Reference
Inhibition of xanthine oxidase assessed as conversion of xanthine to uric acid incubated for 3 min None 4700.0 nM
Antimicrobial activity against Candida albicans at 100 ug after 24 hr by disk diffusion method Candida albicans 0.0 mm
Antimicrobial activity against Corynebacterium accolens at 100 ug after 24 hr by disk diffusion method Corynebacterium accolens 0.0 mm
Antimicrobial activity against Staphylococcus aureus at 100 ug after 24 hr by disk diffusion method Staphylococcus aureus 0.0 mm
Antimicrobial activity against Pectobacterium carotovorum at 100 ug after 24 hr by disk diffusion method Pectobacterium carotovorum 12.0 mm

Cross References

Resources Reference
ChEMBL CHEMBL1939391
PubChem 5487461