Drug details:
Molecular formula: C₂₇H₃₀O₁₆

Standard name: 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

Synonyms:

rutoside Phytomelin Birutan Quercetin 3-rutinoside Sophorin Myrticolorin Eldrin Globulariacitrin Ilixanthin ......

Curated SMILES: C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O

Evidence for compound's anti-virulence activity:

Streptococcus
Related VFcategory: Others
Target: SrtA
Drug effect: Inhibits SrtA-mediated protein anchoring and S. mutans cell aggregation.
Max phase: Preclinical (in vitro)
Publication:
Yang WY, et al., 2016. Flavonoid Glycosides Inhibit Sortase A and Sortase A-Mediated Aggregation of Streptococcus mutans, an Oral Bacterium Responsible for Human Dental Caries. J Microbiol Biotechnol 26(9):1566-9.