Compound ID | 707

Oleuropein

Class: Phenolic sarcolid antioxidant

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: Highly bioavailable with other benefits besides antimicrobial. It is effective against both Gram positives and Gram negatives.
Institute where first reported: University of Athens, Medical School, Greece
Year first mentioned: 2005
Development status: Inactive
Chemical structure(s):
Canonical SMILES: C/C=C/1\[C@H](CC(=O)OCCC2=CC=C(C(=C2)O)O)C(=CO[C@H]1O[C@H]3[C@@H]([C@H]([C@@H]([C@@H](CO)O3)O)O)O)C(=O)OC
Isomeric SMILES: C/C=C/1\[C@@H](C(=CO[C@H]1O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O
InChI: InChI=1S/C25H32O13/c1-3-13-14(9-19(29)35-7-6-12-4-5-16(27)17(28)8-12)15(23(33)34-2)11-36-24(13)38-25-22(32)21(31)20(30)18(10-26)37-25/h3-5,8,11,14,18,20-22,24-28,30-32H,6-7,9-10H2,1-2H3/b13-3+/t14-,18+,20+,21-,22+,24-,25-/m0/s1
InChI Key: RFWGABANNQMHMZ-ZCHJGGQASA-N
Structure link: https://pubchem.ncbi.nlm.nih.gov/compound/5281544
External links:
Guide to Pharmacology: oleuropein
Citations:
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002804/
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC379901/
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