3-Geranyl-4-hydroxy-5-(3'-methyl-2'-butenyl)benzoic acid as an anti-inflammatory compound from Myrsine seguinii.

@article{Dong19993Geranyl4hydroxy53methyl2butenylbenzo,
  title={3-Geranyl-4-hydroxy-5-(3'-methyl-2'-butenyl)benzoic acid as an anti-inflammatory compound from Myrsine seguinii.},
  author={Mei Dong and Maho Nagaoka and Shintaro Miyazaki and Ryozo Iriye and Mitsuru Hirota},
  journal={Bioscience, biotechnology, and biochemistry},
  year={1999},
  volume={63 9},
  pages={
          1650-3
        }
}
Bioassay-guided isolation of anti-inflammatory compounds from the methanol extract of Myrsine seguinii yielded an anti-inflammatory compound (1). The structure of compound 1 was elucidated to be 3-geranyl-4-hydroxy-5-(3'-methyl-2'-butenyl)benzoic acid on the basis of its spectroscopic data. Compound 1 strongly suppressed 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inflammation on mouse ears at a dose of 500 micrograms (inhibitory effect (IE): 65%). The acetate and the methyl ether of 1… 
Antiherbivore prenylated benzoic acid derivatives from Piper kelleyi.
The known prenylated benzoic acid derivative 3-geranyl-4-hydroxy-5-(3″,3″-dimethylallyl)benzoic acid (1) and two new chromane natural products were isolated from the methanolic extract of the leaves
Myrsicorianol, A New Prenylated Benzoic Acid Derivative from Myrsine Coriacea
A new prenylated benzoic acid derivative, named myrsicorianol (1), was isolated from the fruits of Myrsine coriacea and its structure was determined by spectral analysis, including 1D- and 2D-NMR
Myrseguinosides A-E, five new glycosides from the fruits of Myrsine seguinii.
TLDR
Five new glycosides, named myrseguinosides A-E, exhibited 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical-scavenging activity and growth inhibitory activity toward human cancer cells, respectively.
Myrsinoic Acid E, an Anti-inflammatory Compound from Myrsine seguinii
TLDR
Compounds 1-3 suppressed 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inflammation of mouse ears by 59%, 14%, and 69% at a dose of 1.4 μmol.
Studies on the alkylation of phenolate in an organofluorine solvent and its application to the synthesis of myrsinoic acids A and E
ABSTRACT Among the distinct features of organofluorines, solubility properties to molecules often enable unique applications. More importantly, organofluorines can be compatible with chemical
Myrsinoic acid B inhibits the production of hydrogen sulfide by periodontal pathogens in vitro.
TLDR
It is concluded that myrsinoic acid B inhibited the production of both H(2)S and pyruvate by periodontal pathogens.
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