119417-97-9Relevant academic research and scientific papers
Evidence against the structure proposed for a natural phenylethanol isolated from mangrove Avicennia marina
Yang, Yong-Qing
, p. 1263 - 1267 (2016)
In an effort to establish the absolute configuration of a previously reported natural triol, the proposed structure was synthesized in an enantiomerically enriched form. The synthetic sample showed NMR and specific rotation completely incompatible with th
Nelumal A, the active principle from Ligularia nelumbifolia, is a novel farnesoid X receptor agonist
Epifano, Francesco,Genovese, Salvatore,James Squires,Gray, Matthew A.
scheme or table, p. 3130 - 3135 (2012/06/04)
A series of 29 oxyprenylated and azoprenylated phenylpropanoids were chemically synthesized and tested in transfected cultured HepG2 cells by means of the dual-luciferase assay as farnesoid X receptor (FXR) agonists, using the endogenous ligand chenodeoxy
Synthesis and biological activities of prenylated tyrosine derivatives, the metabolites of Pithomyces ellis
Venkateswarlu, Somepalli,Panchagnula, Gopala K.,Subbaraju, Gottumukkala V.
, p. 1063 - 1066 (2007/10/03)
2-[4-(2E)-3-Methylbut-2-enyloxy)phenyl]ethan-1-ol 3 and 3-[4-(2E)-3-methylbut-2-enyloxy) phenyl]-2-(acetylamino)propanoic acid 8 have been synthesized from 4-hydroxyphenylacetic acid 1, L-tyrosine 4, respectively, with an overall yield of 55% and 37%. The spectral data of synthetic 3 and 8 are in good agreement with those of natural 3 and 8, respectively. These synthetic 3 and 8 show significant brine shrimp lethality, but weak antioxidant and antibacterial activities.
