24082-42-6Relevant articles and documents
Molecular design of potent, hydrophilic tyrosinase inhibitors based on the natural dihydrooxyresveratrol skeleton
Tanaka, Yuri,Suzuki, Marina,Kodachi, Yuka,Nihei, Ken-ichi
, p. 42 - 49 (2019)
In this study, dihydrooxyresveratrol glucosides 3–6 were synthesized for the first time to the best of our knowledge by the Wittig reaction and Schmidt glycosylation as key steps for the purpose of developing novel hydrophilic tyrosinase inhibitors. Resul
Identification of dihydrostilbenes in Pholidota chinensis as a new scaffold for GABAA receptor modulators
Rueda, Diana C.,Sch?ffmann, Angela,De Mieri, Maria,Raith, Melanie,J?hne, Evelyn A.,Hering, Steffen,Hamburger, Matthias
, p. 1276 - 1284 (2014/03/21)
A dichloromethane extract of stems and roots of Pholidota chinensis (Orchidaceae) enhanced GABA-induced chloride currents (IGABA) by 132.75 ± 36.69% when tested at 100 μg/mL in a two-microelectrode voltage clamp assay, on Xenopus laevis oocytes
Dimeric cannabinoids with an ethane bridge
Eiden,Gerstlauer
, p. 995 - 1006 (2007/10/02)
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