885053-24-7Relevant academic research and scientific papers
Stilbene analogs as inducers of apolipoprotein-I transcription
Hansen, Henrik C.,Chiacchia, Fabrizio S.,Patel, Reena,Wong, Norman C.W.,Khlebnikov, Vladimir,Jankowska, Renata,Patel, Kalpesh,Reddy, M. Madhava
experimental part, p. 2018 - 2023 (2010/06/19)
Based on the naturally occurring stilbene, Resveratrol, a series of novel stilbene derivatives were synthesized, which have the ability to induce the expression of the ApoA-I gene. Several compounds equally or more potent than Resveratrol were identified. trans-4,4′-Dihydroxy-2-methoxystilbene was the most potent (4.6× more potent than Resveratrol). These compounds provide an early lead into new drugs to treat atherosclerosis.
SELECTIVE ESTROGEN RECEPTOR MODULATORS
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Page/Page column 178-179, (2008/06/13)
The present invention provides a compound represented by the following formula (I); [wherein T represents a single bond, a C1-C4 alkylene group which may have a substituent and the like; formula (I-1) represents a single bond or a double bond; A represents a single bond, a bivalent 5- to 14-membered heterocyclic group which may have a substituent and the like; Y represents a single bond and the like; Z represents a methylene group and the like; ring G represents a phenylene group and the like which may condense with a 5- to 6-membered ring and may have a heteroatom; Ra and Rb are the same as or different from each other and represent a hydrogen atom and the like; W represents a single bond and the like; R' represents 1 to 4 independent hydrogen atoms and the like; and R" represents 1 to 4 independent hydrogen atoms and the like] or a salt thereof, or a hydrate thereof.
A new series of estrogen receptor modulators: Effect of alkyl substituents on receptor-binding affinity
Kamada, Atsushi,Sasaki, Atsushi,Kitazawa, Noritaka,Okabe, Tadashi,Nara, Kazumasa,Hamaoka, Shinichi,Araki, Shin,Hagiwara, Hiroaki
, p. 79 - 88 (2007/10/03)
New types of selective estrogen receptor modulators (SERMs) were synthesized and evaluated for their binding affinity and biological effect on reproductive cells. A proposed lead structure (B) was derivatized to provide compounds 30 and 44, which showed g
