Small molecular inhibitors of miR-1 identified from photocycloadducts of acetylenes with 2-methoxy-1,4-naphthalenequinone
摘要:
Small molecules which can modulate endogenous microRNAs are important chemical tools to study microRNA regulational network. In this Letter we screened the [2+2] photocycloadducts of 2-methoxy-1,4-naphthalenequinone with a series of aryl acetylenes on their activity to modulate endogenous microRNAs. A potent inhibitor of the muscle-specific miR-1 which is closely related with cardiac development and disease was identified. The small molecular inhibitor was the cyclobutene type product derived from the photocycloaddition of 2-methoxy-1,4-naphthalenequinone with tert-butyl (5-(phenylethynyl) quinolin-8-yl) carbonate. Analogues of the small molecular inhibitor were then prepared using similar photocycloaddition reactions for evaluation on inhibition activity on miR-1 to provide structure-activity relationship of the miR-1 inhibitor. (C) 2013 Elsevier Ltd. All rights reserved.
Substituted benzazoles and methods of their use as inhibitors of Raf kinase
申请人:——
公开号:US20040122237A1
公开(公告)日:2004-06-24
New substituted benz-azole compounds, compositions and methods of inhibition of Raf kinase activity in a human or animal subject are provided. The new compounds compositions may be used either alone or in combination with at least one additional agent for the treatment of a Raf kinase mediated disorder, such as cancer.
作者:Yong Yang、Joyce Fen Yan Lim、Xinying Chew、Edward G. Robins、Charles W. Johannes、Yee Hwee Lim、Howard Jong
DOI:10.1039/c5cy00507h
日期:——
and Cy*Phine-nBu), demonstrated exceptional broad-based performance and operational simplicity in the copper-freeSonogashiracross-coupling of challenging (hetero-)aryl chlorides and terminal alkynes. Modifications to the periphery of the ligand scaffold showed modest improvements in the reaction rate when more electron-donating substituents were incorporated, which hints at potential design upgrades
利用演化的间-叔芳基膦配体Cy * Phine的不同变异,开发了三种新颖的钯配合物。这些空气和水分稳定的配合物PdCl 2 L 2(L = Cy * Phine,Cy * Phine-CF 3和Cy * Phine- n Bu)在无铜Sonogashira中表现出优异的广泛性能和操作简便性具有挑战性的(杂)芳基氯化物和末端炔烃的交叉偶联。当引入更多的供电子取代基时,对配体支架外围的修饰显示出反应速率的适度提高,这暗示了未来潜在的设计升级。
[EN] COMPOUNDS USEFUL FOR TREATING A MANNHEIMIA HAEMOLYTICA OR HISTOPHILUS SOMNI INFECTION<br/>[FR] COMPOSÉS UTILES POUR TRAITER UNE INFECTION PAR MANNHEIMIA HAEMOLYTICA OU HISTOPHILUS SOMNI
申请人:INTERVET INT BV
公开号:WO2018115421A1
公开(公告)日:2018-06-28
The present invention discloses compounds of formula (I) that are useful in the treatment of respiratory diseases of animals, especially Bovine or Swine Respiratory disease (BRD and SRD).
synthesis of 2-(3-sulfonatomesityl)-5-sulfonatoindenyl)dicyclohexylphosphine hydrate sodium salt and its use in palladium-catalyzed Suzuki–Miyaura and Sonogashiracoupling reactions in water (and biphasic water–organic solvent mixtures) to prepare a variety of functionalized biaryls and aryl alkynes in excellent yield.
Cu2O/PPh3/TBAB (n-Bu4NBr) system for the cross-couplingreactions of aryl and heteroarylhalides with terminal alkynes has been developed. Four types of Cu2O, including bulky Cu2O, cubic Cu2O nanoparticles, octahedral Cu2O nanoparticles, and spherical Cu2O nanoparticles, were examined, and the octahedral Cu2O nanoparticles were found to be the most effective catalyst for the reaction. In the presence of the octahedral