Adenosine analogues as inhibitors of P2Y12 receptor mediated platelet aggregation
作者:James G. Douglass、J. Bryan deCamp、Emilee H. Fulcher、William Jones、Sanjoy Mahanty、Anna Morgan、Dima Smirnov、José L. Boyer、Paul S. Watson
DOI:10.1016/j.bmcl.2008.01.038
日期:2008.3
Modified adenosine derivatives may lead to the development of P2Y(12) antagonists that are potent, selective, and bind reversibly to the receptor. Analogues of 2',3'-trans-styryl acetal-N6-ureido-adenosine monophosphate were prepared by modification of the 5'-position. The resulting analogues were tested for P2Y(12) antagonism in a plateletaggregation assay.
Garcia Gonzalez; de Castro, Anales de la Real Sociedad Espanola de Fisica y Quimica, 1950, vol. <B>46, p. 68,69,70
作者:Garcia Gonzalez、de Castro
DOI:——
日期:——
The Chemistry of Pyrrolic Compounds. LXXI. Synthesis of the Ring C and the Ring D Demethyl Analogues of Deoxophylloerythroetioporphyrin (dpep)
作者:PS Clezy、A Salek
DOI:10.1071/ch9960265
日期:——
The demethyl analogues (1d,e) of dpep have been prepared by utilizing in each case an oxidative cyclization of an intermediate biladiene -ac to assemble the porphyrin macrocycle.
dpep 的去甲基类似物(1d,e)都是通过中间体双二烯-ac 的氧化环化来组装卟啉大环而制备的。
Garcia Gonzalez; de Castro Brzezicki, Anales de la Real Sociedad Espanola de Fisica y Quimica, 1950, vol. <B> 46, p. 68,71