http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Stereoselective Synthesis of 1'-Functionalized-4'-Thionucleosides
Jeong, Lak Shin,Gunaga, Prashantha,Kim, Hea Ok,Tosh, Dilip K.,Lee, Hyuk Woo,Choe, Seung Ah,Moon, Hyung Ryong,Gao, Zhan-Guo,Jacobson, Kenneth A.,Chun, Moon Woo Taylor Francis 2007 NUCLEOSIDES NUCLEOTIDES AND NUCLEIC ACIDS Vol. No.
<P> Stereoselective functionalization of the 1'-position of 4'-thionucleosides was achieved using a stereoselective SN2 reaction controlled by 5-membered ring coordination.</P>
Jeong, Lak Shin,Choe, Seung Ah,Gunaga, Prashantha,Kim, Hea Ok,Lee, Hyuk Woo,Lee, Sang Kook,Tosh, Dilip K.,Patel, Amit,Palaniappan, Krishnan K.,Gao, Zhan-Guo,Jacobson, Kenneth A.,Moon, Hyung Ryong 이화여자대학교 약학연구소 2008 藥學硏究論文集 Vol.- No.18
Truncated D-4'-thioadenosine derivatives lacking the 4'-hydroxymethylene moiety were synthesized starting from D-mannose, using cyclization to the 4-thiosugar and one-step conversion of the diol to the acetate as key steps At the human A₃ adenosine receptor (AR), N^(6)-substituted purine analogues bound potently and selectively and acted as antagonists in a cyclic AMP functional assay An N^(6)-(3-chlorobenzyl)purine analogue 9b displayed a K, value of 1 66 nM at the human A₃ AR Thus, truncated D-4'-thioadenosine is an excellent template for Ihe design of novel A₃ AR antagonists to act at both human and murine species.
Design and Synthesis of A₃ Adenosine Receptor Ligands, 2´-Fluoro Analogues of Cl-IB-MECA
Kim, Hea Ok,Park, Jae Gyu,Moon, Hyung Ryong,Gunaga, Prashantha,Lim, Moo Hong,Chun, Moon Woo,Jacobson, Kenneth A.,Kim, Hee-Doo,Jeong, Lak Shin 梨花女子大學校 藥學硏究所 2003 藥學硏究論文集 Vol.- No.12
Synthesis of 2'-deoxy-2'-fluoro-N^(6) -substituted adenosines as bioisosteres of Cl-IB-MECA and their binding affinities to A₃ adenosine receptor are described.