Browsing "약학과" byAuthorHou X.

Jump to:
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
  • Sort by:
  • In order:
  • Results/Page
  • Authors/Record:

Showing results 1 to 12 of 12

Issue DateTitleAuthor(s)Type
2007Alternative and improved syntheses of highly potent and selective A 3 adenosine receptor agonists, CI-IB-MECA and thio-CI-IB-MECA정낙신Article
2008Design and synthesis of truncated 4'-thioadenosine derivatives as potent and selective A3 adenosine receptor antagonists.정낙신; 최원준Article
2010Discovery of a new human A2A adenosine receptor agonist, truncated 2-hexynyl-4′-thioadenosine정낙신; 최선Article
2021Dual actions of a2a and a3 adenosine receptor ligand prevents obstruction-induced kidney fibrosis in mice하헌주Article
2008First synthesis of 4′-selenonucleosides showing unusual southern conformation정낙신; 이상국; 권영주Article
2011Regio- and stereoselective synthesis of truncated 3′- aminocarbanucleosides and their binding affinity at the A 3 adenosine receptor정낙신; 최원준Article
2008Stereoselective synthesis and conformational study of novel 2′,3′-didehydro-2′,3′-dideoxy-4′-selenonucleosides정낙신; 최선; 최원준Article
2009Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists정낙신; 이상국; 최원준Article
2012Structure-activity relationships of truncated C2- or C8-substituted adenosine derivatives as dual acting A 2A and A 3 adenosine receptor ligands정낙신; 최선; 최원준Article
2008Structure-activity relationships of truncated D- and L-4′- thioadenosine derivatives as species-independent A3 adenosine receptor antagonists정낙신; 이상국; 최원준Article
2014Synthesis and anti-renal fibrosis activity of conformationally locked truncated 2-hexynyl-N6-substituted-(N)-methanocarba-nucleosides as A3 adenosine receptor antagonists and partial agonists정낙신; 하헌주; 최선Article
2008Synthesis of 2-chloro-N6-substituted-4'-thioadenosine-5'-N, N-dialkyluronamides as potent and selective A3 adenosine receptor antagonists.정낙신; 최원준Article

BROWSE