Shin, DH Lee, HW Park, SS Kim, JH Jeong, LS Chun, MW 2024-01-21T13:40:44Z 2024-01-21T13:40:44Z 2021-09-05 2000-08 0253-6269 https://pubs.kist.re.kr/handle/201004/141211 Based on (-)-neplanocin A with the 5'-hydroxyl substituted with fluoro, azido, or amino group, the corresponding xylo- and arabino derivatives were synthesized from D-ribose using the Mitsunobu reaction as a key step. None of the final nucleosides did show either significant antiviral activities or cytotoxicities. English PHARMACEUTICAL SOCIETY KOREA S-ADENOSYLHOMOCYSTEINE HYDROLASE L-HOMOCYSTEINE HYDROLASE NEPLANOCIN-A TARGET CELLS Synthesis of (-)-neplanocin A analogues as potential antiviral agents Article 10.1007/BF02975438 1 ARCHIVES OF PHARMACAL RESEARCH, v.23, no.4, pp.302 - 309 ARCHIVES OF PHARMACAL RESEARCH 23 4 302 309 scie scopus 000088971900004 2-s2.0-0034251951 Chemistry, Medicinal Pharmacology & Pharmacy Pharmacology & Pharmacy Article S-ADENOSYLHOMOCYSTEINE HYDROLASE L-HOMOCYSTEINE HYDROLASE NEPLANOCIN-A TARGET CELLS neplanocin A nucleosides antiviral activity cytotoxicity S-adenosylhomocysteine hydrolase