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최용석 프로필 사진

최용석

Choi, Yong seok

생명과학대학

생명공학부

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전체 113건 중 101번부터 110번까지의 결과를 표시합니다.

Conference

55. L-Dioxolane thymidine analogues are potent inhibitors against Epstein-Barr virus replication

Yongseok Choi

Conference

Structure-activity relationships of L-dioxolane uracil nucleosides against varicella zoster virus

Yongseok Choi

Conference

Synthesis and potent anti-HIV activity of novel 2’-fluoro-4’-thio-nucleosides

Yongseok Choi

Conference

Synthesis and anti-HIV and HBV activity of 2’-fluoro-2’,3’-unsaturated L-nucleoside(L-F-d4N) analogs

Yongseok Choi

Conference

Synthesis and anti-HIV activity of L-2'-fluoro-2',3'-unsaturated pyrimidine and purine nucleosides

Yongseok Choi

Conference

Structure-activity relationships of (E)-5-(2-bromovinyl)uracil and related pyrimidine nucleosides as anti-varicella zoster virus agents

Yongseok Choi

Conference

59. Synthesis and biological evaluation of 2',3'-dideoxy-2'-fluoro-3'-C-hydroxymethyl-substituted nucleosides

Yongseok Choi

Conference

Structure-activity relationship studies of cytotoxic 5-hydroxy-4-quinolone

Yongseok Choi

Conference

Synthesis and Anti-HIV Activity of D-2’,3’-unsaturated-2’-fluoro-4’-thionucleosides

Yongseok Choi

Conference

The Synthesis of a conformationally locked version of puromycin amino nucleoside

Yongseok Choi

처음 이전 8 9 101112 다음 끝

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최용석

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선택된 필터

55. L-Dioxolane thymidine analogues are potent inhibitors against Epstein-Barr virus replication

Structure-activity relationships of L-dioxolane uracil nucleosides against varicella zoster virus

Synthesis and potent anti-HIV activity of novel 2’-fluoro-4’-thio-nucleosides

Synthesis and anti-HIV and HBV activity of 2’-fluoro-2’,3’-unsaturated L-nucleoside(L-F-d4N) analogs

Synthesis and anti-HIV activity of L-2'-fluoro-2',3'-unsaturated pyrimidine and purine nucleosides

Structure-activity relationships of (E)-5-(2-bromovinyl)uracil and related pyrimidine nucleosides as anti-varicella zoster virus agents

59. Synthesis and biological evaluation of 2',3'-dideoxy-2'-fluoro-3'-C-hydroxymethyl-substituted nucleosides

Structure-activity relationship studies of cytotoxic 5-hydroxy-4-quinolone

Synthesis and Anti-HIV Activity of D-2’,3’-unsaturated-2’-fluoro-4’-thionucleosides

The Synthesis of a conformationally locked version of puromycin amino nucleoside