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최용석 프로필 사진

최용석

Choi, Yong seok

생명과학대학

생명공학부

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전체 113건 중 91번부터 100번까지의 결과를 표시합니다.

2007

Conference

Pyripyropene A derivatives as potent acyl-CoA:Cholesterol Acyltransferase (ACAT) inhibitors and their insecticidal activities

Yongseok Choi

2007-07-10
튀르키예

2003

Book

Antiviral Nucleosides: Chiral Synthesis and Chemotherapy; Ch.1. Recent Advances in Antiviral Nucleosides.

Yongseok Choi

2003-12
Elsevier Science Ltd.

1998

Book

Therapies for Viral Hepatitis; Ch. 32. Preclinical investigation of L-FMAU as an anti-hepatitis B virus agent.

Yongseok Choi

1998-10
International Medical Press

Conference

Asymmetric synthesis of a conformationally locked carbocyclic analogue of L-3’-deoxythymidine that mimicks the south conformation.

Yongseok Choi

Conference

New L-nucleoside b-L-5-vinyl dioxolane uracil (L-VOddU) is the most potent inhibitor of Epstein-Barr virus

Yongseok Choi

Conference

Synthesis and anti-HIV activity of L-2’,3’-didehydro-2’,3’-dideoxy-2’-fluoro-4’-thiocytidine

Yongseok Choi

Conference

48. Inhibition of the growth of varicellar-zoster virus by L-b-5-bromovinyl-(2-hydroxymethyl-1,3-dioxolanyl)uracil

Yongseok Choi

Conference

Asymmetric synthesis of a conformationally locked analogue of 3’-deoxy thymidine and its triphosphate

Yongseok Choi

Conference

Structure-activity relationships of 2'-fluoro-2',3'-unsaturated D-nucleosides as anti-HIV-1 agents.

Yongseok Choi

Conference

2-Substitution of adenine nucleotide analogues containing a bicyclo[3.1.0]hexane ring system locked in a northern conformation

Yongseok Choi

처음 이전 8 91011 12 다음 끝

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최용석

자료 필터

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선택된 필터

Pyripyropene A derivatives as potent acyl-CoA:Cholesterol Acyltransferase (ACAT) inhibitors and their insecticidal activities

Antiviral Nucleosides: Chiral Synthesis and Chemotherapy; Ch.1. Recent Advances in Antiviral Nucleosides.

Therapies for Viral Hepatitis; Ch. 32. Preclinical investigation of L-FMAU as an anti-hepatitis B virus agent.

Asymmetric synthesis of a conformationally locked carbocyclic analogue of L-3’-deoxythymidine that mimicks the south conformation.

New L-nucleoside b-L-5-vinyl dioxolane uracil (L-VOddU) is the most potent inhibitor of Epstein-Barr virus

Synthesis and anti-HIV activity of L-2’,3’-didehydro-2’,3’-dideoxy-2’-fluoro-4’-thiocytidine

48. Inhibition of the growth of varicellar-zoster virus by L-b-5-bromovinyl-(2-hydroxymethyl-1,3-dioxolanyl)uracil

Asymmetric synthesis of a conformationally locked analogue of 3’-deoxy thymidine and its triphosphate

Structure-activity relationships of 2'-fluoro-2',3'-unsaturated D-nucleosides as anti-HIV-1 agents.

2-Substitution of adenine nucleotide analogues containing a bicyclo[3.1.0]hexane ring system locked in a northern conformation