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CHAIN TERMINATORS IN HIV REVERSE TRANSCRIPTION

CHAIN TERMINATORS IN HIV REVERSE TRANSCRIPTION
HIV 逆转录中的链终止子
批准号:
6258822
负责人:
Ramachandra S Hosmane
金额:
$0.01万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-06-01 至 1999-11-30

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中文摘要
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英文摘要
Fat and Slim Nucleosides and Nucleotides as Potential Aticancer and Antiviral Agents: These novel ring-expanded (fat) and ring-contracted (slim) nucleoside analogues, designed and synthesized in this lab, are potential chain-terinators of nucleic acid synthesis when incorporated into a tumor or viral DNA/RNA during transcription (or reverse transcription in case of retroviruses including HIV that causes AIDS). Mode of chain termination, and hence the viral or tumor replication, is believed to be the base-mispairing accompanied by considerable deviation of the base-sugar bond from the natural array. In addition, because of their unique structural, spatial, and conformational characteristics and constraints, fat and slim nucleosides/-tides are excellent probes for nucleic acid metabolism, structure, and function. While we use EI/CI/FAB Mass Spectrometry for routine structural analyses of small molecules, the MALDI TOF mass spectrometer is necessary for the molecular weight determination and purity of oligonucleotides derived from or incorporated with fat or slim nucleotides.
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Inhibition of HCV as an Opportunistic HIV Co-infection
Mechanistic Studies of Anti-HIV Activity of a Novel Ring-Expanded Nucleoside
Mechanistic Studies of Anti-HIV Activity of a Novel Ring-Expanded Nucleoside
Mechanistic Studies of Anti-HIV Activity of a Novel Ring-Expanded Nucleoside
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