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1—环丙基—6—氟—7—取代喹诺酮抗HIV活性的定量构效关系 被引量:1

QSAR of 1 - Cydopropyl - 6 - fluoro - 7 - substituted - 1,4 - dihydro - 4 - oxoquinoline - 3 - carboxylic Acids for Anti - HIV Activity
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摘要 用量子化学AM1法对一系列1-环丙基-6-氟-7-取代-1,4-二氢-4-氧-喹啉-3-羧酸的定量构效关系进行了研究,结果表明该类化合物在对HIV的抑制过程中是一很好的电子给予体,给电子的部位主要是7-位哌嗪基末端氮原子,并进一步指出从抗G+和G-菌活性差的喹诺酮中有望筛选出好的抗HIV化合物.
机构地区 浙江大学化学系
出处 《化学学报》 SCIE CAS CSCD 北大核心 2001年第6期832-835,共4页 Acta Chimica Sinica
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参考文献3

  • 1Li J B,博士论文,1999年
  • 2Yu Q S,药学学报,1994年,29卷,8期,595页
  • 3Guo H Y,中国抗生素杂志,1992年,17卷,2期,99页

同被引文献24

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