Design and Synthesis of Pyrrolo[2,1-c][1,4]benzodiazepine Hybrid Agents

碩士 === 高雄醫學院 === 藥學研究所 === 86 === The pyrrolo[2,1-c][1,4]benzodiazepines (PBDs), a family of potent DNA-binding antitumor antibiotics , are produce by streptomyces species. These drugs react covalently with DNA to form an N2-guanine addu...

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Bibliographic Details
Main Authors: Hsu, Mei Hui, 許美惠
Other Authors: Jeh-Jeng Wang
Format: Others
Language:zh-TW
Published: 1998
Online Access:http://ndltd.ncl.edu.tw/handle/50956882661194243769
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Summary:碩士 === 高雄醫學院 === 藥學研究所 === 86 === The pyrrolo[2,1-c][1,4]benzodiazepines (PBDs), a family of potent DNA-binding antitumor antibiotics , are produce by streptomyces species. These drugs react covalently with DNA to form an N2-guanine adduct that lies within the minor groove of DNA. Although they have the highly antitumor activity, they produce cardiotoxicity, which have precluded their continued clinical application. Therefore , we design and synthesis of hybrid agents base upon the PBD and indole carboxylate (IC). The hybrid agents were synthesized in eleven steps with 19~45% yields. The biological activities of these drugs are under investigation.