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Modular synthesis of heparanase substrates

첫 페이지 보기
  • 발행기관
    한국당과학회 바로가기
  • 간행물
    한국당과학회 학술대회 바로가기
  • 통권
    ACGG 2012 Conference (2012.10)바로가기
  • 페이지
    pp.64-64
  • 저자
    Peng Xu, Weichang Xu, Yuanwei Dai, Biao Yu
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A192870

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원문정보

초록

영어
Heparanase, preferentially expressed in many tumor cells, is an endoβDglucuronidase that cleaves specific sites of heparan sulfate. Elevated levels of heparanase expression correlate with tumor vasculatrity, metastatic potiential, and reduced postoperative survival of cancer patients. Consequencely, heparanase detection is considered a tool for cancer discovery. A library of 20 welldefined Tetra1 analogs were prepared in a convergent “2+2” glycosidation manner utilizing a relatively small number of protected disaccharide donors and acceptors. Among three different donors prepared for the fullprotected tetrasaccharide, trifluoroacetimidate donor was most suitable for the preservation and glycosidation reaction, and in each glycosylation, the yield was good and the major anomer was obtained. After coupling these 12 glycosydic reactions, the observation indicate that the coupling ratio is not only relating to the structure and exact nature of acceptors, but also correlated to the structure and size of donors. Key features of the approach include the use of Bz esters or PMB ethers for those hydroxyls that need sulfation, regioselective opening of the 4,6-O-benzylidene acetal for 4OBn that don’t need sulfation and 6OH that need oxidation, an anomeric TBS group for glycosyl donor synthesis, and benzyl ethers just as permanent protecting groups. The HS oligosaccharides will be employed to probe structural features of HS for cleavage of heparanase.

저자

  • Peng Xu [ State Key Laboratory of Bio-organic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China ]
  • Weichang Xu [ State Key Laboratory of Bio-organic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China ]
  • Yuanwei Dai [ State Key Laboratory of Bio-organic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China ]
  • Biao Yu [ State Key Laboratory of Bio-organic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China ]

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국당과학회 [Korean Society for Glycoscience]
  • 설립연도
    2006
  • 분야
    의약학>약학
  • 소개
    본 학회는 화학, 생화학, 분자생물학, 미생물학, 식품공학, 의학, 약학, 유전공학 및 생물공학, 환경 및 기타 공업 등 전 분야의 탄수화물관련 이론과 기술을 연구 발전시키고 산학협동을 통해 이를 보급하여 국내 관련 산업의 발전 및 국민생활의 과학화에 기여하고자 하며, 이러한 목표와 비젼의 실현을 위해 회원들이 적극적인 참여와 활동을 전개하고자 한다.

간행물

  • 간행물명
    한국당과학회 학술대회
  • 간기
    연간
  • 수록기간
    2006~2022
  • 십진분류
    KDC 517 DDC 614

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