Three New Benzophenone-Xanthone Dimers from the Root of Garcinia dulcis

    • TOSA Hideki
    • Department of Pharmacognosy, Gifu Pharmaceutical University
    • ITO Tetsuro
    • Department of Pharmacognosy, Gifu Pharmaceutical University

    • RISWAN Soedarsono
    • Herbarium Bogoriense, The Indonesian Institute of Science, Research and Development Center for Biology

Abstract

Investigation of the chemical constituents of the roots of Garcinia dulcis resulted in the isolation of three new benzophenone-xanthone dimers named garciduols A-C (1-3) in addition to a new xanthone, 1,3,6-trihydroxy-7-methoxyxanthone (4). Five known xanthones [2,5-dihydroxy-1-methoxy- (5), 1,4,5-trihydroxy- (6), 1,3,5-trihydroxy- (7), 1,3,6-trihydroxy-5-methoxy- (8) and 1,3,6-trihydroxy-8-isoprenyl-7-methoxyxanthone (9)] were also isolated from the roots. Their structures were determined by spectroscopic analysis including two dimensional NMR. The behaviors of chemical shifts caused by acetylation and the position of the methoxyl group in the dimers characterized by model synthetic benzophenones are also discussed.

Journal

Chemical & pharmaceutical bulletin   [List of Volumes]

Chemical & pharmaceutical bulletin 44(9), 1744-1747, 1996-09-15  [Table of Contents]

The Pharmaceutical Society of Japan

References:  16

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Codes

  • NII Article ID (NAID) :
    110003632155
  • NII NACSIS-CAT ID (NCID) :
    AA00602100
  • Text Lang :
    ENG
  • Article Type :
    ART
  • ISSN :
    00092363
  • Databases :
    CJP  NII-ELS 

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