The secondary metabolites of aff Samadera SAC-2825: An Australian Simaroubaceae with unusual chemistry

被引:12
作者
Gibbons, S
Craven, L
Dunlop, C
Gray, AI
Hartley, TG
Waterman, PG
机构
[1] UNIV STRATHCLYDE, DEPT PHARMACEUT SCI, PHYTOCHEM RES LABS, GLASGOW G1 1XW, LANARK, SCOTLAND
[2] AUSTRALIAN NATL HERBARIUM, CANBERRA, ACT 2601, AUSTRALIA
[3] CONSERVAT COMMISS NO TERR, HERBARIUM, PALMERSTON, NT 0831, AUSTRALIA
关键词
SAC-2825 (aff Samadera bidwillii); Simaroubaceae; Rutales; quassinoids; limonoids; 4-quinolone alkaloids; lignans; chemosystematics;
D O I
10.1016/S0031-9422(96)00708-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The phytochemical analysis of two collections of a new species (SAC-2825), tentatively assigned as aff. Samadera bidwillii (Simaroubaceae), has yielded a limonoid (limonin), a quassinoid (2'-acetoxy-glaucarubin), three alkaloids [2-(10'xi-acetoxyundecanyl)-1-acetoxymethyl-4-quinolone, 1-methoxy-10-methyl-acridan-9-one and 1,8-dihydroxyacridan-9-one] and seven bicycle-octane type lignans [(-)-sesamin, (-)-episesamin, fargesin, neofargesin, (-)-kobusin, (-)-epieudesmin and (-)-eudesmin]. The 4-quinolone alkaloid appears to be novel. The metabolites identified are collectively typical of the Rutales, but have a biosynthetic range never previously found together in a single species. Particularly noteworthy is the cooccurrence of limonoids and quassinoids in the same plant, which is currently unique to SAG-2825. Copyright (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:1109 / 1114
页数:6
相关论文
共 18 条
  • [1] QUINOLONE AND ACRIDONE ALKALOIDS FROM BORONIA-LANCEOLATA
    AHSAN, M
    GRAY, AI
    LEACH, G
    WATERMAN, PG
    [J]. PHYTOCHEMISTRY, 1993, 33 (06) : 1507 - 1510
  • [2] H-1 AND C-13 ASSIGNMENTS FROM SENSITIVITY-ENHANCED DETECTION OF HETERONUCLEAR MULTIPLE-BOND CONNECTIVITY BY 2D MULTIPLE QUANTUM NMR
    BAX, A
    SUMMERS, MF
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (08) : 2093 - 2094
  • [3] *CHAPM HALL, 1995, DICT NAT PROD CD ROM
  • [4] STUDIES OF AUSTRALIAN SOFT CORALS .2. NOVEL CEMBRENOID DITERPENE FROM LOBOPHYTUM-MICHAELAE
    COLL, JC
    MITCHELL, SJ
    STOKIE, GJ
    [J]. AUSTRALIAN JOURNAL OF CHEMISTRY, 1977, 30 (08) : 1859 - 1863
  • [5] DA SILVA MFGF, 1988, PLANT SYST EVOL, V161, P97
  • [6] 3-MONOTERPENYL 2,4-DIOXYGENATED QUINOLINE ALKALOIDS FROM THE AERIAL PARTS OF ERIOSTEMON-AUSTRALASIUS SUBSP BANKSII (RUTACEAE)
    DACUNHA, EVL
    ARMSTRONG, JA
    GRAY, AI
    HOCKLESS, DCR
    WATERMAN, PG
    WHITE, AH
    [J]. AUSTRALIAN JOURNAL OF CHEMISTRY, 1993, 46 (10) : 1507 - 1514
  • [7] SIMAROUBACEAE, AN ARTIFICIAL CONSTRUCT - EVIDENCE FROM RBCL SEQUENCE VARIATION
    FERNANDO, ES
    GADEK, PA
    QUINN, CJ
    [J]. AMERICAN JOURNAL OF BOTANY, 1995, 82 (01) : 92 - 103
  • [8] Hegnauer R, 1990, CHEMOTAXONOMIE PFLAN, V9
  • [9] THE DEMETHYLATION OF METHOXYACRIDONES
    HUGHES, GK
    MATHESON, NK
    NORMAN, AT
    RITCHIE, E
    [J]. AUSTRALIAN JOURNAL OF SCIENTIFIC RESEARCH SERIES A-PHYSICAL SCIENCES, 1952, 5 (01): : 206 - 217
  • [10] HYDROPEROXYSESQUITERPENE AND LIGNAN CONSTITUENTS OF MAGNOLIA-KOBUS
    IIDA, T
    NAKANO, M
    ITO, K
    [J]. PHYTOCHEMISTRY, 1982, 21 (03) : 673 - 675