STARFISH SAPONINS .53. A REINVESTIGATION OF THE POLAR STEROIDS FROM THE STARFISH OREASTER-RETICULATUS - ISOLATION OF 16 STEROIDAL OLIGOGLYCOSIDES AND 6 POLYHYDROXYSTEROIDS

被引:31
作者
IORIZZI, M
BIFULCO, G
DERICCARDIS, F
MINALE, L
RICCIO, R
ZOLLO, F
机构
[1] DIPARTIMENTO CHIM SOSTANZE NAT,I-80131 NAPLES,ITALY
[2] UNIV MOLISE,FAC AGRARIA,I-86100 CAMPOBASSO,ITALY
来源
JOURNAL OF NATURAL PRODUCTS-LLOYDIA | 1995年 / 58卷 / 01期
关键词
D O I
10.1021/np50115a002
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
A reinvestigation of the starfish Oreaster reticulatus has led to the isolation of sixteen steroidal oligoglycosides and six polyhydroxysteroids. One steroidal monoglycoside has been identified as asterosaponin-1 [5], previously isolated from the same organism, and one pentaglycoside steroidal sulfate has been identified with the known ophidianoside F [1], previously isolated from starfish species of the family Ophidiasteridae. The novel pentaglycoside steroidal sulfates reticulatosides A [3] and B [4] represent the second examples of asterosaponins containing the 5 alpha-cholesta-9(11)-en-3 beta,6 alpha,20,22-tetraol aglycone. Of the remaining new steroidal oligoglycosides, the majority are characterized by the common (24S)-5 alpha-cholesta-3 beta,6 alpha,8,15 alpha,24-pentaol aglycone, with some having a sulfate group at C-6, and differing in the sugar moiety. Compounds 11, 12, 15,and 16 represent major departures from the more common structural features encountered in steroidal glycosides from starfish with the presence in 11 and 12 of a rare 5-O-methylgalactofuranosyl unit and in 15 and 16 of a 3-O-methyl-2-O-sulfate-xylopyranosyl unit. The latter was shown by nmr data combined with molecular dynamics calculations to exist: in an 8:2 equilibrium mixture of the C-1(4) and C-4(1) conformations.
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页码:10 / 26
页数:17
相关论文
共 34 条
  • [1] CONFIGURATION ASSIGNMENT OF 24R-ISOMERS AND 24S-ISOMERS OF 29-OXYGENATED STEROIDS BY H-1 AND C-13 NMR-SPECTROSCOPY
    ANASTASIA, M
    ALLEVI, P
    CIUFFREDA, P
    RICCIO, R
    [J]. TETRAHEDRON, 1986, 42 (17) : 4843 - 4847
  • [2] HIGH-TEMPERATURE ANNEALED MOLECULAR-DYNAMICS SIMULATIONS AS A TOOL FOR CONFORMATIONAL SAMPLING - APPLICATION TO THE BICYCLIC-222 CRYPTAND
    AUFFINGER, P
    WIPFF, G
    [J]. JOURNAL OF COMPUTATIONAL CHEMISTRY, 1990, 11 (01) : 19 - 31
  • [3] C-13 NUCLEAR MAGNETIC-RESONANCE SPECTROSCOPY OF MONOSACCHARIDES
    BOCK, K
    PEDERSEN, C
    [J]. ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY, 1983, 41 : 27 - 66
  • [4] BRIDGEMAN JE, 1970, J CHEM SOC P1, P950
  • [5] STARFISH SAPONINS .38. STEROIDAL GLYCOSIDES FROM THE STARFISH PYCNOPODIA-HELIANTHOIDES
    BRUNO, I
    MINALE, L
    RICCIO, R
    [J]. JOURNAL OF NATURAL PRODUCTS, 1989, 52 (05): : 1022 - 1026
  • [6] CHO Y, 1992, LIEBIGS ANN CHEM, P79
  • [7] STEREOCHEMICAL ASSIGNMENT AT C-24 AND C-25 OF MARINE 24-ETHYL-26-HYDROXY STEROIDS THROUGH COMPARISON WITH SYNTHETIC (24S,25S)-MODELS, (24S,25R)-MODELS, (24R,25R)-MODELS, AND (24R,25S)-MODELS
    DAURIA, MV
    PALOMA, LG
    MINALE, L
    RICCIO, R
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1990, (11): : 2895 - 2898
  • [8] STARFISH SAPONINS .40. STRUCTURES OF 2 NEW ASTEROSAPONINS FROM THE STARFISH PATIRIA-MINIATA - PATIRIOSIDE-A AND PATIRIOSIDE-B
    DAURIA, MV
    IORIZZI, M
    MINALE, L
    RICCIO, R
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1990, (04): : 1019 - 1023
  • [9] STARFISH SAPONINS .41. STRUCTURE OF 2 NEW STEROIDAL GLYCOSIDE SULFATES (MINIATOSIDE-A AND MINIATOSIDE-B) AND 2 NEW POLYHYDROXYSTEROIDS FROM THE STARFISH PATIRIA-MINIATA
    DAURIA, MV
    IORIZZI, M
    MINALE, L
    RICCIO, R
    URIARTE, E
    [J]. JOURNAL OF NATURAL PRODUCTS, 1990, 53 (01): : 94 - 101
  • [10] POLYOXYGENATED STEROIDS OF MARINE ORIGIN
    DAURIA, MV
    MINALE, L
    RICCIO, R
    [J]. CHEMICAL REVIEWS, 1993, 93 (05) : 1839 - 1895