메뉴 건너뛰기




Volumn 40, Issue 10, 2005, Pages 1075-1079

New ceramides from Rantherium suaveolens

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; LIPIDS; MOLECULAR STRUCTURE; NITROGEN COMPOUNDS; SPECTROSCOPIC ANALYSIS;

EID: 33644877312     PISSN: 00244201     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11745-005-1472-3     Document Type: Article
Times cited : (18)

References (39)
  • 1
    • 33645986548 scopus 로고
    • Tunisian Scientific Publications, Official Press, Republic of Tunisia, Tunis, Tunisia
    • Alapetite, G.P. (1981) Flora of Tunisia, Tunisian Scientific Publications, Official Press, Republic of Tunisia, Tunis, Tunisia.
    • (1981) Flora of Tunisia
    • Alapetite, G.P.1
  • 2
    • 33646003021 scopus 로고
    • Tunisian Scientific Publications, Official Press, Republic of Tunisia, Tunis, Tunisia
    • le Floc'h, E. (1983) Contribution to an Ethnobotanical Study of the Tunisian Flora, pp. 82-83, Tunisian Scientific Publications, Official Press, Republic of Tunisia, Tunis, Tunisia.
    • (1983) Contribution to An Ethnobotanical Study of the Tunisian Flora , pp. 82-83
    • Floc'H, E.1
  • 3
    • 33646008930 scopus 로고    scopus 로고
    • Ministry of the Environment and Territorial Management, State Secretariat of Scientific Research and Technology, Tunisia
    • Issaoui, A., Kallala, A., Naffeti, M., and Akrimi, N. (1996) Plants from South Tunisia, Ministry of the Environment and Territorial Management, p. 174, State Secretariat of Scientific Research and Technology, Tunisia.
    • (1996) Plants from South Tunisia , pp. 174
    • Issaoui, A.1    Kallala, A.2    Naffeti, M.3    Akrimi, N.4
  • 4
    • 33646015437 scopus 로고    scopus 로고
    • Alcools tetrahydropyraniques polyacetyleniques antibacteriens de la plante Rantherium suaveolens poussant dans le sud Tunisien
    • Oueslati, M.H., Ben Jannet, H., Abreu, P.J.M., and Mighri, Z. (2004) Alcools tetrahydropyraniques polyacetyleniques antibacteriens de la plante Rantherium suaveolens poussant dans le sud Tunisien, J. Soc. Alger. Chim. 14, 245-258.
    • (2004) J. Soc. Alger. Chim. , vol.14 , pp. 245-258
    • Oueslati, M.H.1    Ben Jannet, H.2    Abreu, P.J.M.3    Mighri, Z.4
  • 7
    • 51249193286 scopus 로고
    • Methods for methanolysis of sphingolipids and direct determination of long-chain bases by gas chromatography
    • Gaver, R.C., and Sweeley, C.C. (1965) Methods for Methanolysis of Sphingolipids and Direct Determination of Long-Chain Bases by Gas Chromatography, J. Am. Oil Chem. Soc. 42, 294-298.
    • (1965) J. Am. Oil Chem. Soc. , vol.42 , pp. 294-298
    • Gaver, R.C.1    Sweeley, C.C.2
  • 9
    • 0002249585 scopus 로고
    • Crown gall tumours on potato discs and brine shrimp lethality: Two simple bioassays for higher plant screening and fractionation
    • (Emerit, I., and Chance, B., Eds.), Academic, London
    • McLaughlin, J.L. (1991) Crown Gall Tumours on Potato Discs and Brine Shrimp Lethality: Two Simple Bioassays for Higher Plant Screening and Fractionation, in Methods in Plant Biochemistry (Hostettman, K., ed.), Vol. 6, pp 1-32, Academic, London.
    • (1991) Methods in Plant Biochemistryx , vol.6 , pp. 1-32
    • McLaughlin, J.L.1
  • 10
    • 4344666557 scopus 로고    scopus 로고
    • New sphingosines from a gorgonian, Pseudopterogorgia australiensis Ridley, of the Indian Ocean
    • Krishna, N., Muralidhar, P., Kumar, M.M., Rao, D.V., and Rao, C.B. (2004) New Sphingosines from a Gorgonian, Pseudopterogorgia australiensis Ridley, of the Indian Ocean, J. Nat. Prod. 67, 1423-1425.
    • (2004) J. Nat. Prod. , vol.67 , pp. 1423-1425
    • Krishna, N.1    Muralidhar, P.2    Kumar, M.M.3    Rao, D.V.4    Rao, C.B.5
  • 11
    • 1642458527 scopus 로고    scopus 로고
    • New glyceroglycolipid and ceramide from Premna microphylla
    • Zhan, Z.-J., and Yue, J.-M. (2003) New Glyceroglycolipid and Ceramide from Premna microphylla, Lipids 38, 1299-1303.
    • (2003) Lipids , vol.38 , pp. 1299-1303
    • Zhan, Z.-J.1    Yue, J.-M.2
  • 12
    • 1642560875 scopus 로고    scopus 로고
    • A New Tetranortriterpenoid from Dysoxylum lenticellatum
    • Qi, S.-H., Wu, D.-G., Zhang, S., and Luo, X.-D. (2003) A New Tetranortriterpenoid from Dysoxylum lenticellatum, Z. Naturforsch. 58b, 1128-1132.
    • (2003) Z. Naturforsch. , vol.58 , pp. 1128-1132
    • Qi, S.-H.1    Wu, D.-G.2    Zhang, S.3    Luo, X.-D.4
  • 13
    • 0035103748 scopus 로고    scopus 로고
    • A new ceramide from the basidiomycete Russula cyanoxantha
    • Gao, J.-M, Dong, Z.-J., and Liu, J.-K. (2001) A New Ceramide from the Basidiomycete Russula cyanoxantha, Lipids 36, 175-180.
    • (2001) Lipids , vol.36 , pp. 175-180
    • Gao, J.-M.1    Dong, Z.-J.2    Liu, J.-K.3
  • 14
    • 0033936585 scopus 로고    scopus 로고
    • New lipids from the Tunicate Cystodytes cf. dellechiajei, as PLA2 inhibitors
    • Loukaci, A., Bultel-Poncé, V., Longeon, A., and Guyot, M. (2000) New Lipids from the Tunicate Cystodytes cf. dellechiajei, as PLA2 Inhibitors, J. Nat. Prod. 63, 799-802.
    • (2000) J. Nat. Prod. , vol.63 , pp. 799-802
    • Loukaci, A.1    Bultel-Poncé, V.2    Longeon, A.3    Guyot, M.4
  • 15
    • 0034670621 scopus 로고    scopus 로고
    • Sex pheromones of the hair crab Erimacrus isenbeckii. Part 1: Isolation and structures of novel ceramides
    • Asai, N., Fusetani, N., Matsunaga, S., and Sasaki, J. (2000) Sex Pheromones of the Hair Crab Erimacrus isenbeckii. Part 1: Isolation and Structures of Novel Ceramides, Tetrahedron 56, 9895-9899.
    • (2000) Tetrahedron , vol.56 , pp. 9895-9899
    • Asai, N.1    Fusetani, N.2    Matsunaga, S.3    Sasaki, J.4
  • 16
    • 0028371806 scopus 로고
    • Characterization of complex mixture of ceramides by fast atom bombardment and precursor and tandem mass spectrometry
    • Rubino, P.M., Zecca, L., and Sonnino, S. (1994) Characterization of Complex Mixture of Ceramides by Fast Atom Bombardment and Precursor and Tandem Mass Spectrometry, in Mass Spectrometry, Biol. Mass Spectrom. 23, 82-90.
    • (1994) Mass Spectrometry, Biol. Mass Spectrom. , vol.23 , pp. 82-90
    • Rubino, P.M.1    Zecca, L.2    Sonnino, S.3
  • 17
    • 0020065526 scopus 로고
    • 13C NMR spectroscopy for assigning the configuration of C=C double bonds of monoenic or dienic pheromone components and for quantitative determination of ZJE mixtures
    • 13C NMR Spectroscopy for Assigning the Configuration of C=C Double Bonds of Monoenic or Dienic Pheromone Components and for Quantitative Determination of ZJE Mixtures, Tetrahedron 38, 629-644.
    • (1982) Tetrahedron , vol.38 , pp. 629-644
    • Rossi, R.1    Veracini, C.A.2
  • 18
    • 0344741283 scopus 로고    scopus 로고
    • New cerebrosides from Euphorbia peplis, L.: Antimicrobial activity evaluation
    • Cateni, F., Zilic, J., Falsone, G., Scialino, G., and Banfi, E. (2003) New Cerebrosides from Euphorbia peplis, L.: Antimicrobial Activity Evaluation, Bioorg. Med. Chem. Lett. 15, 4345-4350.
    • (2003) Bioorg. Med. Chem. Lett. , vol.15 , pp. 4345-4350
    • Cateni, F.1    Zilic, J.2    Falsone, G.3    Scialino, G.4    Banfi, E.5
  • 19
    • 33947085552 scopus 로고
    • Nuclear magnetic resonance enantiomer reagents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomic mandelate, O-Methylmandelate, and α-Methoxy-α- trifluoromethylphenylacetate (MTPA) Esters
    • Dale, J.A., and Mosher, H.S. (1973) Nuclear Magnetic Resonance Enantiomer Reagents. Configurational Correlations via Nuclear Magnetic Resonance Chemical Shifts of Diastereomic Mandelate, O-Methylmandelate, and α-Methoxy- α-trifluoromethylphenylacetate (MTPA) Esters, J. Am. Chem. Soc. 95, 512-519.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 512-519
    • Dale, J.A.1    Mosher, H.S.2
  • 21
    • 0035956411 scopus 로고    scopus 로고
    • A practical guide for the assignment of the absolute configuration of alcohols, amines and carboxylic acids by NMR
    • Seco, J.M., Quiñoá, E., and Riguera, R. (2001) A Practical Guide for the Assignment of the Absolute Configuration of Alcohols, Amines and Carboxylic Acids by NMR, Tetrahedron: Asymmetry 12, 2915-2925.
    • (2001) Tetrahedron: Asymmetry , vol.12 , pp. 2915-2925
    • Seco, J.M.1    Quiñoá, E.2    Riguera, R.3
  • 23
    • 0043125541 scopus 로고    scopus 로고
    • A glucosylceramide with a novel ceramide and three ceramides from the basidiomycete Cortinarius umidicola
    • Liu, J.-K., Hu, L., and Dong, Z.-J. (2003) A Glucosylceramide with a Novel Ceramide and Three Ceramides from the Basidiomycete Cortinarius umidicola, Lipids 38, 669-675.
    • (2003) Lipids , vol.38 , pp. 669-675
    • Liu, J.-K.1    Hu, L.2    Dong, Z.-J.3
  • 24
    • 0036594820 scopus 로고    scopus 로고
    • Two novel glucosylceramides from gonads and body walls of the patagonian starfish Allostichaster inaequalis
    • De Vivar, M.E.D., Seldes, A.M., and Maier, M.S. (2002) Two Novel Glucosylceramides from Gonads and Body Walls of the Patagonian Starfish Allostichaster inaequalis, Lipids 37, 597-603.
    • (2002) Lipids , vol.37 , pp. 597-603
    • De Vivar, M.E.D.1    Seldes, A.M.2    Maier, M.S.3
  • 25
    • 0030042680 scopus 로고    scopus 로고
    • Glycolipids from Sponges. IV. Immunomodulating Glycosyl Ceramides from the Marine Sponge Agelas dispar
    • Costantino, V., Fattorusso, E., Mangoni, A., Di Rosa, M., Ianaro, A., and Maffia, A. (1996) Glycolipids from Sponges. IV. Immunomodulating Glycosyl Ceramides from the Marine Sponge Agelas dispar, Tetrahedron 52, 1573-1578.
    • (1996) Tetrahedron , vol.52 , pp. 1573-1578
    • Costantino, V.1    Fattorusso, E.2    Mangoni, A.3    Di Rosa, M.4    Ianaro, A.5    Maffia, A.6
  • 26
    • 0028817726 scopus 로고
    • Halicylindrosides, antifungal and cytotoxic cerebrosides from the marine sponge Halichondria cylindrata
    • Li, H.-y., Matsunaga, S., and Fusetani, N. (1995) Halicylindrosides, Antifungal and Cytotoxic Cerebrosides from the Marine Sponge Halichondria cylindrata, Tetrahedron 51, 2273-2280.
    • (1995) Tetrahedron , vol.51 , pp. 2273-2280
    • Li, H.-Y.1    Matsunaga, S.2    Fusetani, N.3
  • 27
    • 0028209483 scopus 로고
    • Ophidiacerebrosides: Cytotoxic glycosphingolipids containing a novel sphingosine from a sea star
    • Jin, W., Rinehart, K.L., and Jares-Erijman, E. (1994) Ophidiacerebrosides: Cytotoxic Glycosphingolipids Containing a Novel Sphingosine from a Sea Star, J. Org. Chem. 59, 144-147.
    • (1994) J. Org. Chem. , vol.59 , pp. 144-147
    • Jin, W.1    Rinehart, K.L.2    Jares-Erijman, E.3
  • 28
    • 0002266172 scopus 로고
    • Isolation and characterization of acanthacerebroside B and structure elucidation of related, nearly homogenous cerebrosides
    • Iguchi, R., Natori, T., and Komori, T. (1990) Isolation and Characterization of Acanthacerebroside B and Structure Elucidation of Related, Nearly Homogenous Cerebrosides, Liebigs Ann. Chem., 51-55.
    • (1990) Liebigs Ann. Chem. , pp. 51-55
    • Iguchi, R.1    Natori, T.2    Komori, T.3
  • 29
    • 84985240041 scopus 로고
    • Asymmetric synthesis of phytosphingosine and phytosphingosine anhydro base: Assignment of the absolute stereochemistry
    • Sugiyama, S., Honda, M., and Komori, T. (1988) Asymmetric Synthesis of Phytosphingosine and Phytosphingosine Anhydro Base: Assignment of the Absolute Stereochemistry, Liebigs Ann. Chem., 619-625.
    • (1988) Liebigs Ann. Chem. , pp. 619-625
    • Sugiyama, S.1    Honda, M.2    Komori, T.3
  • 30
    • 84986695927 scopus 로고
    • Stereochemistry of the four diastereomers of ceramide and ceramide lactoside
    • Sugiyama, S., Honda, M., Higuchi, R., and Komori, T. (1991) Stereochemistry of the Four Diastereomers of Ceramide and Ceramide Lactoside, Liebigs Ann. Chem., 349-356.
    • (1991) Liebigs Ann. Chem. , pp. 349-356
    • Sugiyama, S.1    Honda, M.2    Higuchi, R.3    Komori, T.4
  • 31
    • 0033593382 scopus 로고    scopus 로고
    • Stereocontrolled synthesis of novel phytosphingosine-type glucosaminocerebrosides
    • Murakami, T., and Taguchi, K. (1999) Stereocontrolled Synthesis of Novel Phytosphingosine-type Glucosaminocerebrosides, Tetrahedron 55, 989-1004.
    • (1999) Tetrahedron , vol.55 , pp. 989-1004
    • Murakami, T.1    Taguchi, K.2
  • 32
    • 0033803012 scopus 로고    scopus 로고
    • Current methods for the identification and quantitation of ceramides: An overview
    • Cremesti, A.E., and Fischi, A.S. (2000) Current Methods for the Identification and Quantitation of Ceramides: An Overview, Lipids 35, 937-945.
    • (2000) Lipids , vol.35 , pp. 937-945
    • Cremesti, A.E.1    Fischi, A.S.2
  • 33
    • 0037401646 scopus 로고    scopus 로고
    • Sphingolipids as therapeutics
    • Kester, M., and Kolesnick, R. (2003) Sphingolipids as Therapeutics, Pharmacol. Res. 47, 365-371.
    • (2003) Pharmacol. Res. , vol.47 , pp. 365-371
    • Kester, M.1    Kolesnick, R.2
  • 34
    • 19444377889 scopus 로고    scopus 로고
    • Molecular Associations and surface-active properties of short- and long-N-Acyl chain ceramides
    • Sot, J., Goñi, P.M., and Alonso, A. (2005) Molecular Associations and Surface-Active Properties of Short- and Long-N-Acyl Chain Ceramides, Biochim. Biophys. Acta 1711, 12-19.
    • (2005) Biochim. Biophys. Acta , vol.1711 , pp. 12-19
    • Sot, J.1    Goñi, P.M.2    Alonso, A.3
  • 35
    • 20444386209 scopus 로고    scopus 로고
    • Ceramide induces neuronal apoptosis through mitogen-activated protein kinases and causes release of multiple mitochondrial proteins
    • Stoica, B.A., Movsesyan, V.A., Knoblach, S.M., and Faden, A.I. (2005) Ceramide Induces Neuronal Apoptosis Through Mitogen-Activated Protein Kinases and Causes Release of Multiple Mitochondrial Proteins, Mol. Cell. Neurosci. 29, 355-371.
    • (2005) Mol. Cell. Neurosci. , vol.29 , pp. 355-371
    • Stoica, B.A.1    Movsesyan, V.A.2    Knoblach, S.M.3    Faden, A.I.4
  • 36
    • 0037419356 scopus 로고    scopus 로고
    • Total syntheses of symbioramide derivatives from L-Serine and their antileukemic activities
    • Azuma, H., Takao, R., Niiro, H., Shikata, K., Tamagaki, S., Tachibana, T., and Ogino, K. (2003) Total Syntheses of Symbioramide Derivatives from L-Serine and Their Antileukemic Activities, J. Org. Chem. 68, 2790-2797.
    • (2003) J. Org. Chem. , vol.68 , pp. 2790-2797
    • Azuma, H.1    Takao, R.2    Niiro, H.3    Shikata, K.4    Tamagaki, S.5    Tachibana, T.6    Ogino, K.7
  • 38
    • 0038356303 scopus 로고    scopus 로고
    • Plant sphingolipids: Structural diversity, biosynthesis, first genes and functions
    • Sperling, P., and Heinz, E. (2003) Plant Sphingolipids: Structural Diversity, Biosynthesis, First Genes and Functions, Biochim. Biophys. Acta 1632, 1-15.
    • (2003) Biochim. Biophys. Acta , vol.1632 , pp. 1-15
    • Sperling, P.1    Heinz, E.2
  • 39
    • 0033595881 scopus 로고    scopus 로고
    • Nanogram scale absolute configurational assignment of ceramides by circular dichroism
    • Jiang, H., Huang, X., Nakanishi, K., and Berova, N. (1999) Nanogram Scale Absolute Configurational Assignment of Ceramides by Circular Dichroism, Tetrahedron Lett. 40, 7645-7649.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 7645-7649
    • Jiang, H.1    Huang, X.2    Nakanishi, K.3    Berova, N.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.