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Volumn 20, Issue 9, 2009, Pages 1688-1698

Fragmentation Pathways of Polycyclic Polyisoprenylated Benzophenones and Degradation Profile of Nemorosone by Multiple-Stage Tandem Mass Spectrometry

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGIC ACTIVITIES; CHLOROFORM SOLUTIONS; CYTOTOXIC ACTIVITIES; DEGRADATION PRODUCTS; DEGRADATION PROFILES; DIKETONES; FRAGMENTATION PATHWAYS; MASS MEASUREMENTS; N-HEXANE; NATURAL PRODUCTS; PURIFICATION PROCEDURES; RAPID DEGRADATION; SIDE CHAINS; STORAGE CONDITION; STRUCTURAL CHARACTERIZATION; TANDEM MASS SPECTROMETRY;

EID: 69549111029     PISSN: 10440305     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jasms.2009.05.004     Document Type: Article
Times cited : (27)

References (31)
  • 3
    • 0032934198 scopus 로고    scopus 로고
    • Guttiferone F, the First Prenylated Benzophenone from Allanblackia stuhlmannii
    • Fuller R.W., Blunt J.W., Boswell J.L., Cardellina J.H., and Boyd M.R. Guttiferone F, the First Prenylated Benzophenone from Allanblackia stuhlmannii. J. Nat. Prod. 62 (1999) 130-132
    • (1999) J. Nat. Prod. , vol.62 , pp. 130-132
    • Fuller, R.W.1    Blunt, J.W.2    Boswell, J.L.3    Cardellina, J.H.4    Boyd, M.R.5
  • 4
    • 0036152789 scopus 로고    scopus 로고
    • Natural Products Inhibiting Candida albicans Secreted Aspartic Proteases from Tovomita krukovii
    • Zhang Z., Elsohly H.N., Jacob M.R., Pasco D.S., Walker L.A., and Clark A.M. Natural Products Inhibiting Candida albicans Secreted Aspartic Proteases from Tovomita krukovii. Planta 68 (2002) 49-54
    • (2002) Planta , vol.68 , pp. 49-54
    • Zhang, Z.1    Elsohly, H.N.2    Jacob, M.R.3    Pasco, D.S.4    Walker, L.A.5    Clark, A.M.6
  • 5
    • 0029993740 scopus 로고    scopus 로고
    • Antibacterial Activity of Some Garcinia. Benzophenone Derivatives against Methicillin-Resistant Staphylococcus aureus
    • Iinuma M., Tosa H., Tanaka T., Kanamaru S., Asai F., Kobayashi Y., Miyauchi K.-I., and Shimano R. Antibacterial Activity of Some Garcinia. Benzophenone Derivatives against Methicillin-Resistant Staphylococcus aureus. Biol. Pharm. Bull. 19 (1996) 311-314
    • (1996) Biol. Pharm. Bull. , vol.19 , pp. 311-314
    • Iinuma, M.1    Tosa, H.2    Tanaka, T.3    Kanamaru, S.4    Asai, F.5    Kobayashi, Y.6    Miyauchi, K.-I.7    Shimano, R.8
  • 8
    • 0033948388 scopus 로고    scopus 로고
    • Free Radical Scavenging Activity and Antiulcer Activity of Garcinol from Garcinia indica Fruit Rind
    • Yamaguchi F., Saito M., Ariga T., Yoshimura Y., and Nakazawa H. Free Radical Scavenging Activity and Antiulcer Activity of Garcinol from Garcinia indica Fruit Rind. J. Agric. Food Chem. 48 (2000) 2320-2325
    • (2000) J. Agric. Food Chem. , vol.48 , pp. 2320-2325
    • Yamaguchi, F.1    Saito, M.2    Ariga, T.3    Yoshimura, Y.4    Nakazawa, H.5
  • 9
    • 0033998163 scopus 로고    scopus 로고
    • Antioxidative and Antiglycation Activity of Garcinol from Garcinia indica Fruit Rind
    • Yamaguchi F., Saito M., Ariga T., Yoshimura Y., and Nakazawa H. Antioxidative and Antiglycation Activity of Garcinol from Garcinia indica Fruit Rind. J. Agric. Food Chem. 48 (2000) 180-185
    • (2000) J. Agric. Food Chem. , vol.48 , pp. 180-185
    • Yamaguchi, F.1    Saito, M.2    Ariga, T.3    Yoshimura, Y.4    Nakazawa, H.5
  • 11
    • 0035142784 scopus 로고    scopus 로고
    • Benzophenones and Xanthones with Isoprenoid Groups from Cudrania cochinchinensis
    • Hou A.-J., Fukai T., Shimazaki M., Sakagami H., Sun H.-D., and Nomura T. Benzophenones and Xanthones with Isoprenoid Groups from Cudrania cochinchinensis. J. Nat. Prod. 64 (2001) 65-70
    • (2001) J. Nat. Prod. , vol.64 , pp. 65-70
    • Hou, A.-J.1    Fukai, T.2    Shimazaki, M.3    Sakagami, H.4    Sun, H.-D.5    Nomura, T.6
  • 12
    • 0036325944 scopus 로고    scopus 로고
    • New Cytotoxic Coumarins and Prenylated Benzophenone Derivatives from the Bark of Ochrocarpos punctatus from the Madagascar Rainforest
    • Chaturvedula V.S.P., Schilling J.K., and Kingston D.G.I. New Cytotoxic Coumarins and Prenylated Benzophenone Derivatives from the Bark of Ochrocarpos punctatus from the Madagascar Rainforest. J. Nat. Prod. 65 (2002) 965-972
    • (2002) J. Nat. Prod. , vol.65 , pp. 965-972
    • Chaturvedula, V.S.P.1    Schilling, J.K.2    Kingston, D.G.I.3
  • 14
    • 0033864746 scopus 로고    scopus 로고
    • Structure-Activity Relationship of Polyisoprenyl Benzophenones from Garcinia pyrifera on the Tubulin/Microtubule System
    • Roux D., Hadi H.A., Thoret S., Guenard D., Thoison O., Pais M.H., and Sevenet T. Structure-Activity Relationship of Polyisoprenyl Benzophenones from Garcinia pyrifera on the Tubulin/Microtubule System. J. Nat. Prod. 63 (2000) 1070-1076
    • (2000) J. Nat. Prod. , vol.63 , pp. 1070-1076
    • Roux, D.1    Hadi, H.A.2    Thoret, S.3    Guenard, D.4    Thoison, O.5    Pais, M.H.6    Sevenet, T.7
  • 16
    • 0032925137 scopus 로고    scopus 로고
    • Two Polyisoprenylated Benzophenones from the Floral Resins of Three Clusia Species
    • De Oliveira C.M.A., Porto A.M., Bittrich V., and Marsaioli A.J. Two Polyisoprenylated Benzophenones from the Floral Resins of Three Clusia Species. Phytochemistry 50 (1999) 1073-1079
    • (1999) Phytochemistry , vol.50 , pp. 1073-1079
    • De Oliveira, C.M.A.1    Porto, A.M.2    Bittrich, V.3    Marsaioli, A.J.4
  • 17
    • 0034692455 scopus 로고    scopus 로고
    • Two Polyisoprenylated Benzophenones from the Trunk Latex of Clusia grandiflora (Clusiaceae)
    • Lokvam J., Braddock J.F., Reichardt P.B., and Clausen T.P. Two Polyisoprenylated Benzophenones from the Trunk Latex of Clusia grandiflora (Clusiaceae). Phytochemistry 55 (2000) 29-34
    • (2000) Phytochemistry , vol.55 , pp. 29-34
    • Lokvam, J.1    Braddock, J.F.2    Reichardt, P.B.3    Clausen, T.P.4
  • 19
    • 0036249452 scopus 로고    scopus 로고
    • Polyisoprenylated Benzophenones in Cuban Propolis; Biological Activity of Nemorosone
    • Cuesta-Rubio O., Frontana-Uribeb B.A., Ramirez-Apan T., and Cardenas J. Polyisoprenylated Benzophenones in Cuban Propolis; Biological Activity of Nemorosone. Z. Naturforsch. 57c (2002) 372-378
    • (2002) Z. Naturforsch. , vol.57 c , pp. 372-378
    • Cuesta-Rubio, O.1    Frontana-Uribeb, B.A.2    Ramirez-Apan, T.3    Cardenas, J.4
  • 20
    • 34848858494 scopus 로고    scopus 로고
    • Chemical Characterization of Cuban Propolis by HPLC-PDA, HPLC-MS, and NMR: The Brown, Red, and Yellow Cuban Varieties of Propolis
    • Cuesta-Rubio O., Piccinelli A.L., Fernandez M.C., Hernández I.M., Rosado A., and Rastrelli L. Chemical Characterization of Cuban Propolis by HPLC-PDA, HPLC-MS, and NMR: The Brown, Red, and Yellow Cuban Varieties of Propolis. J. Agric. Food Chem. 55 (2007) 7502-7509
    • (2007) J. Agric. Food Chem. , vol.55 , pp. 7502-7509
    • Cuesta-Rubio, O.1    Piccinelli, A.L.2    Fernandez, M.C.3    Hernández, I.M.4    Rosado, A.5    Rastrelli, L.6
  • 21
    • 0034753678 scopus 로고    scopus 로고
    • Recent Progress in Pharmacological Research of Propolis
    • Banskota A.H., Tezuka Y., and Kadota S. Recent Progress in Pharmacological Research of Propolis. Phytother. Res. 15 (2001) 561-571
    • (2001) Phytother. Res. , vol.15 , pp. 561-571
    • Banskota, A.H.1    Tezuka, Y.2    Kadota, S.3
  • 26
    • 4544271362 scopus 로고    scopus 로고
    • Are Acylphloroglucinols Lead Structures for the Treatment of Degenerative Diseases?
    • Verotta L. Are Acylphloroglucinols Lead Structures for the Treatment of Degenerative Diseases?. Phytochem. Rev. 1 (2002) 389-407
    • (2002) Phytochem. Rev. , vol.1 , pp. 389-407
    • Verotta, L.1
  • 27
    • 0035839238 scopus 로고    scopus 로고
    • High-Performance Liquid Chromatography-Electrospray Ionization Mass Spectrometry and Multiple Mass Spectrometry Studies of Hyperforin Degradation Products
    • Fuzzati N., Gabetta B., Strepponi I., and Villa F. High-Performance Liquid Chromatography-Electrospray Ionization Mass Spectrometry and Multiple Mass Spectrometry Studies of Hyperforin Degradation Products. J. Chromatogr. A 926 (2001) 187-198
    • (2001) J. Chromatogr. A , vol.926 , pp. 187-198
    • Fuzzati, N.1    Gabetta, B.2    Strepponi, I.3    Villa, F.4
  • 28
    • 36749012899 scopus 로고    scopus 로고
    • Differentiation of Nonconventional "Carbanions"-The Total Synthesis of Nemorosone and Clusianone.
    • Tsukano C., Siegel D.R., and Danishefsky S.J. Differentiation of Nonconventional "Carbanions"-The Total Synthesis of Nemorosone and Clusianone. Angew. Chem. Int. Ed. 46 (2007) 8840-8844
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 8840-8844
    • Tsukano, C.1    Siegel, D.R.2    Danishefsky, S.J.3
  • 31
    • 0034062571 scopus 로고    scopus 로고
    • Hyperforin Analogues from St. John's Wort (Hypericum perforatum)
    • Verotta L., Appendino G., Jakupovic J., and Bombardelli E. Hyperforin Analogues from St. John's Wort (Hypericum perforatum). J. Nat. Prod. 63 (2000) 412-415
    • (2000) J. Nat. Prod. , vol.63 , pp. 412-415
    • Verotta, L.1    Appendino, G.2    Jakupovic, J.3    Bombardelli, E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.