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Volumn 43, Issue 8, 2000, Pages 1604-1610

Synthesis, spectroscopy, and cytotoxicity of glycosylated acetogenin derivatives as promising molecules for cancer therapy

Author keywords

[No Author keywords available]

Indexed keywords

ACETOGENIN; ANTINEOPLASTIC AGENT; SQUAMOCIN;

EID: 0034692161     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm990568m     Document Type: Article
Times cited : (22)

References (24)
  • 1
    • 0033521168 scopus 로고    scopus 로고
    • Synthesis of C1-C32 fragment of Aza-solamin, an unnatural analogue of the annonaceous acetogenin solamin
    • Acetogenins from Annonaceae 84. For part 83, see: Pichon, M.; Hocquemiller, R.; Figadère, B. Synthesis of C1-C32 Fragment of Aza-solamin, an Unnatural Analogue of the Annonaceous Acetogenin Solamin. Tetrahedron Lett. 1999, 40, 8567-8570.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 8567-8570
    • Pichon, M.1    Hocquemiller, R.2    Figadère, B.3
  • 3
    • 0030625527 scopus 로고    scopus 로고
    • Acetogenins from annonaceae
    • Herz, W., Kirby, G. W., Moore, R. E., Steglich, W., Tamm, Ch., Eds.; Springer: New York
    • (a) Cavé, A.; Cortes, D.; Figadère, B.; Laurens, A. Acetogenins from Annonaceae. In Progress in the Chemistry of Organic Natural Products; Herz, W., Kirby, G. W., Moore, R. E., Steglich, W., Tamm, Ch., Eds.; Springer: New York, 1997; Vol. 70, pp 81-288.
    • (1997) Progress in the Chemistry of Organic Natural Products , vol.70 , pp. 81-288
    • Cavé, A.1    Cortes, D.2    Figadère, B.3    Laurens, A.4
  • 4
    • 0032891112 scopus 로고    scopus 로고
    • Annonaceous acetogenins: Recent Progress
    • (b) Alali, F. Q.; Liu, X. X. Annonaceous Acetogenins: Recent Progress. J. Nat. Prod. 1999, 62, 504-540.
    • (1999) J. Nat. Prod. , vol.62 , pp. 504-540
    • Alali, F.Q.1    Liu, X.X.2
  • 5
    • 0024209581 scopus 로고
    • Squamocin, a new cytotoxic bis-tetrahydrofuran containing acetogenin from Annona squamosa
    • Fujimoto, Y.; Eguchi, T.; Kakinuma, K.; Ikekawa, N.; Sahai, M.; Gupta, Y. K. Squamocin, a New Cytotoxic Bis-Tetrahydrofuran Containing Acetogenin from Annona squamosa. Chem. Pharm. Bull. 1988, 36, 4802-4806.
    • (1988) Chem. Pharm. Bull. , vol.36 , pp. 4802-4806
    • Fujimoto, Y.1    Eguchi, T.2    Kakinuma, K.3    Ikekawa, N.4    Sahai, M.5    Gupta, Y.K.6
  • 6
    • 0030589537 scopus 로고    scopus 로고
    • Advanced drug delivery reviews: Enzyme prodrug therapy
    • Sherwood, R. F. Advanced Drug Delivery Reviews: Enzyme Prodrug Therapy. Adv. Drug Delivery Rev. 1996, 22, 269-288.
    • (1996) Adv. Drug Delivery Rev. , vol.22 , pp. 269-288
    • Sherwood, R.F.1
  • 8
    • 5244279498 scopus 로고
    • Recent progress in O-glycosylation methods and its application to natural products synthesis
    • Toshima, K.; Tatsuda, K. Recent Progress in O-Glycosylation Methods and its Application to Natural Products Synthesis. Chem. Rev. 1993, 93, 1503-1531.
    • (1993) Chem. Rev. , vol.93 , pp. 1503-1531
    • Toshima, K.1    Tatsuda, K.2
  • 10
    • 0010892703 scopus 로고
    • Chromatography Sciences Series; Marcel Dekker Inc.: New York, Chapter 4
    • Foucault, A. Centrifugal Partition Chromatography, Chromatography Sciences Series; Marcel Dekker Inc.: New York, 1995; Vol. 68, Chapter 4, pp 71-97.
    • (1995) Centrifugal Partition Chromatography , vol.68 , pp. 71-97
    • Foucault, A.1
  • 12
    • 0030874930 scopus 로고    scopus 로고
    • Spinencin, a new bis-tetrahydrofuran acetogenin from the seeds of Annona spinescens
    • Queiroz, E. F.; Roblot, F.; Laprévote, O.; Serani, L.; Cavé, A. Spinencin, a New Bis-Tetrahydrofuran Acetogenin from the Seeds of Annona spinescens. J. Nat. Prod. 1997, 60, 760-765.
    • (1997) J. Nat. Prod. , vol.60 , pp. 760-765
    • Queiroz, E.F.1    Roblot, F.2    Laprévote, O.3    Serani, L.4    Cavé, A.5
  • 13
    • 0028306131 scopus 로고
    • Structural elucidation of acetogenins from annonaceae by fast-atom bombardment mass spectrometry
    • Laprévote, O.; Das, B. C. Structural Elucidation of Acetogenins from Annonaceae by Fast-Atom Bombardment Mass Spectrometry. Tetrahedron 1994, 50, 8479-8490.
    • (1994) Tetrahedron , vol.50 , pp. 8479-8490
    • Laprévote, O.1    Das, B.C.2
  • 14
    • 0021254632 scopus 로고
    • Évaluation de la cytotoxicité d'un antiseptique par une microméthode photométrique
    • Fleury, C.; Cotte-Laffitte, J.; Quéro, A.-M. Évaluation de la Cytotoxicité d'un Antiseptique par une Microméthode Photométrique. Pathol. Biol. 1984, 32, 628-630.
    • (1984) Pathol. Biol. , vol.32 , pp. 628-630
    • Fleury, C.1    Cotte-Laffitte, J.2    Quéro, A.-M.3
  • 15
    • 0018749252 scopus 로고
    • Comparative cytotoxic and antitumoral effects of ellipticine derivatives on mouse L-1210 leukemia
    • Paoletti, C.; Cros, S.; Dat-Xuong, N.; Leconte, P.; Moisand, A. Comparative Cytotoxic and Antitumoral Effects of Ellipticine Derivatives on Mouse L-1210 Leukemia. Chem Biol. Interact. 1979, 25, 45-58.
    • (1979) Chem Biol. Interact. , vol.25 , pp. 45-58
    • Paoletti, C.1    Cros, S.2    Dat-Xuong, N.3    Leconte, P.4    Moisand, A.5
  • 16
    • 0032836893 scopus 로고    scopus 로고
    • Semi-synthesis and cytotoxicity of amino acetogenins and derivatives
    • Duret, P.; Hocquemiller, R.; Gantier, J.-C.; Figadère, B. Semi-synthesis and Cytotoxicity of Amino Acetogenins and Derivatives. Bioorg. Med. Chem. 1999, 7, 1821-1826.
    • (1999) Bioorg. Med. Chem. , vol.7 , pp. 1821-1826
    • Duret, P.1    Hocquemiller, R.2    Gantier, J.-C.3    Figadère, B.4
  • 17
    • 0029132131 scopus 로고
    • Annohexocin, a novel mòno-THF acetogenin with six hydroxyls, from Annona muricata (Annonaceae)
    • Zeng, L.; Wu, F.-E.; McLaughlin, J. L. Annohexocin, a Novel Mòno-THF Acetogenin with Six Hydroxyls, from Annona muricata (Annonaceae). Bioorg. Med. Chem. Lett. 1995, 5, 1865-1868.
    • (1995) Bioorg. Med. Chem. Lett. , vol.5 , pp. 1865-1868
    • Zeng, L.1    Wu, F.-E.2    McLaughlin, J.L.3
  • 18
    • 0031025679 scopus 로고    scopus 로고
    • Coriaheptocins A and B, the first heptahydroxylated acetogenins, isolated from the roots of Annona coriacea
    • Meneses da Silva, E. L.; Roblot, F.; Laprévote, O,; Serani, L.; Cavé, A. Coriaheptocins A and B, the First Heptahydroxylated Acetogenins, Isolated from the Roots of Annona coriacea. J. Nat. Prod. 1997, 60, 162-167.
    • (1997) J. Nat. Prod. , vol.60 , pp. 162-167
    • Meneses Da Silva, E.L.1    Roblot, F.2    Laprévote, O.3    Serani, L.4    Cavé, A.5
  • 19
    • 0033603198 scopus 로고    scopus 로고
    • Antitumoral effects of squamocin on parental and multidrug resistant MCF7 (human breast adenocarcinoma) cell lines
    • (a) Raynaud, S.; Némati, F.; Micoli, L.; Michel, P.; Poupon, M.-F.; Fourneau, C.; Laurens, A.; Hocquemiller, R. Antitumoral Effects of Squamocin on Parental and Multidrug Resistant MCF7 (Human Breast Adenocarcinoma) Cell Lines. Life Sci. 1999, 65, 525-533.
    • (1999) Life Sci. , vol.65 , pp. 525-533
    • Raynaud, S.1    Némati, F.2    Micoli, L.3    Michel, P.4    Poupon, M.-F.5    Fourneau, C.6    Laurens, A.7    Hocquemiller, R.8
  • 20
    • 0031149817 scopus 로고    scopus 로고
    • The annonaceous acetogenin bullatacin is cytotoxic against multidrug resistant human mammary adenocarcinoma cells
    • (b) For precedent, see: Oberlies, N. H.; Croy, V. L.; Harrison, M. L.; McLaughlin, J. L. The Annonaceous Acetogenin Bullatacin is Cytotoxic Against Multidrug Resistant Human Mammary Adenocarcinoma Cells. Cancer Lett. 1997, 775, 73.
    • (1997) Cancer Lett. , vol.775 , pp. 73
    • Oberlies, N.H.1    Croy, V.L.2    Harrison, M.L.3    McLaughlin, J.L.4
  • 21
    • 0031029395 scopus 로고    scopus 로고
    • Isolation of Montecristin, a key metabolite in biogenesis of acetogenins from Annona muricata and its structure elucidation by using tandem mass spectrometry
    • Gleye, C.; Laurens, A.; Hocquemiller, R.; Cavé, A.; Laprévote, O.; Serani, L. Isolation of Montecristin, a Key Metabolite in Biogenesis of Acetogenins from Annona muricata and its Structure Elucidation by Using Tandem Mass Spectrometry. J. Org. Chem. 1997, 63, 510-513.
    • (1997) J. Org. Chem. , vol.63 , pp. 510-513
    • Gleye, C.1    Laurens, A.2    Hocquemiller, R.3    Cavé, A.4    Laprévote, O.5    Serani, L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.