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Volumn 53, Issue 8, 2000, Pages 1067-1073

Aporphinoid alkaloids and other constituents from Lettowianthus stellatus

Author keywords

(Z) 7 Octadecen 9 ynoic acid; 11 Hydroxyguaia 4,6 diene; 11 Methoxylettowianthine; Annonaceae; Aporphinoid alkaloids; Lettowianthine; Lettowianthus stellatus; Methyl (2E,6E,10R) 10,11 dihydroxy 3,7,11 trixnethyl 2,6 dodecadienoate; Methyl (2E,6E,10R) 10,11 epoxy 3,7,11 trimethyl 2,6 dodecadienoate

Indexed keywords

11 HYDROXYGUAIA 4,6 DIENE; 11 METHOXYLETTOWIANTHINE; 11-HYDROXYGUAIA-4,6-DIENE; 11-METHOXYLETTOWIANTHINE; ALKALOID; ALKALOID DERIVATIVE; ANTIMALARIAL AGENT; LETTOWIANTHINE; LETTOWIANTHUS STELLATUS EXTRACT; PLANT EXTRACT; SESQUITERPENE; SESQUITERPENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034716807     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0031-9422(00)00012-1     Document Type: Article
Times cited : (28)

References (26)
  • 1
    • 0343990692 scopus 로고    scopus 로고
    • Oxygenated pyrenes, their potential biosynthetic precursor and benzylated dihydroflavones from two African Uvaria species
    • Achenbach H., Höhn M., Waibel R., Nkunya M.H.H., Jonker S., Muhie S. Oxygenated pyrenes, their potential biosynthetic precursor and benzylated dihydroflavones from two African Uvaria species. Phytochemistry. 44:(2):1997;359-364.
    • (1997) Phytochemistry , vol.44 , Issue.2 , pp. 359-364
    • Achenbach, H.1    Höhn, M.2    Waibel, R.3    Nkunya, M.H.H.4    Jonker, S.5    Muhie, S.6
  • 2
    • 0028878326 scopus 로고
    • Constituents of Isolona maitlandii
    • Achenbach H., Löwel M. Constituents of Isolona maitlandii. Phytochemistry. 40:(3):1995;967-973.
    • (1995) Phytochemistry , vol.40 , Issue.3 , pp. 967-973
    • Achenbach, H.1    Löwel, M.2
  • 4
    • 0011980563 scopus 로고
    • Neue Guajen-Derivate aus Parthenium hysterophorus und ein weiteres Pseudoguajanolid aus Ambrosia cumanensis
    • Bohlmann F., Zdero C., Lonitz M. Neue Guajen-Derivate aus Parthenium hysterophorus und ein weiteres Pseudoguajanolid aus Ambrosia cumanensis. Phytochemistry. 16:(5):1977;575-577.
    • (1977) Phytochemistry , vol.16 , Issue.5 , pp. 575-577
    • Bohlmann, F.1    Zdero, C.2    Lonitz, M.3
  • 5
    • 33947085552 scopus 로고
    • Nuclear magnetic resonance enantiomer reagents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and α-methoxy-α-trifluoromethyl-phenylacetate (MTPA) esters
    • Dale J.A., Mosher H.S. Nuclear magnetic resonance enantiomer reagents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and α-methoxy-α-trifluoromethyl-phenylacetate (MTPA) esters. Journal of the American Chemical Society. 95:(2):1973;512-519.
    • (1973) Journal of the American Chemical Society , vol.95 , Issue.2 , pp. 512-519
    • Dale, J.A.1    Mosher, H.S.2
  • 8
    • 0030581338 scopus 로고    scopus 로고
    • 8-endo Cyclization of (alkoxycarbonyl) methyl radicals: Stereoselective synthesis of (-)-clavukerin A and (-)-11-hydroxyguaiene
    • Lee E., Yoon C.H. 8-endo Cyclization of (alkoxycarbonyl) methyl radicals: stereoselective synthesis of (-)-clavukerin A and (-)-11-hydroxyguaiene. Tetrahedron Letters. 37:(33):1996;5929-5930.
    • (1996) Tetrahedron Letters , vol.37 , Issue.33 , pp. 5929-5930
    • Lee, E.1    Yoon, C.H.2
  • 9
    • 37049100842 scopus 로고
    • A biomimetic synthesis of the novel 6,7-oxazine ring-fused dehydroaporphine alkaloid duguenaine
    • Lenz G.R., Koszyk F.J. A biomimetic synthesis of the novel 6,7-oxazine ring-fused dehydroaporphine alkaloid duguenaine. Journal of the Chemical Society, Perkin Transactions. 1:(6):1984;1273-1277.
    • (1984) Journal of the Chemical Society, Perkin Transactions , vol.1 , Issue.6 , pp. 1273-1277
    • Lenz, G.R.1    Koszyk, F.J.2
  • 10
    • 0029562216 scopus 로고
    • Telisatin A, Telisatin B, and Telitoxinone, three new aporphinoids from Telitoxicum peruvianum
    • Menachery M.D., Blake G.W., Gourley R.C., Freyer A. Telisatin A, Telisatin B, and Telitoxinone, three new aporphinoids from Telitoxicum peruvianum. Journal of Natural Products. 58:(12):1995;1945-1949.
    • (1995) Journal of Natural Products , vol.58 , Issue.12 , pp. 1945-1949
    • Menachery, M.D.1    Blake, G.W.2    Gourley, R.C.3    Freyer, A.4
  • 11
    • 0001057045 scopus 로고
    • Synthesis of both the enantiomers of juvenile hormone III
    • Mori K., Mori H. Synthesis of both the enantiomers of juvenile hormone III. Tetrahedron. 43:(18):1987;4097-4106.
    • (1987) Tetrahedron , vol.43 , Issue.18 , pp. 4097-4106
    • Mori, K.1    Mori, H.2
  • 12
    • 0027140784 scopus 로고
    • Three flavonoids from the stem bark of Uvaria dependens
    • Nkunya M.H.H., Waibel R., Achenbach H. Three flavonoids from the stem bark of Uvaria dependens. Phytochemistry. 34:(3):1993;853-856.
    • (1993) Phytochemistry , vol.34 , Issue.3 , pp. 853-856
    • Nkunya, M.H.H.1    Waibel, R.2    Achenbach, H.3
  • 13
    • 0025823511 scopus 로고
    • Antimalarial activity of Tanzanian plants and their active constituents: The genus Uvaria
    • Nkunya M.H.H., Weenen H., Bray D.H., Mgani Q.A., Mwasumbi L.B. Antimalarial activity of Tanzanian plants and their active constituents: the genus Uvaria. Planta Medica. 57:(4):1991;341-343.
    • (1991) Planta Medica , vol.57 , Issue.4 , pp. 341-343
    • Nkunya, M.H.H.1    Weenen, H.2    Bray, D.H.3    Mgani, Q.A.4    Mwasumbi, L.B.5
  • 14
    • 0006073083 scopus 로고
    • Novel acetylenic acids from the root bark of Paramacrolobium caeruleum: Inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A reductase
    • Patil A.D., Chan J.A., Lois-Flamberg P., Mayer R.J., Westley J.W. Novel acetylenic acids from the root bark of Paramacrolobium caeruleum: inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A reductase. Journal of Natural Products. 52:(1):1989;153-161.
    • (1989) Journal of Natural Products , vol.52 , Issue.1 , pp. 153-161
    • Patil, A.D.1    Chan, J.A.2    Lois-Flamberg, P.3    Mayer, R.J.4    Westley, J.W.5
  • 15
    • 33847088636 scopus 로고
    • Nuclear magnetic resonance determination of enantiomeric composition and absolute configuration of γ-lactones using chiral 2,2,2-trifluoro-1-(9-anthryl)ethanol
    • Pirkle W.H., Sikkenga D.L., Pavlin M.S. Nuclear magnetic resonance determination of enantiomeric composition and absolute configuration of γ-lactones using chiral 2,2,2-trifluoro-1-(9-anthryl)ethanol. Journal of Organic Chemistry. 42:(2):1977;384-387.
    • (1977) Journal of Organic Chemistry , vol.42 , Issue.2 , pp. 384-387
    • Pirkle, W.H.1    Sikkenga, D.L.2    Pavlin, M.S.3
  • 16
    • 84918027722 scopus 로고
    • Duguécalyne et Duguénaïne, alcaloïdes aporphiniques originaux du Duguetia calycina Benoist, Annonaceés
    • Roblot F., Hocquemiller R., Cavé A. Duguécalyne et Duguénaïne, alcaloïdes aporphiniques originaux du Duguetia calycina Benoist, Annonaceés. Comptes Rendus de l'Academie des Sciences, Serie 2. 293:(5):1981;373-376.
    • (1981) Comptes Rendus de l'Academie des Sciences, Serie 2 , vol.293 , Issue.5 , pp. 373-376
    • Roblot, F.1    Hocquemiller, R.2    Cavé, A.3
  • 17
    • 0017880609 scopus 로고
    • Dehydroaporphines: An acylation study
    • Saá J.M., Cava M.P. Dehydroaporphines: an acylation study. Journal of Organic Chemistry. 43:(6):1978;1096-1099.
    • (1978) Journal of Organic Chemistry , vol.43 , Issue.6 , pp. 1096-1099
    • Saá, J.M.1    Cava, M.P.2
  • 18
    • 0022653349 scopus 로고
    • A regioselective entry to 13-substituted 8-oxoprotoberberines. Total synthesis of (±)-corydaline
    • Saá C., Guitián E., Castedo L., Suau R., Saá J.M. A regioselective entry to 13-substituted 8-oxoprotoberberines. Total synthesis of (±)-corydaline. Journal of Organic Chemistry. 51:(14):1986;2781-2784.
    • (1986) Journal of Organic Chemistry , vol.51 , Issue.14 , pp. 2781-2784
    • Saá, C.1    Guitián, E.2    Castedo, L.3    Suau, R.4    Saá, J.M.5
  • 19
    • 50549157850 scopus 로고
    • Dünnschicht-Chromatographie. VI. Mitteilung. Spurenanalyse von Zuckergemischen auf Kieselgur G-Schichten
    • Stahl E., Kaltenbach U. Dünnschicht-Chromatographie. VI. Mitteilung. Spurenanalyse von Zuckergemischen auf Kieselgur G-Schichten. Journal of Chromatography. 5:1961;351-355.
    • (1961) Journal of Chromatography , vol.5 , pp. 351-355
    • Stahl, E.1    Kaltenbach, U.2
  • 21
    • 0343106025 scopus 로고
    • A substituted cinnamoyl ester from Cleistopholis staudtii
    • Tane P., Ayafor J.F., Sondengam B.L. A substituted cinnamoyl ester from Cleistopholis staudtii. Phytochemistry. 27:(12):1988;3986-3988.
    • (1988) Phytochemistry , vol.27 , Issue.12 , pp. 3986-3988
    • Tane, P.1    Ayafor, J.F.2    Sondengam, B.L.3
  • 22
    • 0001207068 scopus 로고
    • Isolation of insect juvenile hormone III from a plant
    • Toong Y.C., Schooley D.A., Baker F.C. Isolation of insect juvenile hormone III from a plant. Nature. 333:1988;170-171.
    • (1988) Nature , vol.333 , pp. 170-171
    • Toong, Y.C.1    Schooley, D.A.2    Baker, F.C.3
  • 24
    • 46549091595 scopus 로고
    • A phytochemist in the African rain forest
    • Waterman P.G. A phytochemist in the African rain forest. Phytochemistry. 25:(1):1986;3-17.
    • (1986) Phytochemistry , vol.25 , Issue.1 , pp. 3-17
    • Waterman, P.G.1
  • 25
    • 0005692188 scopus 로고
    • Sesquiterpenes and alkaloids from Cleistopholis patens
    • Waterman P.G., Muhammad I. Sesquiterpenes and alkaloids from Cleistopholis patens. Phytochemistry. 24:(3):1985;523-527.
    • (1985) Phytochemistry , vol.24 , Issue.3 , pp. 523-527
    • Waterman, P.G.1    Muhammad, I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.