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Volumn 73, Issue 3, 2007, Pages 206-211

Leishmanicidal constituents from the leaves of Piper rusbyi

Author keywords

Chalcones; Kavapyrones; Leishmania; Piper rusbyi; Piperaceae; Reversal of multidrug resistance activities

Indexed keywords

CHALCONE; DIHYDROXY 5,6 DIDEHYDROKAVAIN; EPOXY 5,6 DIDEHYDROKAVAIN; FLAVOKAVAIN B; KAWAIN; NEROLIDOL; PHYTOL; PIPER RUSBYI EXTRACT; PLANT EXTRACT; SPATHULENOL; UNCLASSIFIED DRUG; VIRIDIFLOROL;

EID: 34250366681     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-967123     Document Type: Article
Times cited : (38)

References (26)
  • 1
    • 33750531864 scopus 로고    scopus 로고
    • Innovative lead discovery strategies for tropical diseases
    • Nwaka S, Hudson A. Innovative lead discovery strategies for tropical diseases. Nature Rev Drug Discov 2006; 5: 941-55.
    • (2006) Nature Rev Drug Discov , vol.5 , pp. 941-955
    • Nwaka, S.1    Hudson, A.2
  • 2
    • 0036018927 scopus 로고    scopus 로고
    • Multidrug resistance phenotype mediated by the P-glycoprotein-like transporter in Leishmania: A search for reversal agents
    • Pérez-Victoria JM, Di Prieto A, Barron D, Ravelo AG, Castanys S, Gamarro F. Multidrug resistance phenotype mediated by the P-glycoprotein-like transporter in Leishmania: a search for reversal agents. Curr Drug Targets 2002; 3: 311-33.
    • (2002) Curr Drug Targets , vol.3 , pp. 311-333
    • Pérez-Victoria, J.M.1    Di Prieto, A.2    Barron, D.3    Ravelo, A.G.4    Castanys, S.5    Gamarro, F.6
  • 4
    • 0035179157 scopus 로고    scopus 로고
    • Antiparasitic properties of medicinal plants and other naturally occurring products
    • Townson S. Antiparasitic properties of medicinal plants and other naturally occurring products. Adv Parasitol 2001; 50: 199-295.
    • (2001) Adv Parasitol , vol.50 , pp. 199-295
    • Townson, S.1
  • 6
    • 0006990572 scopus 로고
    • Occurrence of 5,6-dehydrokawain and 7,8-epoxy-5,6-dehydrokawain in Didymocarpus aurentica
    • Adityachaudhury N, Das AK, Daskanungo P. Occurrence of 5,6-dehydrokawain and 7,8-epoxy-5,6-dehydrokawain in Didymocarpus aurentica. Indian J Chem B 1976; 14: 909-11.
    • (1976) Indian J Chem B , vol.14 , pp. 909-911
    • Adityachaudhury, N.1    Das, A.K.2    Daskanungo, P.3
  • 11
    • 37049112046 scopus 로고
    • Analysis of 1H and 13C Nuclear magnetic resonance spectra of sphatulenol by two-dimensional methods
    • Fuyihiko I, Akira A. Analysis of 1H and 13C Nuclear magnetic resonance spectra of sphatulenol by two-dimensional methods. J Chem Soc [Perkin 2]; 1985: 1773-8.
    • (1985) J Chem Soc [Perkin , vol.2 , pp. 1773-1778
    • Fuyihiko, I.1    Akira, A.2
  • 12
    • 34250338453 scopus 로고    scopus 로고
    • Deharo E, Ruiz G, Vargas F, Sagua H, Ortega E, Rojas Aet al. Técnicas de laboratorio para la selección de sustancias antichagas y leishmanicidas. La Paz: Prisa Ltda.-CYTED; 2003.
    • Deharo E, Ruiz G, Vargas F, Sagua H, Ortega E, Rojas Aet al. Técnicas de laboratorio para la selección de sustancias antichagas y leishmanicidas. La Paz: Prisa Ltda.-CYTED; 2003.
  • 13
    • 33645946695 scopus 로고    scopus 로고
    • New administration model of trans-chalcone biodegradable polymers for the treatment of experimental leishmaniasis
    • Piñero J, Temporal RM, Silva-Goncalvez AJ, Jiménez IA, Bazzocchi IL, Oliva A et al. New administration model of trans-chalcone biodegradable polymers for the treatment of experimental leishmaniasis. Acta Trop 2006; 98: 59-65.
    • (2006) Acta Trop , vol.98 , pp. 59-65
    • Piñero, J.1    Temporal, R.M.2    Silva-Goncalvez, A.J.3    Jiménez, I.A.4    Bazzocchi, I.L.5    Oliva, A.6
  • 14
    • 1642540576 scopus 로고    scopus 로고
    • SAR studies of dihydro-β-agarofuran sesquiterpenes as inhibitors of the multridrug-resistance phenotype in a Leishmania tropica line overexpressing a P-glycoprotein-like transporter
    • Cortés-Selva F, Campillo M, Reyes CP, Jiménez IA, Castanys S, Bazzocchi IL et al. SAR studies of dihydro-β-agarofuran sesquiterpenes as inhibitors of the multridrug-resistance phenotype in a Leishmania tropica line overexpressing a P-glycoprotein-like transporter. J Med Chem 2004; 47: 576-87.
    • (2004) J Med Chem , vol.47 , pp. 576-587
    • Cortés-Selva, F.1    Campillo, M.2    Reyes, C.P.3    Jiménez, I.A.4    Castanys, S.5    Bazzocchi, I.L.6
  • 15
    • 0342547236 scopus 로고    scopus 로고
    • Synthesis of 5,6-didehydrokawain-trans-7,8- epoxide and related compounds
    • Achenbach H, Low E. Synthesis of 5,6-didehydrokawain-trans-7,8- epoxide and related compounds. Nat Prod Lett 1997; 10: 79-85.
    • (1997) Nat Prod Lett , vol.10 , pp. 79-85
    • Achenbach, H.1    Low, E.2
  • 16
    • 37049083029 scopus 로고
    • Structural elucidation and absolute configuration of novel β-agafuran (epoxyeudesmene) sesquiterpenes from Maytenus magellanica (Celastraceae)
    • González AG, Nuñez MP, Ravelo AG, Sazatornil JA, Vazquéz JT, Bazzocchi IL et al. Structural elucidation and absolute configuration of novel β-agafuran (epoxyeudesmene) sesquiterpenes from Maytenus magellanica (Celastraceae). J Chem Soc [Perkin 1]; 1992: 1437-41.
    • (1992) J Chem Soc [Perkin , vol.1 , pp. 1437-1441
    • González, A.G.1    Nuñez, M.P.2    Ravelo, A.G.3    Sazatornil, J.A.4    Vazquéz, J.T.5    Bazzocchi, I.L.6
  • 17
    • 34250325468 scopus 로고    scopus 로고
    • PC Model from Serena Software, P.O. Box 3076, Bloomington, IN 47 402-3076.
    • PC Model from Serena Software, P.O. Box 3076, Bloomington, IN 47 402-3076.
  • 18
    • 33748894897 scopus 로고
    • Circular dichroism of (-)-S-trans-1,2-di-4- pyridyloxirane
    • Gottarelli G, Samori B. Circular dichroism of (-)-S-trans-1,2-di-4- pyridyloxirane. J Chem Soc [Perkin 2]; 1972 1998-2001.
    • (1972) J Chem Soc [Perkin , vol.2 , pp. 1998-2001
    • Gottarelli, G.1    Samori, B.2
  • 19
    • 37049086793 scopus 로고
    • An alternative approach to mevinic acid analogues from methyl (3R)-(-)-3-hydroxyhex-5-enoate and an extension to unambiguous syntheses of (6R)-(+)- and (6S)-(-)-goniothalamin
    • Bennett F, Knight DW, Fenton G. An alternative approach to mevinic acid analogues from methyl (3R)-(-)-3-hydroxyhex-5-enoate and an extension to unambiguous syntheses of (6R)-(+)- and (6S)-(-)-goniothalamin. J Chem Soc [Perkin 1]; 1991: 519-23.
    • (1991) J Chem Soc [Perkin , vol.1 , pp. 519-523
    • Bennett, F.1    Knight, D.W.2    Fenton, G.3
  • 20
    • 0028254617 scopus 로고
    • 5-Acetoxyisogoniothalamin oxide, an epoxystyryl lactone from Goniothalamus sesquipedalis
    • Hasam CM, Mia MY, Rashid MA, Connolly JD. 5-Acetoxyisogoniothalamin oxide, an epoxystyryl lactone from Goniothalamus sesquipedalis. Phytochemistry 1994; 37: 1763-4.
    • (1994) Phytochemistry , vol.37 , pp. 1763-1764
    • Hasam, C.M.1    Mia, M.Y.2    Rashid, M.A.3    Connolly, J.D.4
  • 21
    • 0024269565 scopus 로고
    • The stereochemistry of the epoxypropyl side-chain of asperlin
    • Shing TKM, Aloui M. The stereochemistry of the epoxypropyl side-chain of asperlin. J Chem Soc Chem Commun 1988; 23: 1525-26.
    • (1988) J Chem Soc Chem Commun , vol.23 , pp. 1525-1526
    • Shing, T.K.M.1    Aloui, M.2
  • 22
    • 0942277395 scopus 로고    scopus 로고
    • The assignment and absolute configuration by NMR
    • Seco J M, Quiñoá E, Riguera R. The assignment and absolute configuration by NMR. Chem Rev 2004; 104: 17-117.
    • (2004) Chem Rev , vol.104 , pp. 17-117
    • Seco, J.M.1    Quiñoá, E.2    Riguera, R.3
  • 23
    • 0035067048 scopus 로고    scopus 로고
    • In vitro leishmanicidal activity of naturally occurring chalcones
    • Kayser O, Kiderlen AF. In vitro leishmanicidal activity of naturally occurring chalcones. Phytother Res 2001; 15: 148-52.
    • (2001) Phytother Res , vol.15 , pp. 148-152
    • Kayser, O.1    Kiderlen, A.F.2
  • 25
    • 0038548308 scopus 로고    scopus 로고
    • Sructure-activity relationships of antileishmanial and antimalarial chalcones
    • Liu M, Wilairat P, Croft SL, Tan AL-Ch, Go M-L. Sructure-activity relationships of antileishmanial and antimalarial chalcones. Bioorg Med Chem 2003; 11: 2729-38.
    • (2003) Bioorg Med Chem , vol.11 , pp. 2729-2738
    • Liu, M.1    Wilairat, P.2    Croft, S.L.3    Tan, A.L.-C.4    Go, M.-L.5
  • 26
    • 0041589258 scopus 로고    scopus 로고
    • Hermoso A, Jiménez IA, Mamani ZA, Bazzocchi IL, Piñero JE, Ravelo AGet al. Antileishmanial activities of dihydrochalcones from Piper elongatum and synthetic related compounds. Structural requirements for activity. Bioorg Med Chem 2003; 11: 3975-80.
    • Hermoso A, Jiménez IA, Mamani ZA, Bazzocchi IL, Piñero JE, Ravelo AGet al. Antileishmanial activities of dihydrochalcones from Piper elongatum and synthetic related compounds. Structural requirements for activity. Bioorg Med Chem 2003; 11: 3975-80.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.