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Volumn 70, Issue 5, 2009, Pages 590-596

Biosynthesis of antimalarial lignans from Holostylis reniformis

Author keywords

Aristolochiaceae; Aryltetralone lignans; Biosynthesis; Epoxylignans; Holostylis reniformis; Lignans; Neolignans; Propenylphenols

Indexed keywords

ANTIMALARIAL AGENT; LIGNAN;

EID: 64949201138     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2009.02.008     Document Type: Article
Times cited : (56)

References (21)
  • 3
    • 1542375402 scopus 로고    scopus 로고
    • Aryltetralone lignans and 7,8-secolignans from Holostylis reniformis
    • da Silva T., and Lopes L.M.X. Aryltetralone lignans and 7,8-secolignans from Holostylis reniformis. Phytochemistry 65 (2004) 751-759
    • (2004) Phytochemistry , vol.65 , pp. 751-759
    • da Silva, T.1    Lopes, L.M.X.2
  • 4
    • 33646029406 scopus 로고    scopus 로고
    • Aryltetralol and aryltetralone lignans from Holostylis reniformis
    • da Silva T., and Lopes L.M.X. Aryltetralol and aryltetralone lignans from Holostylis reniformis. Phytochemistry 67 (2006) 929-937
    • (2006) Phytochemistry , vol.67 , pp. 929-937
    • da Silva, T.1    Lopes, L.M.X.2
  • 5
    • 64949186923 scopus 로고    scopus 로고
    • Patent PI0404986-1, 2004. Lignanas, lignanas ariltetralônicas, extratos, processos de obtenção de lignanas, processo de obtenção de extratos, uso de lignanas, uso de extratos e composição farmacêutica para prevenir e tratar malária. Rev. Prop. Ind. 2004, p. 1774
    • da Silva, T., Krettli, A.U., Andrade-Neto, V.F., Lopes, L.M.X., Patent PI0404986-1, 2004. Lignanas, lignanas ariltetralônicas, extratos, processos de obtenção de lignanas, processo de obtenção de extratos, uso de lignanas, uso de extratos e composição farmacêutica para prevenir e tratar malária. Rev. Prop. Ind. 2004, p. 1774.
    • da Silva, T.1    Krettli, A.U.2    Andrade-Neto, V.F.3    Lopes, L.M.X.4
  • 6
    • 16844377224 scopus 로고    scopus 로고
    • An historical perspective on lignan biosynthesis: monolignol, allylphenol and hydroxycinnamic acid coupling and downstream metabolism
    • Davin L.B., and Lewis N.G. An historical perspective on lignan biosynthesis: monolignol, allylphenol and hydroxycinnamic acid coupling and downstream metabolism. Phytochem. Rev. 2 (2003) 257-288
    • (2003) Phytochem. Rev. , vol.2 , pp. 257-288
    • Davin, L.B.1    Lewis, N.G.2
  • 7
    • 23444445169 scopus 로고    scopus 로고
    • Dirigent phenoxy radical coupling: advances and challenges
    • Davin L.B., and Lewis N.G. Dirigent phenoxy radical coupling: advances and challenges. Curr. Opin. Biotechnol. 16 (2005) 398-406
    • (2005) Curr. Opin. Biotechnol. , vol.16 , pp. 398-406
    • Davin, L.B.1    Lewis, N.G.2
  • 8
    • 0031031957 scopus 로고    scopus 로고
    • Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center
    • Davin L.B., Wang H.-B., Crowell A.L., Bedgar D.L., Martin D.M., Sarkanen S., and Lewis N.G. Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center. Science 275 (1997) 362-366
    • (1997) Science , vol.275 , pp. 362-366
    • Davin, L.B.1    Wang, H.-B.2    Crowell, A.L.3    Bedgar, D.L.4    Martin, D.M.5    Sarkanen, S.6    Lewis, N.G.7
  • 9
    • 20444385315 scopus 로고    scopus 로고
    • Lignans in plant cell and organ cultures: an overview
    • Fuss E. Lignans in plant cell and organ cultures: an overview. Phytochem. Rev. 2 (2003) 307-320
    • (2003) Phytochem. Rev. , vol.2 , pp. 307-320
    • Fuss, E.1
  • 12
    • 1842817423 scopus 로고    scopus 로고
    • O-Methylation of benzaldehyde derivatives by "lignin specific" caffeic acid 3-O-methyltransferase
    • Kota P., Guo D., Zubieta C., Noel J., and Dixon R.A. O-Methylation of benzaldehyde derivatives by "lignin specific" caffeic acid 3-O-methyltransferase. Phytochemistry 65 (2004) 837-846
    • (2004) Phytochemistry , vol.65 , pp. 837-846
    • Kota, P.1    Guo, D.2    Zubieta, C.3    Noel, J.4    Dixon, R.A.5
  • 13
    • 0034583327 scopus 로고    scopus 로고
    • Nomenclature of lignans and neolignans
    • Moss G.P. Nomenclature of lignans and neolignans. Pure Appl. Chem. 72 (2000) 1493-1523
    • (2000) Pure Appl. Chem. , vol.72 , pp. 1493-1523
    • Moss, G.P.1
  • 15
    • 0028227564 scopus 로고
    • (+)-Pinoresinol synthase: a stereoselective oxidase catalyzing 8,8′-lignan formation in Forsythia intermedia
    • Paré P.W., Wang H.-B., Davin L.B., and Lewis N.G. (+)-Pinoresinol synthase: a stereoselective oxidase catalyzing 8,8′-lignan formation in Forsythia intermedia. Tetrahedron Lett. 27 (1994) 4731-4734
    • (1994) Tetrahedron Lett. , vol.27 , pp. 4731-4734
    • Paré, P.W.1    Wang, H.-B.2    Davin, L.B.3    Lewis, N.G.4
  • 16
    • 0000191645 scopus 로고
    • Further studies on the biosynthesis of pseudoisoeugenols in tissue cultures of Pimpinella anisum
    • Reichling J., and Martin R. Further studies on the biosynthesis of pseudoisoeugenols in tissue cultures of Pimpinella anisum. Z. Naturforsch. 45c (1990) 942-948
    • (1990) Z. Naturforsch. , vol.45 c , pp. 942-948
    • Reichling, J.1    Martin, R.2
  • 17
    • 29844454699 scopus 로고    scopus 로고
    • Reactivity of 4-vinylphenol radical cations in solution: implications for the biosynthesis of lignans
    • Rodríguez-Evora Y., and Schepp N.P. Reactivity of 4-vinylphenol radical cations in solution: implications for the biosynthesis of lignans. Org. Biomol. Chem. 3 (2005) 4444-4449
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 4444-4449
    • Rodríguez-Evora, Y.1    Schepp, N.P.2
  • 19
    • 16844385289 scopus 로고    scopus 로고
    • Diversity in lignan biosynthesis
    • Umezawa T. Diversity in lignan biosynthesis. Phytochem. Rev. 2 (2003) 371-390
    • (2003) Phytochem. Rev. , vol.2 , pp. 371-390
    • Umezawa, T.1
  • 20
    • 33745912517 scopus 로고    scopus 로고
    • Chavicol formation in sweet basil (Ocimum basilicum): cleavage of an esterified C9 hydroxyl group with NAD(P)H-dependent reduction
    • Vassão D.G., Gang D.R., Koeduka T., Jackson B., Pichersky E., Davin L.B., and Lewis N.G. Chavicol formation in sweet basil (Ocimum basilicum): cleavage of an esterified C9 hydroxyl group with NAD(P)H-dependent reduction. Org. Biomol. Chem. 4 (2006) 2733-2744
    • (2006) Org. Biomol. Chem. , vol.4 , pp. 2733-2744
    • Vassão, D.G.1    Gang, D.R.2    Koeduka, T.3    Jackson, B.4    Pichersky, E.5    Davin, L.B.6    Lewis, N.G.7
  • 21
    • 34548009392 scopus 로고    scopus 로고
    • A pinoresinol-lariciresinol reductase homologue from the creosote bush (Larrea tridentata) catalyzes the efficient in vitro conversion of p-coumaryl/coniferyl alcohol esters into the allylphenols chavicol/eugenol, but not the propenylphenols p-anol/isoeugenol
    • Vassão D.G., Kim S.-J., Milhollan J.K., Eichinger D., Davin L.B., and Lewis N.G. A pinoresinol-lariciresinol reductase homologue from the creosote bush (Larrea tridentata) catalyzes the efficient in vitro conversion of p-coumaryl/coniferyl alcohol esters into the allylphenols chavicol/eugenol, but not the propenylphenols p-anol/isoeugenol. Arch. Biochem. Biophys. 465 (2007) 209-218
    • (2007) Arch. Biochem. Biophys. , vol.465 , pp. 209-218
    • Vassão, D.G.1    Kim, S.-J.2    Milhollan, J.K.3    Eichinger, D.4    Davin, L.B.5    Lewis, N.G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.