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Volumn 103, Issue , 2015, Pages 187-191

Cytotoxic prenylated flavonoids from Macaranga indica

Author keywords

Cytotoxicity; Ellagic acid; Euphorbiaceae; Macaranga indica; Prenylated flavonoids

Indexed keywords

CYTOTOXIC AGENT; ELLAGIC ACID; FLAVONOID; FLUOROURACIL; MACARANGA INDICA EXTRACT; MACARINDICIN A; MACARINDICIN B; MACARINDICIN C; PLANT EXTRACT; UNCLASSIFIED DRUG; ANTINEOPLASTIC AGENT;

EID: 84927741198     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2015.04.002     Document Type: Article
Times cited : (21)

References (26)
  • 2
    • 84922515253 scopus 로고    scopus 로고
    • Phytochemistry and pharmacology of the genus Macaranga: A review
    • J.J. Magadula Phytochemistry and pharmacology of the genus Macaranga: a review J. Med. Plant Res. 8 2014 489 503
    • (2014) J. Med. Plant Res. , vol.8 , pp. 489-503
    • Magadula, J.J.1
  • 3
    • 0000693669 scopus 로고
    • Studies on the south east asian ant-plant association Crematogaster borneensis/Macaranga: Adaptations of the ant partner
    • B. Fiala, and U. Maschwitz Studies on the south east asian ant-plant association Crematogaster borneensis/Macaranga: adaptations of the ant partner Insect. Soc. 37 1990 212 231
    • (1990) Insect. Soc. , vol.37 , pp. 212-231
    • Fiala, B.1    Maschwitz, U.2
  • 5
    • 0000983297 scopus 로고
    • Chromenoflavones from Macaranga indica
    • S. Sultana, and M. Ilyas Chromenoflavones from Macaranga indica Phytochemistry 25 1986 953 954
    • (1986) Phytochemistry , vol.25 , pp. 953-954
    • Sultana, S.1    Ilyas, M.2
  • 6
    • 84908596025 scopus 로고    scopus 로고
    • Cytotoxic prenylated bibenzyls and flavonoids from Macaranga kurzii
    • D.S. Yang, J.G. Wei, W.B. Peng, S.M. Wang, C. Sun, Y.P. Yang et al. Cytotoxic prenylated bibenzyls and flavonoids from Macaranga kurzii Fitoterapia 99 2014 261 266
    • (2014) Fitoterapia , vol.99 , pp. 261-266
    • Yang, D.S.1    Wei, J.G.2    Peng, W.B.3    Wang, S.M.4    Sun, C.5    Yang, Y.P.6
  • 7
    • 84922495836 scopus 로고    scopus 로고
    • Denticulatains A and B: Unique stilbene-diterpene heterodimers from Macaranga denticulata
    • D.S. Yang, Z.L. Li, X. Wang, H. Yan, Y.P. Yang, H.R. Luo et al. Denticulatains A and B: unique stilbene-diterpene heterodimers from Macaranga denticulata RSC Adv. 5 2015 13886 13890
    • (2015) RSC Adv. , vol.5 , pp. 13886-13890
    • Yang, D.S.1    Li, Z.L.2    Wang, X.3    Yan, H.4    Yang, Y.P.5    Luo, H.R.6
  • 10
    • 0001777479 scopus 로고
    • Light-induced variation in phenolic levels in foliage of rain-forest plants
    • S. Mole, J.A.M. Ross, and P.G. Waterman Light-induced variation in phenolic levels in foliage of rain-forest plants J. Chem. Ecol. 14 1988 1 21
    • (1988) J. Chem. Ecol. , vol.14 , pp. 1-21
    • Mole, S.1    Ross, J.A.M.2    Waterman, P.G.3
  • 11
    • 79957598613 scopus 로고    scopus 로고
    • Ellagitannins, ellagic acid and their derived metabolites: A review about source, metabolism, functions and health
    • J.M. Landete Ellagitannins, ellagic acid and their derived metabolites: a review about source, metabolism, functions and health Food Res. Int. 44 2011 1150 1160
    • (2011) Food Res. Int. , vol.44 , pp. 1150-1160
    • Landete, J.M.1
  • 12
    • 0034786626 scopus 로고    scopus 로고
    • Five new diprenylated flavonols from the leaves of Broussonetia kazinoki
    • P.C. Zhang, S. Wang, Y. Wu, R.Y. Chen, and D.Q. Yu Five new diprenylated flavonols from the leaves of Broussonetia kazinoki J. Nat. Prod. 64 2001 1206 1209
    • (2001) J. Nat. Prod. , vol.64 , pp. 1206-1209
    • Zhang, P.C.1    Wang, S.2    Wu, Y.3    Chen, R.Y.4    Yu, D.Q.5
  • 15
    • 0001706194 scopus 로고
    • Structures of five new prenylated flavonoids, gancaonins L, M, N, O, and P from aerial parts of Glycyrrhiza uralensis
    • T. Fukai, Q.H. Wang, M. Takayama, and T. Nomura Structures of five new prenylated flavonoids, gancaonins L, M, N, O, and P from aerial parts of Glycyrrhiza uralensis Heterocycles 31 1990 373 382
    • (1990) Heterocycles , vol.31 , pp. 373-382
    • Fukai, T.1    Wang, Q.H.2    Takayama, M.3    Nomura, T.4
  • 18
    • 0035091836 scopus 로고    scopus 로고
    • A facile synthetic approach to prenylated flavanones: First total syntheses of (±)- bonannione A and (±)- sophoraflavanone A
    • Y.Q. Wang, W.F. Tan, W.D.Z. Li, and Y.L. Li A facile synthetic approach to prenylated flavanones: first total syntheses of (±)- bonannione A and (±)- sophoraflavanone A J. Nat. Prod. 64 2001 196 199
    • (2001) J. Nat. Prod. , vol.64 , pp. 196-199
    • Wang, Y.Q.1    Tan, W.F.2    Li, W.D.Z.3    Li, Y.L.4
  • 19
    • 0028304663 scopus 로고
    • Farnesyl acetophenone and flavanone compounds from the aerial parts of Boronia ramosa
    • M. Ahsan, A.I. Gray, P.G. Waterman, and J.A. Armstrong Farnesyl acetophenone and flavanone compounds from the aerial parts of Boronia ramosa J. Nat. Prod. 57 1994 673 676
    • (1994) J. Nat. Prod. , vol.57 , pp. 673-676
    • Ahsan, M.1    Gray, A.I.2    Waterman, P.G.3    Armstrong, J.A.4
  • 20
    • 24344451200 scopus 로고    scopus 로고
    • Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids
    • D. Slade, D. Ferreira, and J.P.J. Marais Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids Phytochemistry 66 2005 2177 2215
    • (2005) Phytochemistry , vol.66 , pp. 2177-2215
    • Slade, D.1    Ferreira, D.2    Marais, J.P.J.3
  • 22
    • 0000422927 scopus 로고
    • Four new prenylated flavonoids, Glyasperins A, B, C, and D from the roots of Glycyrrhiza aspera
    • L. Zeng, T. Fukai, T. Nomura, R.Y. Zhang, and Z.C. Lou Four new prenylated flavonoids, Glyasperins A, B, C, and D from the roots of Glycyrrhiza aspera Heterocycles 34 1992 575 587
    • (1992) Heterocycles , vol.34 , pp. 575-587
    • Zeng, L.1    Fukai, T.2    Nomura, T.3    Zhang, R.Y.4    Lou, Z.C.5
  • 24
    • 77950363308 scopus 로고    scopus 로고
    • Identification of major phenolic compounds from Nephelium lappaceum L. and their antioxidant activities
    • N. Thitilertdecha, A. Teerawutgulrag, J.D. Kilburn, and N. Rakariyatham Identification of major phenolic compounds from Nephelium lappaceum L. and their antioxidant activities Molecules 15 2010 1453 1465
    • (2010) Molecules , vol.15 , pp. 1453-1465
    • Thitilertdecha, N.1    Teerawutgulrag, A.2    Kilburn, J.D.3    Rakariyatham, N.4
  • 25
    • 84903954781 scopus 로고    scopus 로고
    • Chemical constituents from Euphorbia stracheyi and their biological activities
    • D.S. Yang, W.B. Peng, Z.L. Li, X. Wang, J.G. Wei, Q.X. et al. He Chemical constituents from Euphorbia stracheyi and their biological activities Fitoterapia 97 2014 211 218
    • (2014) Fitoterapia , vol.97 , pp. 211-218
    • Yang, D.S.1    Peng, W.B.2    Li, Z.L.3    Wang, X.4    Wei, J.G.5    He, Q.X.6
  • 26
    • 84903954781 scopus 로고    scopus 로고
    • Chemical constituents from Euphorbia stracheyi and their biological activities
    • D.S. Yang, W.B. Peng, Z.L. Li, X. Wang, J.G. Wei, and Q.X. He Chemical constituents from Euphorbia stracheyi and their biological activities Fitoterapia 97 2014 211 218
    • (2014) Fitoterapia , vol.97 , pp. 211-218
    • Yang, D.S.1    Peng, W.B.2    Li, Z.L.3    Wang, X.4    Wei, J.G.5    He, Q.X.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.