메뉴 건너뛰기




Volumn 7, Issue 3, 2012, Pages 389-394

Aurones: Interesting natural and synthetic compounds with emerging biological potential

Author keywords

2 Benzylidenebenzofuran 3(2H) ones; Aurones; Biological activity; Synthesis

Indexed keywords

ANTIINFECTIVE AGENT; ANTIINFLAMMATORY AGENT; ANTIMALARIAL AGENT; ANTINEOPLASTIC AGENT; ANTIVIRUS AGENT; AURONE DERIVATIVE; FLAVONOID; NATURAL PRODUCT; UNCLASSIFIED DRUG;

EID: 84860770231     PISSN: 1934578X     EISSN: 15559475     Source Type: Journal    
DOI: 10.1177/1934578x1200700322     Document Type: Article
Times cited : (66)

References (37)
  • 1
    • 0003816885 scopus 로고
    • Plant flavonoids in biology and medicine: Biochemical, pharmacological, and structure-activity relationships
    • Proceedings of a symposium held in Buffalo, New York, July 22-26, 1985 Liss, New York, USA
    • Cody V, Middleton E. (1986) Plant flavonoids in biology and medicine: biochemical, pharmacological, and structure-activity relationships; Proceedings of a symposium held in Buffalo, New York, July 22-26, 1985. In Progress in Clinical and Biological Research. Liss, New York, USA.
    • (1986) Progress in Clinical and Biological Research
    • Cody, V.1    Middleton, E.2
  • 4
    • 34247863928 scopus 로고    scopus 로고
    • Synthesis and insect antifeedant activity of aurones against Spodoptera litura larvae
    • Morimoto M, Fukumoto H. (2007) Synthesis and insect antifeedant activity of aurones against Spodoptera litura larvae. Journal of Agricultural and Food Chemistry, 55, 700-705.
    • (2007) Journal of Agricultural and Food Chemistry , vol.55 , pp. 700-705
    • Morimoto, M.1    Fukumoto, H.2
  • 5
    • 30444441800 scopus 로고    scopus 로고
    • Discovery of benzylidenebenzofuran-3(2H)-one (aurones) as inhibitors of tyrosinase derived from human melanocytes
    • DOI 10.1021/jm050715i
    • Okombi S, Rival D. (2006) Discovery of benzylidenebenzofuran-3(2H)-one (aurones) as inhibitors of tyrosinase derived from human melanocytes. Journal of Medicinal Chemistry, 49, 329-333. (Pubitemid 43077345)
    • (2006) Journal of Medicinal Chemistry , vol.49 , Issue.1 , pp. 329-333
    • Okombi, S.1    Rival, D.2    Bonnet, S.3    Mariotte, A.-M.4    Perrier, E.5    Boumendjel, A.6
  • 6
    • 9244254822 scopus 로고    scopus 로고
    • Synthesis and antioxidative activity of 3′,4′,6,7- tetrahydroxyaurone, a metabolite of Bidens frondosa
    • DOI 10.1271/bbb.68.2183
    • Venkateswarlu S, Panchagnula GK. (2004) Synthesis and antioxidative activity of 3′,4′,6,7-tetrahydroxyaurone, a metabolite of Bidens frondosa. Bioscience, Biotechnology, and Biochemistry, 68, 2183-2185. (Pubitemid 39547610)
    • (2004) Bioscience, Biotechnology and Biochemistry , vol.68 , Issue.10 , pp. 2183-2185
    • Venkateswarlu, S.1    Panchagnula, G.K.2    Subbaraju, G.V.3
  • 7
    • 0345687480 scopus 로고    scopus 로고
    • Aurones: A subclass of flavones with promising biological potential
    • Boumendjel A. (2003) Aurones: a subclass of flavones with promising biological potential. Current Medicinal Chemistry, 10, 2621-2630.
    • (2003) Current Medicinal Chemistry , vol.10 , pp. 2621-2630
    • Boumendjel, A.1
  • 8
    • 0141433360 scopus 로고    scopus 로고
    • The total synthesis of an aurone isolated from Uvaria hamiltonii: Aurones and flavones as anticancer agents
    • DOI 10.1016/j.bmcl.2003.07.003
    • Lawrence NJ, Rennison D. (2003) The total synthesis of an aurone isolated from Uvaria hamiltonii: aurones and flavones as anticancer agents. Bioorganic & Medicinal Chemistry Letters, 13, 3759-3763. (Pubitemid 37206502)
    • (2003) Bioorganic and Medicinal Chemistry Letters , vol.13 , Issue.21 , pp. 3759-3763
    • Lawrence, N.J.1    Rennison, D.2    McGown, A.T.3    Hadfield, J.A.4
  • 9
    • 0023001362 scopus 로고
    • Inhibition of rat liver iodothyronine deiodinase. Interaction of aurones with the iodothyronine ligand-binding site
    • Auf'mkolk M, Koehrle J. (1986) Inhibition of rat liver iodothyronine deiodinase. Interaction of aurones with the iodothyronine ligand-binding site. The Journal of Biological Chemistry, 261, 11623-11630. (Pubitemid 17206081)
    • (1986) Journal of Biological Chemistry , vol.261 , Issue.25 , pp. 11623-11630
    • Auf'mkolk, M.1    Koehrle, J.2    Hesch, R.-D.3    Cody, V.4
  • 12
    • 78649331023 scopus 로고    scopus 로고
    • Design, synthesis and discovery of 5-hydroxyaurone derivatives as growth inhibitors against HUVEC and some cancer cell lines
    • Cheng H, Zhang L. (2010) Design, synthesis and discovery of 5-hydroxyaurone derivatives as growth inhibitors against HUVEC and some cancer cell lines. European Journal of Medicinal Chemistry, 45, 5950-5957.
    • (2010) European Journal of Medicinal Chemistry , vol.45 , pp. 5950-5957
    • Cheng, H.1    Zhang, L.2
  • 13
    • 0026475479 scopus 로고
    • Alumina-mediated condensation. A simple synthesis of aurones
    • Varma RS, Varma M. (1992) Alumina-mediated condensation. A simple synthesis of aurones. Tetrahedron Letters, 33, 5937-5940.
    • (1992) Tetrahedron Letters , vol.33 , pp. 5937-5940
    • Varma, R.S.1    Varma, M.2
  • 14
    • 0025600973 scopus 로고
    • Synthesis of tunichromes mm-l and mm-2, blood pigments of the iron assimilating tunicate, Molgula manhattensis
    • Kim D, Li Y. (1990) Synthesis of tunichromes mm-l and mm-2, blood pigments of the iron assimilating tunicate, Molgula manhattensis. Tetrahedron Letters, 31, 7119-7122.
    • (1990) Tetrahedron Letters , vol.31 , pp. 7119-7122
    • Kim, D.1    Li, Y.2
  • 15
    • 78449302625 scopus 로고    scopus 로고
    • Divergent approach to flavones and aurones via dihaloacrylic acids. Unexpected dependence on the halogen atom
    • Kraus GA, Gupta V. (2010) Divergent approach to flavones and aurones via dihaloacrylic acids. Unexpected dependence on the halogen atom. Organic letters, 12, 5278-5280.
    • (2010) Organic Letters , vol.12 , pp. 5278-5280
    • Kraus, G.A.1    Gupta, V.2
  • 16
    • 33747071481 scopus 로고    scopus 로고
    • Selected patented cross-coupling reaction technologies
    • Corbet JP, Mignani G. (2006) Selected patented cross-coupling reaction technologies. Chemical Reviews, 106, 2651-2710.
    • (2006) Chemical Reviews , vol.106 , pp. 2651-2710
    • Corbet, J.P.1    Mignani, G.2
  • 17
    • 39349098969 scopus 로고    scopus 로고
    • I- catalyzed cyclization
    • DOI 10.1021/jo702197b
    • Harkat H, Blanc A. (2008) Versatile and expeditious synthesis of aurones via Au I-catalyzed cyclization. The Journal of Organic Chemistry, 73, 1620-1623. (Pubitemid 351263689)
    • (2008) Journal of Organic Chemistry , vol.73 , Issue.4 , pp. 1620-1623
    • Harkat, H.1    Blanc, A.2    Weibel, J.-M.3    Pale, P.4
  • 18
    • 0035142734 scopus 로고    scopus 로고
    • Two new aurones from marine brown alga Spatoglossum variabile
    • Atta ur Rahman, Choudhary MI. (2001) Two new aurones from marine brown alga Spatoglossum variabile. Chemical & Pharmaceutical Bulletin, 49, 105-107.
    • (2001) Chemical & Pharmaceutical Bulletin , vol.49 , pp. 105-107
    • Rahman, A.U.1    Choudhary, M.I.2
  • 19
    • 33744932434 scopus 로고    scopus 로고
    • A new process for the synthesis of aurones by using mercury (II) acetate in pyridine and cupric bromide in dimethyl sulfoxide
    • Agrawal NN, Soni PA. (2006) A new process for the synthesis of aurones by using mercury (II) acetate in pyridine and cupric bromide in dimethyl sulfoxide. Indian Journal of Chemistry, 45B,1301-1303. (Pubitemid 43845095)
    • (2006) Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry , vol.45 , Issue.5 , pp. 1301-1303
    • Agrawal, N.N.1    Soni, P.A.2
  • 20
    • 77953128757 scopus 로고    scopus 로고
    • The scope of thallium nitrate oxidative cyclization of chalcones; synthesis and evaluation of isoflavone and aurone analogs for their inhibitory activity against interleukin-5
    • Thanigaimalai P, Yang HM. (2010) The scope of thallium nitrate oxidative cyclization of chalcones; synthesis and evaluation of isoflavone and aurone analogs for their inhibitory activity against interleukin-5. Bioorganic & Medicinal Chemistry, 18, 4441-4445.
    • (2010) Bioorganic & Medicinal Chemistry , vol.18 , pp. 4441-4445
    • Thanigaimalai, P.1    Yang, H.M.2
  • 21
    • 0037722923 scopus 로고    scopus 로고
    • Structural requirement of isoflavonones for the inhibitory activity of interleukin-5
    • Jung SH, Cho SH. (2003) Structural requirement of isoflavonones for the inhibitory activity of interleukin-5. European Journal of Medicinal Chemistry, 38, 537-545.
    • (2003) European Journal of Medicinal Chemistry , vol.38 , pp. 537-545
    • Jung, S.H.1    Cho, S.H.2
  • 22
    • 34548756783 scopus 로고    scopus 로고
    • The role of alkoxy group on the A ring of isoflavones in the inhibition of interleukin-5
    • Yang HM, Shin HR. (2007) The role of alkoxy group on the A ring of isoflavones in the inhibition of interleukin-5. Archives of Pharmacal Research, 30, 950-954.
    • (2007) Archives of Pharmacal Research , vol.30 , pp. 950-954
    • Yang, H.M.1    Shin, H.R.2
  • 23
    • 0010501503 scopus 로고
    • A novel oxidative cyclization of 2'-hydroxychalcones to 4,5-dialkoxyaurones by thallium(III) nitrate
    • Thakkar K, Cushman M. (1995) A novel oxidative cyclization of 2'-hydroxychalcones to 4,5-dialkoxyaurones by thallium(III) nitrate. The Journal of Organic Chemistry, 60, 6499-6510.
    • (1995) The Journal of Organic Chemistry , vol.60 , pp. 6499-6510
    • Thakkar, K.1    Cushman, M.2
  • 24
    • 71849111943 scopus 로고    scopus 로고
    • Natural and synthetic 2'-hydroxy-chalcones and aurones: Synthesis, characterization and evaluation of the antioxidant and soybean lipoxygenase inhibitory activity
    • Detsi A, Majdalani M. (2009) Natural and synthetic 2'-hydroxy-chalcones and aurones: synthesis, characterization and evaluation of the antioxidant and soybean lipoxygenase inhibitory activity. Bioorganic & Medicinal Chemistry, 17, 8073-8085.
    • (2009) Bioorganic & Medicinal Chemistry , vol.17 , pp. 8073-8085
    • Detsi, A.1    Majdalani, M.2
  • 25
    • 26244463340 scopus 로고    scopus 로고
    • Molecular evolution of the opaque-2 gene in Zea mays L
    • Henry AM, Manicacci D. (2005) Molecular evolution of the opaque-2 gene in Zea mays L. Journal of Molecular Evolution, 61, 551-558.
    • (2005) Journal of Molecular Evolution , vol.61 , pp. 551-558
    • Henry, A.M.1    Manicacci, D.2
  • 26
    • 79951772352 scopus 로고    scopus 로고
    • Genetic engineering of flavonoid pigments to modify flower color in floricultural plants
    • Nishihara M, Nakatsuka T. (2011) Genetic engineering of flavonoid pigments to modify flower color in floricultural plants. Biotechnology Letters, 33, 433-441.
    • (2011) Biotechnology Letters , vol.33 , pp. 433-441
    • Nishihara, M.1    Nakatsuka, T.2
  • 28
    • 84856242643 scopus 로고    scopus 로고
    • Aurones: Small molecule visible range fluorescent probes suitable for biomacromolecules
    • Shanker N, Dilek O. (2011) Aurones: Small molecule visible range fluorescent probes suitable for biomacromolecules. Journal of Fluorescence, 6, 2173-2184.
    • (2011) Journal of Fluorescence , vol.6 , pp. 2173-2184
    • Shanker, N.1    Dilek, O.2
  • 29
    • 80051549637 scopus 로고    scopus 로고
    • The aromatic ketone 4'-hydroxychalcone inhibits TNFalpha-induced NF-kappaB activation via proteasome inhibition
    • Orlikova B, Tasdemir D. (2011) The aromatic ketone 4'-hydroxychalcone inhibits TNFalpha-induced NF-kappaB activation via proteasome inhibition. Biochemical Pharmacology, 82, 620-631.
    • (2011) Biochemical Pharmacology , vol.82 , pp. 620-631
    • Orlikova, B.1    Tasdemir, D.2
  • 30
    • 79956360137 scopus 로고    scopus 로고
    • Dietary chalcones with chemopreventive and chemotherapeutic potential
    • Orlikova B, Tasdemir D. (2011) Dietary chalcones with chemopreventive and chemotherapeutic potential. Genes & Nutrition, 6, 125-147.
    • (2011) Genes & Nutrition , vol.6 , pp. 125-147
    • Orlikova, B.1    Tasdemir, D.2
  • 31
    • 77955428448 scopus 로고    scopus 로고
    • 1-Azaaurones derived from the naturally occurring aurones as potential antimalarial drugs
    • Souard F, Okombi S. (2010) 1-Azaaurones derived from the naturally occurring aurones as potential antimalarial drugs. Bioorganic & Medicinal Chemistry, 18, 5724-5731.
    • (2010) Bioorganic & Medicinal Chemistry , vol.18 , pp. 5724-5731
    • Souard, F.1    Okombi, S.2
  • 32
    • 77954349567 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of a novel series of 2,2-bisaminomethylated aurone analogues as anti-inflammatory and antimicrobial agents
    • Bandgar BP, Patil SA. (2010) Synthesis and biological evaluation of a novel series of 2,2-bisaminomethylated aurone analogues as anti-inflammatory and antimicrobial agents. European Journal of Medicinal Chemistry, 45, 3223-3227.
    • (2010) European Journal of Medicinal Chemistry , vol.45 , pp. 3223-3227
    • Bandgar, B.P.1    Patil, S.A.2
  • 33
    • 48449102581 scopus 로고    scopus 로고
    • Structure-activity relationship of flavonoids as influenza virus neuraminidase inhibitors and their in vitro anti-viral activities
    • Liu AL, Wang HD. (2008) Structure-activity relationship of flavonoids as influenza virus neuraminidase inhibitors and their in vitro anti-viral activities. Bioorganic & Medicinal Chemistry, 16, 7141-7147.
    • (2008) Bioorganic & Medicinal Chemistry , vol.16 , pp. 7141-7147
    • Liu, A.L.1    Wang, H.D.2
  • 34
    • 79961245561 scopus 로고    scopus 로고
    • Discovery of naturally occurring aurones that are potent allosteric inhibitors of hepatitis C virus RNA-dependent RNA polymerase
    • Haudecoeur R, Ahmed-Belkacem A. (2011) Discovery of naturally occurring aurones that are potent allosteric inhibitors of hepatitis C virus RNA-dependent RNA polymerase. Journal of Medicinal Chemistry, 54, 5395-5402.
    • (2011) Journal of Medicinal Chemistry , vol.54 , pp. 5395-5402
    • Haudecoeur, R.1    Ahmed-Belkacem, A.2
  • 35
    • 79960342853 scopus 로고    scopus 로고
    • Synthesis of aurones and their inhibitory effects on nitric oxide and PGE(2) productions in LPS-induced RAW 264.7 cells
    • Shin SY, Shin MC. (2011) Synthesis of aurones and their inhibitory effects on nitric oxide and PGE(2) productions in LPS-induced RAW 264.7 cells. Bioorganic & Medicinal Chemistry Letters, 21, 4520-4523.
    • (2011) Bioorganic & Medicinal Chemistry Letters , vol.21 , pp. 4520-4523
    • Shin, S.Y.1    Shin, M.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.