메뉴 건너뛰기




Volumn 6, Issue 3, 2013, Pages 498-503

Anti-AGEs and antiparasitic activity of an original prenylated isoflavonoid and flavanones isolated from Derris ferruginea

Author keywords

AGEs (advanced glycation endproducts); Antiparasitic; Derris ferruginea; Fabaceae; Flavonoid; Synthesis

Indexed keywords

5 HYDROXY 3 (4 HYDROXYPHENYL) 8 ISOPROPENYL 8,9 DIHYDRO 4H FURO [2,3 H] CHROMEN 4 ONE; ADVANCED GLYCATION END PRODUCT; ANTIPARASITIC AGENT; FLAVANONE DERIVATIVE; ISOFLAVONOID; PHENOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84886871497     PISSN: 18743900     EISSN: 18767486     Source Type: Journal    
DOI: 10.1016/j.phytol.2013.06.002     Document Type: Article
Times cited : (21)

References (44)
  • 1
    • 0038734290 scopus 로고    scopus 로고
    • Synthesis of lupiwighteone via a para-Claisen-Cope rearrangement
    • DOI 10.1016/S0040-4020(03)00579-9
    • Al-Maharik, N., Botting, N.P., 2003. Synthesis of lupiwighteone via a para-Claisen- Cope rearrangement. Tetrahedron 59, 4177-4181. (Pubitemid 36589067)
    • (2003) Tetrahedron , vol.59 , Issue.23 , pp. 4177-4181
    • Al-Maharik, N.1    Botting, N.P.2
  • 2
    • 38949187904 scopus 로고    scopus 로고
    • NMR spectral assignments of a new [C-O-C] isoflavone dimer from Andira surinamensis
    • Almeida, J.G.L., Silveira, E.R., Pessoa, O.D.L., 2008. NMR spectral assignments of a new [C-O-C] isoflavone dimer from Andira surinamensis. Magn. Reson. Chem. 46, 103-106.
    • (2008) Magn. Reson. Chem. , vol.46 , pp. 103-106
    • Almeida, J.G.L.1    Silveira, E.R.2    Pessoa, O.D.L.3
  • 4
    • 69549135067 scopus 로고    scopus 로고
    • Plant-derived antimalarial agents: New leads and efficient phytomedicines. Part II. Non-alkaloidal natural products
    • Batista Jr., R., Oliveira, A.D.J.S., De Oliveira, A.B., 2009. Plant-derived antimalarial agents: new leads and efficient phytomedicines. Part II. Non-alkaloidal natural products. Molecules 14, 3037-3072.
    • (2009) Molecules , vol.14 , pp. 3037-3072
    • Batista Jr., R.1    Oliveira, A.D.J.S.2    De Oliveira, A.B.3
  • 6
    • 77957831206 scopus 로고    scopus 로고
    • Automating a 96-well microtiter plate assay for identification of AGEs inhibitors or inducers: Application to the screening of a small natural compounds library
    • Derbre, S., Gatto, J., Pelleray, A., Coulon, L., Seraphin, D., Richomme, P., 2009. Automating a 96-well microtiter plate assay for identification of AGEs inhibitors or inducers: application to the screening of a small natural compounds library. Anal. Bioanal. Chem. 398, 1747-1758.
    • (2009) Anal. Bioanal. Chem. , vol.398 , pp. 1747-1758
    • Derbre, S.1    Gatto, J.2    Pelleray, A.3    Coulon, L.4    Seraphin, D.5    Richomme, P.6
  • 7
    • 0001639153 scopus 로고
    • Ten isoprenylated and C-methylated flavonoids from the leaves of three Vellozia species
    • Harborne, J.B., Greenham, J., Williams, C.A., Eagles, J., Markham, K.R., 1993. Ten isoprenylated and C-methylated flavonoids from the leaves of three Vellozia species. Phytochemistry 34, 219-226.
    • (1993) Phytochemistry , vol.34 , pp. 219-226
    • Harborne, J.B.1    Greenham, J.2    Williams, C.A.3    Eagles, J.4    Markham, K.R.5
  • 8
    • 0038718469 scopus 로고    scopus 로고
    • Regioselectivity in the ene reaction of singlet oxygen with ortho-prenylphenol derivatives
    • DOI 10.1016/S0040-4020(03)00733-6
    • Helesbeux, J.J., Duval, O., Guilet, D., Seraphin, D., Rondeaub, D., Richomme, P., 2003. Regioselectivity in the ene reaction of singlet oxygen with ortho-prenylphenol derivatives. Tetrahedron 59, 5091-5104. (Pubitemid 36734901)
    • (2003) Tetrahedron , vol.59 , Issue.27 , pp. 5091-5104
    • Helesbeux, J.-J.1    Duval, O.2    Guilet, D.3    Seraphin, D.4    Rondeau, D.5    Richomme, P.6
  • 9
    • 70349186853 scopus 로고    scopus 로고
    • Flavonoids and pterocarpans from the bark of Erythrina fusca
    • Innok, P., Rukachaisirikul, T., Suksamrarn, A., 2009. Flavonoids and pterocarpans from the bark of Erythrina fusca. Chem. Pharm. Bull. 57, 993-996.
    • (2009) Chem. Pharm. Bull. , vol.57 , pp. 993-996
    • Innok, P.1    Rukachaisirikul, T.2    Suksamrarn, A.3
  • 12
    • 0742302442 scopus 로고    scopus 로고
    • A new fluorometric method for anti-Leishmania drug screening on axenic amastigotes
    • Lepape, P., Pagniez, F., Abdala, H., 2003. A new fluorometric method for anti- Leishmania drug screening on axenic amastigotes. Acta Parasitol. 4, 301-305. (Pubitemid 38154189)
    • (2003) Acta Parasitologica , vol.48 , Issue.4 , pp. 301-305
    • Le Pape, P.1    Pagniez, F.2    Abdala-Valencia, H.3
  • 13
    • 0035850950 scopus 로고    scopus 로고
    • Flavonoids from Glycyrrhiza pallidiflora hairy root cultures
    • DOI 10.1016/S0031-9422(01)00268-0, PII S0031942201002680
    • Li, W., Asada, Y., Koike, K., Hirotani, M., Rui, H., Yoshikawa, T., Nikaido, T., 2001. Flavonoids from Glycyrrhiza pallidiflora hairy root cultures. Phytochemistry 58,595-598. (Pubitemid 32904879)
    • (2001) Phytochemistry , vol.58 , Issue.4 , pp. 595-598
    • Li, W.1    Asada, Y.2    Koike, K.3    Hirotani, M.4    Rui, H.5    Yoshikawa, T.6    Nikaido, T.7
  • 14
    • 0026354323 scopus 로고
    • Three new flavonoids, 30-methoxylupinifolin, laxifolin, and isolaxifolin from the roots of Derris laxiflora Benth
    • Lin, Y.L., Chen, Y.L., Kuo, Y.H., 1991. Three new flavonoids, 30-methoxylupinifolin, laxifolin, and isolaxifolin from the roots of Derris laxiflora Benth. Chem. Pharm. Bull. 39, 3132-3135.
    • (1991) Chem. Pharm. Bull. , vol.39 , pp. 3132-3135
    • Lin, Y.L.1    Chen, Y.L.2    Kuo, Y.H.3
  • 15
    • 33845952217 scopus 로고    scopus 로고
    • Trapping reactions of reactive carbonyl species with tea polyphenols in simulated physiological conditions
    • DOI 10.1002/mnfr.200600094
    • Lo, C.Y., Li, S., Tan, D., Pan, M.H., Sang, S., Ho, C.T., 2006. Trapping reactions of reactive carbonyl species with tea polyphenols in simulated physiological conditions. Mol. Nutr. Food Res. 50, 1118-1128. (Pubitemid 46032200)
    • (2006) Molecular Nutrition and Food Research , vol.50 , Issue.12 , pp. 1118-1128
    • Lo, C.-Y.1    Li, S.2    Tan, D.3    Pan, M.-H.4    Sang, S.5    Ho, C.-T.6
  • 16
    • 48749087940 scopus 로고    scopus 로고
    • Isoflavones and their derivatives from the root of Derris elliptica (Roxb.) Benth
    • Lu, H.Y., Liang, J.Y., Yu, P., Qu, W., 2008. Isoflavones and their derivatives from the root of Derris elliptica (Roxb.) Benth. Chin. J. Nat. Med. 6, 265-267.
    • (2008) Chin. J. Nat. Med. , vol.6 , pp. 265-267
    • Lu, H.Y.1    Liang, J.Y.2    Yu, P.3    Qu, W.4
  • 18
    • 2142753011 scopus 로고    scopus 로고
    • A benzil and isoflavone derivatives from Derris scandens Benth
    • DOI 10.1016/j.phytochem.2004.03.006, PII S0031942204001050
    • Mahabusarakam, W., Deachathai, S., Phongpaichit, S., Jansakul, C., Taylor, W.C., 2004. A benzil and isoflavone derivatives from Derris scandens Benth. Phytochemistry 65, 1185-1191. (Pubitemid 38542758)
    • (2004) Phytochemistry , vol.65 , Issue.8 , pp. 1185-1191
    • Mahabusarakam, W.1    Deachathai, S.2    Phongpaichit, S.3    Jansakul, C.4    Taylor, W.C.5
  • 20
    • 0344851580 scopus 로고    scopus 로고
    • Structural requirements of flavonoids for inhibition of protein glycation and radical scavenging activities
    • DOI 10.1016/j.bmc.2003.09.045
    • Matsuda, H., Wang, T., Managi, H., Yoshikawa, M., 2003. Structural requirements of flavonoids for inhibition of protein glycation and radical scavenging activities. Bioorg. Med. Chem. 11, 5317-5323. (Pubitemid 37464658)
    • (2003) Bioorganic and Medicinal Chemistry , vol.11 , Issue.24 , pp. 5317-5323
    • Matsuda, H.1    Wang, T.2    Managi, H.3    Yoshikawa, M.4
  • 21
    • 0347694634 scopus 로고    scopus 로고
    • Antimutagenic activity of phenylpropanoids from clove (Syzygium aromaticum)
    • Miyazawa, M., Hisama, M., 2003. Antimutagenic activity of phenylpropanoids from clove (Syzygium aromaticum). J. Agric. Food Chem. 51, 6413-6422.
    • (2003) J. Agric. Food Chem. , vol.51 , pp. 6413-6422
    • Miyazawa, M.1    Hisama, M.2
  • 22
    • 84857239177 scopus 로고    scopus 로고
    • Preparative isolation, Fast Centrifugal Partition Chromatography purification and biological activity of cajaflavanone from Derris ferruginea stems
    • Morel, S., Landreau, A., Nguyen, V.H., Debre, S., Grellier, P., Pape, P.L., Pagniez, F., Litaudon, M., 2012. Preparative isolation, Fast Centrifugal Partition Chromatography purification and biological activity of cajaflavanone from Derris ferruginea stems. Phytochem. Anal. 23, 152-158.
    • (2012) Phytochem. Anal. , vol.23 , pp. 152-158
    • Morel, S.1    Landreau, A.2    Nguyen, V.H.3    Debre, S.4    Grellier, P.5    Pape, P.L.6    Pagniez, F.7    Litaudon, M.8
  • 26
    • 41849141611 scopus 로고    scopus 로고
    • Cinnamon bark proanthocyanidins as reactive carbonyl scavengers to prevent the formation of advanced glycation endproducts
    • DOI 10.1021/jf073065v
    • Peng, X., Cheng, K.W., Ma, J., Chen, B., Ho, C.T., Lo, C., Chen, F., Wang, M., 2008. Cinnamon bark proanthocyanidins as reactive carbonyl scavengers to prevent the formation of advanced glycation endproducts. J. Agric. Food Chem. 56, 1907-1911. (Pubitemid 351497845)
    • (2008) Journal of Agricultural and Food Chemistry , vol.56 , Issue.6 , pp. 1907-1911
    • Peng, X.1    Cheng, K.-W.2    Ma, J.3    Chen, B.4    Ho, C.-T.5    Lo, C.6    Chen, F.7    Wang, M.8
  • 27
    • 84862833280 scopus 로고    scopus 로고
    • Naturally occurring inhibitors against the formation of advanced glycation end-products
    • Peng, X., Ma, J.Y., Chen, F., Wang, M.F., 2011. Naturally occurring inhibitors against the formation of advanced glycation end-products. Food Funct. 2, 289-301.
    • (2011) Food Funct. , vol.2 , pp. 289-301
    • Peng, X.1    Ma, J.Y.2    Chen, F.3    Wang, M.F.4
  • 28
    • 36849081336 scopus 로고    scopus 로고
    • Antimicrobial phenolic derivatives from Dendranthema zawadskii var latilobum Kitamura (Asteraceae)
    • Rahman, A.A., Moon, S.S., 2007. Antimicrobial phenolic derivatives from Dendranthema zawadskii var. latilobum Kitamura (Asteraceae). Arch. Pharm. Res. 30, 1374-1379.
    • (2007) Arch. Pharm. Res. , vol.30 , pp. 1374-1379
    • Rahman, A.A.1    Moon, S.S.2
  • 29
    • 77951509228 scopus 로고
    • Chemical examination of plant insecticides Part I. Chemical components of Derris ferruginea
    • Rao, N.V.S., Seshadri, T.R., 1946. Chemical examination of plant insecticides. Part I. Chemical components of Derris ferruginea. Proc. Indian Nat. Sci. Acad. 24, 344-348.
    • (1946) Proc. Indian Nat. Sci. Acad. , vol.24 , pp. 344-348
    • Rao, N.V.S.1    Seshadri, T.R.2
  • 30
    • 67650097230 scopus 로고    scopus 로고
    • New furanoflavonoids, intestinal alpha-glucosidase inhibitory and free-radical (DPPH) scavenging, activity from antihyperglycemic root extract of Derris indica (Lam.)
    • Rao, R.R., Tiwari, A.K., Reddy, P.P., Babu, K.S., Ali, A.Z., Madhusudana, K., 2009. New furanoflavonoids, intestinal alpha-glucosidase inhibitory and free-radical (DPPH) scavenging, activity from antihyperglycemic root extract of Derris indica (Lam.). Bioorg. Med. Chem. 17, 5170-5175.
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 5170-5175
    • Rao, R.R.1    Tiwari, A.K.2    Reddy, P.P.3    Babu, K.S.4    Ali, A.Z.5    Madhusudana, K.6
  • 32
    • 33745190013 scopus 로고    scopus 로고
    • Inhibitors of the Maillard reaction and AGE breakers as therapeutics for multiple diseases
    • Reddy, V.P., Beyaz, A., 2006. Inhibitors of the Maillard reaction and AGE breakers as therapeutics for multiple diseases. Drug Discov. Today 11, 646-653.
    • (2006) Drug Discov. Today , vol.11 , pp. 646-653
    • Reddy, V.P.1    Beyaz, A.2
  • 33
    • 62149135335 scopus 로고    scopus 로고
    • N-Terminal 2,3-diaminopropionic acid (Dap) peptides as efficient methylglyoxal scavengers to inhibit advanced glycation endproduct (AGE) formation
    • Sasaki, N.A., Garcia-Alvarez, M.C., Wang, Q., Ermolenko, L., Franck, G., Nhiri, N., Martin, M.T., Audic, N., Potier, P., 2009. N-Terminal 2,3-diaminopropionic acid (Dap) peptides as efficient methylglyoxal scavengers to inhibit advanced glycation endproduct (AGE) formation. Bioorg. Med. Chem. 17, 2310-2320.
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 2310-2320
    • Sasaki, N.A.1    Garcia-Alvarez, M.C.2    Wang, Q.3    Ermolenko, L.4    Franck, G.5    Nhiri, N.6    Martin, M.T.7    Audic, N.8    Potier, P.9
  • 35
    • 55949128773 scopus 로고    scopus 로고
    • Apple polyphenols, phloretin and phloridzin: New trapping agents of reactive dicarbonyl species
    • Shao, X., Bai, N., He, K., Ho, C.T., Yang, C.S., Sang, S., 2008. Apple polyphenols, phloretin and phloridzin: new trapping agents of reactive dicarbonyl species. Chem. Res. Toxicol. 21, 2042-2050.
    • (2008) Chem. Res. Toxicol. , vol.21 , pp. 2042-2050
    • Shao, X.1    Bai, N.2    He, K.3    Ho, C.T.4    Yang, C.S.5    Sang, S.6
  • 36
    • 27144452601 scopus 로고    scopus 로고
    • Neuroprotective flavonoids from Flemingia macrophylla
    • Shiao, Y.J., Wang, C.N., Wang, W.Y., Lin, Y.L., 2005. Neuroprotective flavonoids from Flemingia macrophylla. Planta Med. 71, 835-840.
    • (2005) Planta Med. , vol.71 , pp. 835-840
    • Shiao, Y.J.1    Wang, C.N.2    Wang, W.Y.3    Lin, Y.L.4
  • 39
    • 85008107800 scopus 로고
    • Stereochemical studies on dihydrofuranoisoflavones
    • Tahara, S., Ingham, J.L., Mizutani, J., 1987. Stereochemical studies on dihydrofuranoisoflavones. Agric. Biol. Chem. 51, 211-216.
    • (1987) Agric. Biol. Chem. , vol.51 , pp. 211-216
    • Tahara, S.1    Ingham, J.L.2    Mizutani, J.3
  • 40
    • 70350218974 scopus 로고    scopus 로고
    • An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III
    • The Angiosperm Phylogeny Group
    • The Angiosperm Phylogeny Group, 2009. An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III. Bot. J. Linn. Soc. 161, 105-121.
    • (2009) Bot. J. Linn. Soc. , vol.161 , pp. 105-121
  • 41
    • 0037331582 scopus 로고    scopus 로고
    • Six isoflavones and a 5- deoxyflavonol glycoside from the leaves of Ateleia herbert-smithii
    • Veitch, N.C., Sutton, P.S.E., Kite, G.C., Ireland, H.E., 2003. Six isoflavones and a 5- deoxyflavonol glycoside from the leaves of Ateleia herbert-smithii. J. Nat. Prod. 66, 2003.
    • (2003) J. Nat. Prod. , vol.66 , pp. 2003
    • Veitch, N.C.1    Sutton, P.S.E.2    Kite, G.C.3    Ireland, H.E.4
  • 42
    • 17144387858 scopus 로고    scopus 로고
    • Inhibitory effect of naturally occurring flavonoids on the formation of advanced glycation endproducts
    • Wu, C.H., Yen, G.C., 2005. Inhibitory effect of naturally occurring flavonoids on the formation of advanced glycation endproducts. J. Agric. Food Chem. 53, 3167-3173.
    • (2005) J. Agric. Food Chem. , vol.53 , pp. 3167-3173
    • Wu, C.H.1    Yen, G.C.2
  • 44
    • 67449158736 scopus 로고    scopus 로고
    • Ethnobotanical study on medicinal plants around Mt. Yinggeling, Hainan Island, China
    • Zheng, X.L., Wing, F.W., 2009. Ethnobotanical study on medicinal plants around Mt. Yinggeling, Hainan Island, China. J. Ethnopharmacol. 124, 197-210.
    • (2009) J. Ethnopharmacol. , vol.124 , pp. 197-210
    • Zheng, X.L.1    Wing, F.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.