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Volumn 58, Issue 1, 2010, Pages 202-208

Polyphenols from Broussonetia papyrifera displaying potent α-glucosidase inhibition

Author keywords

glucosidase inhibitor; Broussonetia papyrifera; Flavonoid; Glycosidase

Indexed keywords

ALPHA GLUCOSIDASE; ENZYME INHIBITOR; FLAVONOID; PHENOL DERIVATIVE; PLANT EXTRACT; POLYPHENOLS;

EID: 75249105176     PISSN: 00218561     EISSN: None     Source Type: Journal    
DOI: 10.1021/jf903068k     Document Type: Article
Times cited : (114)

References (27)
  • 1
    • 0034786626 scopus 로고    scopus 로고
    • Five new diprenylated flavonols from the leaves of Broussonetia kazinoki
    • Zhang, P. C.; Wang, S.; Wu, Y.; Chen, R. Y.; Yu, D. Q. Five new diprenylated flavonols from the leaves of Broussonetia kazinoki. J. Nat. Prod. 2001, 64, 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
  • 3
    • 0031659349 scopus 로고    scopus 로고
    • The signal transduction mechanism involved in kazinol B-stimulated superoxide anion generation in rat neutrophils
    • Wang, J. P.; Tsao, L. T.; Raung, S. L.; Lin, C. N. The signal transduction mechanism involved in kazinol B-stimulated superoxide anion generation in rat neutrophils. Br. J. Pharmacol. 1998, 125, 517-525.
    • (1998) Br. J. Pharmacol. , vol.125 , pp. 517-525
    • Wang, J.P.1    Tsao, L.T.2    Raung, S.L.3    Lin, C.N.4
  • 4
    • 0035871960 scopus 로고    scopus 로고
    • Broussochalcone A, a potent antioxidant and effective suppressor of inducible nitric oxide synthase in lipopolysaccharide-activated macrophages
    • Chen, Z. J.; Lin, C. N.; Hwang, T. L.; Teng, C. M. Broussochalcone A, a potent antioxidant and effective suppressor of inducible nitric oxide synthase in lipopolysaccharide-activated macrophages. BioChem. Pharmacol. 2001, 61, 939-946.
    • (2001) BioChem. Pharmacol. , vol.61 , pp. 939-946
    • Chen, Z.J.1    Lin, C.N.2    Hwang, T.L.3    Teng, C.M.4
  • 6
    • 34548255352 scopus 로고    scopus 로고
    • Tyrosinase inhibitors from paper mulberry (Boussonetia papyrifera)
    • Zheng, Z. P.; Cheng, K. W.; Chao, J.; Wu, J.; Wang, M. Tyrosinase inhibitors from paper mulberry (Boussonetia papyrifera). Food Chem. 2008, 106, 529-535.
    • (2008) Food Chem , vol.106 , pp. 529-535
    • Zheng, Z.P.1    Cheng, K.W.2    Chao, J.3    Wu, J.4    Wang, M.5
  • 7
    • 11844294865 scopus 로고    scopus 로고
    • α-Glucosidase inhibitors for patients with type 2 diabetes: Results from a cochrane systematic review and meta-analysis
    • Floris, A. L.; Peter, L. L.; Reinier, P. A.; Eloy, H. L.; Guy, E. R.; Chris, W. α-Glucosidase inhibitors for patients with type 2 diabetes: results from a cochrane systematic review and meta-analysis. Diabetas Care 2005, 28,154-163.
    • (2005) Diabetas Care , vol.28 , pp. 154-163
    • Floris, A.L.1    Peter, L.L.2    Reinier, P.A.3    Eloy, H.L.4    Guy, E.R.5    Chris, W.6
  • 8
    • 0026014062 scopus 로고
    • β1-6 branched oligosaccharides as a marker of tumor progression in human breast and colon neoplasia
    • Fernandes, B.; Sagman, U.; Auger, M.; Demetrio, M.; Dennis, J. W. β1-6 branched oligosaccharides as a marker of tumor progression in human breast and colon neoplasia. Cancer Res. 1991, 51, 718-723.
    • (1991) Cancer Res. , vol.51 , pp. 718-723
    • Fernandes, B.1    Sagman, U.2    Auger, M.3    Demetrio, M.4    Dennis, J.W.5
  • 9
    • 0035112246 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of α-L-fucosidase inhibitors: 5a-carba-α-L-fucopyranosylamine and related compounds
    • (9) Seiichiro, O.; Ayako, M.; Takashi, O.; Hideya, Y.; Hironobu, H. Synthesis and biological evaluation of α-L-fucosidase inhibitors: 5acarba-α-L-fucopyranosylamine and related compounds. Eur. J. Org. Chem. 2001, 5, 967-974. (Pubitemid 32194739)
    • (2001) European Journal of Organic Chemistry , Issue.5 , pp. 967-974
    • Ogawa, S.1    Maruyama, A.2    Odagiri, T.3    Yuasa, H.4    Hashimoto, H.5
  • 10
    • 33745048293 scopus 로고    scopus 로고
    • Structure of the Sulfolobus solfataricus α-Glucosidase: Implications for Domain Conservation and Substrate Recognition in GH31
    • DOI 10.1016/j.jmb.2006.02.056, PII S0022283606002555
    • (10) Ernst, H. A.; Leggio, L. L.; Willemoes, M.; Leonard, G.; Blum, P.; Larsen, S. Structure of the Sulfolobus solfataricus alpha-glucosidase: implications for domain conservation and substrate recognition in GH31. J. Miol. Biol. 2006, 358, 1106-1124. (Pubitemid 44403821)
    • (2006) Journal of Molecular Biology , vol.358 , Issue.4 , pp. 1106-1124
    • Ernst, H.A.1    Lo Leggio, L.2    Willemoes, M.3    Leonard, G.4    Blum, P.5    Larsen, S.6
  • 11
    • 0037336295 scopus 로고    scopus 로고
    • Quality control in the endoplasmic reticulum
    • DOI 10.1038/nrm1052
    • (11) Ellgaard, L.; Helenius, A. Quality control in the endoplasmic reticulum. Nat. Rev. Mol. Cell Biol. 2003, 4, 181-191. (Pubitemid 36288040)
    • (2003) Nature Reviews Molecular Cell Biology , vol.4 , Issue.3 , pp. 181-191
    • Ellgaard, L.1    Helenius, A.2
  • 12
    • 0242287992 scopus 로고    scopus 로고
    • Glycosidase inhibitors: Update and perspectives on practical use
    • Asano, N. Glycosidase inhibitors: update and perspectives on practical use. Glycobiology 2003, 13, 93R-104R.
    • (2003) Glycobiology , vol.13
    • Asano, N.1
  • 14
    • 0028874529 scopus 로고
    • Glycosylation inhibitors in biology and medicine
    • Jacob, G. S. Glycosylation inhibitors in biology and medicine. Curr. Opin. Struct. Biol. 1995, 5, 605-611.
    • (1995) Curr. Opin. Struct. Biol. , vol.5 , pp. 605-611
    • Jacob, G.S.1
  • 15
    • 0001249488 scopus 로고
    • Compounds of Broussonetia papyrifera (L.)
    • Vent. 2. Structure of two new isoprenylated flavans, kazinols A and B
    • Ikut, J.; Hano, Y.; Nomura, T. Compounds of Broussonetia papyrifera (L.) Vent. 2. Structure of two new isoprenylated flavans, kazinols A and B. Heterocycles 1.985, 23, 2835-2842.
    • (1985) Heterocycles , vol.23 , pp. 2835-2842
    • Ikut, J.1    Hano, Y.2    Nomura, T.3
  • 16
    • 0022398938 scopus 로고
    • Components of Broussonetia papyrifera (L.)
    • Vent. I. Structures of two new isoprenylated flavonols and two chalcone derivatives
    • Matsumoto, J.; Fujimoto, T.; Takino, C.; Saitoh, M.; Hano, Y.; Fukai, T.; Nomura, T. Components of Broussonetia papyrifera (L.) Vent. I. Structures of two new isoprenylated flavonols and two chalcone derivatives. Chem. Pharm. Bull. 1985, 33, 3250-3256.
    • (1985) Chem. Pharm. Bull. , vol.33 , pp. 3250-3256
    • Matsumoto, J.1    Fujimoto, T.2    Takino, C.3    Saitoh, M.4    Hano, Y.5    Fukai, T.6    Nomura, T.7
  • 17
    • 0022500292 scopus 로고
    • Components of Broussonetia kazinoki SIEB. I. Structure of two new isoprenylated flavans and five new isoprenylated 1, 3-diphenylpropane derivatives
    • Ikauta, J.; Hano, Y.; Nomura, T.; Kawakami, Y.; Sato, T. Components of Broussonetia kazinoki SIEB. I. Structure of two new isoprenylated flavans and five new isoprenylated 1, 3-diphenylpropane derivatives. Chem. Pharm. Bull. 1986, 34, 1968-1979.
    • (1986) Chem. Pharm. Bull. , vol.34 , pp. 1968-1979
    • Ikauta, J.1    Hano, Y.2    Nomura, T.3    Kawakami, Y.4    Sato, T.5
  • 19
    • 0030774049 scopus 로고    scopus 로고
    • Bioactive constituents of Morus australis and Broussonetia papyrifera
    • Ko, H. H.; Yu, S. M.; Ko, F. N.; Teng, C. M.; Lin, C. N. Bioactive constituents of Morus australis and Broussonetia papyrifera. J. Nat. Prod. 1997, 60, 1008-1011.
    • (1997) J. Nat. Prod. , vol.60 , pp. 1008-1011
    • Ko, H.H.1    Yu, S.M.2    Ko, F.N.3    Teng, C.M.4    Lin, C.N.5
  • 21
    • 0001172735 scopus 로고
    • The flavonoids of Millettia ferruginea subsp. ferruginea and subsp. darassana in Ethiopia
    • Dagne, E.; Bekele, A.; Waterman, P. G. The flavonoids of Millettia ferruginea subsp. ferruginea and subsp. darassana in Ethiopia. Phytochemistry 1989, 28, 1897-1900.
    • (1989) Phytochemistry , vol.28 , pp. 1897-1900
    • Dagne, E.1    Bekele, A.2    Waterman, P.G.3
  • 26
    • 2442532852 scopus 로고    scopus 로고
    • Synthesis of a novel photoaffinity derivative of 1-deoxynojirimycin for active site-directed labeling of glucosidase i
    • Romaniouk, A. V.; Silva, A.; Feng, J.; Vijay, I. K. Synthesis of a novel photoaffinity derivative of 1-deoxynojirimycin for active site-directed labeling of glucosidase I. Glycobiology 2004, 14, 301-310.
    • (2004) Glycobiology , vol.14 , pp. 301-310
    • Romaniouk, A.V.1    Silva, A.2    Feng, J.3    Vijay, I.K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.