메뉴 건너뛰기




Volumn 53, Issue 2, 2013, Pages 492-498

Evaluation of α-glucosidase inhibition potential of some flavonoids fromEpimedium brevicornum

Author keywords

Diabetes; Epimedium; Amylase inhibitors; Glucosidase inhibitors

Indexed keywords

ENZYME INHIBITION; FLAVONOIDS;

EID: 84878108745     PISSN: 00236438     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.lwt.2013.04.002     Document Type: Article
Times cited : (114)

References (40)
  • 1
  • 2
    • 77954667571 scopus 로고    scopus 로고
    • Antidiabetic medicinal plants as a source of alpha glucosidase inhibitors
    • Benalla W., Bellahcen S., Bnouham M. Antidiabetic medicinal plants as a source of alpha glucosidase inhibitors. Current Diabetes Reviews 2010, 6:247-254.
    • (2010) Current Diabetes Reviews , vol.6 , pp. 247-254
    • Benalla, W.1    Bellahcen, S.2    Bnouham, M.3
  • 3
    • 34548224240 scopus 로고    scopus 로고
    • α-Glucosidase and α-amylase inhibitory activities of Nepalese medicinal herb Pakhanbhed (Bergenia ciliata, Haw.)
    • Bhandari M.J., Jong-Anurakkun N., Hong G., Kawabata J. α-Glucosidase and α-amylase inhibitory activities of Nepalese medicinal herb Pakhanbhed (Bergenia ciliata, Haw.). Food Chemistry 2008, 106:247-252.
    • (2008) Food Chemistry , vol.106 , pp. 247-252
    • Bhandari, M.J.1    Jong-Anurakkun, N.2    Hong, G.3    Kawabata, J.4
  • 4
    • 0029609776 scopus 로고
    • The mechanism of alpha glucosidase inhibition in the management of diabetes
    • Bischoff H. The mechanism of alpha glucosidase inhibition in the management of diabetes. Clinical and Investigative Medicine 1995, 18:303-311.
    • (1995) Clinical and Investigative Medicine , vol.18 , pp. 303-311
    • Bischoff, H.1
  • 5
    • 33748708627 scopus 로고    scopus 로고
    • α- and β-Glucosidase inhibitors: chemical structure and biological activity
    • Borges de Melo E., da Silveira Gomes A., Carvalho I. α- and β-Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron 2006, 62(44):10277-10302.
    • (2006) Tetrahedron , vol.62 , Issue.44 , pp. 10277-10302
    • Borges de Melo, E.1    da Silveira Gomes, A.2    Carvalho, I.3
  • 6
    • 0037314783 scopus 로고    scopus 로고
    • An intuitive look at the relationship of Ki and IC50: a more general use for the Dixon plot
    • Burlingham B.T., Widlanski T.S. An intuitive look at the relationship of Ki and IC50: a more general use for the Dixon plot. Journal of Chemical Education 2003, 80:214-218.
    • (2003) Journal of Chemical Education , vol.80 , pp. 214-218
    • Burlingham, B.T.1    Widlanski, T.S.2
  • 7
    • 37749032775 scopus 로고    scopus 로고
    • Arapid method for simultaneous determination of 15 flavonoids in Epimedium using pressurized liquid extraction and ultra-performance liquid chromatography
    • Chen X.J., Ji H., Zhang Q.W., Tu P.F., Wang Y.T., Guo B.L., et al. Arapid method for simultaneous determination of 15 flavonoids in Epimedium using pressurized liquid extraction and ultra-performance liquid chromatography. Journal of Pharmaceutical and Biomedical Analysis 2008, 46:226-235.
    • (2008) Journal of Pharmaceutical and Biomedical Analysis , vol.46 , pp. 226-235
    • Chen, X.J.1    Ji, H.2    Zhang, Q.W.3    Tu, P.F.4    Wang, Y.T.5    Guo, B.L.6
  • 8
    • 77956628381 scopus 로고    scopus 로고
    • Yeast alpha-glucosidase inhibition by isoflavones from plants of Leguminosae as an invitro alternative to acarbose
    • Choi C.W., Choi Y.H., Cha M.R., Yoo D.S., Kim Y.S., Yon G.H., et al. Yeast alpha-glucosidase inhibition by isoflavones from plants of Leguminosae as an invitro alternative to acarbose. Journal of Agricultural and Food Chemistry 2010, 58(18):9988-9993.
    • (2010) Journal of Agricultural and Food Chemistry , vol.58 , Issue.18 , pp. 9988-9993
    • Choi, C.W.1    Choi, Y.H.2    Cha, M.R.3    Yoo, D.S.4    Kim, Y.S.5    Yon, G.H.6
  • 9
    • 7044235743 scopus 로고    scopus 로고
    • Importance of the B ring and its substitution on the α-glucosidase inhibitory activity of baicalein, 5,6,7-trihydroxyflavone
    • Gao H., Kawabata J. Importance of the B ring and its substitution on the α-glucosidase inhibitory activity of baicalein, 5,6,7-trihydroxyflavone. Bioscience, Biotechnology, and Biochemistry 2004, 68(9):1858-1864.
    • (2004) Bioscience, Biotechnology, and Biochemistry , vol.68 , Issue.9 , pp. 1858-1864
    • Gao, H.1    Kawabata, J.2
  • 10
    • 7044235743 scopus 로고    scopus 로고
    • Structure-activity relationship for α-glucosidase inhibition of baicalein, 5,6,7-trihydroxyflavone: the effect of A-ring substitution
    • Gao H., Nishioka T., Kawabata J., Kasai T. Structure-activity relationship for α-glucosidase inhibition of baicalein, 5,6,7-trihydroxyflavone: the effect of A-ring substitution. Bioscience, Biotechnology, and Biochemistry 2004, 68(2):1858-1864.
    • (2004) Bioscience, Biotechnology, and Biochemistry , vol.68 , Issue.2 , pp. 1858-1864
    • Gao, H.1    Nishioka, T.2    Kawabata, J.3    Kasai, T.4
  • 11
    • 0031740355 scopus 로고    scopus 로고
    • The evolving role of alpha-glucosidase inhibitors
    • Goke B., Herrmann-Rinke C. The evolving role of alpha-glucosidase inhibitors. Diabetes Metabolic Reviews 1998, 14(Suppl. 1):S31-S38.
    • (1998) Diabetes Metabolic Reviews , vol.14 , Issue.SUPPL. 1
    • Goke, B.1    Herrmann-Rinke, C.2
  • 15
    • 0842287572 scopus 로고    scopus 로고
    • Anovel alpha-glucosidase inhibitor from pine bark
    • Kim Y.M., Wang M.H., Rhee H.I. Anovel alpha-glucosidase inhibitor from pine bark. Carbohydrate Research 2004, 339(3):715-717.
    • (2004) Carbohydrate Research , vol.339 , Issue.3 , pp. 715-717
    • Kim, Y.M.1    Wang, M.H.2    Rhee, H.I.3
  • 16
    • 20444484201 scopus 로고    scopus 로고
    • Determination of epimedin C in rat plasma by reversed-phase high-performance chromatography after oral administration of Herba Epimedii extract
    • Li Y., Xiong Z., Li F. Determination of epimedin C in rat plasma by reversed-phase high-performance chromatography after oral administration of Herba Epimedii extract. Journal of Chromatography B 2005, 821(2):235-239.
    • (2005) Journal of Chromatography B , vol.821 , Issue.2 , pp. 235-239
    • Li, Y.1    Xiong, Z.2    Li, F.3
  • 17
    • 1942424088 scopus 로고    scopus 로고
    • Natural medicines used in the traditional Chinese medical system for therapy of diabetes mellitus
    • Li W.L., Zheng H.C., Bukuru J., De Kimpe N. Natural medicines used in the traditional Chinese medical system for therapy of diabetes mellitus. Journal of Ethnopharmacology 2004, 92:1-21.
    • (2004) Journal of Ethnopharmacology , vol.92 , pp. 1-21
    • Li, W.L.1    Zheng, H.C.2    Bukuru, J.3    De Kimpe, N.4
  • 18
    • 73349100639 scopus 로고    scopus 로고
    • Comparative evaluation of quercetin, isoquercetin and rutin as inhibitors of α-glucosidase
    • Li Y.Q., Zhou F.C., Gao F., Bian J.S., Shan F. Comparative evaluation of quercetin, isoquercetin and rutin as inhibitors of α-glucosidase. Journal of Agricutural and Food Chemistry 2009, 57:11463-11468.
    • (2009) Journal of Agricutural and Food Chemistry , vol.57 , pp. 11463-11468
    • Li, Y.Q.1    Zhou, F.C.2    Gao, F.3    Bian, J.S.4    Shan, F.5
  • 19
    • 12344310430 scopus 로고    scopus 로고
    • Preparative isolation and purification of three flavonoids from the Chinese medicinal plant Epimedium koreamum Nakai by high-speed counter-current chromatography
    • Liu R., Li A., Sun A., Cui J., Kong L. Preparative isolation and purification of three flavonoids from the Chinese medicinal plant Epimedium koreamum Nakai by high-speed counter-current chromatography. Journal of Chromatography A 2005, 1064:53-57.
    • (2005) Journal of Chromatography A , vol.1064 , pp. 53-57
    • Liu, R.1    Li, A.2    Sun, A.3    Cui, J.4    Kong, L.5
  • 20
    • 45749116594 scopus 로고    scopus 로고
    • Flavonoids for controlling starch digestion: structural requirements for inhibiting human α-amylase
    • Lo Piparo E., Scheib H., Frei N., Williamson G., Grigorov M., Chou C. Flavonoids for controlling starch digestion: structural requirements for inhibiting human α-amylase. Journal of Medicinal Chemistry 2008, 51(12):3555-3561.
    • (2008) Journal of Medicinal Chemistry , vol.51 , Issue.12 , pp. 3555-3561
    • Lo Piparo, E.1    Scheib, H.2    Frei, N.3    Williamson, G.4    Grigorov, M.5    Chou, C.6
  • 21
    • 79954416089 scopus 로고    scopus 로고
    • The genus Epimedium: an ethnopharmacological and phytochemical review
    • Ma H., He X., Yang Y., Li M., Hao D., Jia Z. The genus Epimedium: an ethnopharmacological and phytochemical review. Journal of Ethnopharmacology 2011, 134:519-541.
    • (2011) Journal of Ethnopharmacology , vol.134 , pp. 519-541
    • Ma, H.1    He, X.2    Yang, Y.3    Li, M.4    Hao, D.5    Jia, Z.6
  • 23
    • 77949655880 scopus 로고    scopus 로고
    • Glucosidase inhibitory phenolic compounds from the seed of Psoralea corylifolia
    • Oh K.Y., Lee J.H., Curtis-Long M.J., Cho J.C., Kim J.Y., Lee W.S., et al. Glucosidase inhibitory phenolic compounds from the seed of Psoralea corylifolia. Food Chemistry 2010, 121:940-943.
    • (2010) Food Chemistry , vol.121 , pp. 940-943
    • Oh, K.Y.1    Lee, J.H.2    Curtis-Long, M.J.3    Cho, J.C.4    Kim, J.Y.5    Lee, W.S.6
  • 25
    • 0031657687 scopus 로고    scopus 로고
    • Potential of alpha-glucosidase inhibitors in elderly patients with diabetes mellitus and impaired glucose tolerance
    • Rabasa-Lhoret R., Chiasson L. Potential of alpha-glucosidase inhibitors in elderly patients with diabetes mellitus and impaired glucose tolerance. Drugs and Aging 1998, 13(2):131-143.
    • (1998) Drugs and Aging , vol.13 , Issue.2 , pp. 131-143
    • Rabasa-Lhoret, R.1    Chiasson, L.2
  • 27
    • 34247472210 scopus 로고    scopus 로고
    • Taxonomic, genetic, chemical and estrogenic characteristics of Epimedium species
    • Shen P., Guo B.L., Gong Y., Hong D.Y.Q., Hong Y., Yong E.L. Taxonomic, genetic, chemical and estrogenic characteristics of Epimedium species. Phytochemistry 2007, 68(10):1448-1458.
    • (2007) Phytochemistry , vol.68 , Issue.10 , pp. 1448-1458
    • Shen, P.1    Guo, B.L.2    Gong, Y.3    Hong, D.Y.Q.4    Hong, Y.5    Yong, E.L.6
  • 29
    • 78649472934 scopus 로고    scopus 로고
    • Herba Epimedii: anti-oxidative properties and its medical implications
    • Sze S.C.W., Tong Y., Ng T.B., Cheng C.L.Y., Cheung H.P. Herba Epimedii: anti-oxidative properties and its medical implications. Molecules 2010, 15:7861-7870.
    • (2010) Molecules , vol.15 , pp. 7861-7870
    • Sze, S.C.W.1    Tong, Y.2    Ng, T.B.3    Cheng, C.L.Y.4    Cheung, H.P.5
  • 31
    • 77956629122 scopus 로고    scopus 로고
    • Natural products as α-amylase and α-glucosidase inhibitors and their hypoglycaemic potential in the treatment of diabetes: an update
    • Tundis R., Loizzo M.R., Menichini F. Natural products as α-amylase and α-glucosidase inhibitors and their hypoglycaemic potential in the treatment of diabetes: an update. Mini-Reviews in Medicinal Chemistry 2010, 10:315-331.
    • (2010) Mini-Reviews in Medicinal Chemistry , vol.10 , pp. 315-331
    • Tundis, R.1    Loizzo, M.R.2    Menichini, F.3
  • 32
    • 11844294865 scopus 로고    scopus 로고
    • Alpha-glucosidase inhibitors for patients with type 2 diabetes: results from a Cochrane systematic review and meta-analysis
    • Van de Laar F.A., Lucassen P.L., Akkermans R.P., Van de Lisdonk E.H., Rutten G.E., Van W. Alpha-glucosidase inhibitors for patients with type 2 diabetes: results from a Cochrane systematic review and meta-analysis. Diabetes Care 2005, 28:154-163.
    • (2005) Diabetes Care , vol.28 , pp. 154-163
    • Van de Laar, F.A.1    Lucassen, P.L.2    Akkermans, R.P.3    Van de Lisdonk, E.H.4    Rutten, G.E.5    Van, W.6
  • 33
    • 77952583265 scopus 로고    scopus 로고
    • α-Glucosidase and α-amylase inhibitory activities of guava leaves
    • Wang H., Du Y.-J., Song H.-C. α-Glucosidase and α-amylase inhibitory activities of guava leaves. Food Chemistry 2010, 123:6-13.
    • (2010) Food Chemistry , vol.123 , pp. 6-13
    • Wang, H.1    Du, Y.-J.2    Song, H.-C.3
  • 35
    • 77949293261 scopus 로고    scopus 로고
    • Alpha-glucosidase folding during urea denaturation: enzyme kinetics and computational prediction
    • Wu X.Q., Wang J., Lü Z.R., Tang H.M., Park D., Oh S.H., et al. Alpha-glucosidase folding during urea denaturation: enzyme kinetics and computational prediction. Applied Biochemistry and Biotechnology 2009, 160(5):1341-1355.
    • (2009) Applied Biochemistry and Biotechnology , vol.160 , Issue.5 , pp. 1341-1355
    • Wu, X.Q.1    Wang, J.2    Lü, Z.R.3    Tang, H.M.4    Park, D.5    Oh, S.H.6
  • 36
    • 77958483943 scopus 로고    scopus 로고
    • Inhibition kinetics of flavonoids on yeast α-glucosidase merged with docking simulations
    • Xu H. Inhibition kinetics of flavonoids on yeast α-glucosidase merged with docking simulations. Protein and Peptide Letters 2010, 17(10):1270-1279.
    • (2010) Protein and Peptide Letters , vol.17 , Issue.10 , pp. 1270-1279
    • Xu, H.1
  • 37
    • 80055060410 scopus 로고    scopus 로고
    • Adetermination of potential α-glucosidase inhibitors from azuki beans (Vigna angularis)
    • Yao Y., Chen X., W L., Wang W., Ren G. Adetermination of potential α-glucosidase inhibitors from azuki beans (Vigna angularis). International Journal of Molecular Sciences 2011, 12:6445-6451.
    • (2011) International Journal of Molecular Sciences , vol.12 , pp. 6445-6451
    • Yao, Y.1    Chen, X.2    Wang, W.3    Ren, G.4
  • 38
    • 0029785436 scopus 로고    scopus 로고
    • Areview of the safety and efficacy of acarbose in diabetes mellitus
    • Yee H., Fong N. Areview of the safety and efficacy of acarbose in diabetes mellitus. Pharmacotherapy 1996, 16:792-805.
    • (1996) Pharmacotherapy , vol.16 , pp. 792-805
    • Yee, H.1    Fong, N.2
  • 39
    • 78751580538 scopus 로고    scopus 로고
    • The most abundant polyphenol of soy leaves, coumestrol, displays potent α-glucosidase inhibitory activity
    • Yuk H.J., Lee J.H., Curtis-Long M.J., Lee J.W., Kim Y.S., Ryu H.W., et al. The most abundant polyphenol of soy leaves, coumestrol, displays potent α-glucosidase inhibitory activity. Food Chemistry 2011, 126:1057-1063.
    • (2011) Food Chemistry , vol.126 , pp. 1057-1063
    • Yuk, H.J.1    Lee, J.H.2    Curtis-Long, M.J.3    Lee, J.W.4    Kim, Y.S.5    Ryu, H.W.6
  • 40
    • 44249094229 scopus 로고    scopus 로고
    • Simultaneous extraction of epimedin A, B, C and icariin from Herba Epimedii by ultrasonic technique
    • Zhang H.-F., Yang T.-S., Li Z.-Z., Wang Y. Simultaneous extraction of epimedin A, B, C and icariin from Herba Epimedii by ultrasonic technique. Ultrasonics Sonochemistry 2008, 15:376-385.
    • (2008) Ultrasonics Sonochemistry , vol.15 , pp. 376-385
    • Zhang, H.-F.1    Yang, T.-S.2    Li, Z.-Z.3    Wang, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.