메뉴 건너뛰기




Volumn 171, Issue 3, 2008, Pages 355-362

Influence of chalcone analogues on serum glucose levels in hyperglycemic rats

Author keywords

Analogues; Chalcone; Hyperglycemia; Insulin; Tolbutamide

Indexed keywords

CHALCONE DERIVATIVE; GLUCOSE;

EID: 38549176079     PISSN: 00092797     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbi.2007.11.001     Document Type: Article
Times cited : (39)

References (34)
  • 1
    • 0029859045 scopus 로고    scopus 로고
    • Regulation of gene expression by insulin
    • O'Brien R.M., and Granner D.K. Regulation of gene expression by insulin. Physiol. Rev. 76 (1996) 1109-1161
    • (1996) Physiol. Rev. , vol.76 , pp. 1109-1161
    • O'Brien, R.M.1    Granner, D.K.2
  • 2
    • 33244486544 scopus 로고    scopus 로고
    • Diagnosis and classification of diabetes mellitus
    • American Diabetes Association
    • American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care 29 (2006) 43-48
    • (2006) Diabetes Care , vol.29 , pp. 43-48
  • 3
    • 25844441709 scopus 로고    scopus 로고
    • Type 1 Diabetes Genetics Consortium, Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families
    • Concannon P., Erlich H.A., Julier C., Morahan G., Nerup J., Pociot F., Todd J.A., and Rich S.S. Type 1 Diabetes Genetics Consortium, Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families. Diabetes 54 (2005) 2995-3001
    • (2005) Diabetes , vol.54 , pp. 2995-3001
    • Concannon, P.1    Erlich, H.A.2    Julier, C.3    Morahan, G.4    Nerup, J.5    Pociot, F.6    Todd, J.A.7    Rich, S.S.8
  • 4
    • 0037116638 scopus 로고    scopus 로고
    • Oral antihyperglycemic therapy for type 2 diabetes
    • Inzucchi S.E. Oral antihyperglycemic therapy for type 2 diabetes. JAMA 287 (2002) 360-372
    • (2002) JAMA , vol.287 , pp. 360-372
    • Inzucchi, S.E.1
  • 5
    • 0036701596 scopus 로고    scopus 로고
    • Novel insulins: expanding options in diabetes management
    • Gerich J.E. Novel insulins: expanding options in diabetes management. Am. J. Med. 113 (2002) 308-316
    • (2002) Am. J. Med. , vol.113 , pp. 308-316
    • Gerich, J.E.1
  • 7
    • 9444259786 scopus 로고    scopus 로고
    • Pathways in β-cell stimulus-secretion coupling as targets for therapeutic insulin secretagogues
    • Henquin J.C. Pathways in β-cell stimulus-secretion coupling as targets for therapeutic insulin secretagogues. Diabetes 53 (2004) 48-58
    • (2004) Diabetes , vol.53 , pp. 48-58
    • Henquin, J.C.1
  • 8
    • 0026670081 scopus 로고
    • The fiftieth anniversary of hypoglycaemic sulphonamides: how did the mother compound work?
    • Henquin J.C. The fiftieth anniversary of hypoglycaemic sulphonamides: how did the mother compound work?. Diabetologia 35 (1992) 907-912
    • (1992) Diabetologia , vol.35 , pp. 907-912
    • Henquin, J.C.1
  • 9
    • 25844500308 scopus 로고    scopus 로고
    • Synthesis and evaluation of antiplatelet activity of trihydroxychalcone derivatives
    • Zhao L.M., Jin H.S., Sun L.P., Piao H.R., and Quan Z.S. Synthesis and evaluation of antiplatelet activity of trihydroxychalcone derivatives. Bioorg. Med. Chem. Lett. 15 (2005) 5027-5029
    • (2005) Bioorg. Med. Chem. Lett. , vol.15 , pp. 5027-5029
    • Zhao, L.M.1    Jin, H.S.2    Sun, L.P.3    Piao, H.R.4    Quan, Z.S.5
  • 11
    • 33749609344 scopus 로고    scopus 로고
    • Effects of a-substitutions on structure and biological activity of anticancer chalcones
    • Lawrence N.J., Patterson R.P., Ooi L., Cookc D., and Ducki S. Effects of a-substitutions on structure and biological activity of anticancer chalcones. Bioorg. Med. Chem. Lett. 16 (2006) 5844-5848
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 5844-5848
    • Lawrence, N.J.1    Patterson, R.P.2    Ooi, L.3    Cookc, D.4    Ducki, S.5
  • 12
    • 33645218036 scopus 로고    scopus 로고
    • Chalcone inhibits the proliferation of human breast cancer cell by blocking cell cycle progression and inducing apoptosis
    • Hsu Y.L., Kuo P.L., Tzeng W.S., and Lin C.C. Chalcone inhibits the proliferation of human breast cancer cell by blocking cell cycle progression and inducing apoptosis. Food Chem. Toxicol. 44 (2006) 704-713
    • (2006) Food Chem. Toxicol. , vol.44 , pp. 704-713
    • Hsu, Y.L.1    Kuo, P.L.2    Tzeng, W.S.3    Lin, C.C.4
  • 16
    • 0042705069 scopus 로고    scopus 로고
    • 2-benzyloxychalcone derivatives stimulate glucose uptake in 3T3-L1 adipocytes
    • Kamei R., Kadokura M., and Kitagawa Y. 2-benzyloxychalcone derivatives stimulate glucose uptake in 3T3-L1 adipocytes. Life Sci. 73 (2003) 2091-2099
    • (2003) Life Sci. , vol.73 , pp. 2091-2099
    • Kamei, R.1    Kadokura, M.2    Kitagawa, Y.3
  • 18
    • 0036876269 scopus 로고    scopus 로고
    • Acute effect of Bauhinia forficata on serum glucose levels in normal and alloxan-induced diabetic rats
    • Silva F.R.M.B., Szpoganicz B., Pizzolatti M.G., Willrich M.A.V., and De Sousa E. Acute effect of Bauhinia forficata on serum glucose levels in normal and alloxan-induced diabetic rats. J. Ethnopharmacol. 83 (2002) 33-37
    • (2002) J. Ethnopharmacol. , vol.83 , pp. 33-37
    • Silva, F.R.M.B.1    Szpoganicz, B.2    Pizzolatti, M.G.3    Willrich, M.A.V.4    De Sousa, E.5
  • 24
    • 24344479157 scopus 로고    scopus 로고
    • Stereoselective synthesis of monomeric flavonoids
    • Marais J.P.J., Ferreira D., and Slade D. Stereoselective synthesis of monomeric flavonoids. Phytochemistry 66 (2005) 2145-2176
    • (2005) Phytochemistry , vol.66 , pp. 2145-2176
    • Marais, J.P.J.1    Ferreira, D.2    Slade, D.3
  • 27
    • 0037416109 scopus 로고    scopus 로고
    • A study on CYP1A inhibitory action of E-2-(4′-methoxybenzylidene)-1-benzosuberone and some related chalcones and cyclic chalcone analogues
    • Monostory K., Tamási V., Vereczkey L., and Perjési P. A study on CYP1A inhibitory action of E-2-(4′-methoxybenzylidene)-1-benzosuberone and some related chalcones and cyclic chalcone analogues. Toxicology 184 (2003) 203-210
    • (2003) Toxicology , vol.184 , pp. 203-210
    • Monostory, K.1    Tamási, V.2    Vereczkey, L.3    Perjési, P.4
  • 28
    • 0037470809 scopus 로고    scopus 로고
    • ttCH, a selective inhibitor of inducible nitric oxide synthase expression with antiarthritic properties
    • Rojas J., Payá M., Domínguez J.N., and Ferrándiz M.L. ttCH, a selective inhibitor of inducible nitric oxide synthase expression with antiarthritic properties. Eur. J. Pharmacol. 465 (2003) 183-189
    • (2003) Eur. J. Pharmacol. , vol.465 , pp. 183-189
    • Rojas, J.1    Payá, M.2    Domínguez, J.N.3    Ferrándiz, M.L.4
  • 31
    • 33846194682 scopus 로고    scopus 로고
    • Chalcone based aryloxypropanolamines as potential antihyperglycemic agents
    • Shukla P., Singh A.M., Srivastava A.K., and Pratap R. Chalcone based aryloxypropanolamines as potential antihyperglycemic agents. Bioorg. Med. Chem. Lett. 17 (2007) 799-802
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 799-802
    • Shukla, P.1    Singh, A.M.2    Srivastava, A.K.3    Pratap, R.4
  • 32
    • 0022381067 scopus 로고
    • Effects of chalcone derivatives on lipoxygenase and cyclooxygenase activities of mouse epidermis
    • Nakadate T.O., Aizu E.O., Yamamoto S.O., and Kato R. Effects of chalcone derivatives on lipoxygenase and cyclooxygenase activities of mouse epidermis. Prostaglandins 30 (1985) 357-368
    • (1985) Prostaglandins , vol.30 , pp. 357-368
    • Nakadate, T.O.1    Aizu, E.O.2    Yamamoto, S.O.3    Kato, R.4
  • 33
    • 0029047744 scopus 로고
    • Synthesis and pharmacological evaluation of 2′-hydroxychalcones and flavones as inhibitors of inflammatory mediators generation
    • Ballesteros J.F., Sanz M.J., Ubeda A., Miranda M.A., Iborra S., Paya M., and Alcaraz M.J. Synthesis and pharmacological evaluation of 2′-hydroxychalcones and flavones as inhibitors of inflammatory mediators generation. J. Med. Chem. 14 (1995) 2794-2797
    • (1995) J. Med. Chem. , vol.14 , pp. 2794-2797
    • Ballesteros, J.F.1    Sanz, M.J.2    Ubeda, A.3    Miranda, M.A.4    Iborra, S.5    Paya, M.6    Alcaraz, M.J.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.