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Volumn 1820, Issue 7, 2012, Pages 1021-1026

Liver X receptor and peroxisome proliferator-activated receptor agonist from Cornus alternifolia

Author keywords

Cornus alternifolia; Iridoid glycosides; Liver X receptors; Peroxisome proliferator activated receptors

Indexed keywords

ALTERNOSIDE A; ALTERNOSIDE B; ALTERNOSIDE C; ALTERNOSIDE D; ASTRAGALIN; CORNALTERNOSIDE; CORNOSIDE E; IRIDOID; LIVER X RECEPTOR; LIVER X RECEPTOR AGONIST; MEGASTIGMANE 3 ONE 7 EN 9 O BETA GLUCOPYRANOSIDE; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR ALPHA; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR ALPHA AGONIST; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA AGONIST; PLANT EXTRACT; UNCLASSIFIED DRUG;

EID: 84860665286     PISSN: 03044165     EISSN: 18728006     Source Type: Journal    
DOI: 10.1016/j.bbagen.2012.02.004     Document Type: Article
Times cited : (15)

References (35)
  • 2
    • 55849105651 scopus 로고    scopus 로고
    • Liver X receptors (LXR) as therapeutic targets in dyslipidemia
    • J. Bełtowski Liver X receptors (LXR) as therapeutic targets in dyslipidemia Cardiovasc. Ther. 26 2008 297 316
    • (2008) Cardiovasc. Ther. , vol.26 , pp. 297-316
    • Bełtowski, J.1
  • 3
    • 15744386871 scopus 로고    scopus 로고
    • Nuclear receptors as targets for drug development: Regulation of cholesterol and bile acid metabolism by nuclear receptors
    • M. Makishima Nuclear receptors as targets for drug development: regulation of cholesterol and bile acid metabolism by nuclear receptors J. Pharmacol. Sci. 97 2005 177 183
    • (2005) J. Pharmacol. Sci. , vol.97 , pp. 177-183
    • Makishima, M.1
  • 4
    • 23644456172 scopus 로고    scopus 로고
    • Therapeutic roles of peroxisome proliferator-activated receptor agonists
    • B. Staels, and J.C. Fruchart Therapeutic roles of peroxisome proliferator-activated receptor agonists Diabetes 54 2005 2460 2470
    • (2005) Diabetes , vol.54 , pp. 2460-2470
    • Staels, B.1    Fruchart, J.C.2
  • 5
    • 0036183630 scopus 로고    scopus 로고
    • The mechanisms of action of PPARs
    • J. Berger, and D.E. Moller The mechanisms of action of PPARs Annu. Rev. Med. 53 2002 409 435
    • (2002) Annu. Rev. Med. , vol.53 , pp. 409-435
    • Berger, J.1    Moller, D.E.2
  • 7
    • 0038207195 scopus 로고    scopus 로고
    • Phylogenetic relationships within Cornus (Cornaceae) based on 26S rDNA sequences
    • C. Fan, and Q.Y. Xiang Phylogenetic relationships within Cornus (Cornaceae) based on 26S rDNA sequences Am. J. Bot. 88 2001 1131 1138
    • (2001) Am. J. Bot. , vol.88 , pp. 1131-1138
    • Fan, C.1    Xiang, Q.Y.2
  • 8
    • 29244481658 scopus 로고    scopus 로고
    • Anthocyanins in Cornus alternifolia, Cornus controversa, Cornus kousa and Cornus florida fruits with health benefits
    • S.K. Vareed, M.K. Reddy, R.E. Schutzki, and M.G. Nair Anthocyanins in Cornus alternifolia, Cornus controversa, Cornus kousa and Cornus florida fruits with health benefits Life Sci. 78 2006 777 784
    • (2006) Life Sci. , vol.78 , pp. 777-784
    • Vareed, S.K.1    Reddy, M.K.2    Schutzki, R.E.3    Nair, M.G.4
  • 9
    • 0037165540 scopus 로고    scopus 로고
    • Characterization, quantification, and bioactivities of anthocyanins in cornus species
    • N.P. Seeram, R. Schutzki, A. Chandra, and M.G. Nair Characterization, quantification, and bioactivities of anthocyanins in cornus species J. Agric. Food Chem. 50 2002 2519 2523
    • (2002) J. Agric. Food Chem. , vol.50 , pp. 2519-2523
    • Seeram, N.P.1    Schutzki, R.2    Chandra, A.3    Nair, M.G.4
  • 10
    • 0032986801 scopus 로고    scopus 로고
    • Antioxidant and antiinflammatory activities of anthocyanins and their aglycon, cyanidin, from Tart Cherries
    • H.B. Wang, M.G. Nair, G.M. Strashurg, Y.C. Chang, A.M. Booren, J.I. Gray, and D.L. Dewitt Antioxidant and antiinflammatory activities of anthocyanins and their aglycon, cyanidin, from Tart Cherries J. Nat. Prod. 62 1999 294 296
    • (1999) J. Nat. Prod. , vol.62 , pp. 294-296
    • Wang, H.B.1    Nair, M.G.2    Strashurg, G.M.3    Chang, Y.C.4    Booren, A.M.5    Gray, J.I.6    Dewitt, D.L.7
  • 11
    • 51349128983 scopus 로고    scopus 로고
    • Anthocyanins and their role in cancer prevention
    • L.S. Wang, and G.D. Stoner Anthocyanins and their role in cancer prevention Cancer Lett. 269 2008 281 290
    • (2008) Cancer Lett. , vol.269 , pp. 281-290
    • Wang, L.S.1    Stoner, G.D.2
  • 12
    • 64449085329 scopus 로고    scopus 로고
    • Hypoglycemic activity of a novel anthocyanin-rich formulation from Lowbush blueberry, Vaccinium angustifolium Aiton
    • M.H. Grace, D.M. Ribnicky, P. Kuhn, A. Poulev, S. Logendra, G.G. Yousef, I. Raskin, and M.A. Lila Hypoglycemic activity of a novel anthocyanin-rich formulation from Lowbush blueberry, Vaccinium angustifolium Aiton Phytomedicine 16 2009 406 415
    • (2009) Phytomedicine , vol.16 , pp. 406-415
    • Grace, M.H.1    Ribnicky, D.M.2    Kuhn, P.3    Poulev, A.4    Logendra, S.5    Yousef, G.G.6    Raskin, I.7    Lila, M.A.8
  • 13
    • 33645512781 scopus 로고    scopus 로고
    • Differential effects of isoflavones, from Austragalus membranaceus and Pueraria Thomsonii, on the activation of PPARα, PPARγ, and adipocyte differentiation in vitro
    • P. Shen, M.H. Liu, T.Y. Ng, Y.H. Chan, and E.L. Yong Differential effects of isoflavones, from Austragalus membranaceus and Pueraria Thomsonii, on the activation of PPARα, PPARγ, and adipocyte differentiation in vitro J. Nutr. 136 2006 899 905
    • (2006) J. Nutr. , vol.136 , pp. 899-905
    • Shen, P.1    Liu, M.H.2    Ng, T.Y.3    Chan, Y.H.4    Yong, E.L.5
  • 16
    • 0034624609 scopus 로고    scopus 로고
    • A 9-hydroxyiridoid isolated from Junellia seriphioides (Verbenaceae)
    • H. Franzyk, S.R. Jensen, C.E. Olsen, and J.M. Quiroga A 9-hydroxyiridoid isolated from Junellia seriphioides (Verbenaceae) Org. Lett. 2 2000 699 700
    • (2000) Org. Lett. , vol.2 , pp. 699-700
    • Franzyk, H.1    Jensen, S.R.2    Olsen, C.E.3    Quiroga, J.M.4
  • 18
    • 0036853783 scopus 로고    scopus 로고
    • Caudatosides A-F: New iridoid glucosides from Citharexylum caudatum
    • S. Ayers, and A. Sneden Caudatosides A-F: new iridoid glucosides from Citharexylum caudatum J. Nat. Prod. 65 2002 1621 1626
    • (2002) J. Nat. Prod. , vol.65 , pp. 1621-1626
    • Ayers, S.1    Sneden, A.2
  • 20
    • 0345267196 scopus 로고    scopus 로고
    • Iridoid glucosides from Penstemon secundiflorus and grandiflorus: Revised structure of 10-hydroxy-8-epihastatoside
    • H. Franzyk, S.R. Jensen, and F.R. Stermita Iridoid glucosides from Penstemon secundiflorus and grandiflorus: revised structure of 10-hydroxy-8-epihastatoside Phytochemistry 49 1998 2025 2030
    • (1998) Phytochemistry , vol.49 , pp. 2025-2030
    • Franzyk, H.1    Jensen, S.R.2    Stermita, F.R.3
  • 21
    • 0001656888 scopus 로고
    • Volatile norisoprenoid compounds as constituents of oak woods used in wine and spirit maturation
    • M.A. Sefton, L. Francis, and P.J. Williams Volatile norisoprenoid compounds as constituents of oak woods used in wine and spirit maturation J. Agric. Food Chem. 38 1990 2045 2049
    • (1990) J. Agric. Food Chem. , vol.38 , pp. 2045-2049
    • Sefton, M.A.1    Francis, L.2    Williams, P.J.3
  • 22
    • 0034848949 scopus 로고    scopus 로고
    • Myrsinionosides A-E: Megastigmane glycosides from the leaves of Myrsine seguinii LEV
    • H. Otsaka, X.N. Zhong, E. Hirata, T. Shinzato, and Y. Tokenda Myrsinionosides A-E: megastigmane glycosides from the leaves of Myrsine seguinii LEV Chem. Pharm. Bull. 49 2001 1093 1097
    • (2001) Chem. Pharm. Bull. , vol.49 , pp. 1093-1097
    • Otsaka, H.1    Zhong, X.N.2    Hirata, E.3    Shinzato, T.4    Tokenda, Y.5
  • 23
    • 10644233798 scopus 로고    scopus 로고
    • Megastigmane and phenolic components from Laurus nobilis L. Leaves and their inhibitory effects on nitric oxide production
    • S.D. Marino, N. Borbone, F. Zollo, A. Ionaro, P.D. Meglio, and M. Iorizzi Megastigmane and phenolic components from Laurus nobilis L. Leaves and their inhibitory effects on nitric oxide production J. Agric. Food Chem. 52 2004 7525 7531
    • (2004) J. Agric. Food Chem. , vol.52 , pp. 7525-7531
    • Marino, S.D.1    Borbone, N.2    Zollo, F.3    Ionaro, A.4    Meglio, P.D.5    Iorizzi, M.6
  • 24
    • 0142087956 scopus 로고    scopus 로고
    • 13C NMR resonances of oleanolic acid, 18α-oleanolic acid, ursolic acid and their 11-oxo derivatives
    • 13C NMR resonances of oleanolic acid, 18α-oleanolic acid, ursolic acid and their 11-oxo derivatives Magn. Reson. Chem. 41 2003 636 638
    • (2003) Magn. Reson. Chem. , vol.41 , pp. 636-638
    • Seebacher, W.1    Simic, N.2    Weis, R.3    Saf, R.4    Kunert, O.5
  • 26
    • 84986748726 scopus 로고
    • Studies on the constituents of useful plants. VI. Constituents of the calyx of Diospyros kaki (2), and carbon-13 nuclear magnetic resonance spectra of flavonol glycosides
    • S. Matsuura, and M. Linuma Studies on the constituents of useful plants. VI. Constituents of the calyx of Diospyros kaki (2), and carbon-13 nuclear magnetic resonance spectra of flavonol glycosides Chem. Pharm. Bull. 26 1978 1936 1941
    • (1978) Chem. Pharm. Bull. , vol.26 , pp. 1936-1941
    • Matsuura, S.1    Linuma, M.2
  • 27
    • 0027423239 scopus 로고
    • Secondary metabolites from the stem bark of Celaenodendron mexicanum
    • P. Castaneda, A. Bahena, E. Garcia, D. Chavez, and R. Mata Secondary metabolites from the stem bark of Celaenodendron mexicanum J. Nat. Prod. 56 1993 1575 1579
    • (1993) J. Nat. Prod. , vol.56 , pp. 1575-1579
    • Castaneda, P.1    Bahena, A.2    Garcia, E.3    Chavez, D.4    Mata, R.5
  • 28
    • 34547773253 scopus 로고    scopus 로고
    • Phytochemicals of black bean seed coats: Isolation, structure elucidation, and their antiproliferative and antioxidative activities
    • M. Dong, X.J. He, and R.H. Liu Phytochemicals of black bean seed coats: isolation, structure elucidation, and their antiproliferative and antioxidative activities J. Agric. Food Chem. 55 2007 6044 6051
    • (2007) J. Agric. Food Chem. , vol.55 , pp. 6044-6051
    • Dong, M.1    He, X.J.2    Liu, R.H.3
  • 29
    • 34548628057 scopus 로고    scopus 로고
    • Antioxidative principals of Jussiaea repens: An edible medicinal plant
    • H.L. Huan, D.L. Li, X.M. Li, B. Xu, and B.G. Wang Antioxidative principals of Jussiaea repens: an edible medicinal plant Int. J. Food Sci. Technol. 42 2007 1219 1227
    • (2007) Int. J. Food Sci. Technol. , vol.42 , pp. 1219-1227
    • Huan, H.L.1    Li, D.L.2    Li, X.M.3    Xu, B.4    Wang, B.G.5
  • 30
    • 3242716088 scopus 로고    scopus 로고
    • Flavonol glycosides from the leaves of Eucommia ulmoides O. with glycation inhibitory activity
    • H.Y. Kim, B.H. Moon, H.J. Lee, and D.H. Choi Flavonol glycosides from the leaves of Eucommia ulmoides O. with glycation inhibitory activity J. Ethnopharmacol. 93 2004 227 230
    • (2004) J. Ethnopharmacol. , vol.93 , pp. 227-230
    • Kim, H.Y.1    Moon, B.H.2    Lee, H.J.3    Choi, D.H.4
  • 31
    • 34548248626 scopus 로고    scopus 로고
    • Evaluation of in vitro antioxidant properties of some traditional Sardinian medicinal plants: Investigation of the high antioxidant capacity of Rubus ulmifolius
    • S.D. Acqua, R. Cervellati, M.C. Loi, and G. Innocenti Evaluation of in vitro antioxidant properties of some traditional Sardinian medicinal plants: investigation of the high antioxidant capacity of Rubus ulmifolius Food Chem. 106 2008 745 749
    • (2008) Food Chem. , vol.106 , pp. 745-749
    • Acqua, S.D.1    Cervellati, R.2    Loi, M.C.3    Innocenti, G.4
  • 32
    • 42749089756 scopus 로고    scopus 로고
    • Pharmacological basis for use of Pistacia integerrima leaves in hyperuricemia and gout
    • N.S. Ahmad, M. Farman, M.H. Najmi, K.B. Mian, and A. Hasan Pharmacological basis for use of Pistacia integerrima leaves in hyperuricemia and gout J. Ethnopharmacol. 117 2008 478 482
    • (2008) J. Ethnopharmacol. , vol.117 , pp. 478-482
    • Ahmad, N.S.1    Farman, M.2    Najmi, M.H.3    Mian, K.B.4    Hasan, A.5
  • 33
    • 34247895642 scopus 로고    scopus 로고
    • Potent anti-obese principle from Rosa canina: Structural requirements and mode of action of trans-tiliroside
    • K. Ninomiya, H. Matsuda, M. Kubo, T. Morikawa, N. Nishida, and M. Yoshikawa Potent anti-obese principle from Rosa canina: structural requirements and mode of action of trans-tiliroside Bioorg. Med. Chem. Lett. 17 2007 3059 3064
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 3059-3064
    • Ninomiya, K.1    Matsuda, H.2    Kubo, M.3    Morikawa, T.4    Nishida, N.5    Yoshikawa, M.6
  • 35
    • 0036152763 scopus 로고    scopus 로고
    • Hepatoprotective principles from the flowers of Tilia argentea (Linden): Structure requirements of tiliroside and mechanisms of action
    • H. Matsuda, K. Ninomiya, H. Shimoda, and M. Yoshikawa Hepatoprotective principles from the flowers of Tilia argentea (Linden): structure requirements of tiliroside and mechanisms of action Bioorg. Med. Chem. 10 2002 707 712
    • (2002) Bioorg. Med. Chem. , vol.10 , pp. 707-712
    • Matsuda, H.1    Ninomiya, K.2    Shimoda, H.3    Yoshikawa, M.4


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