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Volumn 31, Issue 5, 2008, Pages 573-578

Heterocyclic compounds from Chrysanthemum coronarium L. and their inhibitory activity on hACAT-1, hACAT-2, and LDL-oxidation

Author keywords

5,5 Dibuthoxy 2,2 bifuran; Adenosine; Chrysathemum coronarium L; HACAT; LDL Oxidation; Methyl trans ferulate; Prunasin; Pterolactam; Sambunigrin

Indexed keywords

5,5' DIBUTOXY 2,2' BIFURAN; 5,5'-DIBUTOXY-2,2'-BIFURAN; ADENOSINE; CAFFEIC ACID DERIVATIVE; CHOLESTEROL ACYLTRANSFERASE; COUMARIC ACID; FERULIC ACID METHYL ESTER; FURAN DERIVATIVE; GLYCOSIDE; LACTAM; LOW DENSITY LIPOPROTEIN; NITRILE; PLANT EXTRACT; PRUNASINE; SAMBUNIGRIN; STEROL O ACYLTRANSFERASE 1; STEROL O ACYLTRANSFERASE 2; STEROL O-ACYLTRANSFERASE 1; STEROL O-ACYLTRANSFERASE 2;

EID: 43749107290     PISSN: 02536269     EISSN: 19763786     Source Type: Journal    
DOI: 10.1007/s12272-001-1195-4     Document Type: Article
Times cited : (38)

References (37)
  • 2
    • 11144232070 scopus 로고
    • Specificity of the cis-isomers of inhibitors of uredospore germination in the rust fungi
    • Allen, P. J., Specificity of the cis-isomers of inhibitors of uredospore germination in the rust fungi. Proc. Nat. Acad. Sci., 69, 3497-3500 (1972).
    • (1972) Proc. Nat. Acad. Sci. , vol.69 , pp. 3497-3500
    • Allen, P.J.1
  • 3
    • 33846568869 scopus 로고    scopus 로고
    • Human ACAT inhibitory effects of shikonin derivatives from Lithospermum erythrorhizon
    • An, S. J., Park, Y. D., Paik, Y. K., Jeong, T. S., and Lee, W. S., Human ACAT inhibitory effects of shikonin derivatives from Lithospermum erythrorhizon. Bioorg. Med. Chem. Lett. 17, 1112-1116 (2007).
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 1112-1116
    • An, S.J.1    Park, Y.D.2    Paik, Y.K.3    Jeong, T.S.4    Lee, W.S.5
  • 4
    • 0342802060 scopus 로고
    • Fluorescent petal constituents of Chrysanthemum coronarium L
    • Anyos, T. and Steelink, C., Fluorescent petal constituents of Chrysanthemum coronarium L. Arch. Biochem. Biophys., 90, 63-67 (1960).
    • (1960) Arch. Biochem. Biophys. , vol.90 , pp. 63-67
    • Anyos, T.1    Steelink, C.2
  • 5
    • 0001498084 scopus 로고
    • Cyanogenic glycosides in leaves of Perilla frutescens var. acuta
    • Aritomi, M., Kumori, T., and Kawasaki, T., Cyanogenic glycosides in leaves of Perilla frutescens var. acuta. Phytochemistry, 24, 2438-2439 (1985).
    • (1985) Phytochemistry , vol.24 , pp. 2438-2439
    • Aritomi, M.1    Kumori, T.2    Kawasaki, T.3
  • 6
    • 0009607502 scopus 로고
    • Neue lyratolester aus Chrysanthemum coronarium
    • Bohlmann, F. and Fritz, U., Neue lyratolester aus Chrysanthemum coronarium. Phytochemistry, 18, 1888-1889 (1979).
    • (1979) Phytochemistry , vol.18 , pp. 1888-1889
    • Bohlmann, F.1    Fritz, U.2
  • 7
    • 0019188967 scopus 로고
    • Properties of acyl-CoA:cholesterol acyltransferase in aortic microsomes from atherosclerotic rabbits
    • Brecher, P. and Chan, C. T., Properties of acyl-CoA:cholesterol acyltransferase in aortic microsomes from atherosclerotic rabbits. Biochim. Biophys. Acta, 617, 458-471 (1980).
    • (1980) Biochim. Biophys. Acta , vol.617 , pp. 458-471
    • Brecher, P.1    Chan, C.T.2
  • 8
    • 0017872475 scopus 로고
    • Microsomal lipid peroxidation
    • Buege, J. A. and Aust, S. D., Microsomal lipid peroxidation. Methods Enzymol., 52, 302 (1978).
    • (1978) Methods Enzymol. , vol.52 , pp. 302
    • Buege, J.A.1    Aust, S.D.2
  • 9
    • 0002452475 scopus 로고
    • Anticancer activity of organotin compounds. 2. Interaction of diorganotin dihalides with nucleic acid bases and nucleosides; The synthesis of adenine, adenosine and 9-methyladenine adducts
    • Cardin, C. J. and Roy, A., Anticancer activity of organotin compounds. 2. Interaction of diorganotin dihalides with nucleic acid bases and nucleosides; the synthesis of adenine, adenosine and 9-methyladenine adducts. Inorg. Chim. Acta, 107, 57-61 (1985).
    • (1985) Inorg. Chim. Acta , vol.107 , pp. 57-61
    • Cardin, C.J.1    Roy, A.2
  • 10
    • 0001761446 scopus 로고
    • Polyoxygenated terpenes and cyanogenic glucosides from Centaurea aspera var. subinermis
    • Cardona, L., Fernández, I., Pedro, J. R., and Vidal, R., Polyoxygenated terpenes and cyanogenic glucosides from Centaurea aspera var. subinermis. Phytochemistry, 31, 3507-3509 (1992).
    • (1992) Phytochemistry , vol.31 , pp. 3507-3509
    • Cardona, L.1    Fernández, I.2    Pedro, J.R.3    Vidal, R.4
  • 11
    • 0027527733 scopus 로고
    • Molecular cloning and functional expression of human acylcoenzyme A:cholesterol acyltransferase cDNA in mutant Chinese hamster ovary cells
    • Chang, C. C., Huh, H. Y., Cadigan, K. M., and Chang, T. Y., Molecular cloning and functional expression of human acylcoenzyme A:cholesterol acyltransferase cDNA in mutant Chinese hamster ovary cells. J. Biol. Chem., 268, 20747-20755 (1993).
    • (1993) J. Biol. Chem. , vol.268 , pp. 20747-20755
    • Chang, C.C.1    Huh, H.Y.2    Cadigan, K.M.3    Chang, T.Y.4
  • 12
    • 0030943621 scopus 로고    scopus 로고
    • Acyl-coenzyme A:cholesterol acyltransferase
    • Chang, T. Y., Chang, C. Y., and Cheng, D., Acyl-coenzyme A:cholesterol acyltransferase. Annu. Rev. Biochem., 66, 613-638 (1997).
    • (1997) Annu. Rev. Biochem. , vol.66 , pp. 613-638
    • Chang, T.Y.1    Chang, C.Y.2    Cheng, D.3
  • 15
    • 3142706550 scopus 로고
    • Purine and pyrimidine bases and nucleosides of germinating Triticum aestivum seeds
    • Grzelczak, Z. and Buchowicz, J., Purine and pyrimidine bases and nucleosides of germinating Triticum aestivum seeds. Phytochemstry, 14, 329-331 (1975).
    • (1975) Phytochemstry , vol.14 , pp. 329-331
    • Grzelczak, Z.1    Buchowicz, J.2
  • 16
    • 33745026603 scopus 로고
    • The distribution and chemical composition of ultracentrifugally separated lipoproteins in human serum
    • Havel, R. J., Edger, H. A., and Bradgon, J., The distribution and chemical composition of ultracentrifugally separated lipoproteins in human serum. J. Clin. Invest., 34, 1345-1353 (1955).
    • (1955) J. Clin. Invest. , vol.34 , pp. 1345-1353
    • Havel, R.J.1    Edger, H.A.2    Bradgon, J.3
  • 17
    • 0001366115 scopus 로고
    • Synthetic electroorganic chemistry. 11. Electrochemical synthesis of semicyclic and cyclic N-acyl N,O-acetals
    • Iwasaki, T., Horikawa, H., Matsumoto, K., and Miyoshi, M., Synthetic electroorganic chemistry. 11. Electrochemical synthesis of semicyclic and cyclic N-acyl N,O-acetals. J. Org. Chem., 44, 1552-1554 (1979).
    • (1979) J. Org. Chem. , vol.44 , pp. 1552-1554
    • Iwasaki, T.1    Horikawa, H.2    Matsumoto, K.3    Miyoshi, M.4
  • 18
    • 3042838346 scopus 로고    scopus 로고
    • Inhibitory effects of mutti-suvstituted benzylidenzethiazolidine-2,4- diones on LDL oxidation
    • Jeong, T. S., Kim, J. R., Kim, K. S., Cho, K. H., Bae, K. H., and Lee, W. S., Inhibitory effects of mutti-suvstituted benzylidenzethiazolidine-2,4-diones on LDL oxidation. Bioorg. Med. Chem., 12, 4017-4023 (2004).
    • (2004) Bioorg. Med. Chem. , vol.12 , pp. 4017-4023
    • Jeong, T.S.1    Kim, J.R.2    Kim, K.S.3    Cho, K.H.4    Bae, K.H.5    Lee, W.S.6
  • 20
    • 0001089464 scopus 로고
    • The constituents of the steam volatile oil from Chrysanthemum coronarium L. var spatiosum
    • Kameoka, H., Kitagawa, C., and Husebe, Y., The constituents of the steam volatile oil from Chrysanthemum coronarium L. var spatiosum. J. Agri. Chem. Soc. Japan, 49, 652-657 (1975).
    • (1975) J. Agri. Chem. Soc. Japan , vol.49 , pp. 652-657
    • Kameoka, H.1    Kitagawa, C.2    Husebe, Y.3
  • 21
    • 0034813893 scopus 로고    scopus 로고
    • Anti-atherogenic effect of citrus flavonoids, naringin and naringenin, associated with hepatic ACAT and aortic VCAM-1 and MCP-1 in high cholesterol-fed rabbits
    • Lee, C. H., Jeong, T.S., Choi, Y. K., Hyun, B. W., Oh, G. T., Kim, E. H., Kin, J. R., Han, J. I., and Bok, S. H., Anti-atherogenic effect of citrus flavonoids, naringin and naringenin, associated with hepatic ACAT and aortic VCAM-1 and MCP-1 in high cholesterol-fed rabbits. Biochem. Biophys. Res. Commun., 284, 681-688 (2001b).
    • (2001) Biochem. Biophys. Res. Commun. , vol.284 , pp. 681-688
    • Lee, C.H.1    Jeong, T.S.2    Choi, Y.K.3    Hyun, B.W.4    Oh, G.T.5    Kim, E.H.6    Kin, J.R.7    Han, J.I.8    Bok, S.H.9
  • 23
    • 33748468822 scopus 로고    scopus 로고
    • Isolation of eudesmanolides derivatives from the flower of Chrysanthemum coronarium L
    • Lee, K. D., Ha, T. J., Park, K. H., and Yang, M. S., Isolation of eudesmanolides derivatives from the flower of Chrysanthemum coronarium L. Kor. J. Medicinal Crop Sci., 9, 269-274 (2001a).
    • (2001) Kor. J. Medicinal Crop Sci. , vol.9 , pp. 269-274
    • Lee, K.D.1    Ha, T.J.2    Park, K.H.3    Yang, M.S.4
  • 24
    • 33748471780 scopus 로고    scopus 로고
    • Isolation of pyrethrosin derivatives from the flower of Chrysanthemum coronarium L
    • Lee, K. D., Park, K. H., Ha, T. J., Han, H. S., and Yang, M. S., Isolation of pyrethrosin derivatives from the flower of Chrysanthemum coronarium L. Agric. Chem. Biotechnol. 46, 76-79 (2003c).
    • (2003) Agric. Chem. Biotechnol. , vol.46 , pp. 76-79
    • Lee, K.D.1    Park, K.H.2    Ha, T.J.3    Han, H.S.4    Yang, M.S.5
  • 25
    • 12144274573 scopus 로고    scopus 로고
    • Cytotoxic activity and structural analogues of guaianolide derivatives from the flower of Chrysanthemum coronarium L
    • Lee, K. D., Park, K. H., Kim, H., Kim, J., Rim, Y., and Yang, M. S., Cytotoxic activity and structural analogues of guaianolide derivatives from the flower of Chrysanthemum coronarium L. Agric. Chem. Biotechnol., 46, 29-32 (2003a).
    • (2003) Agric. Chem. Biotechnol. , vol.46 , pp. 29-32
    • Lee, K.D.1    Park, K.H.2    Kim, H.3    Kim, J.4    Rim, Y.5    Yang, M.S.6
  • 26
    • 0036547826 scopus 로고    scopus 로고
    • Isolation and identification of dihydrochrysanolide and its 1-epimer from the flower of Chrysanthemum coronarium L
    • Lee, K. D., Yang, M. S., Ha, T. J., Park, K. M., and Park, K. H., Isolation and identification of dihydrochrysanolide and its 1-epimer from the flower of Chrysanthemum coronarium L. Biol. Biotech. Biochem., 66, 862-865 (2002).
    • (2002) Biol. Biotech. Biochem. , vol.66 , pp. 862-865
    • Lee, K.D.1    Yang, M.S.2    Ha, T.J.3    Park, K.M.4    Park, K.H.5
  • 27
    • 84954962000 scopus 로고
    • Novel plant growth inhibitors and an insect antifeedant from Chrysanthemum coronarium L
    • Mahahiro, T. and Kazuhiro, C., Novel plant growth inhibitors and an insect antifeedant from Chrysanthemum coronarium L. Agric. Biol. Chem., 48, 1367-1369 (1984).
    • (1984) Agric. Biol. Chem. , vol.48 , pp. 1367-1369
    • Mahahiro, T.1    Kazuhiro, C.2
  • 29
    • 33646462746 scopus 로고    scopus 로고
    • Novel aspects of cyanogenesis in Eucalyptus camphora subsp. humeana
    • Neilson, E. H., Goodger, J. Q. D., and Woodrow, I. E., Novel aspects of cyanogenesis in Eucalyptus camphora subsp. humeana. Functional Plant Biology, 33, 487-496 (2006).
    • (2006) Functional Plant Biology , vol.33 , pp. 487-496
    • Neilson, E.H.1    Goodger, J.Q.D.2    Woodrow, I.E.3
  • 30
    • 0001644682 scopus 로고
    • Photolytic dehydrochlorination of N-chloro-N-alkyl amides: Formation of N-(.alpha.-methoxyalkyl) amides
    • Phan, X. T. and Shannon, P. J., Photolytic dehydrochlorination of N-chloro-N-alkyl amides: formation of N-(.alpha.-methoxyalkyl) amides. J. Org. Chem., 48, 5164-5170 (1983).
    • (1983) J. Org. Chem. , vol.48 , pp. 5164-5170
    • Phan, X.T.1    Shannon, P.J.2
  • 31
    • 0026511875 scopus 로고
    • Susceptibility to low-density lipoprotein oxidation and coronary atherosclerosis in man
    • Regnstrom, J., Nilsson, J., Tornvall, P., Landou, C., and Hamsten, A., Susceptibility to low-density lipoprotein oxidation and coronary atherosclerosis in man. Lancet, 339, 1183-1186 (1992).
    • (1992) Lancet , vol.339 , pp. 1183-1186
    • Regnstrom, J.1    Nilsson, J.2    Tornvall, P.3    Landou, C.4    Hamsten, A.5
  • 33
    • 84986641906 scopus 로고
    • New acetylenes from Chrysanthemum coronarium L
    • Sanz, J. F., Falco, E., and Marco, J. A., New acetylenes from Chrysanthemum coronarium L. Liebigs Ann. Chem., 90, 303-305 (1990).
    • (1990) Liebigs Ann. Chem. , vol.90 , pp. 303-305
    • Sanz, J.F.1    Falco, E.2    Marco, J.A.3
  • 34
    • 43749090075 scopus 로고    scopus 로고
    • Development of biologically active compounds from edible plant sources-VI. Isolation of sterol compounds from the aerial parts of garland (Chrysanthemum coronarium L.)
    • Song, M. C., Hong, Y. H., Kim, D. H., Kim, D. K., Chung, I. S., Kim, S. H., Park, M. H., Kim, I. H., and Baek, N. I., Development of biologically active compounds from edible plant sources-VI. Isolation of sterol compounds from the aerial parts of garland (Chrysanthemum coronarium L.). J. Korean Soc. Agric. Chem. Biotechnol., 46, 376-379 (2003).
    • (2003) J. Korean Soc. Agric. Chem. Biotechnol. , vol.46 , pp. 376-379
    • Song, M.C.1    Hong, Y.H.2    Kim, D.H.3    Kim, D.K.4    Chung, I.S.5    Kim, S.H.6    Park, M.H.7    Kim, I.H.8    Baek, N.I.9
  • 36
    • 0022256566 scopus 로고
    • Role of acyl-CoA: Cholesterol acyltransferase in cellular cholesterol metabolism
    • Suckling, K. E. and Stange, E. F., Role of acyl-CoA: cholesterol acyltransferase in cellular cholesterol metabolism. J. Lipid Res., 26, 647-671 (1985).
    • (1985) J. Lipid Res. , vol.26 , pp. 647-671
    • Suckling, K.E.1    Stange, E.F.2


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