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Volumn 46, Issue 9, 1998, Pages 3509-3516

Antimutagenic Constituents of Casimiroa edulis with Potential Cancer Chemopreventive Activity

Author keywords

(R,S) 5 methoxy 8 (6,7 dihydroxy 3,7 dimethyl 2 octenyl)oxy psoralen; (R,S) 8 (6,7 dihydroxy 3,7 dimethyl 2 octenyl)oxy psoralen; Alkaloids; Antimutagens; Casimiroa edulis; Flavonoids; Furocoumarins; Mouse mammary organ culture assay; Rutaceae

Indexed keywords

CASIMIROA EDULIS; OXY; RUTACEAE; SALMONELLA TYPHIMURIUM; TYPHIMURIUM;

EID: 0000441881     PISSN: 00218561     EISSN: None     Source Type: Journal    
DOI: 10.1021/jf9802373     Document Type: Article
Times cited : (60)

References (75)
  • 1
    • 0003796736 scopus 로고
    • Progress in the chemistry of alkaloids with pharmacological or biological activity
    • Wagner, H., Wolff, P., Eds.; Springer-Verlag: Berlin
    • Achenbach, H. Progress in the chemistry of alkaloids with pharmacological or biological activity. In New Natural Products and Plant Drugs with Pharmacological, Biological or Therapeutical Activity; Wagner, H., Wolff, P., Eds.; Springer-Verlag: Berlin, 1977; pp 108-136.
    • (1977) New Natural Products and Plant Drugs with Pharmacological, Biological or Therapeutical Activity , pp. 108-136
    • Achenbach, H.1
  • 2
    • 84981840254 scopus 로고
    • Über die Isolierung von Casimiroedin aus den Samen von Casimiroa edulis la Llave et Lejarza
    • Aebi, A. Über die Isolierung von Casimiroedin aus den Samen von Casimiroa edulis La Llave et Lejarza. Helv. Chim. Acta 1956, 39, 1495-1500.
    • (1956) Helv. Chim. Acta , vol.39 , pp. 1495-1500
    • Aebi, A.1
  • 3
    • 0029877531 scopus 로고    scopus 로고
    • The effects of dietary ellagic acid on rat hepatic and esophageal mucosal cytochromes P450 and phase II enzymes
    • Ahn, D.; Putt, D.; Kresty, L.; Stoner, G. D.; Fromm, D.; Hollenberg, P. F. The effects of dietary ellagic acid on rat hepatic and esophageal mucosal cytochromes P450 and phase II enzymes. Carcinogenesis 1996, 17, 821-828.
    • (1996) Carcinogenesis , vol.17 , pp. 821-828
    • Ahn, D.1    Putt, D.2    Kresty, L.3    Stoner, G.D.4    Fromm, D.5    Hollenberg, P.F.6
  • 4
    • 0016754798 scopus 로고
    • Inherent specificities of purified cytochromes P-450 and P-448 toward biphenyl hydroxylation and ethoxyresorufin deethylation
    • Burke, M. D.; Mayer, R. T. Inherent specificities of purified cytochromes P-450 and P-448 toward biphenyl hydroxylation and ethoxyresorufin deethylation. Drug Metab. Dispos. 1975, 3, 245-253.
    • (1975) Drug Metab. Dispos. , vol.3 , pp. 245-253
    • Burke, M.D.1    Mayer, R.T.2
  • 5
    • 0022357068 scopus 로고
    • Ethoxy-, pentoxy- and benzyloxyphenoxazones and homologues: A series of substrates to distinguish between different induced cytochromes P-450
    • Burke, M. D.; Thompson, S.; Elcombe, C. R.; Halpert, J.; Haaparanta, T.; Mayer, R. T. Ethoxy-, pentoxy- and benzyloxyphenoxazones and homologues: a series of substrates to distinguish between different induced cytochromes P-450. Biochem. Pharmacol. 1985, 34, 3337-3345.
    • (1985) Biochem. Pharmacol. , vol.34 , pp. 3337-3345
    • Burke, M.D.1    Thompson, S.2    Elcombe, C.R.3    Halpert, J.4    Haaparanta, T.5    Mayer, R.T.6
  • 6
    • 0027432515 scopus 로고
    • Inhibition and inactivation of murine hepatic ethoxy- and pentoxyresorufm O-dealkylase by naturally occurring coumarins
    • Cai, Y.; Bennett, D.; Nair, R. V.; Ceska, O.; Ashwood-Smith, M. J.; DiGiovanni, J. Inhibition and inactivation of murine hepatic ethoxy- and pentoxyresorufm O-dealkylase by naturally occurring coumarins. Chem. Res. Toxicol. 1993, 6, 872-879.
    • (1993) Chem. Res. Toxicol. , vol.6 , pp. 872-879
    • Cai, Y.1    Bennett, D.2    Nair, R.V.3    Ceska, O.4    Ashwood-Smith, M.J.5    DiGiovanni, J.6
  • 7
    • 0023686219 scopus 로고
    • Mechanisms of inhibition of mutagenesis and Carcinogenesis. Classification and overview
    • De Flora, S.; Ramel, C. Mechanisms of inhibition of mutagenesis and Carcinogenesis. Classification and overview. Mutat. Res. 1988, 202, 285-306.
    • (1988) Mutat. Res. , vol.202 , pp. 285-306
    • De Flora, S.1    Ramel, C.2
  • 11
    • 0001223897 scopus 로고
    • Citrus bitter principles. IX. Extractives of Casimiroa edulis Llave et Lex. Structure of zapoterin
    • Dreyer, D. L. Citrus bitter principles. IX. Extractives of Casimiroa edulis Llave et Lex. Structure of zapoterin. J. Org. Chem. 1968, 33, 3577-3582.
    • (1968) J. Org. Chem. , vol.33 , pp. 3577-3582
    • Dreyer, D.L.1
  • 12
    • 0040727758 scopus 로고
    • The structure of zapotin
    • Dreyer, D. L.; Bertelli, D. J. The structure of zapotin. Tetrahedron 1967, 23, 4607-4612.
    • (1967) Tetrahedron , vol.23 , pp. 4607-4612
    • Dreyer, D.L.1    Bertelli, D.J.2
  • 13
    • 0029055363 scopus 로고
    • Disposition of intravenous and oral cyclosporin after administration with grapefruit juice
    • Ducharme, M. P.; Warbasse, L. H.; Edwards, D. J. Disposition of intravenous and oral cyclosporin after administration with grapefruit juice. Clin. Pharmacol. Ther. 1995, 57, 485-491.
    • (1995) Clin. Pharmacol. Ther. , vol.57 , pp. 485-491
    • Ducharme, M.P.1    Warbasse, L.H.2    Edwards, D.J.3
  • 14
    • 0030482468 scopus 로고    scopus 로고
    • Identification of 6′,7′-dihydroxybergamottin, a cytochrome P-450 inhibitor, in grapefruit juice
    • Edwards, D. J.; Bellevue, F. H., III; Woster, P. M. Identification of 6′,7′-dihydroxybergamottin, a cytochrome P-450 inhibitor, in grapefruit juice. Drug Metab. Dispos. 1996, 24, 1287-1290.
    • (1996) Drug Metab. Dispos. , vol.24 , pp. 1287-1290
    • Edwards, D.J.1    Bellevue III, F.H.2    Woster, P.M.3
  • 15
    • 0001507117 scopus 로고
    • 13C NMR chemical shifts and carbon-proton coupling constants of some furocoumarins and furochromones
    • 13C NMR chemical shifts and carbon-proton coupling constants of some furocoumarins and furochromones. Phytochemistry 1979, 18, 139-143.
    • (1979) Phytochemistry , vol.18 , pp. 139-143
    • Elgamal, M.H.A.1    Elewa, N.H.2    Elkhrisy, E.A.M.3    Duddeck, H.4
  • 16
    • 0021227912 scopus 로고
    • High-performance liquid chromatographic study of Casimiroa edulis. II. Determination of furocoumarins
    • Enríquez, R. G.; Romero, M. L.; Escobar, L. L; Joseph-Nathan, P.; Reynolds, W. F. High-performance liquid chromatographic study of Casimiroa edulis. II. Determination of furocoumarins. J. Chromatogr. 1984, 287, 209-214.
    • (1984) J. Chromatogr. , vol.287 , pp. 209-214
    • Enríquez, R.G.1    Romero, M.L.2    Escobar, L.L.3    Joseph-Nathan, P.4    Reynolds, W.F.5
  • 17
    • 0000664079 scopus 로고
    • Constituents of Casimiroa edulis Llave et Lex. VIII. The structures of zapotin and zapotinin
    • Garratt, P. J.; Scheinmann, F.; Sondheimer, F. Constituents of Casimiroa edulis Llave et Lex. VIII. The structures of zapotin and zapotinin. Tetrahedron 1967, 23, 2413-2416.
    • (1967) Tetrahedron , vol.23 , pp. 2413-2416
    • Garratt, P.J.1    Scheinmann, F.2    Sondheimer, F.3
  • 20
    • 0027055359 scopus 로고
    • Effects of phenethyl isothiocyanate, a carcinogenesis inhibitor, on xenobiotic-metabolizing enzymes and nitrosoamine metabolism in rat
    • Guo, Z.; Smith, T. J.; Wang, E.; Sadrieh, N.; Ma, Q.; Thomas, P. E.; Yang, C. S. Effects of phenethyl isothiocyanate, a carcinogenesis inhibitor, on xenobiotic-metabolizing enzymes and nitrosoamine metabolism in rat. Carcinogenesis 1992, 13, 2205-2210.
    • (1992) Carcinogenesis , vol.13 , pp. 2205-2210
    • Guo, Z.1    Smith, T.J.2    Wang, E.3    Sadrieh, N.4    Ma, Q.5    Thomas, P.E.6    Yang, C.S.7
  • 21
    • 0023693118 scopus 로고
    • Mutagenicity of furoquinoline alkaloids in the Salmonella/microsome assay. Mutagenicity of dictamnine is modified by various enzyme inducers and inhibitors
    • Hafele, F.; Schimmer O. Mutagenicity of furoquinoline alkaloids in the Salmonella/microsome assay. Mutagenicity of dictamnine is modified by various enzyme inducers and inhibitors. Mutagenesis 1988, 3, 349-353.
    • (1988) Mutagenesis , vol.3 , pp. 349-353
    • Hafele, F.1    Schimmer, O.2
  • 22
    • 0013190603 scopus 로고
    • Alkaloids of the Australian Rutaceae: Lunasia quercifolia
    • Hart, K. N.; Johns, R. S.; Lamberton, A. J.; Price, R. J. Alkaloids of the Australian Rutaceae: Lunasia quercifolia. Aust J. Chem. 1968, 21, 1389-1391.
    • (1968) Aust J. Chem. , vol.21 , pp. 1389-1391
    • Hart, K.N.1    Johns, R.S.2    Lamberton, A.J.3    Price, R.J.4
  • 23
    • 84889193469 scopus 로고
    • Food Phytochemicals for Cancer Prevention II Teas, Spices, and Herbs; American Chemical Society: Washington, DC
    • Ho, C.-T., Osawa, T., Huang, M.-T., Rosen, R. T., Eds. Food Phytochemicals for Cancer Prevention II Teas, Spices, and Herbs; ACS Symposium Series 547; American Chemical Society: Washington, DC, 1994.
    • (1994) ACS Symposium Series 547
    • Ho, C.-T.1    Osawa, T.2    Huang, M.-T.3    Rosen, R.T.4
  • 24
    • 84889183577 scopus 로고
    • Food Phytochemicals for Cancer Prevention I. Fruits and Vegetables; American Chemical Society: Washington, DC
    • Huang, M.-T., Osawa, T., Ho, C.-T., Rosen, R. T., Eds. Food Phytochemicals for Cancer Prevention I. Fruits and Vegetables; ACS Symposium Series 546; American Chemical Society: Washington, DC, 1994.
    • (1994) ACS Symposium Series 546
    • Huang, M.-T.1    Osawa, T.2    Ho, C.-T.3    Rosen, R.T.4
  • 25
    • 0542415293 scopus 로고
    • The constituents of Casimiroa edulis Llave et Lex. Part II. The Bark
    • Iriarte, J.; Kincl, F. A.; Rosenkranz, G.; Sondheimer, F, The constituents of Casimiroa edulis Llave et Lex. Part II. The Bark. J. Chem. Soc. 1956, 4170-4173.
    • (1956) J. Chem. Soc. , pp. 4170-4173
    • Iriarte, J.1    Kincl, F.A.2    Rosenkranz, G.3    Sondheimer, F.4
  • 27
    • 0022459566 scopus 로고
    • Antimutagens and their modes of action
    • Shankel, D. M., Hartman, P. E., Kada, T., Hollaender, A., Eds.; Plenum Press: New York
    • Kada, Y.; Inoue, T.; Ohta, T.; Shirasu, Y. Antimutagens and their modes of action. In Antimutagenesis and Anticarcinogenesis Mechanisms; Shankel, D. M., Hartman, P. E., Kada, T., Hollaender, A., Eds.; Plenum Press: New York, 1986; pp 181-196.
    • (1986) Antimutagenesis and Anticarcinogenesis Mechanisms , pp. 181-196
    • Kada, Y.1    Inoue, T.2    Ohta, T.3    Shirasu, Y.4
  • 28
    • 0022609905 scopus 로고
    • Further study on mutagenic furoquinoline alkaloids of Dictamni Radicis cortex: Isolation of skimmianine and high-performance liquid Chromatographic analysis
    • Kanamori, H.; Sakamoto, I.; Mizuta, M. Further study on mutagenic furoquinoline alkaloids of Dictamni Radicis cortex: isolation of skimmianine and high-performance liquid Chromatographic analysis. Chem. Pharm. Bull. 1986, 34, 1826-1829.
    • (1986) Chem. Pharm. Bull. , vol.34 , pp. 1826-1829
    • Kanamori, H.1    Sakamoto, I.2    Mizuta, M.3
  • 29
    • 0020567821 scopus 로고
    • Furocoumarins of Heracleum laciniatum: Isolation, phototoxicity, absorption and action spectra studies
    • Kavli, G.; Raa, J.; Johnson, B. E.; Volden, G.; Haugsbo, S. Furocoumarins of Heracleum laciniatum: isolation, phototoxicity, absorption and action spectra studies. Contact Dermatitis 1983, 9, 257-262.
    • (1983) Contact Dermatitis , vol.9 , pp. 257-262
    • Kavli, G.1    Raa, J.2    Johnson, B.E.3    Volden, G.4    Haugsbo, S.5
  • 31
    • 0013560741 scopus 로고
    • The constituents of Casimiroa edulis Llave et Lex. Part I. The seeds
    • Kind, F. A.; Romo, J.; Rosenkranz, G.; Sondheimer, F. The constituents of Casimiroa edulis Llave et Lex. Part I. The seeds. J. Chem. Soc. 1956, 4163-4169.
    • (1956) J. Chem. Soc. , pp. 4163-4169
    • Kind, F.A.1    Romo, J.2    Rosenkranz, G.3    Sondheimer, F.4
  • 32
    • 0023727642 scopus 로고
    • Antimutagenesis by factors affecting DNA repair in bacteria
    • Kuroda, Y.; Inoue, T. Antimutagenesis by factors affecting DNA repair in bacteria. Mutat. Res. 1988, 202, 387-391.
    • (1988) Mutat. Res. , vol.202 , pp. 387-391
    • Kuroda, Y.1    Inoue, T.2
  • 33
    • 0020366827 scopus 로고
    • Genetic evidence that a phorbol ester tumor promoter stimulates ornithine decarboxylase activity by a pathway that is independent of cyclic AMP-dependent protein kinases in CHO cells
    • Lichti, U.; Gottesman, M. M. Genetic evidence that a phorbol ester tumor promoter stimulates ornithine decarboxylase activity by a pathway that is independent of cyclic AMP-dependent protein kinases in CHO cells. J. Cell. Physiol. 1982, 113, 433-439.
    • (1982) J. Cell. Physiol. , vol.113 , pp. 433-439
    • Lichti, U.1    Gottesman, M.M.2
  • 35
    • 0026061827 scopus 로고
    • Pharmacology of Casimiroa edulis. Part I. Blood pressure and heart rate effects in anesthetized rat
    • Magos, G. A.; Vidrio, H. Pharmacology of Casimiroa edulis. Part I. Blood pressure and heart rate effects in anesthetized rat. Planta Med. 1991, 57, 20-24.
    • (1991) Planta Med. , vol.57 , pp. 20-24
    • Magos, G.A.1    Vidrio, H.2
  • 36
    • 0029001845 scopus 로고
    • Pharmacology of Casimiroa edulis. III. Relaxant and contractile effects in rat aortic rings
    • Magos, G. A.; Vidrio, H.; Enriquez, R, Pharmacology of Casimiroa edulis. III. Relaxant and contractile effects in rat aortic rings. J. Ethnopharmacol. 1995, 47, 1-8.
    • (1995) J. Ethnopharmacol. , vol.47 , pp. 1-8
    • Magos, G.A.1    Vidrio, H.2    Enriquez, R.3
  • 37
    • 0020533372 scopus 로고
    • Revised methods for the Salmonella mutagenicity test
    • Maron, D. M.; Ames, B. N. Revised methods for the Salmonella mutagenicity test. Mutat Res. 1983, 113, 173-215.
    • (1983) Mutat Res. , vol.113 , pp. 173-215
    • Maron, D.M.1    Ames, B.N.2
  • 39
    • 0025788487 scopus 로고
    • Influence of thiols and inhibitors of prostaglandin biosynthesis on the carcinogen-induced development of mammary lesions in vitro
    • Mehta, R. G.; Steele, V.; Kelloff, G. J.; Moon, R. C. Influence of thiols and inhibitors of prostaglandin biosynthesis on the carcinogen-induced development of mammary lesions in vitro. Anticancer Res. 1991, 11, 587-592.
    • (1991) Anticancer Res. , vol.11 , pp. 587-592
    • Mehta, R.G.1    Steele, V.2    Kelloff, G.J.3    Moon, R.C.4
  • 40
    • 0542439200 scopus 로고
    • The constituents of Casimiroa edulis Llave et Lex. III. The structure of casimiroin
    • Meisels, A.; Sondheimer, F. The constituents of Casimiroa edulis Llave et Lex. III. The structure of casimiroin. J. Am. Chem. Soc. 1957, 79, 6328-6333.
    • (1957) J. Am. Chem. Soc. , vol.79 , pp. 6328-6333
    • Meisels, A.1    Sondheimer, F.2
  • 41
    • 0017642367 scopus 로고
    • Oral methoxsalen photochemotherapy for the treatment of psoriasis: A cooperative clinical trial
    • Melski, J. W.; Tanenbaum, L.; Parrish, J. A.; Fitzpatrick, T. B.; Bleich, H. L. Oral methoxsalen photochemotherapy for the treatment of psoriasis: a cooperative clinical trial. J. Invest. Dermatol. 1977, 68, 328-335.
    • (1977) J. Invest. Dermatol. , vol.68 , pp. 328-335
    • Melski, J.W.1    Tanenbaum, L.2    Parrish, J.A.3    Fitzpatrick, T.B.4    Bleich, H.L.5
  • 42
    • 0022385516 scopus 로고
    • Mutagenic activities of dictamnine and γ-fagarine from Dictamni Radicis cortex (Rutaceae)
    • Mizuta, M.; Kanamori, H. Mutagenic activities of dictamnine and γ-fagarine from Dictamni Radicis cortex (Rutaceae). Mutat. Res. 1985, 144, 221-225.
    • (1985) Mutat. Res. , vol.144 , pp. 221-225
    • Mizuta, M.1    Kanamori, H.2
  • 43
    • 0542367910 scopus 로고
    • Spectra and stereo-chemistry. XXIX. The structure of zapoterin
    • Murphy, J. W.; Toube, T.; Cross, D. A. Spectra and stereo-chemistry. XXIX. The structure of zapoterin. Tetrahedron 1968, 49, 5153-5156.
    • (1968) Tetrahedron , vol.49 , pp. 5153-5156
    • Murphy, J.W.1    Toube, T.2    Cross, D.A.3
  • 44
    • 0000768084 scopus 로고
    • Synthetic application of lithiation reactions. VI. New synthesis of linear furoquinoline alkaloids
    • Narasimhan, N. S.; Mali, R. S. Synthetic application of lithiation reactions. VI. New synthesis of linear furoquinoline alkaloids. Tetrahedron 1974, 30, 4153-4157.
    • (1974) Tetrahedron , vol.30 , pp. 4153-4157
    • Narasimhan, N.S.1    Mali, R.S.2
  • 45
    • 0028905528 scopus 로고
    • Anticonvulsant activity of Casimiroa edulis in comparison to phenytoin and phenobarbital
    • Navarro, R. A.; Bastidas, R. B. E.; Garcia, E. J.; Garcia, L. P.; Garzon, P. Anticonvulsant activity of Casimiroa edulis in comparison to phenytoin and phenobarbital. J. Ethnopharmacol. 1995, 45, 199-206.
    • (1995) J. Ethnopharmacol. , vol.45 , pp. 199-206
    • Navarro, R.A.1    Bastidas, R.B.E.2    Garcia, E.J.3    Garcia, L.P.4    Garzon, P.5
  • 46
    • 0342940037 scopus 로고
    • Alkaloids of the stem bark of Hesperethusa crenulata
    • Nayar, M. N. S., Sutar, C. V.; Bhan, M. K. Alkaloids of the stem bark of Hesperethusa crenulata. Phytochemistry 1971, 10, 2843-2844.
    • (1971) Phytochemistry , vol.10 , pp. 2843-2844
    • Nayar, M.N.S.1    Sutar, C.V.2    Bhan, M.K.3
  • 47
    • 84889208018 scopus 로고
    • Alterations in the metabolism of 7,12-dimethylbenz-[a]anthracene and various xenobiotics by rat hepatic microsomes following Sudan III treatment in vivo
    • O'Dowd, J. J.; Burnett, A. K.; Weston, A.; Bulleid, N. J.; Craft, J. A. Alterations in the metabolism of 7,12-dimethylbenz-[a]anthracene and various xenobiotics by rat hepatic microsomes following Sudan III treatment in vivo. Carcinogenesis 1988, 9, 1485-1491.
    • (1988) Carcinogenesis , vol.9 , pp. 1485-1491
    • O'Dowd, J.J.1    Burnett, A.K.2    Weston, A.3    Bulleid, N.J.4    Craft, J.A.5
  • 48
    • 0015936914 scopus 로고
    • The total synthesis of the alkaloid casimiroedine, an imidazole nucleoside
    • Panzica, R. P.; Townsend, L. B. The total synthesis of the alkaloid casimiroedine, an imidazole nucleoside. J. Am. Chem. Soc. 1973, 95, 8737-8740.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 8737-8740
    • Panzica, R.P.1    Townsend, L.B.2
  • 49
    • 0023371882 scopus 로고
    • Mutagenic compounds in an extract from Rutae Herba (Ruta graveolens L.). I. Mutagenicity is partially caused by furoquinoline alkaloids
    • Paulini, H.; Eilert, U.; Schimmer, O. Mutagenic compounds in an extract from Rutae Herba (Ruta graveolens L.). I. Mutagenicity is partially caused by furoquinoline alkaloids. Mutagenesis 1987, 2, 271-273.
    • (1987) Mutagenesis , vol.2 , pp. 271-273
    • Paulini, H.1    Eilert, U.2    Schimmer, O.3
  • 50
    • 0024468664 scopus 로고
    • Mutagenicity and structure-mutagenicity relationships of furoquinolines, naturally occurring alkaloids of the Rutaceae
    • Paulini, H.; Waiber, R.; Schimmer, O. Mutagenicity and structure-mutagenicity relationships of furoquinolines, naturally occurring alkaloids of the Rutaceae. Mutat. Res. 1989, 227, 179-186.
    • (1989) Mutat. Res. , vol.227 , pp. 179-186
    • Paulini, H.1    Waiber, R.2    Schimmer, O.3
  • 51
    • 0020418553 scopus 로고
    • Etude de quelques Rutacees a alcaloides. II. Ruta graveolens: Revue botanique, chimique et pharmacologique. (Etude particuliere des alcaloides quaternaires quinoleiques)
    • Petit-Paly, G.; Rideau, M.; Chenieux, C. J, Etude de quelques Rutacees a alcaloides. II. Ruta graveolens: Revue botanique, chimique et pharmacologique. (Etude particuliere des alcaloides quaternaires quinoleiques). Plant. Med. Phytother. 1982, 16, 55-72.
    • (1982) Plant. Med. Phytother. , vol.16 , pp. 55-72
    • Petit-Paly, G.1    Rideau, M.2    Chenieux, C.J.3
  • 52
    • 0001828070 scopus 로고
    • Natural product cancer chemopreventive agents
    • Arnason, J. T., Mata, R., Romeo, J. T., Eds.; Plenum Press: New York
    • Pezzuto, J. M. Natural product cancer chemopreventive agents. In Recent Advances in Phytochemistry, Vol. 29, Phytochemistry of Medicinal Plants; Arnason, J. T., Mata, R., Romeo, J. T., Eds.; Plenum Press: New York, 1995; pp 19-45.
    • (1995) Recent Advances in Phytochemistry, Vol. 29, Phytochemistry of Medicinal Plants , vol.29 , pp. 19-45
    • Pezzuto, J.M.1
  • 53
    • 0013494539 scopus 로고
    • The consituents of the seeds of Casimiroa edulis
    • Power, F. B.; Callan, T. The consituents of the seeds of Casimiroa edulis. J. Chem. Soc. 1911, 1993-2012.
    • (1911) J. Chem. Soc. , pp. 1993-2012
    • Power, F.B.1    Callan, T.2
  • 55
    • 33947469101 scopus 로고
    • α-Dimethylhistamine, a hypotensive principle in Casimiroa edulis Llave et Lex
    • α-Dimethylhistamine, a hypotensive principle in Casimiroa edulis Llave et Lex. J. Org. Chem. 1958, 23, 1564-1565.
    • (1958) J. Org. Chem. , vol.23 , pp. 1564-1565
    • Randolph, T.M.1    Friedrich, D.2
  • 56
    • 0021982621 scopus 로고
    • Alkaloids and coumarins of Casimiroa edulis
    • Rizvi, S. H.; Kapil, R. S.; Shoeb, A. Alkaloids and coumarins of Casimiroa edulis. J. Nat. Prod. 1985, 48, 146.
    • (1985) J. Nat. Prod. , vol.48 , pp. 146
    • Rizvi, S.H.1    Kapil, R.S.2    Shoeb, A.3
  • 57
    • 0542367907 scopus 로고
    • High-performance liquid chomatographic study of Casimiroa edulis. I. Determination of imidazole derivatives and rutin in aqueous and organic extracts
    • Romero, M. L.; Escobar, L. L; Lozoya, X.; Enríquez, R. G. High-performance liquid chomatographic study of Casimiroa edulis. I. Determination of imidazole derivatives and rutin in aqueous and organic extracts. J. Chromatogr. 1983, 281, 245-251.
    • (1983) J. Chromatogr. , vol.281 , pp. 245-251
    • Romero, M.L.1    Escobar, L.L.2    Lozoya, X.3    Enríquez, R.G.4
  • 58
    • 0016169629 scopus 로고
    • On the mass spectra of several furanocoumarins having various isoprenoidal residues
    • Saiki, Y.; Uchida, M.; Okegawa, O.; Fukushima, S. On the mass spectra of several furanocoumarins having various isoprenoidal residues. Chem. Pharm. Bull. 1974, 22, 1227-1232.
    • (1974) Chem. Pharm. Bull. , vol.22 , pp. 1227-1232
    • Saiki, Y.1    Uchida, M.2    Okegawa, O.3    Fukushima, S.4
  • 59
    • 84889229523 scopus 로고
    • Gamma-Fagarin, ein Furochinolinalkaloid aus Ruta graveolens L., induziert SCE in menschlichen lymphocyten in vitro
    • Schimmer, O.; Leimeister, U, Gamma-Fagarin, ein Furochinolinalkaloid aus Ruta graveolens L., induziert SCE in menschlichen lymphocyten in vitro. Arch. Pharm. 1988, 321, 637.
    • (1988) Arch. Pharm. , vol.321 , pp. 637
    • Schimmer, O.1    Leimeister, U.2
  • 60
    • 0026042491 scopus 로고
    • Inhibitory effects of furocoumarins in Salmonella typhimurium TA98 on the mutagenicity of dictamnine and rutacridone, promutagens from Ruta graveolens L
    • Schimmer, O.; Kiefer, J.; Paulini, H. Inhibitory effects of furocoumarins in Salmonella typhimurium TA98 on the mutagenicity of dictamnine and rutacridone, promutagens from Ruta graveolens L. Mutagenesis 1991, 6, 501-506.
    • (1991) Mutagenesis , vol.6 , pp. 501-506
    • Schimmer, O.1    Kiefer, J.2    Paulini, H.3
  • 61
    • 0028568405 scopus 로고
    • A correlative approach for the identification of antimutagens that demonstrate chemopreventive activity
    • Shamon, L. A.; Chen, C.; Mehta, R. G.; Steele, V.; Moon, R. C.; Pezzuto, J. M. A correlative approach for the identification of antimutagens that demonstrate chemopreventive activity. Anticancer Res. 1994, 14, 1775-1778.
    • (1994) Anticancer Res. , vol.14 , pp. 1775-1778
    • Shamon, L.A.1    Chen, C.2    Mehta, R.G.3    Steele, V.4    Moon, R.C.5    Pezzuto, J.M.6
  • 62
    • 0024541342 scopus 로고
    • Evidence for cytochrome P-450NF, the nifedipine oxidase, being the principal enzyme involved in the bioactivation of aflatoxins in the human liver
    • Shimada, T.; Guengerich, F. P. Evidence for cytochrome P-450NF, the nifedipine oxidase, being the principal enzyme involved in the bioactivation of aflatoxins in the human liver. Proc. Natl. Acad. Sci. U.S.A. 1989, 86, 462-465.
    • (1989) Proc. Natl. Acad. Sci. U.S.A. , vol.86 , pp. 462-465
    • Shimada, T.1    Guengerich, F.P.2
  • 63
    • 0025354746 scopus 로고
    • The mode of the activity of naturally occurring furanocoumarins on hepatic cytochrome P-450 enzyme system
    • Shin, K. H.; Woo, W. S. The mode of the activity of naturally occurring furanocoumarins on hepatic cytochrome P-450 enzyme system. Kor. J. Pharmacog. 1990, 211, 74-82.
    • (1990) Kor. J. Pharmacog. , vol.211 , pp. 74-82
    • Shin, K.H.1    Woo, W.S.2
  • 64
    • 1842321714 scopus 로고
    • Relative sensitivities of forward and reverse mutation assays in Salmonella typhimurium
    • Skopek, T. R.; Liber, H. L.; Kaden, D. A.; Thilly, W. G. Relative sensitivities of forward and reverse mutation assays in Salmonella typhimurium. Proc. Natl. Acad. Sci U.S.A. 1978, 75, 4465-4469.
    • (1978) Proc. Natl. Acad. Sci U.S.A. , vol.75 , pp. 4465-4469
    • Skopek, T.R.1    Liber, H.L.2    Kaden, D.A.3    Thilly, W.G.4
  • 65
    • 0343695974 scopus 로고
    • The constituents of Casimiroa edulis Llave et Lex. IV. Identification of edulin with 7-methyl-1-methyl-2-phenyl-4-quinolone
    • Sondheimer, F.; Meisels, A. The constituents of Casimiroa edulis Llave et Lex. IV. Identification of edulin with 7-methyl-1-methyl-2-phenyl-4-quinolone. J. Org. Chem. 1958, 23, 762-763.
    • (1958) J. Org. Chem. , vol.23 , pp. 762-763
    • Sondheimer, F.1    Meisels, A.2
  • 66
    • 0542415294 scopus 로고
    • Constituents of Casimiroa edulis Llave et Lex. VI. 2′,5′,6-trimethoxy flavone, 2′,5,6,7-tetra-methoxyflavone (zapotin) and 5-hydroxy-2′,6,7-trimethoxyflavone (zapotinin)
    • Sondheimer, F.; Meisels, A. Constituents of Casimiroa edulis Llave et Lex. VI. 2′,5′,6-trimethoxy flavone, 2′,5,6,7-tetra-methoxyflavone (zapotin) and 5-hydroxy-2′,6,7-trimethoxyflavone (zapotinin). Tetrahedron 1960, 9, 139-144.
    • (1960) Tetrahedron , vol.9 , pp. 139-144
    • Sondheimer, F.1    Meisels, A.2
  • 67
    • 0542391670 scopus 로고
    • Constituents of Casimiroa edulis Llave et Lex. V. Identity of casimirolid and obacunone
    • Sondheimer, F.; Meisels, A.; Kincl, F. A. Constituents of Casimiroa edulis Llave et Lex. V. Identity of casimirolid and obacunone. J. Org. Chem. 1959, 24, 870.
    • (1959) J. Org. Chem. , vol.24 , pp. 870
    • Sondheimer, F.1    Meisels, A.2    Kincl, F.A.3
  • 68
    • 0017136711 scopus 로고
    • Prevention of chemical carcinogenesis by vitamin A and its synthetic analogs (retinoids)
    • Sporn, M. B.; Dunlop, N. M.; Newton, D. L.; Smith, J. M. Prevention of chemical carcinogenesis by vitamin A and its synthetic analogs (retinoids). Fed. Proc. 1976, 35, 1332-1338.
    • (1976) Fed. Proc. , vol.35 , pp. 1332-1338
    • Sporn, M.B.1    Dunlop, N.M.2    Newton, D.L.3    Smith, J.M.4
  • 69
    • 0029064407 scopus 로고
    • Discovery of natural product chemopreventive agents using HL-60 cell differentiation as a model
    • Suh, N.; Luyengi, L.; Fong, H. H. S.; Kinghorn, A. D.; Pezzuto, J. M. Discovery of natural product chemopreventive agents using HL-60 cell differentiation as a model. Anticancer Res. 1995, 15, 233-238.
    • (1995) Anticancer Res. , vol.15 , pp. 233-238
    • Suh, N.1    Luyengi, L.2    Fong, H.H.S.3    Kinghorn, A.D.4    Pezzuto, J.M.5
  • 70
    • 0006262948 scopus 로고
    • The structures of edulitine and edulinine. XXIV. Spectra and stereochemistry
    • Toube, T. P.; Murphy, J. W.; Cross, A. D. The structures of edulitine and edulinine. XXIV. Spectra and stereochemistry. Tetrahedron 1967, 23, 2061-2065.
    • (1967) Tetrahedron , vol.23 , pp. 2061-2065
    • Toube, T.P.1    Murphy, J.W.2    Cross, A.D.3
  • 71
    • 0025779874 scopus 로고
    • Pharmacology of Casimiroa edulis. II. Cardiovascular effects in the anesthesized dog
    • Vidrio, H.; Magos, G. A. Pharmacology of Casimiroa edulis. II. Cardiovascular effects in the anesthesized dog. Planta Med. 1991, 57, 217-220.
    • (1991) Planta Med. , vol.57 , pp. 217-220
    • Vidrio, H.1    Magos, G.A.2
  • 72
    • 0026447635 scopus 로고
    • Antimutagenic agents from natural products
    • Wall, M. E. Antimutagenic agents from natural products. J. Nat. Prod. 1992, 55, 1561-1568.
    • (1992) J. Nat. Prod. , vol.55 , pp. 1561-1568
    • Wall, M.E.1
  • 74
    • 0006539828 scopus 로고
    • Heterocyclic compounds. V. The synthesis of casimiroin
    • Weinstein, B.; Hylton, T. A. Heterocyclic compounds. V. The synthesis of casimiroin. Tetrahedron 1964, 20, 1725-1728.
    • (1964) Tetrahedron , vol.20 , pp. 1725-1728
    • Weinstein, B.1    Hylton, T.A.2
  • 75
    • 0008295684 scopus 로고
    • 5-Hydroxy-6,2′-dimethoxyflavone from Primula denticulata
    • Wollenweber, E.; Iinuma, M.; Tanaka, T.; Mizuno, M. 5-Hydroxy-6,2′-dimethoxyflavone from Primula denticulata. Phytochemistry 1990, 29, 633-637.
    • (1990) Phytochemistry , vol.29 , pp. 633-637
    • Wollenweber, E.1    Iinuma, M.2    Tanaka, T.3    Mizuno, M.4


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