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Volumn 68, Issue 15, 2007, Pages 2101-2111

Lignans, an amide and anti-platelet activities from Piper philippinum

Author keywords

(+) Bornyl caffeate; Amide; Anti platelet activity; Lignan; Philippinamide; Piper philippinum; Piperaceae; Piperphilippinins I VI; Stem

Indexed keywords

AMIDE; ANTITHROMBOCYTIC AGENT; LIGNAN; PLANT EXTRACT;

EID: 34447542701     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2007.05.003     Document Type: Article
Times cited : (59)

References (43)
  • 1
    • 0001536125 scopus 로고
    • Über die Isolierung von zwei neuen Pyrrolididen aus Rauschpfeffer (Piper methysticum Forst.)
    • Achenbach H., and Karl W. Über die Isolierung von zwei neuen Pyrrolididen aus Rauschpfeffer (Piper methysticum Forst.). Chem. Ber. 103 (1970) 2535-2540
    • (1970) Chem. Ber. , vol.103 , pp. 2535-2540
    • Achenbach, H.1    Karl, W.2
  • 2
    • 0022585458 scopus 로고
    • Constituents of tropical medicinal plants, IXX GC/MS-investigations of the constituents of Piper amalago - 30 new amides of the piperine-type
    • Achenbach H., Fietz W., Wörth J., Waibel R., and Portecop J. Constituents of tropical medicinal plants, IXX GC/MS-investigations of the constituents of Piper amalago - 30 new amides of the piperine-type. Planta Med. 52 (1986) 12-18
    • (1986) Planta Med. , vol.52 , pp. 12-18
    • Achenbach, H.1    Fietz, W.2    Wörth, J.3    Waibel, R.4    Portecop, J.5
  • 4
    • 0001235697 scopus 로고
    • Palladium-catalyzed formylation of organic halides with carbon monoxide and tin hydride
    • Baillargeon V.P., and Stille J.K. Palladium-catalyzed formylation of organic halides with carbon monoxide and tin hydride. J. Am. Chem. Soc. 108 (1986) 452-461
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 452-461
    • Baillargeon, V.P.1    Stille, J.K.2
  • 5
    • 33751385800 scopus 로고
    • A simple and highly stereoselective route to E-α,β-unsaturated aldehydes
    • Bellassoued M., and Majidi A. A simple and highly stereoselective route to E-α,β-unsaturated aldehydes. J. Org. Chem. 58 (1993) 2517-2522
    • (1993) J. Org. Chem. , vol.58 , pp. 2517-2522
    • Bellassoued, M.1    Majidi, A.2
  • 6
    • 0010463546 scopus 로고
    • Neue Terpen-Inhaltsstoffe aus Verbesina-Arten
    • Bohlmann F., and Zdero C. Neue Terpen-Inhaltsstoffe aus Verbesina-Arten. Phytochemistry 15 (1976) 1310-1311
    • (1976) Phytochemistry , vol.15 , pp. 1310-1311
    • Bohlmann, F.1    Zdero, C.2
  • 9
    • 1542344485 scopus 로고    scopus 로고
    • A new aristolactam alkaloid and anti-platelet aggregation constituents from Piper taiwanense
    • Chen Y.C., Chen J.J., Chang Y.L., Teng C.M., Lin W.Y., Wang E.C., and Chen I.S. A new aristolactam alkaloid and anti-platelet aggregation constituents from Piper taiwanense. Planta Med. 70 (2004) 174-177
    • (2004) Planta Med. , vol.70 , pp. 174-177
    • Chen, Y.C.1    Chen, J.J.2    Chang, Y.L.3    Teng, C.M.4    Lin, W.Y.5    Wang, E.C.6    Chen, I.S.7
  • 11
    • 4243173397 scopus 로고
    • Two phenolic amides in the seed balls of sugar beet (Beta vulgaris L. var. saccharifera Alefeld)
    • Chiji H., Giga T., Izawa M., and Kiriyama S. Two phenolic amides in the seed balls of sugar beet (Beta vulgaris L. var. saccharifera Alefeld). Agric. Biol. Chem. 48 (1984) 1653-1654
    • (1984) Agric. Biol. Chem. , vol.48 , pp. 1653-1654
    • Chiji, H.1    Giga, T.2    Izawa, M.3    Kiriyama, S.4
  • 12
    • 0001532649 scopus 로고
    • Aristolactams and 4,5-dioxoaporphines from Piper longum
    • Desai S.J., Prabsu B.R., and Mulchandani N.B. Aristolactams and 4,5-dioxoaporphines from Piper longum. Phytochemistry 27 (1988) 1511-1515
    • (1988) Phytochemistry , vol.27 , pp. 1511-1515
    • Desai, S.J.1    Prabsu, B.R.2    Mulchandani, N.B.3
  • 14
    • 0001311379 scopus 로고
    • Haplomyrtin and (-)-haplomyrfolin: two lignans from Haplophyllum myrtifolium
    • Evcim U., Gözler B., Freyer A.J., and Shamma M. Haplomyrtin and (-)-haplomyrfolin: two lignans from Haplophyllum myrtifolium. Phytochemistry 25 (1986) 1949-1951
    • (1986) Phytochemistry , vol.25 , pp. 1949-1951
    • Evcim, U.1    Gözler, B.2    Freyer, A.J.3    Shamma, M.4
  • 15
    • 0031763237 scopus 로고    scopus 로고
    • Steroidal constituents of Ganoderma applanatum and Ganoderma neo-japonicum
    • Gan K.H., Kuo S.H., and Lin C.N. Steroidal constituents of Ganoderma applanatum and Ganoderma neo-japonicum. J. Nat. Prod. 61 (1998) 1421-1422
    • (1998) J. Nat. Prod. , vol.61 , pp. 1421-1422
    • Gan, K.H.1    Kuo, S.H.2    Lin, C.N.3
  • 17
    • 0000618669 scopus 로고
    • Isodaurinol, an arylnaphthalene lignan from Haplophyllum cappadocicum
    • Gözler B., Arar G., Gözler T., and Hesse M. Isodaurinol, an arylnaphthalene lignan from Haplophyllum cappadocicum. Phytochemistry 31 (1992) 2473-2475
    • (1992) Phytochemistry , vol.31 , pp. 2473-2475
    • Gözler, B.1    Arar, G.2    Gözler, T.3    Hesse, M.4
  • 18
    • 0034711463 scopus 로고    scopus 로고
    • A 38 kDa allylic alcohol dehydrogenase from the cultured cells of Nicotiana tabacum
    • Hirata T., Tamura Y., Yokobatake N., Shimoda K., and Ashida Y. A 38 kDa allylic alcohol dehydrogenase from the cultured cells of Nicotiana tabacum. Phytochemistry 55 (2000) 297-303
    • (2000) Phytochemistry , vol.55 , pp. 297-303
    • Hirata, T.1    Tamura, Y.2    Yokobatake, N.3    Shimoda, K.4    Ashida, Y.5
  • 19
    • 0000449373 scopus 로고
    • Biosynthesis of Podophyllum lignans-i. Cinnamic acid precursors of podophyllotoxin in Podophyllum hexandrum
    • Jackson D.E., and Dewick P.M. Biosynthesis of Podophyllum lignans-i. Cinnamic acid precursors of podophyllotoxin in Podophyllum hexandrum. Phytochemistry 23 (1984) 1029-1035
    • (1984) Phytochemistry , vol.23 , pp. 1029-1035
    • Jackson, D.E.1    Dewick, P.M.2
  • 20
    • 0025266068 scopus 로고
    • Fern constituents: cheilanthenetriol and cheilanthenediol. Sesterterpenoids isolated from the leaves of Aleuritopteris khunii
    • Kamaya R., and Ageta H. Fern constituents: cheilanthenetriol and cheilanthenediol. Sesterterpenoids isolated from the leaves of Aleuritopteris khunii. Chem. Pharm. Bull. 38 (1990) 342-346
    • (1990) Chem. Pharm. Bull. , vol.38 , pp. 342-346
    • Kamaya, R.1    Ageta, H.2
  • 21
    • 0343106462 scopus 로고
    • Quassinoids from Picrasma javanica
    • Koike K., and Ohmoto T. Quassinoids from Picrasma javanica. Phytochemistry 29 (1990) 2617-2621
    • (1990) Phytochemistry , vol.29 , pp. 2617-2621
    • Koike, K.1    Ohmoto, T.2
  • 22
    • 44949267313 scopus 로고
    • Sterol glucosides from Prunella vulgaris
    • Kojima H., Sato N., Hatano A., and Ogura H. Sterol glucosides from Prunella vulgaris. Phytochemistry 29 (1990) 2351-2355
    • (1990) Phytochemistry , vol.29 , pp. 2351-2355
    • Kojima, H.1    Sato, N.2    Hatano, A.3    Ogura, H.4
  • 23
    • 0036635202 scopus 로고    scopus 로고
    • New lignans from the heartwood of Chamaecyparis obtusa var. formosana
    • Kuo Y.H., Chen C.H., and Lin Y.L. New lignans from the heartwood of Chamaecyparis obtusa var. formosana. Chem. Pharm. Bull. 50 (2002) 978-980
    • (2002) Chem. Pharm. Bull. , vol.50 , pp. 978-980
    • Kuo, Y.H.1    Chen, C.H.2    Lin, Y.L.3
  • 25
    • 34447553299 scopus 로고    scopus 로고
    • Lin, T.T., Lu, S.Y., 1996. Piperaceae in Flora of Taiwan, second ed. Editorial Committee of the Flora of Taiwan, Taipei, Taiwan, vol. 2, pp. 624-631.
  • 26
    • 0000633244 scopus 로고
    • Dibenzylbutyrolactone lignans from Virola sebifera
    • Lopes L.M.X., Yoshida M., and Gottlieb O.R. Dibenzylbutyrolactone lignans from Virola sebifera. Phytochemistry 22 (1983) 1516-1518
    • (1983) Phytochemistry , vol.22 , pp. 1516-1518
    • Lopes, L.M.X.1    Yoshida, M.2    Gottlieb, O.R.3
  • 27
    • 15144352590 scopus 로고    scopus 로고
    • Anti-inflammatory activity of phenylpropanoids from Coreopsis mutica var. mutica
    • Maldonado E., Apan M.T.R., and Pérez-Castorena A.L. Anti-inflammatory activity of phenylpropanoids from Coreopsis mutica var. mutica. Planta Med. 64 (1998) 660-661
    • (1998) Planta Med. , vol.64 , pp. 660-661
    • Maldonado, E.1    Apan, M.T.R.2    Pérez-Castorena, A.L.3
  • 28
    • 0018584464 scopus 로고
    • The Piperaceae amides I: structure of pipercide, a new insecticidal amide from Piper nigrum L
    • Miyakado M., Nakayama I., Yoshioka H., and Nakatani N. The Piperaceae amides I: structure of pipercide, a new insecticidal amide from Piper nigrum L. Agric. Biol. Chem. 43 (1979) 1609-1611
    • (1979) Agric. Biol. Chem. , vol.43 , pp. 1609-1611
    • Miyakado, M.1    Nakayama, I.2    Yoshioka, H.3    Nakatani, N.4
  • 29
    • 0001194480 scopus 로고    scopus 로고
    • Suppression of SOS-inducing activity of chemical mutagens by cinnamic acid derivatives from Scrophularia ningpoensis in the Salmonella typhimurium TA1535/pSK1002 umu test
    • Miyazawa M., Okuno Y., Nakamura S., and Kameoka H. Suppression of SOS-inducing activity of chemical mutagens by cinnamic acid derivatives from Scrophularia ningpoensis in the Salmonella typhimurium TA1535/pSK1002 umu test. J. Agric. Food Chem. 46 (1998) 904-910
    • (1998) J. Agric. Food Chem. , vol.46 , pp. 904-910
    • Miyazawa, M.1    Okuno, Y.2    Nakamura, S.3    Kameoka, H.4
  • 30
    • 0001332609 scopus 로고
    • Platelet aggregation II. Some results from a new method of study
    • O'Brien J.R. Platelet aggregation II. Some results from a new method of study. J. Clin. Path. 15 (1962) 452-455
    • (1962) J. Clin. Path. , vol.15 , pp. 452-455
    • O'Brien, J.R.1
  • 31
    • 0030926256 scopus 로고    scopus 로고
    • Neolignans, styrylpyrones and flavonoids from an Aniba species
    • Rossi M.H., Yoshida M., and Maia J.G.S. Neolignans, styrylpyrones and flavonoids from an Aniba species. Phytochemistry 45 (1997) 1263-1269
    • (1997) Phytochemistry , vol.45 , pp. 1263-1269
    • Rossi, M.H.1    Yoshida, M.2    Maia, J.G.S.3
  • 32
    • 7344223255 scopus 로고    scopus 로고
    • A practical and efficient synthetic route to dihydropipercide and pipercide
    • Rotherham L.W., and Semple J.E. A practical and efficient synthetic route to dihydropipercide and pipercide. J. Org. Chem. 63 (1998) 6667-6672
    • (1998) J. Org. Chem. , vol.63 , pp. 6667-6672
    • Rotherham, L.W.1    Semple, J.E.2
  • 33
    • 0025994652 scopus 로고
    • Isolation, structure and synthesis of new diarylbutane lignans from Phyllanthus niruri: synthesis of 5′-desmethoxy niranthin and an antitumour extractive
    • Satyanarayana P., and Venkateswarlu S. Isolation, structure and synthesis of new diarylbutane lignans from Phyllanthus niruri: synthesis of 5′-desmethoxy niranthin and an antitumour extractive. Tetrahedron 47 (1991) 8931-8940
    • (1991) Tetrahedron , vol.47 , pp. 8931-8940
    • Satyanarayana, P.1    Venkateswarlu, S.2
  • 34
    • 0034740850 scopus 로고    scopus 로고
    • Three-component synthesis of (E)-α,β-unsaturated amides of the piperine family
    • Schobert R., Siegfried S., and Gordon G.J. Three-component synthesis of (E)-α,β-unsaturated amides of the piperine family. J. Chem. Soc., Perkin Trans. 1 (2001) 2393-2397
    • (2001) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 2393-2397
    • Schobert, R.1    Siegfried, S.2    Gordon, G.J.3
  • 35
    • 34447571611 scopus 로고    scopus 로고
    • Shih, M.H., 1991. Ph.D. Thesis. National Tsing Hua University, Hsinchu, Taiwan, pp. 216-224.
  • 36
    • 0019841997 scopus 로고
    • Diphenyl ether herbicides remarkably elevate the content in Spinacia oleracea of (E)-3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-2-propenamide
    • Suzuki T., Holden I., and Casida J.E. Diphenyl ether herbicides remarkably elevate the content in Spinacia oleracea of (E)-3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-2-propenamide. J. Agric. Food Chem. 29 (1981) 992-995
    • (1981) J. Agric. Food Chem. , vol.29 , pp. 992-995
    • Suzuki, T.1    Holden, I.2    Casida, J.E.3
  • 39
    • 0029360451 scopus 로고
    • Antimalarial sesquiterpenes from tubers of Cyperus rotundus: structure of 10,12-peroxycalamenene, a sesquiterpene endoperoxide
    • Thebtaranonth C., Thebtaranonth Y., Wanauppathamkul S., and Yuthavong Y. Antimalarial sesquiterpenes from tubers of Cyperus rotundus: structure of 10,12-peroxycalamenene, a sesquiterpene endoperoxide. Phytochemistry 40 (1995) 125-128
    • (1995) Phytochemistry , vol.40 , pp. 125-128
    • Thebtaranonth, C.1    Thebtaranonth, Y.2    Wanauppathamkul, S.3    Yuthavong, Y.4
  • 40
    • 21344469115 scopus 로고    scopus 로고
    • New cytotoxic cyclobutanoid amides, new furanoid lignan and anti-platelet aggregation constituents from Piper arborescens
    • Tsai I.L., Lee F.P., Wu C.C., Duh C.Y., Ishikawa T., Chen J.J., Chen Y.C., Seki H., and Chen I.S. New cytotoxic cyclobutanoid amides, new furanoid lignan and anti-platelet aggregation constituents from Piper arborescens. Planta Med. 71 (2005) 535-542
    • (2005) Planta Med. , vol.71 , pp. 535-542
    • Tsai, I.L.1    Lee, F.P.2    Wu, C.C.3    Duh, C.Y.4    Ishikawa, T.5    Chen, J.J.6    Chen, Y.C.7    Seki, H.8    Chen, I.S.9
  • 41
    • 0023239401 scopus 로고
    • Annoquinone-A, an antimicrobial and cytotoxic principle from Annona montana
    • Wu T.S., Jong T.T., Tien H.J., Kuoh C.S., Furukawa H., and Lee K.H. Annoquinone-A, an antimicrobial and cytotoxic principle from Annona montana. Phytochemistry 26 (1987) 1623-1625
    • (1987) Phytochemistry , vol.26 , pp. 1623-1625
    • Wu, T.S.1    Jong, T.T.2    Tien, H.J.3    Kuoh, C.S.4    Furukawa, H.5    Lee, K.H.6
  • 42
    • 0242380663 scopus 로고    scopus 로고
    • Transformation of arctiin to estrogenic and antiestrogenic substances by human intestinal bacteria
    • Xie L.H., Ahn E.M., Akao T., Abdel-Hafez A.A.M., Nakamura N., and Hattori M. Transformation of arctiin to estrogenic and antiestrogenic substances by human intestinal bacteria. Chem. Pharm. Bull. 51 (2003) 378-384
    • (2003) Chem. Pharm. Bull. , vol.51 , pp. 378-384
    • Xie, L.H.1    Ahn, E.M.2    Akao, T.3    Abdel-Hafez, A.A.M.4    Nakamura, N.5    Hattori, M.6
  • 43
    • 0642340664 scopus 로고    scopus 로고
    • Biotransformation of pinoresinol diglucoside to mammalian lignans by human intestinal microflora, and isolation of Enterococcus faecalis strain PDG-1 responsible for the transformation of (+)-pinoresinol to (+)-lariciresinol
    • Xie L.H., Akao T., Hamasaki K., Deyama T., and Hattori M. Biotransformation of pinoresinol diglucoside to mammalian lignans by human intestinal microflora, and isolation of Enterococcus faecalis strain PDG-1 responsible for the transformation of (+)-pinoresinol to (+)-lariciresinol. Chem. Pharm. Bull. 51 (2003) 508-515
    • (2003) Chem. Pharm. Bull. , vol.51 , pp. 508-515
    • Xie, L.H.1    Akao, T.2    Hamasaki, K.3    Deyama, T.4    Hattori, M.5


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