메뉴 건너뛰기




Volumn 4, Issue 3, 2011, Pages 271-274

Constituents from Chimonanthus praecox (wintersweet)

Author keywords

Calycanthaceae; Chimonanthus praecox; Dimeric tryptamine related alkaloids; Sesquiterpenoids

Indexed keywords

3 EUDESMEN BETA,11 DIOL; 3 HYDROXY 5,6 EPOXY BETA IONOL 3 O BETA DEXTRO GLUCOPYRANOSIDE; 3 METHYLCARBOXYMETHYL INDOLE 1 N BETA DEXTRO GLUCOPYRANOSIDE; 4 EPI BULLATANTRIOL (1BETA,4ALPHA,11 OPPOSITANETRIOL); 4 EUDESMEN BETA,11 DIOL; 4(15 EUDESMEN BETA,11 DIOL(SELIN 4 (15) EN BETA,11 DIOL; ALKALOID; BENZYL BETA PRIMEVEROSIDE; BRIDELIONOSIDE B; BULLATANTRIOL; CALYCANTHIDINE; CALYCANTHINE; CHIMONANTHINE; FLUOROURACIL; FOLICANTHINE; GLYCOSIDE; HOMALOMENOL A; HOMALOMENOL C; LINOCINNAMARIN; METHYL 4 BETA DEXTRO GLUCOPYRANOSYL FERULATE; OPLODIOL; SESQUITERPENOID; UNCLASSIFIED DRUG;

EID: 80053324378     PISSN: 18743900     EISSN: 18767486     Source Type: Journal    
DOI: 10.1016/j.phytol.2011.04.012     Document Type: Article
Times cited : (40)

References (26)
  • 1
    • 0001461165 scopus 로고
    • A new sesquiterpene alcohol from Pterocarpus marsupium
    • D. Adinarayana, and K.V. Syamasundar A new sesquiterpene alcohol from Pterocarpus marsupium Phytochemistry 21 1982 1083 1085
    • (1982) Phytochemistry , vol.21 , pp. 1083-1085
    • Adinarayana, D.1    Syamasundar, K.V.2
  • 2
    • 0024847919 scopus 로고
    • Cytotoxicity on human leukemic and rat hepatoma cell lines of alkaloid extracts of Psychotria forsteriana
    • Y. Adjibadé, B. Kuballa, P. Cabalion, M.L. Jung, J.P. Beck, and R. Anton Cytotoxicity on human leukemic and rat hepatoma cell lines of alkaloid extracts of Psychotria forsteriana Planta Med. 55 1989 567 568 (Pubitemid 20059705)
    • (1989) Planta Medica , vol.55 , Issue.6 , pp. 567-568
    • Adjibade, Y.1    Kuballa, B.2    Cabalion, P.3    Jung, M.L.4    Beck, J.P.5    Anton, R.6
  • 3
    • 33947298484 scopus 로고
    • Methyl-1-(β-d-glucopyranosy)-3-indoleacetate
    • R.L. Franklin, and H.M. Sell Methyl-1-(β-d-glucopyranosy)-3- indoleacetate J. Chem. Eng. Data 14 1969 267 269
    • (1969) J. Chem. Eng. Data , vol.14 , pp. 267-269
    • Franklin, R.L.1    Sell, H.M.2
  • 4
    • 34848913109 scopus 로고    scopus 로고
    • Chemical synthesis of hydroxycinnamic acid glucosides and evaluation of their ability to stabilize natural colors via anthocyanin copigmentation
    • DOI 10.1021/jf071205v
    • S. Galland, N. Mora, M. Abert-Vian, N. Rakotomanomana, and O. Dangles Chemical synthesis of hydroxycinnamic acid glucosides and evaluation of their ability to stabilize natural colors via anthocyanin copigmentation J. Agric. Food Chem. 55 2007 7573 7579 (Pubitemid 47492317)
    • (2007) Journal of Agricultural and Food Chemistry , vol.55 , Issue.18 , pp. 7573-7579
    • Galland, S.1    Mora, N.2    Abert-Vian, M.3    Rakotomanomana, N.4    Dangles, O.5
  • 5
    • 0028489368 scopus 로고
    • (S)-Linalyl, 2-phenylethyl, and benzyl disaccharide glycosides isolated as aroma precursors from Oolong tea leaves
    • W. Guo, R. Hosoi, K. Sakata, N. Watanabe, A. Yagi, K. Ina, and S. Luo (S)-Linalyl, 2-phenylethyl, and benzyl disaccharide glycosides isolated as aroma precursors from Oolong tea leaves Biosci. Biotechnol. Biochem. 58 1994 1532 1534
    • (1994) Biosci. Biotechnol. Biochem. , vol.58 , pp. 1532-1534
    • Guo, W.1    Hosoi, R.2    Sakata, K.3    Watanabe, N.4    Yagi, A.5    Ina, K.6    Luo, S.7
  • 6
    • 0000160597 scopus 로고
    • Sesquiterpene alcohols and triterpenoids from Liatris microcephala
    • W. Herz, and K. Watanabe Sesquiterpene alcohols and triterpenoids from Liatris microcephala Phytochemistry 22 1983 1457 1459
    • (1983) Phytochemistry , vol.22 , pp. 1457-1459
    • Herz, W.1    Watanabe, K.2
  • 7
    • 0003658331 scopus 로고
    • Jiangsu New Medical College Shanghai Science and Technology Publishing House Shanghai p. 1863, 2553
    • Jiangsu New Medical College Dictionary of the Chinese Materia Medica 1986 Shanghai Science and Technology Publishing House Shanghai p. 1863, 2553
    • (1986) Dictionary of the Chinese Materia Medica
  • 8
    • 33645756584 scopus 로고    scopus 로고
    • Two new tryptamine-derived alkaloids from Chimonanthus praecox f. concolor
    • M. Kitajima, I. Mori, K. Arai, N. Kogure, and H. Takayama Two new tryptamine-derived alkaloids from Chimonanthus praecox f. concolor Tetrahedron Lett. 47 2006 3199 3202
    • (2006) Tetrahedron Lett. , vol.47 , pp. 3199-3202
    • Kitajima, M.1    Mori, I.2    Arai, K.3    Kogure, N.4    Takayama, H.5
  • 10
    • 0344056809 scopus 로고
    • Isolation of a new terpene glucoside, 3-hydroxy-5,6-epoxy-β-ionyl- β-d-glucopyranoside from flue-cured tobacco
    • H. Kodama, T. Fujimori, and K. Kat Isolation of a new terpene glucoside, 3-hydroxy-5,6-epoxy-β-ionyl-β-d-glucopyranoside from flue-cured tobacco Agric. Biol. Chem. 45 1981 941 944
    • (1981) Agric. Biol. Chem. , vol.45 , pp. 941-944
    • Kodama, H.1    Fujimori, T.2    Kat, K.3
  • 11
    • 7444271125 scopus 로고
    • Bullatantriol, a sesquiterpene from Annona bullata
    • L. Kutschabsky, D. Sandoval, and H. Ripperger Bullatantriol, a sesquiterpene from Annona bullata Phytochemistry 24 1985 2724 2725
    • (1985) Phytochemistry , vol.24 , pp. 2724-2725
    • Kutschabsky, L.1    Sandoval, D.2    Ripperger, H.3
  • 13
    • 0011491353 scopus 로고
    • Biomimetic transformation of hodgkinsine, a pyrrolidinoindoline alkaloid
    • F. Libot, N. Kunesch, J. Poisson, M. Kaiser, and H. Duddeck Biomimetic transformation of hodgkinsine, a pyrrolidinoindoline alkaloid Heterocycles 27 1988 2381 2386
    • (1988) Heterocycles , vol.27 , pp. 2381-2386
    • Libot, F.1    Kunesch, N.2    Poisson, J.3    Kaiser, M.4    Duddeck, H.5
  • 15
    • 0033603864 scopus 로고    scopus 로고
    • Direct stereo- and enantiocontrolled synthesis of vicinal stereogenic quaternary carbon centers. Total syntheses of meso- and (-)-chimonanthine and (+)-calycanthine [4]
    • DOI 10.1021/ja991714g
    • L.E. Overman, D.V. Paone, and B.A. Stearns Direct stereo- and enantiocontrolled synthesis of vicinal stereogenic quaternary carbon centers. Total syntheses of meso- and (-)-Chimonanthine and (+)-Calycanthine J. Am. Chem. Soc. 121 1999 7702 7703 (Pubitemid 29413735)
    • (1999) Journal of the American Chemical Society , vol.121 , Issue.33 , pp. 7702-7703
    • Overman, L.E.1    Paone, D.V.2    Stearns, B.A.3
  • 16
    • 34249849535 scopus 로고    scopus 로고
    • Isolation, structure determination, and sensory activity of mouth-drying and astringent nitrogen-containing phytochemicals isolated from red currants (Ribes rubrum)
    • B. Schwarz, and T. Hofmann Isolation, structure determination, and sensory activity of mouth-drying and astringent nitrogen-containing phytochemicals isolated from red currants (Ribes rubrum) J. Agric. Food Chem. 55 2007 1405 1410
    • (2007) J. Agric. Food Chem. , vol.55 , pp. 1405-1410
    • Schwarz, B.1    Hofmann, T.2
  • 17
    • 0028888392 scopus 로고
    • Sesquiterpenes from leaves of Cryptomeria japonica
    • W.-C. Su, J.-M. Fang, and Y.-S. Cheng Sesquiterpenes from leaves of Cryptomeria japonica Phytochemistry 39 1995 603 607
    • (1995) Phytochemistry , vol.39 , pp. 603-607
    • Su, W.-C.1    Fang, J.-M.2    Cheng, Y.-S.3
  • 18
    • 0034060694 scopus 로고    scopus 로고
    • Megastigmane, benzyl and phenethyl alcohol glycosides, and 4,4'-dimethoxy-β-truxinic acid catalpol diester from the leaves of Premna subscandens Merr
    • H. Sudo, T. Ide, H. Otsuka, E. Hirata, A. Takushi, T. Shinzato, and Y. Takeda Megastigmane, benzyl and phenethyl alcohol glycosides, and 4,4′-dimethoxy-β-truxinic acid catalpol diester from the leaves of Premna subscandens Merr Chem. Pharm. Bull. 48 2000 542 546 (Pubitemid 30246312)
    • (2000) Chemical and Pharmaceutical Bulletin , vol.48 , Issue.4 , pp. 542-546
    • Sudo, H.1    Ide, T.2    Otsuka, H.3    Hirata, E.4    Takushi, A.5    Shinzato, T.6    Takeda, Y.7
  • 19
    • 33750175548 scopus 로고    scopus 로고
    • Bridelionosides A-F: Megastigmane glucosides from Bridelia glauca f. balansae
    • DOI 10.1016/j.phytochem.2006.09.007, PII S0031942206005711
    • E. Sueyoshi, H. Liu, K. Matsunami, H. Otsuka, T. Shinzato, M. Aranoto, and Y. Takeda Bridelionosides A-F:Megastigmane glucosides from Bridelia glauca f. balansae Phytochemistry 67 2006 2483 2493 (Pubitemid 44602135)
    • (2006) Phytochemistry , vol.67 , Issue.22 , pp. 2483-2493
    • Sueyoshi, E.1    Liu, H.2    Matsunami, K.3    Otsuka, H.4    Shinzato, T.5    Aramoto, M.6    Takeda, Y.7
  • 22
    • 0346969633 scopus 로고    scopus 로고
    • Isolation, structure elucidation, and total synthesis of two new Chimonanthus alkaloids, chimonamidine and chimonanthidine
    • DOI 10.1016/j.tet.2003.11.034
    • H. Takayama, Y. Matsuda, K. Masubuchi, A. Ishida, M. Kitajima, and N. Aimi Isolation, structure elucidation, and total synthesis of two new Chimonanthus alkaloids, chimonamidine and chimonanthidine Tetrahedron 60 2004 893 900 (Pubitemid 38068307)
    • (2004) Tetrahedron , vol.60 , Issue.4 , pp. 893-900
    • Takayama, H.1    Matsuda, Y.2    Masubuchi, K.3    Ishida, A.4    Kitajima, M.5    Aimi, N.6
  • 23
    • 84987564508 scopus 로고
    • The volatile constituents of the flower concrete of Chimonanthus praecox Link. from China
    • Y. Ueyama, S. Hashimoto, H. Nii, and K. Furukawa The volatile constituents of the flower concrete of Chimonanthus praecox Link. from China Flavour Fragr. J. 5 1990 85 88
    • (1990) Flavour Fragr. J. , vol.5 , pp. 85-88
    • Ueyama, Y.1    Hashimoto, S.2    Nii, H.3    Furukawa, K.4
  • 25
    • 78650189141 scopus 로고    scopus 로고
    • Triterpenoids and steroids from the fruits of Melia toosendan and their cytotoxic effects on two human cancer cell lines
    • S.-B. Wu, J.-J. Su, L.-H. Sun, W.-X. Wang, Y. Zhao, H. Li, S.-P. Zhang, G.-H. Dai, C.-G. Wang, and J.-F. Hu Triterpenoids and steroids from the fruits of Melia toosendan and their cytotoxic effects on two human cancer cell lines J. Nat. Prod. 73 2010 1898 1906
    • (2010) J. Nat. Prod. , vol.73 , pp. 1898-1906
    • Wu, S.-B.1    Su, J.-J.2    Sun, L.-H.3    Wang, W.-X.4    Zhao, Y.5    Li, H.6    Zhang, S.-P.7    Dai, G.-H.8    Wang, C.-G.9    Hu, J.-F.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.