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Volumn 74, Issue , 2012, Pages 140-145

Indole alkaloids from Ervatamia chinensis

Author keywords

Apocynaceae; Bisindole alkaloids; Cytotoxicity; Ervachinines A D; Ervatamia chinensis

Indexed keywords

ALKALOID; ANTINEOPLASTIC AGENT; CISPLATIN; INDOLE DERIVATIVE; PLANT EXTRACT;

EID: 84855941638     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2011.11.002     Document Type: Article
Times cited : (64)

References (29)
  • 1
    • 0028251962 scopus 로고
    • Indole alkaloids from Tabernaemontana glandulosa
    • H. Achenbach, R. Waibel, and M. Zwanzger Indole alkaloids from Tabernaemontana glandulosa Phytochemistry 37 1994 1737 1743
    • (1994) Phytochemistry , vol.37 , pp. 1737-1743
    • Achenbach, H.1    Waibel, R.2    Zwanzger, M.3
  • 3
    • 0242386588 scopus 로고    scopus 로고
    • Natural, semisynthetic and synthetic microtubule inhibitors for cancer therapy
    • DOI 10.1358/dof.2003.028.08.744356
    • T. Beckers, and S. Mahboobi Natural, semisynthetic and synthetic microtuble inhibitors for cancer therapy Drugs Future 28 2003 767 785 (Pubitemid 37345316)
    • (2003) Drugs of the Future , vol.28 , Issue.8 , pp. 767-785
    • Beckers, T.1    Mahboobi, S.2
  • 4
    • 0034273688 scopus 로고    scopus 로고
    • Synthesis of strychnine
    • J. Bonjoch, and D. Sole Synthesis of strychnine Chem. Rev. 100 2000 3455 3482
    • (2000) Chem. Rev. , vol.100 , pp. 3455-3482
    • Bonjoch, J.1    Sole, D.2
  • 7
    • 0000671245 scopus 로고
    • Determining the chiralities of optically active glycols
    • N. Harada, and K. Nakanishi Determining the chiralities of optically active glycols J. Am. Chem. Soc. 91 1969 3989 3991
    • (1969) J. Am. Chem. Soc. , vol.91 , pp. 3989-3991
    • Harada, N.1    Nakanishi, K.2
  • 11
    • 0037250073 scopus 로고    scopus 로고
    • New bisindole alkaloids from Tabernaemontana corymbosa
    • T.S. Kam, K.M. Sim, and H.S. Pang New bisindole alkaloids from Tabernaemontana corymbosa J. Nat. Prod. 66 2003 11 16
    • (2003) J. Nat. Prod. , vol.66 , pp. 11-16
    • Kam, T.S.1    Sim, K.M.2    Pang, H.S.3
  • 12
    • 0019782451 scopus 로고
    • CONTRIBUTION A L'ETUDE DES TABERNAEMONTANEES AMERICAINES. III. ALCALOIDES DE ANARTIA CF. MEYERI
    • F. Ladhar, M. Damak, A. Ahond, C. Poupat, P. Potier, and C. Moretti Study of American Tanbernaemontana. III. Alkaloids from Anartia cf. meyeri J. Nat. Prod. 44 1981 459 465 (Pubitemid 12230436)
    • (1981) Journal of Natural Products , vol.44 , Issue.4 , pp. 459-465
    • Ladhar, F.1    Damak, M.2    Ahond, A.3
  • 14
    • 71049175371 scopus 로고    scopus 로고
    • Structure, biological activity, and a biomimetic partial synthesis of the lirofolines, novel pentacylic indole alkaloids from Tabernaemontana
    • Y.Y. Low, K.H. Lim, Y.M. Choo, H.S. Pang, T. Etoch, M. Hayashi, K. Komiyama, and T.S. Kam Structure, biological activity, and a biomimetic partial synthesis of the lirofolines, novel pentacylic indole alkaloids from Tabernaemontana Tetrahedron Lett. 51 2010 269 272
    • (2010) Tetrahedron Lett. , vol.51 , pp. 269-272
    • Low, Y.Y.1    Lim, K.H.2    Choo, Y.M.3    Pang, H.S.4    Etoch, T.5    Hayashi, M.6    Komiyama, K.7    Kam, T.S.8
  • 17
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • T. Mosmann Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays J. Immunol. Methods 65 1983 55 63 (Pubitemid 14203433)
    • (1983) Journal of Immunological Methods , vol.65 , Issue.1-2 , pp. 55-63
    • Mosmann, T.1
  • 19
    • 0026795942 scopus 로고
    • Analgesic components bornean medicinal plants, Tabernaemontana pauciflora Blume and Tabernaemontana pandacaqui Poir
    • E. Okuyama, L.H. Gao, and M. Yamazaki Analgesic components bornean medicinal plants, Tabernaemontana pauciflora Blume and Tabernaemontana pandacaqui Poir Chem. Pharm. Bull. 40 1992 2075 2079
    • (1992) Chem. Pharm. Bull. , vol.40 , pp. 2075-2079
    • Okuyama, E.1    Gao, L.H.2    Yamazaki, M.3
  • 20
    • 33745158157 scopus 로고
    • A simple method of estimating fifty percent end points
    • L.J. Reed, and H. Muench A simple method of estimating fifty percent end points Am. J. Hyg. 27 1938 493 497
    • (1938) Am. J. Hyg. , vol.27 , pp. 493-497
    • Reed, L.J.1    Muench, H.2
  • 21
    • 0029346971 scopus 로고
    • Recent progress in the chemistry of the monoterpenoid indole alkaloids
    • J.E. Saxton Recent progress in the chemistry of the monoterpenoid indole alkaloids Nat. Prod. Rep. 12 1995 385 411
    • (1995) Nat. Prod. Rep. , vol.12 , pp. 385-411
    • Saxton, J.E.1
  • 22
    • 0036321335 scopus 로고    scopus 로고
    • New alkaloids of the sarpagine group from Rauvolfia serpentina hairy root culture
    • DOI 10.1021/np0200919
    • Y. Sheludko, I. Gerasimenko, H. Kolshorn, and J. Stockigt New alkaloids of the sarpagine group from Rauvolfia serpentina hairy root J. Nat. Prod. 65 2002 1006 1010 (Pubitemid 34827487)
    • (2002) Journal of Natural Products , vol.65 , Issue.7 , pp. 1006-1010
    • Sheludko, Y.1    Gerasimenko, I.2    Kolshorn, H.3    Stockigt, J.4
  • 26
    • 70349513454 scopus 로고    scopus 로고
    • Biscarpamontamines A and B, an aspidosperma-iboga bisindole alkaloid and an aspidosperma-aspidosperma bisindole alkaloids, from Tabernaemontana sphaerocarpa
    • K. Zaima, T. Hirata, T. Hosoya, Y. Hirasawa, K. Koyama, A. Rahman, I. Kusumawati, N.C. Zaini, M. Shiro, and H. Morita Biscarpamontamines A and B, an aspidosperma-iboga bisindole alkaloid and an aspidosperma-aspidosperma bisindole alkaloids, from Tabernaemontana sphaerocarpa J. Nat. Prod. 72 2009 1686 1690
    • (2009) J. Nat. Prod. , vol.72 , pp. 1686-1690
    • Zaima, K.1    Hirata, T.2    Hosoya, T.3    Hirasawa, Y.4    Koyama, K.5    Rahman, A.6    Kusumawati, I.7    Zaini, N.C.8    Shiro, M.9    Morita, H.10
  • 27
    • 33847040326 scopus 로고    scopus 로고
    • Indole alkaloids form three species of the Ervatamia genus: E. Officinalis, E. divaricata, and E. divaricata Gouyahua
    • H. Zhang, X.N. Wang, L.P. Lin, J. Ding, and J.M. Yue Indole alkaloids form three species of the Ervatamia genus: E. Officinalis, E. divaricata, and E. divaricata Gouyahua J. Nat. Prod. 70 2007 54 59
    • (2007) J. Nat. Prod. , vol.70 , pp. 54-59
    • Zhang, H.1    Wang, X.N.2    Lin, L.P.3    Ding, J.4    Yue, J.M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.