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Volumn 64, Issue 4, 2000, Pages 894-898

Two Novel taxane diterpenoids from the needles of japanese yew, taxu

Author keywords

Ntitumour compound; Taxaceaediterpenoidtaxane; Taxus cuspidata

Indexed keywords

1,7 DIHYDROXYTAXININE; 1,7-DIHYDROXYTAXININE; BRIDGED COMPOUND; DITERPENE; PLANT EXTRACT; TAXANE; TAXOID;

EID: 0034168775     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.64.894     Document Type: Article
Times cited : (11)

References (17)
  • 1
    • 0015211527 scopus 로고
    • Plant antitumor agents. IV. The isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia
    • Wani, M. C., Taylor, H. L., Wall, M. E., Coggon, P., and Mcphail, A. T., Plant antitumor agents. IV. The isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia. J. Am. Chem. Soc., 93, 2325-2327 (1971).
    • (1971) J. Am. Chem. Soc , vol.93 , pp. 2325-2327
    • Wani, M.C.1    Taylor, H.L.2    Wall, M.E.3    Coggon, P.4    Mc Phail, A.T.5
  • 2
    • 0001881989 scopus 로고
    • Current status of clinical trials with paclitaxel and docetaxel
    • Georg, G. I., Chen, T. T., Ojima, I., and Vyas, D. M., ACS Symposium Series 583, American Chemical Society, Washington, DC
    • Holmes, F. A., Kudelka, A. P., Kavanagh, J. J., Huber, M. H., Ajani, J. A., and Valero, V., Current status of clinical trials with paclitaxel and docetaxel. In “Taxane Anticancer Agents: Basic Science and Current Status," eds. Georg, G. I., Chen, T. T., Ojima, I., and Vyas, D. M., ACS Symposium Series 583, American Chemical Society, Washington, DC, pp. 31-57 (1995).
    • (1995) “Taxane Anticancer Agents: Basic Science and Current Status , pp. 31-57
    • Holmes, F.A.1    Kudelka, A.P.2    Kavanagh, J.J.3    Huber, M.H.4    Ajani, J.A.5    Valero, V.6
  • 4
    • 0029346876 scopus 로고
    • The phytochemistry of the yew tree
    • Appendino, G., The phytochemistry of the yew tree. Nat. Prod. Rep., 12, 349-360 (1995).
    • (1995) Nat. Prod. Rep , vol.12 , pp. 349-360
    • Appendino, G.1
  • 5
    • 85007703409 scopus 로고
    • A novel taxane diterpenoid from Japanese yew, Taxus cuspidata
    • Sugiyama, T., Oritani, T., and Oritani, T., A novel taxane diterpenoid from Japanese yew, Taxus cuspidata. Biosci. Biotechnol. Biochem., 58, 1923-1924 (1994).
    • (1994) Biosci. Biotechnol. Biochem , vol.58 , pp. 1923-1924
    • Sugiyama, T.1    Oritani, T.2    Oritani, T.3
  • 6
    • 0032406661 scopus 로고    scopus 로고
    • Two new taxanes from Taxus chinensis var. Mairei
    • Shi, Q.-W., Oritani, T., Sugiyama, T., and Kiyota, H., Two new taxanes from Taxus chinensis var. mairei. Plant a Medica, 64, 766-769 (1998).
    • (1998) Plant a Medica , vol.64 , pp. 766-769
    • Shi, Q.-W.1    Oritani, T.2    Sugiyama, T.3    Kiyota, H.4
  • 8
    • 0032845969 scopus 로고    scopus 로고
    • Six new taxane diterpenoids from the seeds of Taxus chinensis var. Mairei and Taxus yunnanensis
    • Shi, Q.-W., Oritani, T., Sugiyama, T., Murakami, R., and Wei, H.-Q., Six new taxane diterpenoids from the seeds of Taxus chinensis var. mairei and Taxus yunnanensis. J. Nat. Prod., 62, 1114-1118 (1999).
    • (1999) J. Nat. Prod , vol.62 , pp. 1114-1118
    • Shi, Q.-W.1    Oritani, T.2    Sugiyama, T.3    Murakami, R.4    Wei, H.-Q.5
  • 9
    • 0001288515 scopus 로고    scopus 로고
    • A novel rearranged taxoid from the needles of Japanese yew, Taxus cuspidata Sieb. Et Zucc
    • Murakami, R., Shi, Q.-W., Oritani, T., Horiguchi, T., and Oritani, T., A novel rearranged taxoid from the needles of Japanese yew, Taxus cuspidata Sieb. et Zucc. Biosci. Biotechnol. Biochem., 63, 1660-1663 (1999).
    • (1999) Biosci. Biotechnol. Biochem , vol.63 , pp. 1660-1663
    • Murakami, R.1    Shi, Q.-W.2    Oritani, T.3    Horiguchi, T.4    Oritani, T.5
  • 10
    • 0033117563 scopus 로고    scopus 로고
    • Three new rearranged taxane diterpenoids from the bark of Taxus chinensis var. Mairei and the needles of Taxus cuspidata
    • Shi, Q.-W., Oritani, T., Sugiyama, T., Horiguchi, T., and Kiyota, H., Three new rearranged taxane diterpenoids from the bark of Taxus chinensis var. mairei and the needles of Taxus cuspidata. Heterocycles, 51, 841-850 (1999).
    • (1999) Heterocycles , vol.51 , pp. 841-850
    • Shi, Q.-W.1    Oritani, T.2    Sugiyama, T.3    Horiguchi, T.4    Kiyota, H.5
  • 11
    • 0033412595 scopus 로고    scopus 로고
    • Three novel bicyclic taxoids from the needles of the Chinensis yew, Taxus chinensis var. Mairei
    • Shi, Q.-W., Oritani, T., Sugiyama S, and Cheng, Q., Three novel bicyclic taxoids from the needles of the Chinensis yew, Taxus chinensis var. mairei. Chin. Chem. Lett, 10, 481-484 (1999).
    • (1999) Chin. Chem. Lett , vol.10 , pp. 481-484
    • Shi, Q.-W.1    Oritani, T.2    Sugiyama, S.3    Cheng, Q.4
  • 12
    • 0033538629 scopus 로고    scopus 로고
    • Three new taxane diterpenoids from the seeds of Taxus yunnanensis Cheng et L. K. Fu and T. Cuspidata Sieb et Zucc
    • Shi, Q.-W., Oritani, T., Sugiyama, T., Horiguchi, T., Murakami, R., Zhao, D., and Oritani, T., Three new taxane diterpenoids from the seeds of Taxus yunnanensis Cheng et L. K. Fu and T. cuspidata Sieb et Zucc. Tetrahedron, 55, 8365-8376 (1999).
    • (1999) Tetrahedron , vol.55 , pp. 8365-8376
    • Shi, Q.-W.1    Oritani, T.2    Sugiyama, T.3    Horiguchi, T.4    Murakami, R.5    Zhao, D.6    Oritani, T.7
  • 13
    • 0033536679 scopus 로고    scopus 로고
    • PrO)3 TiCl-induced reactions of a- and /?-4(20)-epoxy-5-hydroxytriacetyltaxicin-I
    • 3TiCl-induced reactions of a- and /?-4(20)-epoxy-5-hydroxytriacetyltaxicin-I. Tetrahedron, 55, 12099-12108 (1999).
    • (1999) Tetrahedron , vol.55 , pp. 12099-12108
    • Cheng, Q.1    Oritani, T.2    Horiguchi, T.3
  • 14
    • 0034387320 scopus 로고    scopus 로고
    • Et2AlCl-mediated reaction of a-4(20)-epoxy-5-hydroxy Taxi-nine B
    • Cheng, Q., Oritani, T., and Horiguchi, T., Et2AlCl-mediated reaction of a-4(20)-epoxy-5-hydroxy Taxi-nine B. Chin. Chem. Lett., in press (1999).
    • (1999) Chin. Chem. Lett
    • Cheng, Q.1    Oritani, T.2    Horiguchi, T.3
  • 16
    • 33947315483 scopus 로고
    • The nuclear overhauser effect, a unique method of defining the relative stereochemistry and conformation of taxane derivatives
    • Woods, M. C., Chiang, H.-C., Nakadaira, Y., and Nakanishi, K., The nuclear overhauser effect, a unique method of defining the relative stereochemistry and conformation of taxane derivatives. J. Am. Chem. Soc., 90, 522-523 (1968).
    • (1968) J. Am. Chem. Soc , vol.90 , pp. 522-523
    • Woods, M.C.1    Chiang, H.-C.2    Nakadaira, Y.3    Nakanishi, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.