1982
DOI: 10.1021/np50022a019
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New Taxanes From Taxus brevifolia

Abstract: The isolation of two taxanes from Taxus brevifolia Nutt. is described, together with the isolation of two acetylated taxol derivatives from an acetylated fraction from the same plant. The compounds were identified on the basis of their spectroscopic properties as taxa-4(20),11-diene-2 alpha, 5 alpha, 7 beta, 9 alpha, 10 beta, 13 alpha-hexaol 2,7,9,10,13-pentaacetate (1) (decinnamoyltaxinine J), 10-deacetylbaccatin III (2), taxol 2',7-diacetate (3), and 10-deacetyltaxol 2',7-diacetate (4).

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Cited by 69 publications
(27 citation statements)
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“…On one hand, extensive experience relating to TCMs may facilitate the identification of novel active substances. This approach has already proven successful by many established cytostatic compounds of natural origin [27], e.g., Vinca alkaloids from Vinca major [28], epipodophyllotoxins from Podophyllum peltatum [29,30], taxanes from Taxus brevifolia [31,32], camptothecin from Camptotheca acuminate [33,34], and so on. On the other hand, TCMs in conjunction with chemotherapy or TCMs alone may be beneficial in terms of improvement in marrow suppression and immune system, and may improve overall state of the quality of life (see review by Zhang et al [6]).…”
Section: Discussionmentioning
confidence: 99%
“…On one hand, extensive experience relating to TCMs may facilitate the identification of novel active substances. This approach has already proven successful by many established cytostatic compounds of natural origin [27], e.g., Vinca alkaloids from Vinca major [28], epipodophyllotoxins from Podophyllum peltatum [29,30], taxanes from Taxus brevifolia [31,32], camptothecin from Camptotheca acuminate [33,34], and so on. On the other hand, TCMs in conjunction with chemotherapy or TCMs alone may be beneficial in terms of improvement in marrow suppression and immune system, and may improve overall state of the quality of life (see review by Zhang et al [6]).…”
Section: Discussionmentioning
confidence: 99%
“…A wide range of compounds interact with the α and β tubulin subunits and some function as antimitotic agents, inhibiting cellular replication (Jordan and Wilson 2004; by Wall and Wani (Kingston et al 1982;Parekh and Simpkins 1997;Roytta et al 1984;Wani et al 1971), is such a compound with an ability to stabilize polymerized α-β tubulin heterodimers in microtubules and inhibit polymer disassembly (Orr et al 2003;Schiff and Horwitz 1980). Because of the requirement for microtubule rapid disassembly and dynamic behavior during cell division (Reinecke et al 1997), paclitaxel is effective as a cancer treatment drug (Ramalingam and Belani 2008).…”
Section: Introductionmentioning
confidence: 99%
“…The C-13 side chain was retained based on the knowledge that this unit, and especially the C-2 0 hydroxyl group, is essential to bioactivity [183,184]. These simplified analogs were reported to show reduced activity in inhibition of tubulin depolymerization, but no detailed data were presented.…”
Section: Synthetic Attempts To Make Simplified Paclitaxel Analogsmentioning
confidence: 99%