Zobrazeno 1 - 10
of 209
pro vyhledávání: '"Koppaka V"'
Autor:
Koppaka V. Rao, James H. Johnson
Publikováno v:
Phytochemistry. 49:1361-1364
Taxiflorine, originally isolated from the needles of Taxus floridana and described previously, has its structure revised to that of taxchinin M. Four other known taxanes also isolated were: 1-deoxy baccatin IV, 1-hydroxy baccatin 1, 10-deacetyl pacli
Autor:
James H. Johnson, Koppaka V. Rao
Publikováno v:
Tetrahedron Letters. 39:4611-4614
Paclitaxel and some of its natural analogues are readily converted to their respective nitrate esters when reacted with nitric acid in acetic anhydride at 25° C in 30 minutes. Under milder conditions. partially esterified products can be prepared. T
Autor:
Koppaka V. Rao
Publikováno v:
Journal of Heterocyclic Chemistry. 34:675-680
Paclitaxel, an antitumor drug effective on ovarian and breast carcinomas, is currently being produced both by direct isolation from the bark of Taxus brevifolia and by semi-synthesis from a natural precursor, 10-deacetyl baccatin III. Although other
Publikováno v:
Phytochemistry. 43:439-442
The chloroform-soluble portion of the methanolic extract of the needles of Taxus x media was chromatographed on a C-18 reverse-phase column and the major components were separated by direct crystallization. Further fractionation by chromatography on
Autor:
Charles P. Rock, Koppaka V. Rao
Publikováno v:
Journal of Heterocyclic Chemistry. 33:447-458
Streptonigrin is an antitumor antibiotic with significant in vitro and in vivo antitumor activity spectrum. Besides the total syntheses, numerous syntheses of the partial structures have been carried out in order to assess the structural requirements
Publikováno v:
Phytochemistry. 41:863-866
Large-scale processing of the chloroform extract of the bark of Taxus brevifolia by reversed phase column chromatography on C-18 bonded silica using acetonitrile/water mixtures, gave a taxane-rich fraction which emerged just after the elution of pacl
Publikováno v:
Journal of Medicinal Chemistry. 38:3411-3414
10-Deacetylpaclitaxel, isolated from the bark of Taxus brevifolia, was converted into paclitaxel in one composite step (trimethylsilylation, acetylation, and desilylation) and in an overall yield of 80-85%. A series of 10-monoesters of 10-deacetylpac
Autor:
Ronald Baxley, Koppaka V. Rao, Mark Stoy, Claudio Alvarez, Jampani B. Hanuman, Richard M. Davies, John Juchum
Publikováno v:
Pharmaceutical Research. 12:1003-1010
Purpose. In view of the demonstrated antitumor activity of taxol, ready availability of the drug is important. The current isolation methods starting from the bark of Taxus brevifolia involve multiple manipulations, leading to only taxol and in a yie
Autor:
Koppaka V. Rao
Publikováno v:
Pharmaceutical Research. 10:521-524
The published procedures for the isolation of taxol from the Pacific yew (Taxus brevifolia) and other species of Taxus are cumbersome, and the yields of taxol are in the range of 0.0075–0.01%. This paper describes a simple and efficient procedure f
Autor:
Koppaka V. Rao
Publikováno v:
ChemInform. 28
Paclitaxel, an antitumor drug effective on ovarian and breast carcinomas, is currently being produced both by direct isolation from the bark of Taxus brevifolia and by semi-synthesis from a natural precursor, 10-deacetyl baccatin III. Although other