CAS 90332-65-3
:7-Xilosil-10-desacetiltaxol C
Descrição:
7-Xilosil-10-desacetiltaxol C, com o número CAS 90332-65-3, é um composto químico que pertence à família dos taxanos, conhecida por seu papel no tratamento do câncer devido à sua capacidade de inibir a divisão celular. Este composto apresenta um grupo xilosil, que é uma porção de açúcar, ligado à estrutura do taxano, aumentando sua solubilidade e potencialmente sua atividade biológica. A presença da forma desacetilada indica que carece de um grupo acetila, o que pode influenciar sua farmacocinética e eficácia terapêutica. Os taxanos, incluindo derivados como este, geralmente exibem propriedades antitumorais significativas ao estabilizar microtúbulos e prevenir sua despolimerização, interrompendo assim o processo mitótico normal nas células cancerosas. As características específicas, como solubilidade, estabilidade e atividade biológica, dependeriam de sua estrutura molecular e dos grupos funcionais presentes. Estudos adicionais seriam necessários para elucidar completamente seu perfil farmacológico e aplicações potenciais em oncologia.
Fórmula:C49H63NO17
InChI:InChI=1S/C49H63NO17/c1-7-8-11-20-33(53)50-35(27-16-12-9-13-17-27)38(56)44(60)64-30-22-49(61)42(66-43(59)28-18-14-10-15-19-28)40-47(6,41(58)37(55)34(25(30)2)46(49,4)5)31(21-32-48(40,24-63-32)67-26(3)51)65-45-39(57)36(54)29(52)23-62-45/h9-10,12-19,29-32,35-40,42,45,52,54-57,61H,7-8,11,20-24H2,1-6H3,(H,50,53)/t29-,30+,31+,32-,35+,36+,37-,38-,39-,40+,42+,45+,47-,48+,49-/m1/s1
Chave InChI:InChIKey=XGWGQEYABFGJID-UVDBIDMBSA-N
SMILES:O(C(C)=O)[C@]12[C@@]3([C@@](C)([C@@H](O[C@H]4[C@H](O)[C@@H](O)[C@H](O)CO4)C[C@]1(OC2)[H])C(=O)[C@H](O)C=5C(C)(C)[C@](O)([C@H]3OC(=O)C6=CC=CC=C6)C[C@H](OC([C@@H]([C@@H](NC(CCCCC)=O)C7=CC=CC=C7)O)=O)C5C)[H]
Sinónimos:- 10-Deacetyl-7-xylosyltaxol C
- 10-Deacetylpaclitaxel C 7-xyloside
- 10-Deacetyltaxol C 7-xyloside
- 7,11-Methano-1H-cyclodeca[3,4]benz[1,2-b]oxete, benzenepropanoic acid deriv.
- 7-(b-Xylosyl)-10-deacetyltaxol C
- 7-Xylosyl-10-deacetyltaxol C
- Benzenepropanoic acid, α-hydroxy-β-[(1-oxohexyl)amino]-, (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-12b-(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-6,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-4-(β-<span class="text-smallcaps">D</span>-xylopyranosyloxy)-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, (αR,βS)-
- Benzenepropanoic acid, α-hydroxy-β-[(1-oxohexyl)amino]-, 12b-(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-6,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-4-(β-<span class="text-smallcaps">D</span>-xylopyranosyloxy)-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, [2aR-[2aα,4β,4aβ,6β,9α(αR*,βS*),11α,12α,12aα,12bα]]-
- Benzenepropanoicacid, a-hydroxy-b-[(1-oxohexyl)amino]-,12b-(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-6,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-4-(b-D-xylopyranosyloxy)-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-ylester, [2aR-[2aa,4b,4ab,6b,9a(aR*,bS*),11a,12a,12aa,12ba]]-
- Benzenepropanoic acid, α-hydroxy-β-[(1-oxohexyl)amino]-, 12b-(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-6,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-4-(β-D-xylopyranosyloxy)-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, [2aR-[2aα,4β,4aβ,6β,9α(αR*,βS*),11α,12α,12aα,12bα]]-
- Benzenepropanoic acid, α-hydroxy-β-[(1-oxohexyl)amino]-, (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-12b-(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-6,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-4-(β-D-xylopyranosyloxy)-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, (αR,βS)-
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3 produtos.
7-Xylosyl-10-deacetyltaxol C
CAS:7-Xylosyl-10-deacetyltaxol C is a natural product from Taxus wallichiana Zucc.Fórmula:C49H63NO17Pureza:98%Cor e Forma:SolidPeso molecular:938.033Deacetyl-7-xylosyltaxol C
CAS:Deacetyl-7-xylosyltaxol C is a complex taxol derivative, which is a naturally occurring compound obtained from the bark of the Pacific yew tree, Taxus brevifolia, and other related species. This unique derivative is structurally modified by the removal of an acetyl group and the addition of a xylose moiety, which is characteristic of its taxonomy.Fórmula:C49H63NO17Pureza:Min. 95%Peso molecular:938 g/mol


