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Chemical investigation on the root bark of Bombax malabarica

机译:轰炸马巴卡博马克根吠的化学研究

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Ten compounds were isolated from the root bark of Bombax malabarica, including two new compounds, born-bamalin (1) and 3,4,5-trimethoxypheno1-1[beta-xylopyranosyl-(1 -> 2)]beta-glucopyranoside (3), and shorealactone (4), a rare dehydroascorbic acid fused 1-epsilon-viniferin. Compound 1 is an unusual bissesquiterpene, containing a 1,4-dioxene ring formed by fusing isohemigossypol with ent-cadinen-2-one. Their structures were elucidated by extensive spectroscopic analysis. This chemical reinvestigation is of value for chemotaxonomy of the Bombax genus, in particular the finding of the unusual 1 and rare 4. Among the isolates, shorealactone (4), bepicatechin 5-O-beta-D-xyloside (5), and 2-C-U3-D-apiosyl-(1 -> 6)1- beta-D-glucosyl)-1,3,6-trihydroxy-7-methoxyxanthone (6) displayed some inhibition against alpha-glucosidase with IC50 values of 224, 345, and 285 mu M, respectively.
机译:从Bomax Malabarica的根吠声中分离十种化合物,包括两个新化合物,出生的Bamalin(1)和3,4,5-三甲氧基苯甲烯β-吡喃葡萄糖苷(3 )和Shorealactone(4),一种罕见的脱氢血脂酸融合1-EPSILON-VINIFERIN。 化合物1是一种不寻常的BissesquitePene,其含有通过熔化肌肉-2-one融合的Isohemigossypol而形成的1,4-二恶烯环。 通过广泛的光谱分析阐明了它们的结构。 这种化学再征收对致弹性的趋化性有价值,特别是发现不寻常的1和罕见的4.分离物,Shorealactere(4),BepicateChin 5-O-Beta-D-木糖苷(5)和2 -C-U3-D- apiosyl-(1 - > 6)1-Beta-D-葡萄糖基)-1,3,6-三羟基-7-甲氧基琥珀酮(6)显示出对α-葡糖苷酶的一些抑制作用IC50值224 345和285 mu m。

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