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Antiallergic agent from natural sources. Structures and inhibitory effect of histamine release of naphthopyrone glycosides from seeds of Cassia obtusifolia L.

机译:天然来源的抗过敏剂。决明子种子中萘并吡喃糖苷的组胺释放结构和抑制作用

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摘要

Two new naphthopyrones, cassiasides B2 (1) and C2 (2), were isolated from the seeds (Cassiae Semen) of Cassia obtusifolia L. The structures of the two new compounds 1 and 2 were established as rubrofusarin 6-O-beta-D- glucopyranosyl-(1-->6)-O-beta-D-glucopyranosyl-(1-->3)-O-beta-D- glucopyranosyl-(1-->6)-O-beta-D-glucopyranoside and toralactone 9-O-beta-D-glucopyranosyl-(1-->6)-O-beta-D-glucopyranosyl- (1-->3)-O-beta-D-glucopyranosyl-(1-->6)-O-beta-D-glucopyranoside, respectively, on the basis of spectral and chemical evidence. Compound 2 was found to inhibit the histamine release from rat peritoneal exudate mast cells induced by antigen-antibody reaction.
机译:从决明子的种子(Cassiae Semen)中分离出两个新的萘并吡喃酮,即决明子苷B2(1)和C2(2)。这两个新化合物1和2的结构被确定为Rubrofusarin 6-O-beta-D -吡喃葡萄糖基-(1-> 6)-O-β-D-吡喃葡萄糖基-(1-> 3)-O-β-D-吡喃葡萄糖基-(1-> 6)-O-β-D-吡喃葡糖苷和托拉内酯9-O-β-D-吡喃葡萄糖基-(1-> 6)-O-β-D-吡喃葡萄糖基-(1-> 3)-O-β-D-吡喃葡萄糖基-(1-> 6 )-O-β-D-吡喃葡萄糖苷分别基于光谱和化学证据。发现化合物2抑制由抗原-抗体反应诱导的组胺从大鼠腹膜渗出液肥大细胞中的释放。

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