[Study on chemical constituents of Rhododendri Mollis Flos].

Q3 Pharmacology, Toxicology and Pharmaceutics
Peng-Yu Guo, Yang Song, Hai-Qiang Wang, Shi-Shan Yu
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引用次数: 0

Abstract

This study investigated the chemical constituents of Rhododendri Mollis Flos. The n-butanol fraction of 95% ethanol extract of Rhododendri Mollis Flos was separated and purified using chromatographic techniques, including normal-phase silica gel, ODS, and Sephadex LH-20 column chromatography. The structures of the isolated compounds were identified by spectroscopic techniques. Seven compounds were isolated and identified as rhodomollein LXⅦ(1), rhodomollein X(2), nivalenol(3),(3S,6S)-cis-linalool-3,7-oxide-β-D-glucopyranoside(4), thymidine(5), cyclo(Ala-Tyr)(6), and(S)-5-hydroxypyrrolidin-2-one(7). Among them, compound 1 was identified as a new compound, and compound 3 was isolated from this plant for the first time. The analgesic activity of compound 1 was evaluated using the acetic acid-induced writhing test. At a dose of 5.0 mg·kg~(-1), compound 1 showed a 75.4% inhibition rate in the writhing test, indicating significant analgesic activity.

[杜鹃花化学成分的研究]。
对杜鹃花的化学成分进行了研究。采用正相硅胶、ODS、Sephadex LH-20柱层析等色谱技术对杜鹃花95%乙醇提取物正丁醇部分进行分离纯化。分离得到的化合物通过光谱技术进行了结构鉴定。分离得到7个化合物,分别为rhodomollein LXⅦ(1)、rhodomollein X(2)、nivalenol(3)、(3S,6S)-顺式芳樟醇-3,7-oxide-β-D-glucopyranoside(4)、胸腺嘧啶(5)、cycloo (Ala-Tyr)(6)和(S)-5- hydroxypyrrolitin -2-one(7)。其中化合物1为新化合物,化合物3为首次从该植物中分离得到。采用醋酸扭体法评价化合物1的镇痛活性。在5.0 mg·kg~(-1)剂量下,化合物1在扭体实验中抑制率为75.4%,具有明显的镇痛作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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