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来自……根部的三种新的具有镇痛作用的二萜类化合物。 (原句不完整,“from the roots of.”后面应该还有具体植物名称等信息)

Three new antinociceptive diterpenoids from the roots of .

作者信息

Chai Bing, Li Yong, Yu Shi-Shan

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union, Medical College, Beijing 100050, China.

出版信息

J Asian Nat Prod Res. 2020 Oct;22(10):895-904. doi: 10.1080/10286020.2020.1777545. Epub 2020 Jun 13.

Abstract

Two new grayanane-type ( and ) and one new kalmane-type diterpenoids (), together with 16 known compounds, were isolated from the roots of The structures of new compounds were fully determined on the basis of spectroscopic analysis, including HRESIMS, 1 D and 2 D NMR data. An acetic acid-induced writhing test in mice was proceeded to evaluate the antinociceptive activities of compounds , , and . Compared to vehicle-injected mice, compounds , , and 1 showed significant antinociceptive effects with writhe inhibition rates of 45.8%-64.2% at a dose of 0.1 mg/kg, and compounds , and showed significant antinociceptive effects with writhe inhibition rates of 33.9%-64.8% at a dose of 5 mg/kg. Compound showed potent antinociceptive effects with writhe inhibition rates of 86.1% and 54.7% at doses of 8 mg/kg and 0.8 mg/kg, respectively. [Formula: see text].

摘要

从 的根部分离出两种新的木藜芦烷型( 和 )和一种新的卡拉烷型二萜类化合物( ),以及16种已知化合物。基于光谱分析,包括高分辨电喷雾电离质谱(HRESIMS)、一维和二维核磁共振数据,完全确定了新化合物的结构。进行了乙酸诱导的小鼠扭体试验,以评估化合物 、 、 和 的抗伤害感受活性。与注射赋形剂的小鼠相比,化合物 、 、 和1在剂量为0.1mg/kg时显示出显著的抗伤害感受作用,扭体抑制率为45.8%-64.2%,化合物 、 和 在剂量为5mg/kg时显示出显著的抗伤害感受作用,扭体抑制率为33.9%-64.8%。化合物 在剂量为8mg/kg和0.8mg/kg时分别显示出强效的抗伤害感受作用,扭体抑制率分别为86.1%和54.7%。[分子式:见正文]

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