Polyoxygenated cyclohexene derivatives and other constituents of Uvaria rufa stem

被引:2
|
作者
Gurgul, Aleksandra [1 ,7 ]
Wu, Zhenlong [2 ]
Han, Kyu-Yeon [3 ]
Shetye, Gauri [4 ]
Sydara, Kongmany [5 ]
Souliya, Onevilay [5 ]
Johnson, Jeremy J. [6 ]
Che, Chun -Tao [1 ]
机构
[1] Univ Illinois, Coll Pharm, Dept Pharmaceut Sci, Chicago, IL 60612 USA
[2] Jinan Univ, Inst Tradit Chinese Med & Nat Prod, Coll Pharm, Guangzhou 510632, Peoples R China
[3] Univ Illinois, Illinois Eye & Ear Infirm, Dept Ophthalmol & Visual Sci, Chicago, IL 60612 USA
[4] Univ Illinois, Inst TB Res, Coll Pharm, Chicago, IL 60612 USA
[5] Minist Hlth, Inst Tradit Med, Viangchan, Laos
[6] Univ Illinois, Coll Pharm, Dept Pharm Pract, Chicago, IL 60612 USA
[7] 833 South Wood St, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
Uvaria rufa; Annonaceae; Polyoxygenated cyclohexenes; Cytotoxicity; Antimycobacterial; Anti-inflammatory; LIGNAN GLYCOSIDE; ESSENTIAL OILS; NITRIC-OXIDE; FLAVONOIDS; LEAVES; 2-PHENYLNAPHTHALENES; ELUCIDATION; ANNONACEAE; EXTRACTS; ROOTS;
D O I
10.1016/j.phytochem.2023.113884
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Six undescribed compounds, uvarirufols D and E, (+)-uvarigranol B, (-)-uvarigranol E, 6-acetoxy-5-hydroxy-7-methoxyflavanone and cherrevenaphthalene D, along with twelve known compounds, including polyoxygenated cyclohexenes, flavonoids, and lignans, were isolated from the methanol extract of Uvaria rufa stems. Their structures were elucidated by spectroscopic analyses and the absolute configurations were determined using electronic circular dichroism. Several isolates were evaluated for cytotoxic, antitubercular and anti-inflammatory potentials. (-)-6-Acetylzeylenol showed moderate inhibitory activity against Mycobacterium tuberculosis, with MIC value of 47.10 mu g/mL. Cherrevenaphthalene D exhibited weak antimycobacterial activity and potent inhibitory effect on lipopolysaccharide-induced nitric oxide (NO) production in RAW 264.7 cells (EC50 = 8.54 mu M). 8-Hydroxy-5,7-dimethoxyflavanone displayed moderate level of NO inhibition (EC50 = 43.62 mu M) with little cytotoxicity. The polyoxygenated cyclohexenes and lignans were inactive against HCT 116 and 22Rv1 cancer cells (IC50 > 100 mu M).
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页数:10
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