Bioactive constituents from the rhizomes of Atractylodes macrocephala

被引:13
作者
Zhang, Haixin [1 ]
Lin, Chunyu [1 ]
Yin, Luying [1 ]
Si, Jinguang [1 ]
Yu, Meng [1 ]
Li, Jingrong [1 ,3 ]
Li, Lingyu [1 ]
Zhang, Tao [1 ,2 ]
Zou, Zhongmei [1 ,2 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Plant Dev, Beijing 100193, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, State Key Lab Bioact Subst & Funct Nat Med, Beijing 100050, Peoples R China
[3] Guizhou Med Univ, Med Sci, Guiyang 550000, Peoples R China
基金
中国国家自然科学基金;
关键词
Compositae; Atractylodes macrocephala Koidz; Sesquiterpene; Norneolignan; SESQUITERPENOIDS; IRIDOIDS;
D O I
10.1016/j.fitote.2023.105431
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Twelve undescribed compounds including five sesquiterpenes (1-5), one monoterpene (6), and four lignans (7a/ 7b and 8a/8b), along with two other types (9 and 10) were isolated from the rhizomes of Atractylodes macro-cephala. Among them, two pairs of enantiomers (7a/7b and 8a/8b) were successfully separated by chiral-phase HPLC, while racemate 9 could not be resolved. Their structures and absolute configurations were unambiguously elucidated by spectroscopic data analysis and electronic circular dichroism (ECD) calculations. Notably, com-pounds 1 and 2 are rare sesquiterpene hybrids featuring an eudesmanolactam linked to a resorcinol or methyl 2-methylpentanoat through a C-N bond. Compound 3 represents the first example of eudesmanolide sesquiter-pene with an oxygen-bridge between C-8 and C-14. Compounds 7a and 7b are a pair of rare enantiomeric benzodioxane norneolignans. Additionally, compound 2 exhibited weak cytotoxicity against SGC-7901 cells. Compound 4 significantly promoted the proliferation of LPS-induced IEC-6 cells with the rate of 117.2%.
引用
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页数:11
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