Antioxidant and Anti-Inflammatory Constituents from Rhamnus crenata

被引:1
作者
Chin, Chih-Hui [1 ,2 ]
Liaw, Chia-Ching [3 ]
Chang, Tsung-Hsien [4 ]
Shu, Chih-Wen [5 ]
Sung, Ping-Jyun [6 ]
Cheng, Ming-Jen [7 ]
Wang, I-Chou [8 ]
Chen, Jih-Jung [9 ,10 ]
机构
[1] Cathay Gen Hosp, Cardiovasc Ctr, Taipei 106, Taiwan
[2] Fu Jen Catholic Univ, Sch Med, New Taipei City 242, Taiwan
[3] Natl Res Inst Chinese Med, Div Chinese Mat Med Dev, Taipei 112, Taiwan
[4] Natl Def Med Ctr, Inst Microbiol & Immunol, Taipei 114, Taiwan
[5] Natl Sun Yat Sen Univ, Inst BioPharmaceut Sci, Kaohsiung 804, Taiwan
[6] Natl Museum Marine Biol & Aquarium, Pingtung 944, Taiwan
[7] Fu Jen Catholic Univ, Dept Life Sci, New Taipei City 242, Taiwan
[8] Kaohsiung Vet Gen Hosp Tainan Branch, Dept Phys Med & Rehabil, Tainan 710, Taiwan
[9] Natl Yang Ming Chiao Tung Univ, Sch Pharmaceut Sci, Dept Pharm, Taipei 112, Taiwan
[10] China Med Univ, China Med Univ Hosp, Dept Med Res, Taichung 404, Taiwan
关键词
Rhamnus crenata; Rhamnaceae; naphthalene derivative; antioxidant; anti-inflammatory activity;
D O I
10.1007/s10600-024-04251-4
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A new naphthalene derivative, 7-acetyl-8-hydroxy-3-methoxy-6-methylnaphthalen-1-yl acetate (1), has been isolated from the stem of Rhamnus crenata, together with eight known compounds 2-9. The structure of new compound 1 was determined through spectroscopic and MS analyses. Among the isolates, emodin (3), physcion (4), quercetin 3-O-alpha-L-rhamnopyranoside (5), and quercetin 7-O-alpha-L-rhamnopyranoside (6) showed potent inhibition with IC50 values of 33.18 +/- 2.73, 35.52 +/- 3.27, 28.05 +/- 1.85, and 26.41 +/- 3.01 mu M, respectively, against LPS-induced NO generation. In addition, compounds 3, 5, and 6 also showed potent DPPH radical scavenging activities with IC50 values of 95.47 +/- 6.18, 68.27 +/- 5.38, and 66.25 +/- 4.20 mu M, respectively.
引用
收藏
页码:50 / 54
页数:5
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