Planta Med 2014; 80(18): 1732-1738
DOI: 10.1055/s-0034-1383253
Natural Product Chemistry
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Antioxidant and Tyrosinase Inhibitory Effects of Neolignan Glycosides from Crataegus pinnatifida Seeds

Xiao-Xiao Huang*
1   Department of Natural Products Chemistry, Shenyang Pharmaceutical University, Shenyang, P. R. China
2   Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, P. R. China
,
Qing-Bo Liu*
1   Department of Natural Products Chemistry, Shenyang Pharmaceutical University, Shenyang, P. R. China
2   Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, P. R. China
,
Jie Wu
1   Department of Natural Products Chemistry, Shenyang Pharmaceutical University, Shenyang, P. R. China
2   Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, P. R. China
,
Li-Hong Yu
1   Department of Natural Products Chemistry, Shenyang Pharmaceutical University, Shenyang, P. R. China
2   Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, P. R. China
,
Qian Cong
1   Department of Natural Products Chemistry, Shenyang Pharmaceutical University, Shenyang, P. R. China
2   Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, P. R. China
,
Yan Zhang
3   School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang, P. R. China
,
Li-Li Lou
1   Department of Natural Products Chemistry, Shenyang Pharmaceutical University, Shenyang, P. R. China
2   Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, P. R. China
,
Ling-Zhi Li
1   Department of Natural Products Chemistry, Shenyang Pharmaceutical University, Shenyang, P. R. China
2   Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, P. R. China
,
Shao-Jiang Song
1   Department of Natural Products Chemistry, Shenyang Pharmaceutical University, Shenyang, P. R. China
2   Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, P. R. China
› Author Affiliations
Further Information

Publication History

received 22 March 2014

accepted 12 October 2014

Publication Date:
06 November 2014 (online)

Abstract

In our efforts to find an inhibitor of melanin formation and develop potential depigmenting agents for skin-protecting cosmetics and medicinal products from natural resources, we focused on the seeds of Crataegus pinnatifida which showed antioxidant and tyrosinase-inhibiting activities. By activity-guided fractionation of an extract of C. pinnatifida seeds, four new neolignan glycosides, pinnatifidaninsides A–D (14), along with two known compounds (56), were isolated. Their structures were elucidated by spectroscopic analyses, especially 1D, 2D NMR and CD spectra. The antioxidant and tyrosinase-inhibiting activities of all isolates were assayed. Compound 6 showed good activity against 2,2-diphenyl-1-pikrylhydrazyl, while compounds 1, 2, 5, and 6 exhibited strong 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) free radical scavenging activity, being as effective as, or even more effective than the positive control Trolox. Moreover, compounds 5 and 6 displayed a moderate mushroom tyrosinase inhibitory activity.

* These authors made equal contribution to the article.


Supporting Information

 
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