Published August 31, 2019
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Fig. 7 in Hyperforatins L-U: Prenylated acylphloroglucinols with a terminal double bond from Hypericum perforatum L. (St John's Wort)
Authors/Creators
- 1. ∗ & ∗∗ & Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and & H, C, Dept, Hsqc, Hmbc, & H- & H COSY, and NOESY experiments). Their absolute configurations were determined by comprehensive analyses of their experimental ECD spectra in conjunction with a modified Mosher's method. Evaluation of their neuroprotective activities highlighted hyperforatin L, which displayed mild activity at a concentration of 10 μM.
Description
Fig. 7. Neuroprotective effects of selected compounds (10 μM) and desipramine (positive control, PC) against corticosterone (CORT)-induced injury in PC12 cells. *p <0.05, **p <0.01, ***p <0.001 vs negative control (NC) group; ###p <0.001 vs blank.
Notes
Published as part of Guo, Yi, Zhang, Na, Duan, Xueyan, Cao, Yunfang, Xue, Yongbo, Luo, Zengwei, Zhu, Hucheng, Chen, Chunmei, Wang, Jianping & Zhang, Yonghui, 2019, Hyperforatins L-U: Prenylated acylphloroglucinols with a terminal double bond from Hypericum perforatum L. (St John's Wort), pp. 41-49 in Phytochemistry 164 on page 45, DOI: 10.1016/j.phytochem.2019.04.011, http://zenodo.org/record/10482801
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- Journal article: 10.1016/j.phytochem.2019.04.011 (DOI)
- Journal article: urn:lsid:plazi.org:pub:FFB9FFCFA074FFB9FFB9FB69FFB1FFCD (LSID)
- Journal article: https://zenodo.org/record/10482801 (URL)