Published August 31, 2019
| Version v1
Figure
Open
Fig. 3 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. 3. Values of δS–δR for Mosher's MTPA esters of compounds 1, 3, 5, 6, and 8.
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 44, DOI: 10.1016/j.phytochem.2019.04.011, http://zenodo.org/record/10482801
Files
figure.png
Files
(417.1 kB)
| Name | Size | Download all |
|---|---|---|
|
md5:b5c5b776fd00226750030c883ea41ac4
|
417.1 kB | Preview Download |
Linked records
Additional details
Related works
- Is part of
- 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)