Neophathalides A and B, two pairs of unusual phthalide analog enantiomers from Ligusticum chuanxiong
Author:
Affiliation:
1. State Key Laboratory of Bioactive Substance and Function of Natural Medicines
2. Institute of Materia Medica
3. Chinese Academy of Medical Sciences and Peking Union Medical College
4. Beijing 100050
5. People’s Republic of China
Abstract
Two pairs of unusual phthalide analog enantiomers, (+)- and (−)-neophathalides A and B [(+)- and (−)-1 and 2], were isolated from the rhizome of Ligusticum chuanxiong Hort.
Funder
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB01014F
Reference17 articles.
1. Phthalides and Phthalans: Synthetic Methodologies and Their Applications in the Total Synthesis
2. l-3-n-butylphthalide alleviates hydrogen peroxide-induced apoptosis by PKC pathway in human neuroblastoma SK-N-SH cells
3. l-3-n-Butylphthalide ameliorates β-amyloid-induced neuronal toxicity in cultured neuronal cells
4. Relaxation effects of ligustilide and senkyunolide A, two main constituents of Ligusticum chuanxiong, in rat isolated aorta
5. Phthalide Lactones fromLigusticum chuanxiongInhibit Lipopolysaccharide-Induced TNF-α Production and TNF-α-Mediated NF-κB Activation
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