2016
DOI: 10.1016/j.phytochem.2016.02.005
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Tetrandrine – A molecule of wide bioactivity

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Cited by 168 publications
(119 citation statements)
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“…Identification that PyVs share a conserved requirement with EBOV suggests that NAADP-sensitive TPC inhibition represents a therapeutic target for viruses and pathogens that traffic through the ER during entry stages. Although tetrandrine is not widely available and there are currently limited studies into the efficacy of treatment in vivo , the identification of endosomal-ER fusion as a requirement for a variety of pathogens provides a common target that could potentially be exploited (60, 61).…”
Section: Discussionmentioning
confidence: 99%
“…Identification that PyVs share a conserved requirement with EBOV suggests that NAADP-sensitive TPC inhibition represents a therapeutic target for viruses and pathogens that traffic through the ER during entry stages. Although tetrandrine is not widely available and there are currently limited studies into the efficacy of treatment in vivo , the identification of endosomal-ER fusion as a requirement for a variety of pathogens provides a common target that could potentially be exploited (60, 61).…”
Section: Discussionmentioning
confidence: 99%
“…To date, the published literature has focused principally on the alkaloids and extracts of S. tetrandra. The molecules that have received the greatest in-depth study of their pharmacological activity are tetrandrine (Yang et al 2018a;Bhagya and Chandrashekar 2016;Wang et al 2017a;Xing et al 2014;Cai et al 2011), fangchinoline (Desgrouas et al 2014a;Wang et al 2017a;Xing et al 2014) and cepharanthine (Bailly 2019;Wang et al 2017a). Not only are these compounds found in S. tetrandra, but also in other plants known to have medicinal properties (Table 2).…”
Section: Pharmacological Propertiesmentioning
confidence: 99%
“…17 It has been demonstrated that low pH is required for the GP-mediated membrane fusion. 2), a very well-known remedy in Traditional Chinese Medicine (TCM) for the treatment of a number of diseases such as tuberculosis, dysentery, malaria, cancer, and fever, 19 isolated from different species of plants from the Menispermaceae family, was shown to inhibit EBOV entry into host cells and infection of human macrophages (EC 50 ¼ 55 nM) by binding to TPC. 2) and clathrin-mediated endocytosis chlorpromazine have been shown to inhibit EBOV entry into the host cells in an in vitro replication-competent viral assay (inferred EC 50 values around 10 nM and 13 μM, respectively), providing a promising scaffold for the development of novel EBOV therapeutics.…”
Section: Endocytosis And/or Macropinocytosis Inhibitorsmentioning
confidence: 99%