Literature DB >> 21561425

Perspectives on sesquiterpene lactones in inflammation and cancer.

Irmgard Merfort1.   

Abstract

Sesquiterpene lactones are a large group of secondary plant metabolites mostly known from the Asteraceae family. They exert a broad variety of different biological activities. This review attempts to critically summarise the knowledge on the anti-inflammatory and cytotoxic activity of SLs, with a special focus on parthenolide and helenalin. Recent advances on their molecular modes of action, allergic potential and also QSAR studies with SLs are presented. Therapeutic areas are highlighted in which SLs may play a role in the future. Thus, SLs may possess therapeutic relevance as single components for the local treatment of inflammation, such as rheumatoid complaints. In cancer therapy, SLs may be favourable in dual therapy or in the inhibition of leukaemia cell growth. In each case, native SLs serve as leads that have to be optimised in terms of their specificity, pharmacokinetics and absorption, distribution, metabolism and excretion (=ADME) properties. Finally, appropriate in vivo studies will decide whether SLs will become therapeutics or remain interesting research compounds.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21561425     DOI: 10.2174/138945011798109437

Source DB:  PubMed          Journal:  Curr Drug Targets        ISSN: 1389-4501            Impact factor:   3.465


  55 in total

1.  Chemoenzymatic synthesis and antileukemic activity of novel C9- and C14-functionalized parthenolide analogs.

Authors:  Vikas Tyagi; Hanan Alwaseem; Kristen M O'Dwyer; Jessica Ponder; Qi Ying Li; Craig T Jordan; Rudi Fasan
Journal:  Bioorg Med Chem       Date:  2016-06-16       Impact factor: 3.641

2.  Glutamate Toxicity to Differentiated Neuroblastoma N2a Cells Is Prevented by the Sesquiterpene Lactone Achillolide A and the Flavonoid 3,5,4'-Trihydroxy-6,7,3'-Trimethoxyflavone from Achillea fragrantissima.

Authors:  Anat Elmann; Alona Telerman; Rivka Ofir; Yoel Kashman
Journal:  J Mol Neurosci       Date:  2017-04-11       Impact factor: 3.444

3.  Halocarbocyclization entry into the oxabicyclo[4.3.1]decyl exomethylene-δ-lactone cores of linearifolin and zaluzanin A: exploiting combinatorial catalysis.

Authors:  Sandeep K Ginotra; Jacob A Friest; David B Berkowitz
Journal:  Org Lett       Date:  2012-02-08       Impact factor: 6.005

4.  Synthesis of deoxyelephantopin analogues.

Authors:  Roman Lagoutte; Christelle Serba; Nicolas Winssinger
Journal:  J Antibiot (Tokyo)       Date:  2017-11-01       Impact factor: 2.649

5.  Identification of a melampomagnolide B analog as a potential lead molecule for treatment of acute myelogenous leukemia.

Authors:  Zaineb A F Albayati; Venumadhav Janganati; Zheng Chen; Jessica Ponder; Philip J Breen; Craig T Jordan; Peter A Crooks
Journal:  Bioorg Med Chem       Date:  2016-12-26       Impact factor: 3.641

Review 6.  Development of Anticancer Agents from Plant-Derived Sesquiterpene Lactones.

Authors:  Yulin Ren; Jianhua Yu; A Douglas Kinghorn
Journal:  Curr Med Chem       Date:  2016       Impact factor: 4.530

7.  Targeting NF-κB p65 with a Helenalin Inspired Bis-electrophile.

Authors:  John C Widen; Aaron M Kempema; Peter W Villalta; Daniel A Harki
Journal:  ACS Chem Biol       Date:  2016-11-28       Impact factor: 5.100

8.  Sesquiterpene lactones and scopoletins from Artemisia scoparia Waldst. & Kit. and their angiotensin I-converting enzyme inhibitory activities.

Authors:  Jeong-Yong Cho; Seung-Jae Jeong; Hee La Lee; Kyung-Hee Park; Do Young Hwang; Sun-Young Park; Yu Geon Lee; Jae-Hak Moon; Kyung-Sik Ham
Journal:  Food Sci Biotechnol       Date:  2016-12-31       Impact factor: 2.391

9.  Selective cytotoxicity, inhibition of cell cycle progression, and induction of apoptosis in human breast cancer cells by sesquiterpenoids from Inula lineariifolia Turcz.

Authors:  Jiang-Jiang Qin; Hui-Zi Jin; Ying Huang; Shou-De Zhang; Lei Shan; Sukesh Voruganti; Subhasree Nag; Wei Wang; Wei-Dong Zhang; Ruiwen Zhang
Journal:  Eur J Med Chem       Date:  2013-08-11       Impact factor: 6.514

10.  Conditions for a Rh(I)-catalyzed [2 + 2 + 1] cycloaddition reaction with methyl substituted allenes and alkynes.

Authors:  Sarah M Wells; Kay M Brummond
Journal:  Tetrahedron Lett       Date:  2015-06-03       Impact factor: 2.415

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.