2015
DOI: 10.1039/c4np00101j
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Triterpenoids

Abstract: This review covers the isolation and structure determination of triterpenoids reported during 2012 including squalene derivatives, lanostanes, holostanes, cycloartanes, cucurbitanes, dammaranes, euphanes, tirucallanes, tetranortriterpenoids, quassinoids, lupanes, oleananes, friedelanes, ursanes, hopanes, serratanes, isomalabaricanes and saponins; 348 references are cited.

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Cited by 56 publications
(34 citation statements)
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References 320 publications
(154 reference statements)
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“…This pharmacological significance has made triterpenoids one of the most studied families of natural products in recent decades (Hill and Connolly, 2015;Han and Peng, 2014;Nazaruk and Borzym-Kluczyk, 2014;Salvador et al, 2014;Parmar et al, 2013;Petronelli et al, 2009).…”
Section: Introductionmentioning
confidence: 98%
“…This pharmacological significance has made triterpenoids one of the most studied families of natural products in recent decades (Hill and Connolly, 2015;Han and Peng, 2014;Nazaruk and Borzym-Kluczyk, 2014;Salvador et al, 2014;Parmar et al, 2013;Petronelli et al, 2009).…”
Section: Introductionmentioning
confidence: 98%
“…Hence, a comprehensive medicinal chemistry tools and analysis methodology are employed herein to assess the various limonin biosynthetic products. Degraded limonoids (e.g., isobenzofuranones sharing structural features with limonoids [91]) and other tetranortriterpenoids extracted from different genera and/or not belonging to the limonin biosynthetic group will not be considered and hence readers are rather directed to relevant recent reviews [15,37,[92][93][94][95][96][97][98][99][100][101].…”
Section: Medicinal Chemistry Toolsmentioning
confidence: 99%
“…Also, they identified 13 phenolic compounds with higher concentration in the leaves (4.6 g kg −1 dry matter [DM]), from which 3.1 g kg −1 DM were sulfated flavonoids. A rare triterpenic ketone with pharmaceutical properties (Hill & Connolly 2015) was found at high concentrations (2.8 g kg −1 DM) in the roots, namely the molecule hop-17(21)-en-3-one (Vilela et al 2014). Rodrigues et al (2014) looked at the bioactivity of H. portulacoides extracts and found high radical scavenging activity (IC50 = 0.9 mg ml −1 ) against the radical ABTS and a decrease in nitric oxide production after incubation of macro phages with lipopolysaccharide and a chlo roform extract Cambrollé et al (2012a,b), Sousa et al (2010, 2011), Válega et al (2008a (IC50 = 109 µg ml −1 ), indicative of anti-inflammatory properties.…”
Section: The Potential Of Halimione Portulacoidesmentioning
confidence: 99%