| Literature DB >> 32417524 |
Fabiola A López-Huerta1, Antonio Nieto-Camacho1, Félix Morales-Flores1, Simón Hernández-Ortega1, María Isabel Chávez1, Carlos A Méndez Cuesta2, Ignacio Martínez3, Bertha Espinoza3, Francisco J Espinosa-García4, Guillermo Delgado5.
Abstract
Chemical investigation of the aerial parts of Cnidoscolus spinosus resulted in the isolation of relatively infrequent hopane-type triterpenes, 3β-acetoxy-hop-22(29)-ene (1), first reported here as natural product, together with 3-oxo-hop-22(29)-ene (2), and 3β-hydroxy-hop-22(29)-ene (3). β-Amyrin palmitate and three phytosterols were also characterized. The structures of the compounds were established using spectroscopic methods, and those of 1 and 2 were confirmed by crystallographic analysis. Selected biological activities for the isolated hopane-type triterpenes were tested through a series of assays for determining the cytotoxic, anti-inflammatory, α-glucosidase inhibition and antiparasitic activities. Compounds 1-3 did not show cytotoxic activity, compound 1 displayed an important inhibitory effect in the mouse ear induced inflammation assay, and significantly inhibited the yeast α-glucosidase activity in vitro and in silico. Additionally, compounds 2 and 3 showed marginal activities against Trypanosoma cruzi and Leishmania mexicana. Therefore, the bioactivities of hopane-type triterpenes deserve further investigation, particularly their anti-inflammatory properties.Entities:
Keywords: 3β-acetoxy-hop-22(29)-ene; Anti-inflammation; Cnidoscolus spinosus; Hopanes; Triterpenes
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Year: 2020 PMID: 32417524 DOI: 10.1016/j.bioorg.2020.103919
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275