Nove limonóides foram isolados de Carapa guianensis e Cedrela fissilis. Entre eles, a 1,2-diidro-3β-hidroxi-7-desacetoxi-7-oxogedunina é uma substância inédita. Além disso, alguns deslocamentos químicos da xilocensina k foram corrigidos e os dados de RMN 1 H da 7-desacetilgedunina são descritos pela primeira vez na literatura. Seis dos limonóides isolados foram submetidos a ensaios com formigas Atta sexdens rubropilosa e apresentaram atividade inseticida moderada. Nine limonoids were isolated from Carapa guianensis and Cedrela fissilis. Among them, 1,2-dihydro-3β-hydroxy-7-deacetoxy-7-oxogedunin is a new compound. Moreover, the assignments of some chemical shifts of xyloccensin k have been corrected and 1 H NMR data of 7-deacetylgedunin have been assigned for the first time. These isolated limonoids were assayed on Atta sexdens rubropilosa workers showing moderate insecticidal activities.
Chagas' disease is an illness that affects millions of people in Central and South America. The search for both a prophylactic drug to be added to human blood as well as a safe and reliable therapeutic drug are greatly needed to control such disease. Herein, we report the trypanocidal activity of 15 crude extracts and 14 compounds (limonoids and triterpenes) as well as the isolation of 25 known compounds (6 limonoids, 12 triterpenes, 1 sesquiterpene, 5 steroids, and 1 flavonoid) from Cedrela fissilis. The present study shows that this plant is a promising source of active compounds for the control of Chagas' disease. The inhibitory activity found for odoratol indicates that it is potentially useful as an alternative for the chemoprophylactic gentian violet.
cells play a pivotal role in host responses against primary Denv infection in mice. after infection, μMt −/− mice showed increased viral loads followed by severe disease manifestation characterized by intense thrombocytopenia, hemoconcentration, cytokine production and massive liver damage that culminated in death. In addition, we show that poly and monoclonal anti-Denv-specific antibodies can sufficiently increase viral replication through a suppression of early innate antiviral responses and enhance disease manifestation, so that a mostly non-lethal illness becomes a fatal disease resembling human DHF/Dss. Finally, treatment with intravenous immunoglobulin containing anti-Denv antibodies confirmed the potential enhancing capacity of Abstract Dengue is a mosquito-borne disease caused by one of four serotypes of Dengue virus (Denv-1-4). epidemiologic and observational studies demonstrate that the majority of severe dengue cases, dengue hemorrhagic fever and dengue shock syndrome (DHF/Dss), occurs predominantly in either individuals with cross-reactive immunity following a secondary heterologous infection or in infants with primary Denv infections born from dengue-immune mothers, suggesting that B-cell-mediated and antibody responses impact on disease evolution. We demonstrate here that B Electronic supplementary material the online version of this article
The trypanocidal activity of crude extracts and fractions from the leaves and stems of Peperomia obtusifolia (Piperaceae) was evaluated in vitro against the epimastigote forms of Trypanosoma cruzi. Bioactivity-guided fractionation of the most active extracts afforded seven known compounds, including three chromanes, two furofuran lignans and two flavone C-diglycosides. The most active compounds were the chromanes peperobtusin A and 3,4-dihydro-5-hydroxy-2,7-dimethyl-8-(2''-methyl-2''-butenyl)-2-(4'-methyl-1',3'-pentadienyl)-2 H-1-benzopyran-6-carboxylic acid, with IC (50) values of 3.1 microM (almost three times more active than the positive control benznidazole, IC (50) 10.4 microM) and 27.0 microM, respectively. Cytotoxicity assays using peritoneal murine macrophages indicated that the chromanes were not toxic at the level of the IC (50) for trypanocidal activity. This is the first report on the trypanocidal activity besides unspecific cytotoxicity of chromanes from Peperomia species. Additionally it represents the first time isolation of 3,4-dihydro-5-hydroxy-2,7-dimethyl-8-(2''-methyl-2''-butenyl)-2-(4'-methyl-1',3'-pentadienyl)-2 H-1-benzopyran-6-carboxylic acid from P. obtusifolia.
Ni‐Mn‐based Heusler alloys exhibit a variety of features related to martensitic transformations and are materials that are sought to be employed in actuation applications. To be able to exploit their properties, it is necessary to understand the rich variety and subtle magnetic coupling mechanisms occurring in these alloys. We review complementary neutron polarization analysis and ferromagnetic resonance experiments and give an account on the complex magnetism of these alloys in the austenite and martensite states.
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