Cargando…

Morita-Baylis-Hillman Adducts Display Anti-Inflammatory Effects by Modulating Inflammatory Mediator Expression in RAW264.7 Cells

Inflammatory response plays an important role not only in the normal physiology but also in pathologies such as cancers. The Morita-Baylis-Hillman adducts (MBHA) are a novel group of synthetic molecules that have demonstrated many biological activities against some parasitic cells such as Plasmodium...

Descripción completa

Detalles Bibliográficos
Autores principales:	Faheina-Martins, Glaucia V., Leite, Jacqueline Alves, Dantas, Bruna Braga, Lima-Júnior, Cláudio G., Vasconcellos, Mário L. A. A., Rodrigues-Mascarenhas, Sandra, Araújo, Demetrius A. M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2017
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529643/ https://www.ncbi.nlm.nih.gov/pubmed/28785138 http://dx.doi.org/10.1155/2017/6898505

Ejemplares similares

Regio- and Stereoselective Electrochemical Alkylation of Morita–Baylis–Hillman Adducts
por: Bertuzzi, Giulio, et al.
Publicado: (2022)

Enantioselective, Organocatalytic Morita-Baylis-Hillman and Aza-Morita-Baylis-Hillman Reactions: Stereochemical Issues
por: Mansilla, Javier, et al.
Publicado: (2010)

Morita–Baylis–Hillman reaction of acrylamide with isatin derivatives
por: Singh, Radhey Mohan, et al.
Publicado: (2014)

Naphthalenes and Quinolines by Domino Reactions of Morita–Baylis–Hillman Acetates
por: Annor-Gyamfi, Joel K., et al.
Publicado: (2020)

Application of 7-azaisatins in enantioselective Morita–Baylis–Hillman reaction
por: He, Qing, et al.
Publicado: (2016)

Engineering an Efficient and Enantioselective Enzyme for the Morita-Baylis-Hillman Reaction
por: Crawshaw, Rebecca, et al.
Publicado: (2022)

Trypanosoma cruzi Cell Death Induced by the Morita-Baylis-Hillman Adduct 3-Hydroxy-2-Methylene-3-(4-Nitrophenylpropanenitrile)
por: Sandes, Jana M., et al.
Publicado: (2014)

Dihydroquinolines, Dihydronaphthyridines and Quinolones by Domino Reactions of Morita-Baylis-Hillman Acetates
por: Annor-Gyamfi, Joel K., et al.
Publicado: (2021)

Organocatalytic asymmetric allylic amination of Morita–Baylis–Hillman carbonates of isatins
por: Zhang, Hang, et al.
Publicado: (2012)

2-Fluoroenones via an Umpolung Morita–Baylis–Hillman Reaction of Enones
por: Maity, Subrata, et al.
Publicado: (2023)

Synthesis and In Vitro Anti Leishmania amazonensis Biological Screening of Morita-Baylis-Hillman Adducts Prepared from Eugenol, Thymol and Carvacrol
por: Xavier, Francisco José Seixas, et al.
Publicado: (2016)

Synthesis of 16 New Hybrids from Tetrahydropyrans Derivatives and Morita-Baylis-Hillman Adducts: In Vitro Screening against Leishmania donovani
por: de Oliveira Sousa, Suervy Canuto, et al.
Publicado: (2017)

Remarkable influence of microwave heating on Morita-baylis-Hillman reaction in PEG-200
por: Aravind, A, et al.
Publicado: (2012)

Antimicrobial activity of allylic thiocyanates derived from the Morita-Baylis-Hillman reaction
por: Sá, Marcus Mandolesi, et al.
Publicado: (2014)

Expedient Organocatalytic Aza-Morita–Baylis–Hillman Reaction through Ball-Milling
por: Williams, Matthew T. J., et al.
Publicado: (2020)

One-Electron Reduction Potentials: Calibration of Theoretical Protocols for Morita–Baylis–Hillman Nitroaromatic Compounds in Aprotic Media
por: Francisco da Silva, Amauri, et al.
Publicado: (2018)

The Morita–Baylis–Hillman reaction for non-electron-deficient olefins enabled by photoredox catalysis
por: Li, Long-Hai, et al.
Publicado: (2022)

Chiral Phosphine Catalyzed Allylic Alkylation of Benzylidene Succinimides with Morita–Baylis–Hillman Carbonates
por: Liu, Chang, et al.
Publicado: (2023)

Lipase‐Catalysed Enzymatic Kinetic Resolution of Aromatic Morita‐Baylis‐Hillman Derivatives by Hydrolysis and Transesterification
por: Mathebula, Nompumelelo P., et al.
Publicado: (2022)

Asymmetric allylic alkylation of Morita–Baylis–Hillman carbonates with α-fluoro-β-keto esters
por: Yan, Lin, et al.
Publicado: (2013)

Pentapeptide Nanoreactor as a Platform for Halogenations, Diels–Alder Reaction, and Morita–Baylis–Hillman Reaction
por: Debnath, Mintu, et al.
Publicado: (2019)

The Morita-Baylis-Hillman Reaction: Insights into Asymmetry and Reaction Mechanisms by Electrospray Ionization Mass Spectrometry
por: Carrasco-Sanchez, Verónica, et al.
Publicado: (2009)

A Facile and Mild Synthesis of Trisubstituted Allylic Sulfones from Morita-Baylis-Hillman Carbonates
por: Jiang, Lin, et al.
Publicado: (2015)

Amino acid ionic liquids as catalysts in a solvent-free Morita–Baylis–Hillman reaction
por: Pereira, Mathias Prado, et al.
Publicado: (2018)

Phosphine-mediated enantioselective [1 + 4]-annulation of Morita–Baylis–Hillman carbonates with 2-enoylpyridines
por: Wang, Tao, et al.
Publicado: (2018)

A Case Study of the Mechanism of Alcohol-Mediated Morita Baylis–Hillman Reactions. The Importance of Experimental Observations
por: Plata, R. Erik, et al.
Publicado: (2015)

A Convenient One-Pot Preparation of 2-Methyl-3-(phenylthio- methyl)quinolines from Morita-Baylis-Hillman Adducts and Their Oxidation to the Corresponding Sulfones
por: Ramesh, Chintakunta, et al.
Publicado: (2012)

Azidophosphonium salt-directed chemoselective synthesis of (E)/(Z)-cinnamyl-1H-triazoles and regiospecific access to bromomethylcoumarins from Morita–Baylis–Hillman adducts
por: Karthikeyan, Soundararajan, et al.
Publicado: (2020)

Chiral multifunctional thiourea-phosphine catalyzed asymmetric [3 + 2] annulation of Morita–Baylis–Hillman carbonates with maleimides
por: Deng, Hong-Ping, et al.
Publicado: (2012)

First DMAP-mediated direct conversion of Morita–Baylis–Hillman alcohols into γ-ketoallylphosphonates: Synthesis of γ-aminoallylphosphonates
por: Ayadi, Marwa, et al.
Publicado: (2016)

Metal catalyst-free N-allylation/alkylation of imidazole and benzimidazole with Morita–Baylis–Hillman (MBH) alcohols and acetates
por: Mhasni, Olfa, et al.
Publicado: (2023)

Synthesis of Functionalized Thieno[2,3-b]indoles via One-Pot Reaction of Indoline-2-thiones with Morita–Baylis–Hillman and Rauhut–Currier Adducts of Nitroalkenes
por: Mane, Vaijinath, et al.
Publicado: (2018)

Et(3)B-mediated and palladium-catalyzed direct allylation of β-dicarbonyl compounds with Morita–Baylis–Hillman alcohols
por: Abidi, Ahlem, et al.
Publicado: (2016)

Morita–Baylis–Hillman reaction of 3-formyl-9H-pyrido[3,4-b]indoles and fluorescence studies of the products
por: Devi, Nisha, et al.
Publicado: (2022)

Facile and innovative catalytic protocol for intramolecular Friedel–Crafts cyclization of Morita–Baylis–Hillman adducts: Synergistic combination of chiral (salen)chromium(III)/BF(3)·OEt(2) catalysis
por: Soundararajan, Karthikeyan, et al.
Publicado: (2021)

Synthetic Access to Cyclopenta[a]inden-2(1H)-ones from Morita–Baylis–Hillman Products of 2-Alkynyl Benzaldehydes
por: Raji Reddy, Chada, et al.
Publicado: (2018)

Combining palladium and ammonium halide catalysts for Morita–Baylis–Hillman carbonates of methyl vinyl ketone: from 1,4-carbodipoles to ion pairs
por: Yang, Yang, et al.
Publicado: (2021)

Synthesis, antitubercular and anticancer activity of new Baylis–Hillman adduct-derived N-cinnamyl-substituted isatin derivatives
por: Kumar, Sriramoju Bharath, et al.
Publicado: (2013)

Regioselective S(N)2' Mitsunobu reaction of Morita–Baylis–Hillman alcohols: A facile and stereoselective synthesis of α-alkylidene-β-hydrazino acid derivatives
por: Xu, Silong, et al.
Publicado: (2014)

DABCO-Catalyzed Mono-/Diallylation of N-Unsubstituted Isatin N,N′-Cyclic Azomethine Imine 1,3-Dipoles with Morita-Baylis-Hillman Carbonates
por: Wang, Qiumi, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_0iji1f6750e3m0ln4pv47hg4a4