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1.
Artigo em Inglês | MEDLINE | ID: mdl-38079363

RESUMO

The selective hydrogenation of aldehydes and olefins plays a crucial role in the synthesis of various industrial products. Immobilizing noble metal catalysts on solid supports has been pursued to overcome the challenges associated with catalyst separation and recovery. In this study, we explore the use of metal-organic frameworks (MOFs) as supports for the immobilization of molecular ruthenium catalysts in the hydrogenation of olefins and aldehydes. We designed a mixed-linker MOF by incorporating the picolylamine moiety, which is a ligand known for its excellent catalytic activity. The ruthenium catalysts were prepared via a simple metal-ligand coordination process without the need for additional treatments. The resulting catalysts exhibit high catalytic activity and a uniform distribution of ruthenium sites on the MOF crystals. The choice of ruthenium precursor has a significant influence on the catalytic performance, with even lower metal content resulting in higher activity. The catalysts achieve high conversion rates and selectivities in the hydrogenation of various olefins. However, in the hydrogenation of aldehydes, due to the harsher conditions required, the formation of small nanoparticles is observed after the reaction. Overall, our findings highlight the potential of picolylamine-modified MOFs as effective supports for the development of highly active heterogeneous catalysts for selective hydrogenation reactions.

2.
Bioorg Chem ; 124: 105754, 2022 07.
Artigo em Inglês | MEDLINE | ID: mdl-35469631

RESUMO

Inflammation is a natural response of the organism to an infection, trauma, or cellular stress. Pain is the first symptom of acute and chronic inflammation. The standard class of medication to treat inflammatory pain is the nonsteroidal anti-inflammatory drug (NSAID). These drugs are associated with severe side effects such as gastric ulcers, gastritis, or internal bleeding. One of NSAIDs, Dipyrone® (metamizole) is largely used in many European and South American countries despite its dubious effectivity and its withdrawal from the market of several countries. Here, aiming to identify a new anti-inflammatory drug prototype based on Dipyrone® structure, a set of 27 molecules were virtually screened, and 4 compounds containing the active metabolite 4-aminoantipyrine and 1,4-dioxo-2-butenyl fragment were selected for docking, synthesis, and biological evaluation. The selection was based on the number of H-bonds and π- π stacking interactions between the inhibitor and the amino acids within the binding site of the enzyme. Carrageenan-induced paw edema, acetic acid-induced writhing, and formalin assays were used to evaluate inflammation and pain response. The selected compounds 1-4 inhibited the involvement of biogenic amines in the formation of paw edema. Compounds 1-4 also reduced pain in the inflammatory response phase. It has to be noted that 4-AA may cause agranulocytosis, which should be borne in mind when developing drug candidates of similar structure. Our new drug prototypes based on 4-aminoantipyrine and 1,4-dioxo-2-butenyl moieties open a gate for developing a prototype of nonsteroidal anti-inflammatory drugs.


Assuntos
Ampirona , Dipirona , Aminas/uso terapêutico , Analgésicos/química , Analgésicos/farmacologia , Analgésicos/uso terapêutico , Anti-Inflamatórios/química , Anti-Inflamatórios/farmacologia , Anti-Inflamatórios/uso terapêutico , Anti-Inflamatórios não Esteroides/uso terapêutico , Carragenina , Dipirona/efeitos adversos , Edema/induzido quimicamente , Edema/tratamento farmacológico , Humanos , Inflamação/tratamento farmacológico , Dor/induzido quimicamente , Dor/tratamento farmacológico
3.
Chem Commun (Camb) ; 58(19): 3101-3121, 2022 Mar 03.
Artigo em Inglês | MEDLINE | ID: mdl-35195128

RESUMO

Metal catalyzed C-H functionalization offers a versatile platform for methodology development and a wide variety of reactions now exist for the chemo- and site-selective functionalization of organic molecules. Cyclopentadienyl-metal (CpM) complexes of transition metals and their correlative analogues have found widespread application in this area, and herein we highlight several key applications of commonly used transition-metal Cp-type catalysts. In addition, an understanding of transition metal Cp-type catalyst synthesis is important, particularly where modifications to the catalyst structure are required for different applications, and a summary of this aspect is given.

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