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Wyszukujesz frazę "Jankowska, Anna." wg kryterium: Autor


Wyświetlanie 1-3 z 3
Tytuł:
Kataliza procesów hydrosililowania z udziałem cieczy jonowych
Catalysis of hydrosilylation processes with the participation of ionic liquids
Autorzy:
Bartlewicz, Olga
Szymańska, Anna
Jankowska-Wajda, Magdalena
Dąbek, Izabela
Maciejewski, Hieronim
Powiązania:
https://bibliotekanauki.pl/articles/1413312.pdf
Data publikacji:
2021
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
hydrosililowanie
kompleksy Rh
kompleksy Pt
ciecze jonowe
SILPC
kataliza heterogeniczna
hydrosilylation
Rh complexes
Pt complexes
ionic liquids
heterogeneous catalysis
Opis:
Hydrosilylation is a fundamental and elegant method for the laboratory and industrial synthesis of organosilicon compounds. The hydrosilylation reaction is usually performed in a single-phase homogeneous system. A major problem, particularly in homogeneous catalysis, is the separation of catalyst from the reaction mixture. The presence of metals in the reaction products, even in trace quantities, is unacceptable for many applications, therefore efforts have been made at applying heterogeneous catalysts or immobilised metal complexes in order to obtain high catalytic activity and easy product isolation at the same time. One of the methods for producing such catalysts is the employment of ionic liquids as agents for the immobilization of metal complexes. Biphasic catalysis in a liquid-liquid system is an ideal approach through which to combine the advantages of both homogeneous and heterogeneous catalysis. The ionic liquids (ILs) generally form the phase in which the catalyst is dissolved and immobilized. In our research we have obtained a number of catalytic systems of such a type which were based on rhodium and platinum complexes dissolved in phosphonium, imidazolium, pyridinium and ammonium liquids. Currently, there has a common trend to obtain heterogenized systems that combine advantages of homogeneous and heterogeneous catalysis, which makes the hydrosilylation process more cost- effective. Such integration of homo- and heterogeneous catalysts is realized in several variants, as supported IL phase catalysts (SILPC) and solid catalysts with ILs layer (SCILL). Although all the above systems show high catalytic activities, their structure is unknown. This is why we have made attempts to modify selected ionic liquids (corresponding to our most effective systems) and we have applied them as ligands in the synthesis of platinum and rhodium complexes. Another group of catalysts comprises anionic complexes of rhodium and platinum which were obtained by reactions between halide complexes of metals and a respective ionic liquid. Most of the obtained complexes are solids insoluble in hydrosilylation reagents and are characterized by a high catalytic activity. A considerable development of heterogeneous catalysts of this type and their application in many hydrosilylation processes can be expected in the future. This mini-review briefly describes the recent progress in the design and development of catalysts based on the presence of ionic liquids and their applications for hydrosilylation processes.
Źródło:
Wiadomości Chemiczne; 2021, 75, 1-2; 5-29
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Biologia i chemia nowotworu płuca
Biology and chemistry of lung cancer
Autorzy:
Musiał, Claudia
Zaucha, Renata
Kuban-Jankowska, Alicja
Kamm, Anna
Górska-Ponikowska, Magdalena
Powiązania:
https://bibliotekanauki.pl/articles/972293.pdf
Data publikacji:
2019
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
farmakoprewencja raka płuca
biologia raka płuca
chemia raka płuca
indukcja hormonalna
2-metoksyestradiol
lung cancer pharmacoprevention
biology of lung cancer
chemistry of lung cancer
hormonal induction
2-methoxyestradiol
Opis:
Lung cancer is the most common fatal cancer disease in the world. A characteristic feature of lung cancer is genetic diversity. In the overwhelming majority of cases, smoking is the most important etiopathogenic factor. Lung cancer is a cancer with a very bad prognosis regarding long-term survival. The risk of lung cancer depends primarily on active or passive exposure to the carcinogenic components of tobacco smoke. According to available data, the development of lung cancer in addition to active and passive smoking is directly affected by environmental pollution such as smog and fumes, ionizing radiation, mycotoxins and long-term exposure to asbestos (occupational exposure). Research on the pharmacoprevention of lung cancer began over 30 years ago. The first nutrient that the researchers said could inhibit the development of lung cancer was beta carotene. Unfortunately, long-term regular supplementation with high doses of antioxidant in the form of beta-carotene brought the opposite effect. An increase in the incidence of lung cancer was found in people who received beta carotene in the form of a synthetic food supplement. The other component tested was N-acetylcysteine. It is a sulfur compound and a powerful antioxidant that supports the synthesis of glutathione and cysteine, with destructive effects on carcinogenic substances. N-acetyl-cysteine, used in the form of NAC adduct and epigallocatechin-3-gallate, showed efficacy in inhibiting the development of lung cancer only in animal models. In the pharmacoprevention of lung cancer, the use of vitamin E was also tested in the form of tocotrienol and tocopherol. The following work also shows the existence of a high concentration correlation which belongs to the steroid hormone, mainly estrogen, in the blood and the development of lung cancer in women. An increased risk of lung cancer has been observed in women undergoing long-term hormone replacement therapy. The results show that 2-methoxyestradiol, the endogenous metabolite of 17ß-estradiol, shows positive results that inhibit the growth of lung cancer cell lines. The aim of the work was to present the correlation between tobacco abuse and passive smoking and lung cancer, pharmacoprevention of lung cancer and the association of elevated estrogen concentration in women with an increased risk of lung cancer.
Źródło:
Wiadomości Chemiczne; 2019, 73, 7-8; 505-522
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Czynniki wirulencji bakterii - białkowe fosfatazy tyrozynowe : jako cel terapeutyczny w odpowiedzi na rozwijającą się antybiotykooporność
Protein tyrosine phosphatases - factors of bacterial virulence : as a therapeutic target in response to increasing antibiotic resistance
Autorzy:
Kostrzewa, Tomasz
Styszko, Joanna
Przychodzeń, Paulina
Kamm, Anna
Górska-Ponikowska, Magdalena
Kuban-Jankowska, Alicja
Powiązania:
https://bibliotekanauki.pl/articles/171488.pdf
Data publikacji:
2019
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
antybiotykooporność
czynniki wirulencji bakterii
białkowe fosfatazy tyrozynowe
inhibitory PTPs
antibiotic resistance
virulence factors
protein tyrosine phosphatases
PTPs inhibitors
Opis:
Microbial virulence is the ability of pathogen to penetrate, replicate, multiplícate and, as a consequence, damage the cells of the infected organism. In recent years, rapid progress in bacterial genome sequencing has led to the discovery and characterization of many new virulence factors. One of the many mechanisms of bacterial virulence is the activity of bacterial kinases and phosphatases. These enzymes phosphorylate and dephosphorylate various amino acid residues in proteins, most commonly serine, tyrosine and threonine. Reversible phosphorylation and dephosphorylation can control the activity of target proteins, either directly, by inducing conformational changes in proteins, or indirectly, by regulating protein-protein interactions. Due to the increasing antibiotic resistance, new substances that could be used to treat diseases caused by resistant bacterial strains are sought. One of the possibilities seems to be the inhibition of bacterial tyrosine phosphatases. Phosphorylation of proteins containing tyrosine residues is a key post-translational modification that controls the numerous cellular functions in bacteria. So far, many tyrosine phosphatases have been found to be responsible for the virulence of various bacterial strains. Many bacterial species use protein tyrosine phosphatases activity in host-pathogen interaction, by affecting signalling pathways and subsequent induction of the infection process. Many studies are devoted to the search for tyrosine phosphatases inhibitors in the context of possible support of the current antibacterial treatment. This article presents a review of reports on bacterial virulence factors-protein tyrosine phosphatases as potential therapeutic targets.
Źródło:
Wiadomości Chemiczne; 2019, 73, 11-12; 679-699
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-3 z 3

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