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Wyświetlanie 1-15 z 54
Tytuł:
Pochodne 1,2,3-triazolu. Potencjalne leki?
Derivatives of 1,2,3-triazole. Potential drugs?
Autorzy:
Bankowska, E.
Wróblewski, A. E.
Powiązania:
https://bibliotekanauki.pl/articles/171634.pdf
Data publikacji:
2012
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
pochodne 1,2,3-triazolu
aktywność przeciwbakteryjna
aktywność przeciwgrzybicza
aktywność przeciwgruźlicza
aktywność przeciwpsychotyczna
aktywność przeciwdrgawkowa
aktywność przeciwzapalna
aktywność hipoglikemiczna
aktywność przeciwnowotworowa
aktywność przeciwwirusowa
1,2,3-triazole derivatives
antibacterial activity
antifungal activity
antitubercular activity
antipsychotic activity
anticonvulsant activity
anti-inflammatory activity
hypoglycemic activity
anticancer activity
antiviral activity
Opis:
Recently, 1,2,3-triazoles have gained an increased attention in the field of drug discovery because several derivatives have already been marketed as medications (e.g. tazobactam, cefatrizine, rufinamide) [1, 2] and many of them appeared to be very active in diverse biological studies including plinambulin 69 currently in the last stage of the clinical trials [60]. In this review very recent investigations of antibacterial, antitubercular, antifungal, antipsychotic, antiepileptic, anti-inflammatory, hypoglycemic, anticancer and antiviral properties of 1,2,3-triazole derivatives are discussed. These studies allowed to select several compounds which were found to be more active in comparison to the already used drugs.
Źródło:
Wiadomości Chemiczne; 2012, 66, 11-12; 993-1022
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Syntezy wybranych zasad Mannicha o aktywności przeciwbakteryjnej i przeciwgrzybiczej in vitro
Synthesis and antibacterial and antifungal activity in vitro of selected Mannich bases
Autorzy:
Nowicka, A.
Liszkiewicz, H.
Nawrocka, W. P.
Powiązania:
https://bibliotekanauki.pl/articles/172209.pdf
Data publikacji:
2014
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
zasada Mannicha
aktywność przeciwbakteryjna
aktywność przeciwgrzybicza
Mannich bases
antibacterial activity
antifungal activity
Opis:
The Mannich reaction is a three-component condensation reaction involving an active hydrogen containing compound, formaldehyde and a primary or a secondary amine. The Mannich reaction is one of the most important basic reaction types in organic chemistry. This kind of aminoalkylation is important for the synthesis and modification of biologically active compounds. Many studies have shown that Mannich bases possesses potent biological activities: antibacterial, antifungal, anti-inflammatory and antimalarial properties. Mannich bases – substituted products containing different heterocyclic moiety in their structures seem to be suitable candidates for further chemical modifications and might be of interest as pharmacologically active compounds. The main goal of this article is to present synthesis and antimicrobial activity of selected Mannich bases. The Mannich reaction is known to be very useful for the synthesis of antibacterial compounds. The Mannich bases, containing various heterocyclic systems were identified as potent antimicrobial agents. Obtained in Mannich reaction derivatives of antibacterial drugs: ciprofloxacine, norfloxacine demonstrate higher antibacterial activity than used drugs, while derivatives of drugs: ibuporofen or phenytoine changed the profile of action of new synthesized compounds.
Źródło:
Wiadomości Chemiczne; 2014, 68, 3-4; 161-186
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Biokoniugaty antybiotykow jonoforowych : cele, strategie syntezy i właściwości
Bioconjugates of ionophore antibiotics : goals, synthesis strategies and properties
Autorzy:
Antoszczak, M.
Kordylas, M.
Huczyński, A.
Powiązania:
https://bibliotekanauki.pl/articles/172178.pdf
Data publikacji:
2018
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
antybiotyki jonoforowe
jonofory
biokoniugacja
hybrydy
aktywność przeciwbakteryjna
aktywność przeciwnowotworowa
ionophore antibiotics
ionophores
bioconjugation
hybrids
antibacterial
activity
anticancer activity
Opis:
Polyether ionophore antibiotics (ionophores) represent a large group of naturally- occurring lipophilic compounds which are able to form complexes with the metal cations and transport them across the lipid membranes. This process disturbs the intercellular Na+/K+ concentration gradient and intracellular pH, and leads to the mitochondrial damages, cell swelling, vacuolization and finally to apoptosis process. For this reason, ionophores are commonly used in veterinary medicine as the non-hormonal growth-promoting as well as coccidiostatic agents. In this group particularly interesting are monensin and salinomycin (Fig. 1) because of their proved anti-tumour activity, including efficiency against multidrug- -resistant cancer cells and cancer stem cells of different origin. Improved synthetic derivatives of both polyether ionophores are thus of considerable current interest. Selective derivatization of these structures whose display multiple reactive functional groups and, in the case of salinomycin, a sensitive tricyclic spiroketal ring system is however non-trivial. Even so, semi-synthetic analogs reported to date includes i.a. selective derivatization of the carboxyl group, the three hydroxyl groups, the ketone group, the alkene, and epimerization of the characteristic tricyclic salinomycin unit (for more details see: M. Antoszczak, A. Huczyński, B. Brzezinski, Wiad. Chem., 2017, 71, 629). On the other hand, as part of the original program to develop innovatory anti- -cancer pro-drugs and prompted by the idea that cancer cells may be individually effectively killed by monensin and salinomycin, a very interesting direction of research is bioconjugation of these ionophores. In this context, our review article is focused on the possible role of hybrids of both ionophore antibiotics with other biologically active substances (natural amino acids, Cinchona alkaloids, flavonoids, nucleosides) in anti-bacterial and anti-cancer treatment, and gives an overview of their properties.
Źródło:
Wiadomości Chemiczne; 2018, 72, 1-2; 1-28
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Właściwości antyoksydacyjne, antybakteryjne i przeciwgrzybicze związków kompleksowych miedzi(II)
Antioxidant, antibacterial and antifungal properties of complex compounds of copper(II)
Autorzy:
Piotrowska, A.
Drzeżdżon, J.
Jacewicz, D.
Chmurzyński, L.
Powiązania:
https://bibliotekanauki.pl/articles/171722.pdf
Data publikacji:
2017
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
związki kompleksowe
miedź(II)
antyoksydanty
aktywność antybakteryjna
aktywność przeciwgrzybicza
copper(II) complexes
antioxidants
antibacterial activity
antifungal activity
Opis:
Since late 1930s copper has been recognized as an essential trace metal in living organisms. Copper(II) cation plays the role as a coordination center not only in the single-nuclear complexes, but also in the multinuclear coordination compounds with a particular emphasis on the polymers as ligands. The selected complex compounds of copper(II) with ligands which are organic and inorganic species have been characterized taking into account their physico-chemical properties. In addition, the complex compounds containing ligands such as Schiff ’s bases, hydrocarbons, organic bases, and also polycarboxylic anions: oxydiacetate, thiodiacetate, iminodiacetate and dipicolinate have been described considering their role in the biological systems. Nowadays tested coordination compounds of copper(II) have interesting antibacterial activities against bacteria strains that are antagonistic to the human. The antibacterial activity of copper(II) complex is stronger than some of the known antibacterial substances e.g. ciprofloxacin. In addition, copper(II) complex compounds exhibit a 64-fold greater antimicrobial properties than copper(II) chloride. Moreover, these compounds have antifungal and antioxidant properties. The activities of antibacterial, antifungal, and antioxidant complex compounds of copper( II) have been compared to the reactivities of these compounds with complexes used as reference substances, e.g. L-ascorbic acid, in the assay using nitrotetrazolium blue.
Źródło:
Wiadomości Chemiczne; 2017, 71, 3-4; 219-240
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Naturalne hydroksy- i chlorolaktony terpenoidowe : ich występowanie i właściwości
Natural terpenoid hydroxyand chlorolactones : their occurrence and properties
Autorzy:
Grabarczyk, M.
Wińska, K.
Mączka, W.
Powiązania:
https://bibliotekanauki.pl/articles/172249.pdf
Data publikacji:
2014
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
hydroksylaktony
chlorolaktony
aktywność biologiczna
hydroxylactones
chlorolactones
biological activity
Opis:
The world around us is composed of a variety of organic compounds that form the animal and plant species. One of the larger groups amongst them are terpenoid compounds, either the structurally simplest monoterpenoids, or sesquiterpenoids containing several atoms or even di- and triterpenoids composed of several carbon atoms. Many of these compounds contain lactone moiety in their structure [1–27]. Equally often, a component of their structure is a hydroxyl group [1–23]. Sometimes, the structural element can also be a halogen atom [24–27]. Many of the hydroxylactones exhibit interesting biological properties, such as antimicrobial (Fig. 1, 2, 12, 13), [2, 3, 19, 21], cytotoxic (Fig. 4, 6, 8), [8, 12, 14], anti-inflammatory (Fig. 1, 4, 11, 14), [3, 9, 18, 22], anti-fungal (112 Fig. 13), [19, 21] or liver protection (Fig. 4, 9) [8, 15]. Some of these compounds also exist as flavoring or taste agents in food (Fig. 3, 10), [7, 16], inhibitors of overproduction nitrogen sulfide (5, 6, 11), [10, 12, 18] or pesticides (Fig. 2, 13), [6, 20]. Hydroxylactones are usually isolated from plants, in many cases, those that are used in traditional folk medicine (Fig. 1, 4, 6, 7, 9, 11, 14, 15, 17), [1, 3, 8, 9, 12, 13, 15, 18, 22, 23, 25, 26], and sometimes from the other organisms, such as microorganisms or fungi (Fig. 2, 5), [6, 10]. Lactones that contain a chlorine atom in their structure, in addition to or instead of the hydroxy group usually have cytotoxic properties (16, 17), [15, 25, 27]. They are found in both land- -based plants, mainly belonging to the family Asteraceae (Fig. 17) [25–27] as well as in marine organisms (Fig. 16), [24], in which the presence of chlorine atoms can be a result of the presence of salt (chloride) in seawater. The following article presents an overview of the various sources from which hydroxylactones and chlorolactones were isolated and also biological properties of these compounds.
Źródło:
Wiadomości Chemiczne; 2014, 68, 1-2; 117-131
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Otrzymywanie i właściwości biologiczne racemicznych i optycznie czynnych laktonów z pierścieniem aromatycznym w pozycji β
Synthesis and biological properties of racemic and optically active lactones with aromatic ring on β-position
Autorzy:
Gładkowski, Witold
Powiązania:
https://bibliotekanauki.pl/articles/27310041.pdf
Data publikacji:
2023
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
laktony
synteza chemoenzymatyczna
konfiguracja absolutna
aktywność antyproliferacyjna
aktywność antyfidantna
lactones
chemoenzymatic synthesis
absolute configuration
antiproliferative activity
antifeedant activity
Opis:
Natural and synthetic lactones containing an aromatic ring exhibit a number of biological properties, e.g. antiproliferative, antifeedant or antimicrobial activity. This review deals with the synthesis and biological properties of lactones containing an aromatic substituent in the β-position of the lactone ring. The described group of compounds includes halolactones, hydroxylactones, unsaturated lactones and products of reductive dehalogenation of iodolactones. In addition to chemical transformations, biotechnological methods for obtaining optically active lactones have also been described, including the use of lipases in the chemoenzymatic pathway leading to the production of halolactones, kinetic separation of hydroxylactones in the process of enzymatic transesterification, microbial hydrolytic dehalogenation of iodolactones and enantioselective hydrolysis of the lactone ring. The biological activity of the obtained β-aryllactones was also briefly characterized.
Źródło:
Wiadomości Chemiczne; 2023, 77, 5-6; 509--531
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Synteza i aktywność biologiczna pochodnych salinomycyny
Synthesis and biological activity of salinomycin derivatives
Autorzy:
Antoszczak, M.
Huczyński, A.
Brzezinski, B.
Powiązania:
https://bibliotekanauki.pl/articles/171728.pdf
Data publikacji:
2017
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
antybiotyki jonoforowe
jonofory
struktura molekularna
aktywność przeciwbakteryjna
aktywność przeciwnowotworowa
ionophore antibiotics
ionophores
molecular structure
antibacterial activity
anticancer activity
Opis:
Polyether ionophore antibiotics (ionophores) represent a large group of naturally- occurring lipid-soluble compounds isolated from actinomycetes strains of Streptomyces genus. Ionophores are able to form complexes with the metal cations, especially sodium and potassium, and transport them across the lipid membranes according to electroneutral or electrogenic transport mechanism. This process disturbs the intercellular Na+/K+ concentration gradient and intracellular pH, leads to the mitochondrial injuries, cell swelling, vacuolization and finally to programmed cell death (apoptosis). For this reason, ionophore antibiotics found commercial use in veterinary medicine as coccidiostatic agents and non-hormonal growth promoters. In addition to the industrial use of ionophores, some of them effectively and selectively inhibit properties of different cancer cells as well as enhance the anti-cancer effects of radio- and/or chemotherapy. In this group, particularly interesting is salinomycin because of its potent anti-microbial and anti-cancer activity, including efficiency against multi-drug resistant cancer cells and cancer stem cells. A very interesting direction of research is the chemical modification of ionophore antibiotics, which can lead to obtaining various derivatives with better biological activity and lower toxicity than those of the starting substances. Because biological activity of ionophore antibiotics and their derivatives is strictly connected with the ability to form characteristic pseudocyclic structures around the complexed cations (host-guest complex), it is also important to establish the detailed information on these structures. In this context, our review article is focused on the possible role of salinomycin and its derivatives in anti-microbial as well as anti-cancer therapy, and gives an overview of the properties of this antibiotic.
Źródło:
Wiadomości Chemiczne; 2017, 71, 7-8; 629-661
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Naturalne i syntetyczne laktony o aktywności przeciwnowotworowej i przeciwdrobnoustrojowej
Natural and synthetic lactones with anticancer and antimicrobial activity
Autorzy:
Mazur, M.
Powiązania:
https://bibliotekanauki.pl/articles/171876.pdf
Data publikacji:
2011
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
laktony aktywne biologicznie
laktony seskwiterpenowe
aktywność przeciwnowotworowa
aktywność przeciwdrobnoustrojowa
biologically active lactones
sesquiterpene lactones
anticancer activity
antimicrobial activity
Opis:
Medicine is one of the most developing branches of knowledge. But even now there are still some diseases which are impossible to cure. Different cancers, antibiotic resistant bacterial infections and fungal pathogenesis infections are still everlasting problems. Thus, two ways of solutions are proposed. First is the return to natural medicines. From the ancient times plants have been used in medicine and the natural products have been an important source of drugs. Nowadays isolation and identification of these compounds, together with the determination of their biological activity, also play an important role. Lactones are the cyclic esters with a wide range of carbon atoms in a lactone ring. They are a very interesting group of compounds which reveal a wide spectrum of biological activity. Terpenoid, especially sesquiterpene lactones and coumarin derivatives, are found in plants of the Asteraceae and Apiaceae families as well as in many others organisms. The naturally occurring lactones often possess anti-inflamatory [1, 2], phytotoxic [3, 4], antiprotozoal [5], and antiviral activities [6]. They are also well known for their anticancer [7, 8] and antimicrobial activities [9, 10]. The second way of obtaining new biologically active lactones is the chemical synthesis of new potent structural analogs of natural bioactive compounds. However, the complexity of natural products and their derivatives may lead to limited supplies, especially when they have the chiral centers which are one of the most important factors influencing their biological activity. It also causes difficulties to determine the mechanism of action. For those reasons, structural simplification plays an important role in the development of analog design. This review is focused on novel literature data about synthetic and natural lactones which reveal anticancer, antibacterial and antifungal activities. Presented compounds show potent biological activity and high selectivity with holding promises for further applications.
Źródło:
Wiadomości Chemiczne; 2011, 65, 1-2; 135-149
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Syntezy i aktywność biologiczna wybranych zasad Mannicha
Synthesis and biological activity of selected Mannich bases
Autorzy:
Nawrocka, W. P.
Nowicka, A.
Powiązania:
https://bibliotekanauki.pl/articles/172259.pdf
Data publikacji:
2014
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
zasada Mannicha
aktywność biologiczna
syntezy
Mannich bases
biological activity
synthesis
Opis:
The Mannich reaction is important for the synthesis and modification of biologically active compounds. Mannich bases – substituted products containing different heterocyclic system in their structures seem to be suitable candidates for further chemical modifications and might be of interest as pharmacologically active compounds. The main goal of this article is to present synthesis and biological activity of selected Mannich bases. Based on a review of the chemical literature, Mannich bases showed a multipharmacological effects. The Mannich bases, containing various heterocyclic systems were identified as potent anticancer agents. Presented compounds exhibit cytotoxic, antiproliferate in vitro, anticonvulsant, antioxidative, antiinflaminatory and analgesic activity. Some of them can be used in a treatment of diabetes and hypertension.
Źródło:
Wiadomości Chemiczne; 2014, 68, 11-12; 981-1008
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Naturalne i syntetyczne analogi strukturalne jononów
Natural and synthetic structural analogs of ionones
Autorzy:
Grabarczyk, M.
Wińska, K.
Mączka, W.
Powiązania:
https://bibliotekanauki.pl/articles/172354.pdf
Data publikacji:
2015
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
pochodne jononów
aktywność biologiczna
biotransformacja
ionone derivatives
biological activity
biotransformation
Opis:
Both plants and animals in the process of evolution gained the ability to produce compounds that affect their existence in the wild. These compounds may affect the organisms producing them, and may also be used by completely different individuals. Among huge number of molecules characterized by extremely essential features are, among others, ionones and their derivatives. Ionones are ketones composed of 13 carbon atoms. They are found in many essential oils being the products of degradation of carotenoids. Both they and their structural analogues can play various biological functions such as being deterrent to other individuals or, conversely, atractant. Compounds found in plants, containing like ionone carbon skeleton, and having in their structure additional hydroxyl groups or epoxide ring (4)–(23) often exhibit allelopathic activity [1–15] (Fig. 2–5). Marine animals may in turn use them as ichtyotoxic compounds (27) and (28) [19] (Fig. 7). A compound called luciferin Latia (29) is responsible for the bioluminescent properties of marine snail [20] (Fig. 8). Plants used for centuries in traditional folk medicine of different countries are a source of glycoside derived α- and β-ionone (37)–(55) [22–31] (Fig. 11–14). These compounds may also be used in modern medicine, inter alia, in the regulation of neurodegenerative diseases or for the treatment of osteoporosis. Because of the potential biological properties of structural analogs of ionones they are also obtained by chemical synthesis (56)–(69) [32–39] (Fig. 15–18) or biotransformation (70)–(89) [40–47] (Fig. 19–25), and then subjected to careful examination of their biological activities. By applying these methods we can also obtain a molecules whose acquisition from natural sources is unprofitable. We have received such derivatives which have no counterpart in nature.
Źródło:
Wiadomości Chemiczne; 2015, 69, 11-12; 997-1018
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Oznaczanie aktywności przeciwutleniającej metodami in-vitro
Determination of antioxidant activity with in-vitro methods
Autorzy:
Malinowski, Jacek
Drzeżdżon, Joanna
Chmurzyński, Lech
Jacewicz, Dagmara
Powiązania:
https://bibliotekanauki.pl/articles/972307.pdf
Data publikacji:
2019
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
aktywność przeciwutleniająca
metoda in vitro
antioxidant activity
in vitro methods
Opis:
In - vitro methods of determination of the antioxidant activity of complex compounds are very interesting and not fully investigated areas of knowledge from the borderline of chemistry and biology. Methods used for determination of the activity of antioxidant complex compounds are modified due to the conditions of the experiments in which they should be carried out, e.g. reactions at physiological pH. Civilization diseases, stress related to the fast pace of life and increasing requirements of our lives cause the formation of free radicals in our body, i.e. particles characterized by a high reactivity. The methods of determination of the antioxidant activity of complexes discussed in this work apply tests carried out in laboratory conditions - in - vitro.
Źródło:
Wiadomości Chemiczne; 2019, 73, 9-10; 523-542
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Terapeutyczny potencjał pochodnych izotiazolowych : wpływ struktury związku na aktywność
The terapeutic potential of isothiazole derivatives : the effect of compound structure on activity
Autorzy:
Jęśkowiak, I.
Mączyński, M.
Ryng, S.
Powiązania:
https://bibliotekanauki.pl/articles/172092.pdf
Data publikacji:
2018
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
izotiazol
struktura
aktywność biologiczna
isothiazole
chemical structure
biological activity
Opis:
Isothiazole derivatives are compounds with potentially interesting biological activity. The work on the isothiazole ring was successfully conducted by Machoń from the Department of Organic Chemistry at Wrocław Medical University. Machoń received an isothiazole derivative – Denotivirum, which is an original Polish drug. This compound has antiviral, anti-inflammatory and bacteriostatic activity against Staphylococcus aureus. Within the group of isothiazolpyrimidine derivatives, Machoń selected a compound with a very strong antitumor effect (IP-10). This combination has gone through a preclinical study. The high antitumor activity was confirmed by the Bethesda USA Research Center, which qualified him for clinical trials [1–5]. The aim of the study was to review and evaluate the latest scientific works in the field of isothiazole derivatives and, above all, the dependence of their structure on activity. The Chemical Abstracts Database and Reaxys, together with other sources of information, was searched using isothiazole keyword. As a result of the search, the majority of works describing isothiazole derivatives for the anticancer (Tab. 1), immunological among other anti-inflammatory, immunosuppressive (Tab. 2) and antiviral (Tabs 3 and 4) activity were selected. Some substances have been tested for antibacterial, antifungal, insecticidal, antiparasitic, analgesic, antidiabetic and neuroprotective properties (Tab. 5). Analyzed were only compounds containing the isothiazole ring, which are not belong to condensed heterocyclic compounds such as benzoisothiazoles, isothiazolpyridines or furoisothiazoles. In conclusion, the most interesting works presented herein illustrate a wide range of activities of isothiazole derivatives depending on their structure, which also extend the scope of biological research revealing previously barren activities of this group of compounds.
Źródło:
Wiadomości Chemiczne; 2018, 72, 11-12; 867-885
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Oznaczanie aktywności przeciwutleniającej metodami in-vitro
Determination of antioxidant activity with in-vitro methods
Autorzy:
Malinowski, Jacek
Drzeżdżon, Joanna
Chmurzyński, Lech
Jacewicz, Dagmara
Powiązania:
https://bibliotekanauki.pl/articles/972311.pdf
Data publikacji:
2019
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
aktywność przeciwutleniająca
metoda in vitro
antioxidant activity
in vitro methods
Opis:
In - vitro methods of determination of the antioxidant activity of complex compounds are very interesting and not fully investigated areas of knowledge from the borderline of chemistry and biology. Methods used for determination of the activity of antioxidant complex compounds are modified due to the conditions of the experiments in which they should be carried out, e.g. reactions at physiological pH. Civilization diseases, stress related to the fast pace of life and increasing requirements of our lives cause the formation of free radicals in our body, i.e. particles characterized by a high reactivity. The methods of determination of the antioxidant activity of complexes discussed in this work apply tests carried out in laboratory conditions - in - vitro.
Źródło:
Wiadomości Chemiczne; 2019, 73, 9-10; 523-542
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Aktywność biologiczna pochodnych 2-amino -1H-benzimidazolu. Część II
Biological activity of 2-amino -1Hbenzimidazole derivatives. Part II
Autorzy:
Nawrocka, W. P.
Nowicka, A.
Liszkiewicz, H.
Powiązania:
https://bibliotekanauki.pl/articles/171652.pdf
Data publikacji:
2012
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
pochodne 2-aminobenzimidazolu
aktywność biologiczna
2-aminobenzimidazole derivatives
biological activity
Opis:
2-Aminobenzimidazole occur in a broad spectrum of drugs and pharmacological agents with hypotensive [26], antihistaminic, immunotropic [16], antiarrhythmic [25], analgesic [21, 22] or antiaggregatory properties [27]. There are 30 drugs, 2-aminobenzimidazole derivatives, registered in the world which exhibit diverse pharmacological activities. Carbendazim is an antifungal drug, but in 2003 it has been registered as anticancer [1]. They are also voltage sensitive calcium channel blockers [33], inhibitors of vascular endothelial growth factor [12]. The main goal of this article is to present a various biological activity of 2-aminobenzimidazole derivatives. During the past 20 years the biological activity of 2-aminobenzimidazole have been studied. Based on a review of the chemical literature, derivatives of 2-aminobenzimidazole showed a multipharmacological effects such as hypotensive effect [28], antiinflammatory effect [20] or antibacterial activity. Some chemical compounds, which contain in their structure 2-aminobenzimidazole system inhibit neurodegeneration and in the future they may be used in a treatment of Alzheimer’s disease or Parkinson’s disease [32]. Some of described derivatives of 2-aminobenimidazole can be used in a treatment of metabolic syndrome and diabetes [38]. Synthesis of new 2-aminobenzimidazole derivatives with anticancer activity is now one of the most important direction of research conducted on this group of compounds. Present compounds exhibit anticancer, antiproliferate, neuroprotetic and antiinflaminatory activity. Some of them can be used in a treatment of diabetes and hypertension.
Źródło:
Wiadomości Chemiczne; 2012, 66, 9-10; 840-865
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Aktywność biologiczna pochodnych 2-amino -1H-benzimidazolu. Część I
Biological activity of 2-amino -1H-benzimidazole derivatives. Part I
Autorzy:
Nawrocka, W. P.
Nowicka, A.
Liszkiewicz, H.
Powiązania:
https://bibliotekanauki.pl/articles/171654.pdf
Data publikacji:
2012
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
pochodne 2-aminobenzimidazolu
aktywność biologiczna
2-aminobenzimidazole derivatives
biological activity
Opis:
The main goal of this article is to present a various biological activity of 2-aminobenzimidazole derivatives. During the past 20 years the biological activity of 2-aminobenzimidazole have been studied. 2-Aminobenzimidazole occurs in a broad spectrum of drugs and pharmacological agents with anticancer [21], antibacterial [14], antiviral [10], analgesic or antiaggregatory properties. There are 30 drugs, 2-aminobenzimidazole derivatives, registered in the world. Mebendazole represents a big group of antiparasitic drugs [25]. Antihistaminic II-nd generation drug with selective activity towards H1 receptors represents Astemizol [2]. Antiviral drugs are: Enviroksym and its isomer Zinviroksym and Enviraden [3–5]. Synthesized 2-aminobenzimidazole derivatives are active against HCV [7], HIV [8, 9] or HCHV [11]. Selected compounds exhibit antiviral [3–5], antifungal [22–24] and antiparasitic [26–28] activity. Some of them can be used in the treatment of bacterial infections [12–14]. Many of 2-aminobenzimidazole analogues are histamine H1, H2, H3 and also H4 receptor antagonists [30, 33, 35, 39].
Źródło:
Wiadomości Chemiczne; 2012, 66, 9-10; 811-838
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
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