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    Wyświetlanie 1-15 z 15
    Tytuł:
    Novel Synthesis, spectral, characterization of 4,5-diphenyl-1-((tetrahydrofuran-2-yl)methyl)-2-(3,4,5-trichlorophenyl)-1H-imidazole and its applications of molecular docking, anticancer activity
    Autorzy:
    Dhineshkumar, E.
    doss, M. Arockia
    Uma, D.
    Powiązania:
    https://bibliotekanauki.pl/articles/1031882.pdf
    Data publikacji:
    2020
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    HepG2
    Imidazole
    cytotoxicity
    molecular docking
    Opis:
    In the present study of 4,5-diphenyl-1-((tetrahydrofuran-2-yl)methyl)-2-(3,4,5-trichlorophenyl)-1H-imidazole 1 was synthesized. The synthesized imidazole compound 1 has been characterized by FT-IR, 1H, 13C NMR and ESI-Mass spectral studies. Molecular docking is also performed in order to explain the over-expression of estrogen receptor in 70% of liver cancer. The imidazole scaffold is a privileged scaffold for exploration of anticancer agents. The objective of the present study is to evaluate the anticancer activity of imidazole 1 in human liver cancer cell lines HepG2.
    Źródło:
    World News of Natural Sciences; 2020, 30, 2; 203-212
    2543-5426
    Pojawia się w:
    World News of Natural Sciences
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Acid-Promoted Synthesis of Imidazolyl-Pyrazole Derivatives via a Multicomponent Reaction Using Ultra Sound Irradiation
    Autorzy:
    Baria, B.
    Viradiya, D.
    Kotadiya, V.
    Kakadiya, R.
    Shah, A.
    Powiązania:
    https://bibliotekanauki.pl/articles/412490.pdf
    Data publikacji:
    2014
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    Imidazole
    ultrasound irradiation
    Imidazolyl-Pyrazole
    Benzil
    Opis:
    Some new imidazolyl pyrazole derivatives have been synthesized using benzil, ammonium acetate, and heterocyclic aldehyde in ethanol and acetic acid under ultra sound irradiation. The obtained products using this approach are having high purity and good in yield. By conducting the reactions in ethanol, the solid products were precipitated out and could be isolated simply by filtration. The synthesized compounds were characterized by various analytical techniques such as 1H and 13C NMR and further supported by mass spectroscopy.
    Źródło:
    International Letters of Chemistry, Physics and Astronomy; 2014, 11, 3; 277-283
    2299-3843
    Pojawia się w:
    International Letters of Chemistry, Physics and Astronomy
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Flotation separation of quartz from phosphorite using an imidazole ionic liquid collector and its adsorption mechanism
    Autorzy:
    Zhao, Yuanyuan
    Xu, Wei
    Mei, Guangjun
    Yu, Mingming
    Yang, Siyuan
    He, Zhan
    Powiązania:
    https://bibliotekanauki.pl/articles/2146857.pdf
    Data publikacji:
    2022
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    reverse flotation
    imidazole ionic liquid
    desilication
    phosphorite
    quartz
    Opis:
    In this study, an imidazole ionic liquid (dodecyl-tri-methylimidazolium chloride) was employed as a collector to separate quartz from phosphorite. The micro-flotation experiments of a single mineral found that it had selective collecting ability for quartz than phosphorite. Mixed mineral flotation experiments confirmed that efficient separation results could be obtained using the imidazole ionic liquid as the collector. A concentrate with a 31.44% grade of phosphorite could be obtained with a 0.285 kg/Mg collector dosage at neutral pH, which was much better than the traditional collector dodecylamine. The adsorption mechanism of the imidazole ionic liquid on the surface of phosphorite and quartz was investigated by contact angle and zeta potential measurements, Fourier transform infrared and X-ray photoelectron spectroscopy analyses. These results showed that the adsorption of imidazole ionic liquid at the quartz surface was stronger than that of phosphorite, and the collector adsorbability difference between quartz and phosphorite resulted in the efficient flotation separation. Consequently, the dodecyl-tri-methylimidazolium chloride salt is an effective collector for reverse flotation of quartz from phosphorite.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2022, 58, 1; 159--168
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Some High Nitrogen Derivatives of Nitrotetrazolylimidazole as New High Performance Energetic Compounds
    Autorzy:
    Zohari, N.
    Keshavarz, M. H.
    Seyedsadjadi, S. A.
    Powiązania:
    https://bibliotekanauki.pl/articles/358162.pdf
    Data publikacji:
    2014
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    nitrotetrazolyl-imidazole
    high energy material
    performance
    safety
    thermochemical property
    Opis:
    This work introduces important properties of some new derivatives of nitrotetrazolyl-imidazole as high nitrogen energetic compounds, which are evaluated and discussed using some reliable models. The predicted properties are also compared with 1,3,5,7-tetranitro-1,3,5,7-tetraazacyclooctane (HMX). It is shown that some of these compounds can be seen as interesting organic explosives with relatively high performance and low sensitivity, which could be used for important industrial applications. Since some of the new compounds have a relatively good oxygen balance, the calculated specific impulses confirm that these compounds can be considered as suitable oxidizers in solid propellants.
    Źródło:
    Central European Journal of Energetic Materials; 2014, 11, 3; 349-362
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Antiplatelet action of losartan involves TXA2 receptor antagonism but not TXA2 synthase inhibition
    Autorzy:
    Chlopicki, S.
    Koda, M.
    Chabielska, E.
    Buczko, W.
    Gryglewski, R.J.
    Powiązania:
    https://bibliotekanauki.pl/articles/70180.pdf
    Data publikacji:
    2000
    Wydawca:
    Polskie Towarzystwo Fizjologiczne
    Tematy:
    thromboxane A2
    synthase inhibition
    imidazole
    antiplatelet action
    losartan
    platelet
    Źródło:
    Journal of Physiology and Pharmacology; 2000, 51, 4,1
    0867-5910
    Pojawia się w:
    Journal of Physiology and Pharmacology
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Protochlorophyllide photoreduction in angiosperms: focus on protochlorophyllide – surroundings interaction in model system
    Autorzy:
    Mysliwa-Kurdziel, B.
    Gabruk, M.
    Kruk, J.
    Strzalka, K.
    Powiązania:
    https://bibliotekanauki.pl/articles/79978.pdf
    Data publikacji:
    2013
    Wydawca:
    Polska Akademia Nauk. Czytelnia Czasopism PAN
    Tematy:
    conference
    protochlorophyllide
    angiosperm
    chlorophyll
    photosynthetic reaction
    fluorescence intensity
    imidazole
    model system
    Źródło:
    BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology; 2013, 94, 3
    0860-7796
    Pojawia się w:
    BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Application of polymer inclusion membranes doped with 1-hexyl-4-methylimidazole for pertraction of zinc(II) and other transition metal ions
    Autorzy:
    Ulewicz, M.
    Radzyminska-Lenarcik, E.
    Powiązania:
    https://bibliotekanauki.pl/articles/110567.pdf
    Data publikacji:
    2015
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    polymer inclusion membrane
    PIM
    metal ions separation
    zinc(II)
    transition metal ions
    imidazole derivatives
    Opis:
    Transport of Zn(II) from unary aqueous chloride solutions and from solutions which contain mixtures of Cd(II), Co(II) and Ni(II) ions in source phases (cMe = 0.001 mol/dm3, pH = 6.0) across polymer inclusion membranes (PIMs) doped with 1-hexyl-4-methylimidazole as ion carrier was studied. The use of 1-hexyl-4-methylimidazole enables the separation of 98.5% Zn(II) from a unary solution and 96.9% from a quaternary solution of Zn(II)-Cd(II)-Co(II)-Ni(II) after running the process for 24 hours. Using that ion carrier, the metals are transported in the following order: Zn(II) > Cd(II) > Ni(II) > Co(II), and the selectivity coefficients of Zn(II)/Cd(II), Zn(II)/Ni(II), and Zn(II)/Co(II) are 12.9, 23.4 and 40.8, respectively. Findings of atomic force microscopy (AFM) examinations as well as thermograms of a polymer inclusion membrane containing 1-hexyl-4-methylimidazole are also presented. A membrane with 1.0 mol/dm3 of carrier has a porosity of 15.8%, and roughness of 6.6 nm. The membranes remain thermally stable at temperatures up to 200oC. The findings were compared with earlier-reported results for 1-hexylimidazole.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2015, 51, 2; 447-460
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Spectroscopic study of a bis(imidazole) (octaethylporphyrinato)iron(III) complex
    Autorzy:
    Rutkowska, I.
    Dziliński, K.
    Kaczmarzyk, T.
    Stanek, J.
    Powiązania:
    https://bibliotekanauki.pl/articles/146898.pdf
    Data publikacji:
    2013
    Wydawca:
    Instytut Chemii i Techniki Jądrowej
    Tematy:
    electron paramagnetic resonance (EPR) spectroscopy
    Mössbauer spectroscopy
    low-spin iron porphyrin
    imidazole axial ligands
    Opis:
    Low-spin ferric octaethylporphyrinatoiron complex with two imidazole axial ligands [Fe(III)(OEP)(Im)2]+ has been investigated by electron paramagnetic resonance (EPR) and Mössbauer spectroscopies. It was found that the ground spin state corresponds to the electron configuration (dxy)2 (dxz, dyz)3 and planes of the imidazole axial ligands have a parallel mutual orientation. Ethyl groups bonded to pyrrole rings, as peripheral substituents, effect on the ground electron spin state of the complex studied and the relative orientation of the the imidazole axial ligands in a similar way like the phenyl substituents bonded to meso-carbon atoms of the porphyrin macrocycle. The temperature dependence of the Mössbauer spectra is discussed in terms of magnetic relaxation processes.
    Źródło:
    Nukleonika; 2013, 58, 3; 419-423
    0029-5922
    1508-5791
    Pojawia się w:
    Nukleonika
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Search for the possibility of utilizing the differences in complex-forming capacities of alkylimidazoles for selective extraction of some metal ions from aqueous solutions
    Autorzy:
    Radzymińska-Lenarcik, E.
    Powiązania:
    https://bibliotekanauki.pl/articles/778263.pdf
    Data publikacji:
    2008
    Wydawca:
    Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
    Tematy:
    ekstrakcja selektywna
    alkiloimidazol
    jony metali przejściowych
    selective extraction
    alkyl imidazole derivatives
    transition metals ions
    Opis:
    Alkyl substituents in position 1 of the imidazole ring distinctly affect the hydrophobic properties of the molecule and strengthen its basicity. Hence, 1-alkylimidazoles have been used as extractants of a number of metal ions. Again, a methyl substituent in position 2 of the imidazole ring raises by an order of magnitude the basicity. At the same time, the substituent impedes the formation of the 2-alkylimidazole complexes with metal ions due to the steric effect. By the substitution of alkyl groups in position 1 or 2 of the imidazole ring it is possible to program the extraction properties of extractants and to control the selectivity of extraction.
    Źródło:
    Polish Journal of Chemical Technology; 2008, 10, 1; 73-78
    1509-8117
    1899-4741
    Pojawia się w:
    Polish Journal of Chemical Technology
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Greener, facile and ultrasound assisted synthesis of 1,2,3-triazole via CuAAC of 2-(azidomethyl)-1H-benzo[d]imidazole and alkynes and their evaluation of antimicrobial activity
    Autorzy:
    Kapupara, Vimalkumar H.
    Kalavadiya, Prakash L.
    Gojiya, Dinesh G.
    Parmar, Nilesh D.
    Joshi, Hitendra S.
    Powiązania:
    https://bibliotekanauki.pl/articles/1075696.pdf
    Data publikacji:
    2019
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    1
    1H-benzo[d]imidazole azide
    2
    3-triazol-1-yl)methyl)-1H-benzo[d]imidazole
    3-triazole via CuAAC
    4-disubstituted 1H-1
    alkynes
    antimicrobial
    copper(I) catalyst
    Opis:
    An expeditious room temperature protocol for the synthesis of 1,4-disubstituted 1H-1,2,3-triazol-1-yl)methyl)-1H-benzo[d]imidazole from [3+2] cyclization by using 1H-benzo[d]imidazole azide and various substituted terminal alkynes and copper(I) as a catalyst. This synthetic approach has been various prominent features such as fewer reaction steps, Good Yield, simple reaction condition and no any further purification required. Characterizations of all the synthesized compounds were done by various spectroscopic techniques like FT-IR, NMR and Mass spectrometry. All the synthesized targeted compounds were screened and evaluated for their antimicrobial activities.
    Źródło:
    World Scientific News; 2019, 119; 139-167
    2392-2192
    Pojawia się w:
    World Scientific News
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Epoxy adhesive formulations using latent imidazole metal cation complexes
    Autorzy:
    Pilawka, R.
    Maka, H.
    Powiązania:
    https://bibliotekanauki.pl/articles/779382.pdf
    Data publikacji:
    2011
    Wydawca:
    Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
    Tematy:
    kleje epoksydowe
    utwardzacze
    kompleksy imidazoli
    wytrzymałość na ścinanie
    epoxy adhesives
    latent curing agent
    imidazole complexes
    pot life
    shear strength
    Opis:
    Complexes of 2-methylimidazole with cations from several metal sulfates were prepared and investigated as curing agents for epoxy resins. The reactivity of one-part formulations of these complexes with a bisphenol A type epoxy resin was determined by the differential scanning calorimetry and the pot life observed by viscosity measurements. Tensile lap shear tests at room temperature and at 120°C were used to evaluate the adhesive strength of the formulations directly after preparation as well as after one and three months of storage at room temperature. The DSC measurements showed much lower reactivity (7 - 32%) and higher reaction temperatures of the complex formulations in comparison to the mixtures with pure 2-methylimidazole. The viscosity of most formulations remained almost unchanged over the observed period of three months. The adhesive strength of the freshly prepared complex formulations is comparable to a formulation with pure 2-methylimidazole and decreases over time, depending on the type of metal cation and the cation-to-imidazole molar ratio. The obtained results indicate that complexes of 2-methylimidazole with cations are suitable as latent curing agents for epoxy resins.
    Źródło:
    Polish Journal of Chemical Technology; 2011, 13, 1; 63-66
    1509-8117
    1899-4741
    Pojawia się w:
    Polish Journal of Chemical Technology
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Determination of in vitro metabolism of new non-imidazole histamine H3 receptor antagonist 1-[3-(4-tert-butylphenoxy)propyl]piperidine
    Autorzy:
    Kryczyk-Poprawa, Agata
    Szafarz, Małgorzata
    Palak, Aneta Palak
    Łażewska, Dorota
    Kuś, Kamil
    Opoka, Włodzimierz
    Szymura-Oleksiak, Joanna
    Powiązania:
    https://bibliotekanauki.pl/articles/895240.pdf
    Data publikacji:
    2019-10-30
    Wydawca:
    Polskie Towarzystwo Farmaceutyczne
    Tematy:
    1-[3-(4-tert-butylphenoxy)propyl]piperidin
    well-stirred model
    parallel tube model
    non-imidazole histamine H3 receptor antagonist
    Opis:
    Early understanding of the pharmacokinetics of drug candidates is essential during the evaluation of drug development process. DL76 1-[3-(4-tert-butylphenoxy)propyl]piperidine is a novel promising non-imidazole H3 receptor antagonist. Presented study was undertaken to compare with each other the predicted hepatic clearance values of DL76 calculated, using two most common mathematical models “well-stirred” and “parallel tube”, based on the data obtained in in vitro experiments. The metabolic intrinsic clearance of DL76 equaled to 0.4848 mL/min/mg protein was scaled up and the values of hepatic clearance estimated from "well-stirred" and "parallel tube" models were 55.47 mL/min/kg and 58.80 mL/min/kg, respectively. They were further compared with pharmacokinetic parameters calculated based on the concentration-time profile obtained following intravenous administration of DL76 to rats at the dose of 6 mg/kg. The estimated systemic serum clearance value of 144.5 mL/h/kg and blood clearance value of 81.17 mL/min/kg indicate the potential extrahepatic metabolism of the investigated compound. This study demonstrates the utility of rat liver microsomes for the prediction of DL76 hepatic clearance.
    Źródło:
    Acta Poloniae Pharmaceutica - Drug Research; 2019, 76, 5; 877-884
    0001-6837
    2353-5288
    Pojawia się w:
    Acta Poloniae Pharmaceutica - Drug Research
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Otrzymywanie i badanie właściwości 4,4',5,5'-tetranitro-2,2'-bi-1H-imidazolu (TNBI)
    Synthesis and properties of 4,4',5,5'-tetranitro-2,2'-bi-1H-imidazole
    Autorzy:
    Szala, M.
    Lewczuk, R.
    Powiązania:
    https://bibliotekanauki.pl/articles/210793.pdf
    Data publikacji:
    2013
    Wydawca:
    Wojskowa Akademia Techniczna im. Jarosława Dąbrowskiego
    Tematy:
    tetranitrobiimidazol
    nitrowanie
    małowrażliwe materiały wybuchowe
    4,4',5,5'-tetranitro-2,2'-bi-1H-imidazole
    nitration
    low sensitivity explosives
    Opis:
    Wykonano przegląd metod nitrowania 2,2'-biimidazolu od jego odkrycia do roku 2012. Zaproponowano dwie nowe ścieżki nitrowania 2,2'-biimidazolu do 4,4',5,5'-tetranitro-2,2'-bi-1H-imidazolu (TNBI). Strukturę produktu pośredniego i TNBI określono na podstawie wyników badań spektroskopowych (¹H, ¹³C NMR, IR). Stwierdzono, że TNBI tworzy stabilny hydrat, który ulega odwodnieniu w temperaturze ok. 80°C. Na podstawie wyników badania DTA /TG określono, że TNBI zachowuje stabilność do temperatury 277°C po czym bez topnienia ulega egzotermicznemu rozkładowi. Zmierzona prędkość detonacji TNBI wynosi 7950 m/s przy gęstości 1,72 g/cm³.
    The known synthesis methods of 4,4',5,5'-tetranitro-2,2'-bi-1H-imidazole (TNBI) are reviewed. Two novel nitration methods of 2,2'-biimidazole to TNBI were presented. Solid products of reactions were analyzed using ¹H, ¹³C NMR and IR spectroscopy. Thermal stability has been studied by DTA. Friction sensitivity of main product was examined. Heat of combustion was measured and standard enthalpy of formation was calculated. Detonation velocity of TNBI for the density of 1.72 g/cm³ was measured.
    Źródło:
    Biuletyn Wojskowej Akademii Technicznej; 2013, 62, 1; 34-43
    1234-5865
    Pojawia się w:
    Biuletyn Wojskowej Akademii Technicznej
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Synthesis and characterization of novel pyrimidine derivatives of N-pentyl-2,7-diphenyl-3,8a-dihydroimidazo[1,2-a]pyrimidin-3-amine via 4-phenylpyrimidin-2-amine
    Autorzy:
    Ramade, Kadachha Raju
    Rojivadiya, Atul J.
    Naliapara, Yogesh T.
    Babariya, Jayesh S.
    Powiązania:
    https://bibliotekanauki.pl/articles/1839572.pdf
    Data publikacji:
    2021
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    imidazole
    pyrimidine
    N-pentyl-2.7-diphenyl-3.8a-dihydroimidazo[1.2-a]pyrimidin-3-amine
    4-phenylpyrimidin-2-amine
    triflouro acetic acid
    benzyldehyde
    Opis:
    The target compound N-pentyl-2,7-diphenyl-3,8a-dihydroimidazo[1,2-a]pyrimidin-3-amine have been synthesized by4-phenylpyrimidin-2-amine with Triflouro acetic acid and benzyldehyde. The obtained products were characterized by 1H NMR, Mass and IR Spectra. Purity of all the compounds has been checked on thin layer chromatographic plate and NMR analysis technique.
    Źródło:
    World News of Natural Sciences; 2021, 37; 92-101
    2543-5426
    Pojawia się w:
    World News of Natural Sciences
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Receptor histaminowy H3 – budowa, funkcje, aktywne ligandy
    Histamine H3 receptor – structure, functions, active ligands
    Autorzy:
    Masłowska-Lipowicz, Iwona
    Powiązania:
    https://bibliotekanauki.pl/articles/412777.pdf
    Data publikacji:
    2019
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Skórzanego
    Tematy:
    histamina
    receptor histaminowy H3
    agonista receptora H3
    odwrotny agonista receptora H3
    imidazol
    histamine
    H3 receptor
    agonists histamine H3
    inverse agonists histamine H3 receptor
    imidazole
    Opis:
    Receptor histaminowy H3 został odkryty w 1983 roku przez Schwartza [1]. Od tego czasu w wielu ośrodkach naukowych trwają poszukiwania aktywnych ligandów H3. Literatura opisuje liczne związki, które są aktywne (antagoniści/odwrotni agoniści) wobec H3, jednak w chwili obecnej niewiele leków znajduje się w rutynowej praktyce klinicznej (betahistyna, pitolisant). Antagoniści/odwrotni agoniści H3 stanowią atrakcyjny cel w poszukiwaniu nowych leków. Dane przedkliniczne i kliniczne wskazują na ich potencjalną przydatność w leczeniu różnych chorób ośrodkowego układu nerwowego (OUN) takich, jak: narkolepsja, katalepsja, ADHD, choroba Alzheimera, a ponadto zaburzeń metabolicznych czy alergii.
    The histamine H3 receptor was discovered in 1983 by Schwartz and coauthors [1]. In many scientific centers, the search for active H3ligands is continued to this day. The literature describes a many compounds that are active (antagonists/inverse antagonists) against H3, however at present, only few drugs are found in routine clinical practice (betahistine, pitolisant). H3 antagonists/inverse agonists are an attractive target in the search for new drugs. Preclinical and clinical data indicate their potential usefulness in the treatment of various central nervous system (CNS) diseases, such as narcolepsy, catalepsy, ADHD, Alzheimer’s disease, as well as metabolic disorders or allergies.
    Źródło:
    Technologia i Jakość Wyrobów; 2019, 64; 14-23
    2299-7989
    Pojawia się w:
    Technologia i Jakość Wyrobów
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
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