Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Maria Dobosz"'
Publikováno v:
Journal of cosmetic dermatologyREFERENCES. 21(10)
Motivations for getting aesthetic medicine treatments concern not only the improvement of the physical appearance but also internal aspects such as feeling more confident or happier. Body dysmorphic disorder (BDD) is a disorder that affects from 5 to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6e575d0b854a32fdc858b9508b0b814
https://pubmed.ncbi.nlm.nih.gov/35243745
https://pubmed.ncbi.nlm.nih.gov/35243745
Autor:
Katarzyna Marta Bocian-Ostrzycka, Anna Maria Łasica, Stanisław eDunin-Horkawicz, Magdalena Joanna Grzeszczuk, Karolina eDrabik, Aneta Maria Dobosz, Renata eGodlewska, Elżbieta eNowak, Jean-Francois eCollet, Elżbieta Katarzyna Jagusztyn-Krynicka
Publikováno v:
Frontiers in Microbiology, Vol 6 (2015)
Helicobacter pylori does not encode the classical DsbA/DsbB oxidoreductases that are crucial for oxidative folding of extracytoplasmic proteins. Instead, this microorganism encodes an untypical two proteins playing a role in disulfide bond formation
Externí odkaz:
https://doaj.org/article/0ba850196c5c4b0c9eca812b188a162a
Publikováno v:
Medicinal Chemistry Research
This study presents the synthesis and spectral analysis of new derivatives of 1,2,4-triazole-3-thione and 1,3,4-thiadiazole. New compounds were prepared by cyclization reaction of acyl thiosemicarbazide derivatives in the presence of alkaline and aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73ae0cb430ae893d29490eb6edb9f33c
http://europepmc.org/articles/PMC3661924
http://europepmc.org/articles/PMC3661924
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 187:468-481
1,2,4-triazole and 1,3,4-thiadiazole derivatives are still considered a viable lead structure for the synthesis of more efficient antimicrobial agents having a broad spectrum of activity. This study presents the synthesis and antimicrobial evaluation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27467f72334da9f0e078c3c400b20414
https://doi.org/10.1080/10426507.2011.625511
https://doi.org/10.1080/10426507.2011.625511
Autor:
Liliana Mazur, Ewa Jagiełło-Wójtowicz, Zofia Rzączyńska, Anna Chodkowska, Łukasz Popiołek, Maria Dobosz, Anna Malm, Urszula Kosikowska
Publikováno v:
Journal of Heterocyclic Chemistry. 48:339-346
Reaction of 4-phenyl-4H-1,2,4-triazole-3-thione with ethyl bromoacetate has led to the formation of ethyl [(4-phenyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetate 1, the structure of which was confirmed by X-ray analysis. In the next reaction with 80% hydra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5b86985cad96f2de3c38bb4488b2ac9
https://doi.org/10.1002/jhet.563
https://doi.org/10.1002/jhet.563
Publikováno v:
Acta Chromatographica. 22:37-55
Summary Some new derivatives of thiosemicarbazide and the 1,2,4-triazole of sulphanylacetic acid have been chromatographed on RP-18 HPTLC plates with mobile phases containing water and an organic modifier (methanol, dioxane, acetone, 2-propanol, or t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef3ec697d27594bd8d18482f938862ab
https://doi.org/10.1556/achrom.22.2010.1.3
https://doi.org/10.1556/achrom.22.2010.1.3
Publikováno v:
Heteroatom Chemistry. 21:521-532
On a four series of 1-azolil-4-aryl/alkyl-thiosemicabazides, a study on the influence of azole moiety on the capability for intramolecular cyclization and its direction was carried out. It was found that for 4-aryl/alkyl-thiosemicabazides with triazo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::332bc5dd71c9ebefbfdc2961c43a90b6
https://doi.org/10.1002/hc.20643
https://doi.org/10.1002/hc.20643
Autor:
Maria Dobosz, Piotr Paneth, Agata Siwek, Monika Wujec, Ewa Jagiełło-Wójtowicz, Anna Chodkowska, Agnieszka Kleinrok
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 183:2669-2677
Three 3-(thiophen-2-yl)-4-substituted-Δ 2 -1,2,4-triazoline-5-thiones were synthesized by intramolecular cyclization of 1-(thiophen-2-ylcarbonyl)-4-substituted thiosemicarbazides in alkaline medium. Their effects on the central nervous system (CNS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc086443b46b52d87982bb0cba0cb1bb
https://doi.org/10.1080/10426500801968136
https://doi.org/10.1080/10426500801968136
Autor:
Monika Wujec, Ewa Jagiełło-Wójtowicz, Agnieszka Kleinrok, Maria Dobosz, Agata Siwek, Piotr Paneth, Anna Chodkowska
Publikováno v:
Open Chemistry. 6:47-53
By the reaction of 2-methyl-furan-3-carboxylic acid hydrazide with isothiocyanates, 1-[(2-methyl-furan-3-yl)carbonyl]-4-substituted thiosemicarbazides 1 were obtained. Further cyclization with 2% NaOH led to the formation of 3-(2-methyl-furan-3-yl)-4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79cf9c0d7f928d3e34681b9f39351450
https://doi.org/10.2478/s11532-007-0058-0
https://doi.org/10.2478/s11532-007-0058-0
Publikováno v:
Heteroatom Chemistry. 19:337-344
The synthesis of 4-[3-(2-methyl-furan-3-yl)-5-thioxo-1,2,4-triazolin-4-yl]acetic acid, its structural study in the solid state, and the thiol–thione tautomeric recognition on the basis of spectroscopic data and theoretical calculations are presente
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::359fc0eb9b4447cd3d18f16ef17abf53
https://doi.org/10.1002/hc.20433
https://doi.org/10.1002/hc.20433