Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Marek L. Główka"'
Publikováno v:
Acta Crystallographica Section E, Vol 70, Iss 10, Pp o1081-o1082 (2014)
The characteristic feature of the title molecule, C16H23NO4, is the syn configuration of the partially double amide C—N bond [C—N—C—O torsion angle = −14.8 (2)°]. The crystal packing is determined by intermolecular O—H...O and N—H...O
Externí odkaz:
https://doaj.org/article/807dcafee1c841198352b6474132f957
Autor:
Ida Mazerant-Politowicz, Andrzej Olczak, Marek L. Główka, Henryk Foks, Katarzyna Gobis, Dagmara Ziembicka, Izabela Korona-Glowniak, Małgorzata Szczesio
Publikováno v:
Acta Crystallographica Section C Structural Chemistry. 76:673-680
Four new picolinohydrazonamide derivatives, namely, 6-methyl-N′-(morpholine-4-carbonothioyl)picolinohydrazonamide, C12H17N5OS, 6-chloro-N′-(morpholine-4-carbonothioyl)picolinohydrazonamide methanol monosolvate, C11H14ClN5OS·CH3OH, 6-chloro-N′-
Autor:
Katarzyna Gobis, Małgorzata Szczesio, Andrzej Olczak, Izabela Korona-Głowniak, Ewa Augustynowicz-Kopeć, Ida Mazernt-Politowicz, Dagmara Ziembicka, Marek L. Główka
Publikováno v:
Materials; Volume 15; Issue 9; Pages: 3085
Four novel methyl 4-phenylpicolinoimidate derivatives of hydrazone have been synthesized and evaluated for their antimicrobial activity, including tuberculostatic activity. The compounds obtained are condensates of hydrazonamide or hydrazide with 5-n
Autor:
Katarzyna Gobis, Małgorzata Szczesio, Andrzej Olczak, Tomasz Pawlak, Ewa Augustynowicz-Kopeć, Malwina Krause, Marek L. Główka
Publikováno v:
Materials
Materials, Vol 15, Iss 349, p 349 (2022)
Materials; Volume 15; Issue 1; Pages: 349
Materials, Vol 15, Iss 349, p 349 (2022)
Materials; Volume 15; Issue 1; Pages: 349
Tuberculosis remains one of the most common diseases affecting developing countries due to difficult living conditions, the rapidly increasing resistance of M. tuberculosis strains and the small number of effective anti-tuberculosis drugs. This study
Publikováno v:
Acta Crystallographica Section C Structural Chemistry. 73:797-802
The search for new tuberculostatics is important considering the occurrence of drug-resistant strains of Mycobacterium tuberculosis. Three polymorphs of N′-(1,3-dithiolan-2-ylidene)-4-nitrobenzohydrazide (a potentially tuberculostatic agent), C10H9
Autor:
Karol Jędrzejczak, Janusz Zabrocki, Beata Kolesinska, Iwona Kochanowska, Michał Zimecki, Małgorzata Szczesio, Krzysztof Huben, Marek L. Główka, Paweł Hrynczyszyn, Jolanta Artym, Maja Kocięba, Stefan Jankowski, Tomasz Jastrząbek
Publikováno v:
Bioorganic & Medicinal Chemistry. 25:4265-4276
Cyclolinopeptide A (CLA), an immunosuppressive nonapeptide derived from linen seeds, was modified with S or R-γ4-bis(homo-phenylalanine) in positions 3 or 4, or both 3 and 4. These modifications changed the flexibility of new analogues and distribut
Autor:
Małgorzata Szczesio, Katarzyna Gobis, Ida Mazerant, Andrzej Olczak, Marek L. Główka, Henryk Foks
Publikováno v:
Acta Crystallographica Section C Structural Chemistry. 73:84-90
Searches for new tuberculostatic agents are important considering the occurrence of drug-resistant strains ofMycobacterium tuberculosis. The structures of three new potentially tuberculostatic compounds, namely isopropyl methyl (2-hydroxybenzoyl)carb
Autor:
Marek L. Główka, Henryk Foks, Katarzyna Gobis, Andrzej Olczak, Malwina Krause, Sylwia Kałużyńska, Małgorzata Szczesio
Publikováno v:
Acta crystallographica. Section C, Structural chemistry. 74(Pt 12)
Tuberculosis still remains a very important problem, especially its multidrug resistant varieties (MDR-TB). Among the potential tuberculostatics, there are two benzimidazole derivatives, namely 5,6-dimethyl-2-phenylethylbenzo[d]imidazole (1) and (E)-
Autor:
Marek L. Główka
Publikováno v:
Acta Crystallographica Section A Foundations and Advances. 75:e292-e292
Autor:
Marek L. Główka, Ewa Kwapisz, Andrzej Olczak, Katarzyna Gobis, Agnieszka Bogdanowicz, Anna Kędzia, Henryk Foks
Publikováno v:
Journal of Heterocyclic Chemistry. 50:544-550
2-Bromo-4-(pyrrolidin-1-yl)pyridine-3-carbonitrile obtained from 2-(1,3-bis(pyrrolidin-1-yl)allylidene)malononitrile has been used as a substrate for the synthesis of new cyanopyridine derivatives: 2-methoxy, 2-phenoxy, 2-aminoethylthio, and 2-thioxo