-
1دورية أكاديمية
المساهمون: McKenna, Robert [Univ. of Florida, Gainesville, FL (United States)]
المصدر: Biochemistry; 54; 43
وصف الملف: Medium: ED; Size: 6631-6638
-
2دورية أكاديمية
المؤلفون: Linda J. Urbanski, Daniela Vullo, Seppo Parkkila, Claudiu T. Supuran
المصدر: Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 1088-1092 (2021)
مصطلحات موضوعية: β-carbonic anhydrase, staphylococcus aureus, kinetics, inhibition, anions, Therapeutics. Pharmacology, RM1-950
وصف الملف: electronic resource
-
3دورية أكاديمية
المؤلفون: Ashok Aspatwar, Milka Hammaren, Mataleena Parikka, Seppo Parkkila, Fabrizio Carta, Murat Bozdag, Daniela Vullo, Claudiu T. Supuran
المصدر: Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 35, Iss 1, Pp 65-71 (2020)
مصطلحات موضوعية: β-carbonic anhydrase, monothiocarbamates (mtcs), dithiocarbamate (dtcs), in vitro inhibition, zebrafish larvae, Therapeutics. Pharmacology, RM1-950
وصف الملف: electronic resource
-
4دورية أكاديمية
المؤلفون: Linda J. Urbanski, Silvia Bua, Andrea Angeli, Marianne Kuuslahti, Vesa. P. Hytönen, Claudiu T. Supuran, Seppo Parkkila
المصدر: Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 35, Iss 1, Pp 1834-1839 (2020)
مصطلحات موضوعية: β-carbonic anhydrase, staphylococcus aureus, kinetics, inhibition, sulphonamides, Therapeutics. Pharmacology, RM1-950
وصف الملف: electronic resource
-
5دورية أكاديمية
المؤلفون: Andrea Angeli, Marta Ferraroni, Mariana Pinteala, Stelian S. Maier, Bogdan C. Simionescu, Fabrizio Carta, Sonia Del Prete, Clemente Capasso, Claudiu T. Supuran
المصدر: Molecules; Volume 25; Issue 10; Pages: 2269
مصطلحات موضوعية: β-Carbonic Anhydrase, Burkholderia pseudomallei, crystal structure, type II CA
جغرافية الموضوع: agris
وصف الملف: application/pdf
العلاقة: Bioorganic Chemistry; https://dx.doi.org/10.3390/molecules25102269Test
-
6دورية أكاديمية
المؤلفون: Verônica da Silva Cardoso, Alane Beatriz Vermelho, Eduardo Ricci Junior, Igor Almeida Rodrigues, Ana Maria Mazotto, Claudiu T. Supuran
المصدر: Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 33, Iss 1, Pp 850-857 (2018)
مصطلحات موضوعية: Sulphonamide, Leishmania, nanoemulsions, β-carbonic anhydrase, Therapeutics. Pharmacology, RM1-950
وصف الملف: electronic resource
-
7دورية أكاديمية
المؤلفون: Ashok Aspatwar, Milka Hammarén, Sanni Koskinen, Bruno Luukinen, Harlan Barker, Fabrizio Carta, Claudiu T. Supuran, Mataleena Parikka, Seppo Parkkila
المصدر: Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 832-840 (2017)
مصطلحات موضوعية: Dithiocarbamates, Mycobacterium marinum, β-carbonic anhydrase, in vivo inhibition, zebrafish embryos, Therapeutics. Pharmacology, RM1-950
وصف الملف: electronic resource
-
8دورية أكاديمية
المؤلفون: Hiromi Kato, Makoto Yoshida, Ryuka Iizuka, Takahiro Ogawa, Yasuhiko Matsushita, Yoko Katayama, Yoshihito Masaki, Yuka Kojima
المصدر: Microbes and Environments. 2021, 36(2):20058
-
9دورية أكاديمية
المؤلفون: Akdemir, ATİLLA, ANGELI, A, GÖKTAŞ, F, Eraslan, Elma, KARALı, N, SUPURAN, CT
المساهمون: Inhibition of the b-carbonic anhydrase (CA, EC 4.2.1.1) from pathogenic Candida glabrata (CgNce103) by 1H-indole-2,3-dione 3- N-(4-sulfamoylphenyl)thiosemicarbazones 4a–m was investigated. All the compounds were found to be potent inhibitors of CgNce103, with inhibition constants in the range of 6.4- 63.9 nM. The 5,7-dichloro substituted derivative 4l showed the most effective inhibition (KI of 6.4 nM) as well as the highest selectivity for inhibiting CgNce103 over the cytosolic human (h) isoforms hCA I and II. A possible binding interaction of compound 4l within the active site of CgNce103 has been proposed based on docking studies., AKDEMİR, ATİLLA
مصطلحات موضوعية: Akdemir A., ANGELI A., GÖKTAŞ F., Eraslan E., KARALı N., SUPURAN C., Novel 2-indolinones containing a sulfonamide moiety as selective inhibitors of candida β-carbonic anhydrase enzyme.-, Journal of enzyme inhibition and medicinal chemistry, cilt.34, ss.528-531
الوقت: 2019
وصف الملف: application/pdf
العلاقة: https://hdl.handle.net/20.500.12645/3777Test; WOS:000457960800001; 85061106138
الإتاحة: https://doi.org/20.500.12645/3777Test
https://doi.org/10.3233/dma-2011-0800Test
https://doi.org/10.1080/14756366.2018.1564045Test
https://hdl.handle.net/20.500.12645/3777Test -
10
المؤلفون: Claudiu T. Supuran, Mataleena Parikka, Milka Hammaren, Seppo Parkkila, Daniela Vullo, Murat Bozdag, Ashok Aspatwar, Fabrizio Carta
المساهمون: Lääketieteen ja terveysteknologian tiedekunta - Faculty of Medicine and Health Technology, Tampere University
المصدر: Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 35, Iss 1, Pp 65-71 (2020)مصطلحات موضوعية: in vitro inhibition, Biolääketieteet - Biomedicine, RM1-950, 01 natural sciences, dithiocarbamate (DTCs), Mycobacterium tuberculosis, monothiocarbamates (MTCs), Drug Discovery, Zebrafish larvae, Dithiocarbamate, Zebrafish, Pharmacology, chemistry.chemical_classification, β-carbonic anhydrase, biology, 010405 organic chemistry, Chemistry, Embryo, General Medicine, biology.organism_classification, In vitro, 0104 chemical sciences, 010404 medicinal & biomolecular chemistry, Biochemistry, Toxicity, zebrafish larvae, Therapeutics. Pharmacology, Carbonic anhydrase 3, Research Paper
وصف الملف: fulltext
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8cd186d0288cd0369a33e73a2d55d01Test
http://europepmc.org/articles/PMC6830242Test