Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Huba Kalasz"'
Autor:
Tiyyaba Furqan, Sidra Batool, Rabia Habib, Mamoona Shah, Huba Kalasz, Ferenc Darvas, Kamil Kuca, Eugenie Nepovimova, Sajida Batool, Syed M Nurulain
Publikováno v:
Biomolecules, Vol 10, Iss 5, p 758 (2020)
The study documented here was aimed to find the molecular interactions of some of the cannabinoid constituents of cannabis with acetylcholinesterase (AChE). Molecular docking and LogP determination were performed to predict the AChE inhibitory effect
Externí odkaz:
https://doaj.org/article/5803cafa02a24cb89d312111a6821fcf
Publikováno v:
Molecular and cellular biochemistry. 476(12)
Allium species, belonging to Alliaceae family, are among the oldest cultivated vegetables used as food. Garlic, onions, leeks and chives, which belong to this family, have been reported to have medicinal properties. The Allium species constituents ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b88cc82774c8e58b021e549872b15acd
https://pubmed.ncbi.nlm.nih.gov/34420186
https://pubmed.ncbi.nlm.nih.gov/34420186
Autor:
Miklos, Krepuska, Marta, Hubay, Endre, Zima, Aniko, Kovacs, Violetta, Kekesi, Huba, Kalasz, Brigitta, Szilagyi, Bela, Merkely, Peter, Sotonyi
Publikováno v:
The Open Medicinal Chemistry Journal
Introduction: Tinuvin 770 [bis(2,2,6,6-tetramethyl-4-piperidinyl) sebacate, Ciba-Geigy, Basel, Switzerland] is a UV light stabilizer that is a component of many plastic materials used world-wide in the medical and food industries. We report on the ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ff7c39e3a5f41bc9324b0f40c841d7a
https://pubmed.ncbi.nlm.nih.gov/30288180
https://pubmed.ncbi.nlm.nih.gov/30288180
Publikováno v:
Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology. 13(2)
Clinical effect of drugs is influenced by the composition of the pharmaceutical preparation but substantially by the fate of the drug in the body. Metabolism of the xenobiotic drug compounds may result in pharmacologically inactive metabolites, howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c36aecdacec0469e3864948d138be9a0
https://pubmed.ncbi.nlm.nih.gov/21677324
https://pubmed.ncbi.nlm.nih.gov/21677324
Autor:
Hitoshi Nakayama, Arnold Schwartz, Toshiro Watanabe, Kazuaki Naito, Huba Kalasz, Pal L. Vaghy, Kiyoshi Itagaki, Hideo Yabana
Publikováno v:
FEBS letters. 331(1-2)
Calcium channel blockers are drugs that bind to the alpha 1 subunit of L-type calcium channels and selectively inhibit ion movements through these channels. Determination of the mechanism of channel blockade requires localization of drug-binding site
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d9092ec910704bba222dd96d8765ef6
https://pubmed.ncbi.nlm.nih.gov/8405401
https://pubmed.ncbi.nlm.nih.gov/8405401
Autor:
Ernest Adeghate, Crystal M. D’Souza, Zulqarnain Saeed, Saeeda Al Jaberi, Saeed Tariq, Huba Kalász, Kornélia Tekes, Ernest A. Adeghate
Publikováno v:
Biology, Vol 10, Iss 7, p 621 (2021)
Nociceptin (NC) consists of 17 amino acids (aa) and takes part in the processing of learning and memory. The role of NC in the induction of endogenous antioxidants in still unclear. We examined the effect of NC on the expression of endogenous antioxi
Externí odkaz:
https://doaj.org/article/28aa97d2335544c189a8f9a062cf04fb
Publikováno v:
Molecules, Vol 25, Iss 5, p 1250 (2020)
Our aim was to find chlorine-substituted antidotes against organophosphate poisoning and compare their pharmacokinetics to their parent compound, K-203. White male Wistar rats were intramuscularly injected with K-203, K-867 or K-870. Serum, brain, ki
Externí odkaz:
https://doaj.org/article/c21957877b1f487383940831ab53e8d6
Autor:
John L. Mershon, Akihiko Kuniyasu, Toshiro Watanabe, Huba Kalasz, Arnold Schwartz, Hitoshi Nakayama, Kiyoshi Itagaki, Kazuaki Naito, Pal L. Vaghy, Hideo Yabana
Publikováno v:
FEBS Letters. (3):261-264
[3H]Azidobutyryl clentiazem, a new photoactivable diltiazem derivative, has a higher binding affinity than azidobutyryl diltiazem. It can be covalently incorporated into the alpha 1 subunit of the skeletal muscle calcium channel by UV irradiation, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af7be90cf2d33ab2ed3f93fce7a7e587
Periodical
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