Zobrazeno 1 - 10 of 47 pro vyhledávání: '"Farid S. G. Soliman"'
2
An Overview and Update of COVID-19: Can SARS-Coronavirus-2 Infect Farm Animals?
Autor: Karim El-Sabrout, Noha Mitwally, Sarah Aggag, Farid S. G. Soliman
Publikováno v: Journal of Animal Health and Production. 8
Coronaviruses have been recognized as causing pathological conditions to humans and animals since the 1960s and 1970s Coronaviruses discovered from avian species are classified to the Genera Gamma-and Delta Coronaviruses which include the highly cont
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d67b28b426dc84a1298f593db8852a75
https://doi.org/10.17582/journal.jahp/2020/8.3.89.92
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3
Association of single-nucleotide polymorphism of melanocortin gene with feed intake in rabbit (Oryctolagus cuniculus)
Autor: Karim El-Sabrout, Farid S. G. Soliman
Publikováno v: Journal of animal physiology and animal nutrition. 102(2)
The aim of the study was to investigate the association of two parts of melanocortin gene (MC4R-1, MC4R-2) and feed intake for V-line rabbits. V-line rabbits were grouped into high and low daily feed intake during the period from 30 to 63 days of age
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::402c759d4deab34f38f8edcc27b54ba4
https://pubmed.ncbi.nlm.nih.gov/28990229
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4
Synthesis of some substituted furan-2(5H)-ones and derived quinoxalinones as potential anti-microbial and anti-cancer agents
Autor: Yasser S. Abdel-Ghany, Alaa A. El-Tombary, Farid S. G. Soliman, S. A. Shams El-Dine, Ahmad S. F. Belal
Publikováno v: Medicinal Chemistry Research. 20:865-876
In search for novel anti-cancer and anti-microbial agents with promising pharmacotoxicological profile, the synthesis of some substituted 4-halofuran-2(5H)-ones (8a–l, 9, 11) and derived halogenated quinoxalin-2(1H)-ones (12a–d) is described. Som
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8502e68e6845476148c7b7bc58a06dff
https://doi.org/10.1007/s00044-010-9394-2
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5
Synthesis of new series of pyrazolo[4,3-d]pyrimidin-7-ones and pyrido[2,3-d]pyrimidin-4-ones for their bacterial and cyclin-dependent kinases (CDKs) inhibitory activities
Autor: Doaa A. E. Issa, Raafat Soliman, Detlef Geffken, Farid S. G. Soliman, Magdi M. Abdel-Khalek
Publikováno v: Medicinal Chemistry Research. 20:408-420
Two series of pyrazolo[4,3-d]pyrimidin-7-ones and pyrido[2,3-d]pyrimidin-4-ones were designed, synthesised, and evaluated for their antibacterial activities and CDKs inhibitory activities. The pyridazine derivative: 6-phenyl-5-phenylhydrazono-2,3,4,5
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c5cd4e1a86ebfa337b502b706a0a5261
https://doi.org/10.1007/s00044-010-9328-z
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6
Novel potential nonsedating H1 antagonists related to the gauche rotamer of PROS-NH-histamine
Autor: Rasha Y. Elbayaa, R. M. Shafik, Mona M. El-Semary, Manal N. S. Saudi, Farid S. G. Soliman
Publikováno v: Medicinal Chemistry Research. 18:187-205
On the basis of the most stable stereorotameric (R) forms of πNH-histamine (2), the trans (1-TR) and gauche (1-GR) forms have both been reported to be involved in potentiation of H1-receptors. Apart from the known classic models of H1-antagonists th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2cd57ab0a72fcaeb20d6e29bdf551bb6
https://doi.org/10.1007/s00044-008-9119-y
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7
Synthesis and 5-HT2A Antagonist Activity of Derivatives of the Novel Heterocycles Indolo[3,2-d]pyrrolo[3,2-g]azecine and Benzo[d]pyrrolo[3,2-g]azecine compared to the Benz[d]indolo[2,3-g]azecine Derivative LE 300
Autor: Sigurd Elz, Sherif A. F. Rostom, Farid S. G. Soliman, Jochen Lehmann, Mona M. El-Semary, Ahmed M. Farghaly
Publikováno v: Archiv der Pharmazie. 334:241-247
An indolo[3,2-d]pyrrolo[3,2-g]azecine and a benzo[d]pyrrolo[3,2-g]azecine analogue of the potent dopamine receptor antagonist LE 300 (7-methyl-6,7,8,9,14,15-hexahydro-5H-benz[d]indolo[2,3-g]azecine) have been prepared in multi-step reactions via C-N
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ca14df9fc1834f6c02e579e7223cb09f
https://doi.org/10.1002/1521-4184(200107)334:7<241::aid-ardp241>3.0.co
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10
ChemInform Abstract: Synthesis and 5-HT2A Antagonist Activity of Derivatives of the Novel Heterocycles Indolo[3,2-d]pyrrolo[3,2-g]azecine and Benzo[d]pyrrolo[3,2-g]azecine Compared to the Benz[d]indolo[2,3-g]azecine Derivative LE 300
Autor: Ahmed M. Farghaly, Mona M. El-Semary, Sigurd Elz, Sherif A. F. Rostom, Jochen Lehmann, Farid S. G. Soliman
Publikováno v: ChemInform. 32
An indolo[3,2-d]pyrrolo[3,2-g]azecine and a benzo[d]pyrrolo[3,2-g]azecine analogue of the potent dopamine receptor antagonist LE 300 (7-methyl-6,7,8,9,14,15-hexahydro-5H-benz[d]indolo[2,3-g]azecine) have been prepared in multi-step reactions via C-N
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1d97ea7047ae3f6796b328027d4a85d9
https://doi.org/10.1002/chin.200144167
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