Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Eman R. El-Bendary"'
Publikováno v:
Molecules, Vol 19, Iss 3, Pp 3417-3435 (2014)
A new series of oxime ethers 4a–z was designed and synthesized to test the blocking activity against β1 and β2-adrenergic receptors. Docking of these ether derivatives into the active site of the identified 3D structures of β1 and β2-adrenergic
Externí odkaz:
https://doaj.org/article/6076fafffcec432d95b0200da905bfa1
Autor:
Nadia S. El-Gohary, Eman R. El-Bendary, Said M. Bayomi, Alaa A. Abd Elhameed, Mona I. Shaaban
Publikováno v:
Bioorganic Chemistry. 81:299-310
New thiazolopyrimidine and dithiazolopyrimidinone derivatives 2-11 were synthesized and estimated for antimicrobial activity against S. aureus, B. cereus, E. coli, C. albicans, A. fumigatus and A. terreus. The attained results proved that 4, 8a and 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7348157db4591abf75f119b4305a5b7a
https://doi.org/10.1016/j.bioorg.2018.08.013
https://doi.org/10.1016/j.bioorg.2018.08.013
Autor:
Saadia M. El-Ashry, Eman R. El-Bendary, Nadia S. El-Gohary, Mona I. Shaaban, Somaya A. Abdel-Rahman
Publikováno v:
European Journal of Medicinal Chemistry. 140:200-211
New series of cyclopenta(hepta)[b]thiophene and fused cyclohepta[b]thiophene analogs were synthesized. The new analogs were assessed for antibacterial efficacy toward Escherichia coli ATCC 12435, Bacillus cereus UW 85 and Staphylococcus aureus. Compo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e4396d97fd89bc870bc7d354700f528
https://doi.org/10.1016/j.ejmech.2017.08.066
https://doi.org/10.1016/j.ejmech.2017.08.066
Publikováno v:
Chinese Chemical Letters. 27:380-386
A new series of benzothiazole Schiff bases 3–29 was synthesized and screened for antitumor activity against cervical cancer (Hela) and kidney fibroblast cancer (COS-7) cell lines. Results indicated that compounds 3, 14, 19, 27 and 28 have promising
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3420d18e05e1d7bd1e99fcc0fb1a883b
https://doi.org/10.1016/j.cclet.2015.12.033
https://doi.org/10.1016/j.cclet.2015.12.033
Autor:
Ghada M. Suddek, Ihsan A. Shehata, Mohamed M. El-Kerdawy, Mahasen M. Fouad, Eman R. El-Bendary
Publikováno v:
Bioorganic chemistry. 81
New thiophene ( 2 – 13 ) and thienopyrimidine ( 15 – 27 ) derivatives have been synthesized. Twenty three compounds were screened against five cell lines namely; hepatocellular carcinoma (liver) HepG-2, epidermoid carcinoma (larynx) Hep-2, mammar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::043e53319dbe6ec8c35b01b5e6eb6e72
https://pubmed.ncbi.nlm.nih.gov/30248510
https://pubmed.ncbi.nlm.nih.gov/30248510
Autor:
Nanting Ni, Nadia S. El-Gohary, Moustafa T. Gabr, Eman R. El-Bendary, Mona I. Shaaban, Mohammed M. El-Kerdawy
New isatin-β-thiocarbohydrazone hybrids 4-17 were designed relied on isatin scaffold to generate various analogs with expected antimicrobial activity. The new hybrids were estimated for antibacterial effectiveness over S. aureus, B. cereus and E. co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b6ebcbfb196b84b378e31212b12886e
Autor:
Eman R. El-Bendary, Nadia S. El-Gohary, Mona I. Shaaban, Nanting Ni, Moustafa T. Gabr, Mohamed M. El-Kerdawy
Publikováno v:
Chinese Chemical Letters. 26:1522-1528
New series of benzothiazole derivatives were designed and synthesized. The newly synthesized compounds were screened for their antibacterial activity against Escherichia coli, Staphylococcus aureus and Bacillus cereus. Compounds 6j and 6o showed the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be68f1d5fc79db0ee9666802bfc27572
https://doi.org/10.1016/j.cclet.2015.09.004
https://doi.org/10.1016/j.cclet.2015.09.004
Publikováno v:
European Journal of Medicinal Chemistry. 85:576-592
New series of benzothiazole and pyrimido[2,1- b ]benzothiazole derivatives were synthesized and characterized by analytical and spectrometrical methods (IR, HRMS, 1 H and 13 C NMR). Nineteen of the synthesized compounds were selected by the National
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cb94b5825df732ce02609375a742be3
https://doi.org/10.1016/j.ejmech.2014.07.097
https://doi.org/10.1016/j.ejmech.2014.07.097
Publikováno v:
Medicinal Chemistry Research. 24:860-878
New series of benzothiazole and pyrimido[2,1-b]benzothiazole derivatives were synthesized and characterized by analytical and spectrometrical methods (IR, HRMS, 1H, and 13C NMR). Eleven of the synthesized compounds were selected by the National Cance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2581bd65359d82b0d5a65722a6878dd
https://doi.org/10.1007/s00044-014-1114-x
https://doi.org/10.1007/s00044-014-1114-x
Publikováno v:
Molecules, Vol 19, Iss 3, Pp 3417-3435 (2014)
Molecules; Volume 19; Issue 3; Pages: 3417-3435
Molecules
Molecules; Volume 19; Issue 3; Pages: 3417-3435
Molecules
A new series of oxime ethers 4a – z was designed and synthesized to test the blocking activity against β 1 and β 2 -adrenergic receptors. Docking of these ether derivatives into the active site of the identified 3D structures of β 1 and β 2 -ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe4b0ffaba9c3273d62501d583b2b970
http://www.mdpi.com/1420-3049/19/3/3417
http://www.mdpi.com/1420-3049/19/3/3417