Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Almeqdad Y. Habashneh"'
Autor:
Ahmad H. Abdullah, Ahmad K. Alarareh, Mahmoud A. Al-Sha’er, Almeqdad Y. Habashneh, Firas F. Awwadi, Sanaa K. Bardaweel
Publikováno v:
Pharmacia, Vol 71, Iss , Pp 1-12 (2024)
A group of new amidrazone compounds that include a quinoline component was produced through the reaction of hydrazonyl chloride, derived from 6-aminoquinoline, with appropriate secondary cyclic amines. The new compounds were confirmed through 1H-NMR,
Externí odkaz:
https://doaj.org/article/536af494252e4cfebd21f6ae78808ab0
Autor:
Tayel A. Al Hujran, Mousa K. Magharbeh, Almeqdad Y. Habashneh, Rasha S. Al-Dmour, Ashraf Aboelela, Hesham M. Tawfeek
Publikováno v:
Molecules, Vol 27, Iss 14, p 4425 (2022)
The study aims to assess the interaction between fluconazole and sulfonatocalix[4]naphthalene towards enhancing its dissolution performance and antimycotic activity. A solubility study was carried out at different pH conditions, and the results revea
Externí odkaz:
https://doaj.org/article/f0f8f462e01b46efab7e685cf3994929
Publikováno v:
Medicinal Chemistry Research. 32:271-287
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42fe38086b5219f0e43278e5f88efa9c
https://doi.org/10.1007/s00044-022-03001-x
https://doi.org/10.1007/s00044-022-03001-x
Publikováno v:
Medicinal Chemistry. 14:468-477
BACKGROUND Amidrazones have been reported to have significant anti-tumor properties against several cancer cell lines. OBJECTIVES The current project aims to profile the structure-anticancer activity relationship of phenyl-amidrazons. METHODS Fifteen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aed12c0e6af73fd39ff285c884d2b4b2
https://doi.org/10.2174/1573406414666171204143157
https://doi.org/10.2174/1573406414666171204143157
Autor:
Deeb Taher, Marcus Korb, Heinrich Lang, J. Matthäus Speck, Firas F. Awwadi, Sultan T. Abu-Orabi, Mousa Al-Noaimi, Emad M. Hamed, Kurt Merzweiler, Mohammad El-khateeb, Almeqdad Y. Habashneh, Christoph Wagner
Publikováno v:
Journal of Organometallic Chemistry. 847:59-67
The synthesis and characterization of four ferrocenyl thiocarboxylate complexes are reported. Thus, treatment of [Fe(η5-C5H5)(η5-C5H4S−)] (1) with one equivalent of the acid chlorides 2-ClC(O)-cC4H3X(2a, X = O; 2b, X = NMe) gave [Fe(η5-C5H5)(η5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b8e9d0197304eadc57543f7199d0ba0
https://doi.org/10.1016/j.jorganchem.2017.03.053
https://doi.org/10.1016/j.jorganchem.2017.03.053
Autor:
Deeb Taher, Marcus Korb, Dieter Schaarschmidt, Almeqdad Y. Habashneh, Heinrich Lang, Sultan T. Abu-Orabi, Firas F. Awwadi, Mousa Al-Noaimi, Saddam Weheabby, J. Matthäus Speck, Mohammad El-khateeb
Publikováno v:
Journal of Organometallic Chemistry. 845:55-62
Treatment of two equiv. of [Fe(η5-C5H5)(η5-C5H4SeSiMe3)] (1) with one equiv. of 2,5-(ClC(O))2-cC4H2X (2) produced the corresponding ferrocenyl carboselenolates 2,5-[(FcSeC(O))2-cC4H2X] (3) ([Fc = Fe(η5-C5H5)(η5-C5H4)]; a, X = O; b, X = NMe; c, X
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d170d848c9d8b711fbdda827a73a2d8f
https://doi.org/10.1016/j.jorganchem.2017.02.024
https://doi.org/10.1016/j.jorganchem.2017.02.024
Publikováno v:
Archiv der Pharmazie. 347:415-422
A new series of N1-(flavon-6-yl)amidrazones were synthesized by reacting the hydrazonoyl chloride derived from 6-aminoflavone with the appropriate sec-cyclic amines. The antitumor activities of these compounds were evaluated on breast cancer (MCF-7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::955681a28ef2bf4e936d93a85a4b038e
https://doi.org/10.1002/ardp.201300326
https://doi.org/10.1002/ardp.201300326
Publikováno v:
Zeitschrift für Naturforschung B. 68:1049-1055
A model N-ethyl-1,10-dioxo-3-phenylpyrano[3,2- f ]quinoline-9-carboxylic acid (8) and the isomeric (2-substituted) pyrano[2,3- f ]quinoline-9-carboxylic acids (6 and 7) were prepared from the corresponding 6/7-aminochromen-4-ones via the Gould-Jacobs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f61c3838d1558890b5df87e91ef4a3a0
https://doi.org/10.5560/znb.2013-3122
https://doi.org/10.5560/znb.2013-3122
Publikováno v:
Zeitschrift für Naturforschung B. 67:725-730
A synthesis of 4-methylpyrano[2,3-e]indole-2,8,9-trione (5) is achieved from 7-amino-4- methylcoumarin by adopting the classical Sandmeyer methodology. The cyclocondensation reaction of pyrano-isatin 5 with the appropriately substituted o-phenylenedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47f32c354a387896ff9803cfc122e831
https://doi.org/10.5560/znb.2012-0131
https://doi.org/10.5560/znb.2012-0131
Publikováno v:
Synthetic Communications. 39:4221-4229
Suzuki–Miyaura double cross-coupling to form teraryls of interest as Schiff-base precursors can be achieved efficiently in near-quantitative yields using a low mol% amount of Pd(PPh3)4 and easily accessible dibromoaryls.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90c2d086f1fe5c3843c56c44fd9eb06b
https://doi.org/10.1080/00397910902898577
https://doi.org/10.1080/00397910902898577