Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Bahjat A. Saeed"'
Publikováno v:
Molecules, Vol 15, Iss 11, Pp 8425-8430 (2010)
Novel 2,3-dihydro-4-pyridinones were synthesized via the reaction of curcumin and primary amines or amine acetates under microwave irradiation. Montmorillonite K-10 was used as a catalyst. Reaction times did not exceed 120 s. The structures of the co
Externí odkaz:
https://doaj.org/article/f1143f6b457741eb99b6b4262082e7d8
Autor:
Ibrahim A. Musad, Bahjat A. Saeed
Publikováno v:
Molecules, Vol 14, Iss 6, Pp 2278-2285 (2009)
Symmetrical and non-symmetrical diimines derived from dimedone were synthesized by the reaction of their corresponding enaminothiones with primary amines. The synthesized compounds were characterized using micro analytical data and NMR spectroscopy.
Externí odkaz:
https://doaj.org/article/c73152e970d54985a4481ca214a99ddf
Autor:
Alaa M. Al-Roumy, F. A. Al-Saymari, H. A. Sultan, Qusay M.A. Hassan, Rita S. Elias, Tahseen A. Alsalim, Bahjat A. Saeed, C. A. Emshary, M. A. Mahdi
Publikováno v:
Journal of Fluorescence.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a12d61b78b9ee2ac04dca120511a3263
https://doi.org/10.1007/s10895-023-03257-5
https://doi.org/10.1007/s10895-023-03257-5
Autor:
Raad S. Jihad, Nabeel A. Abdul-Rida, Amer M. J. Al-Shamari, Najim A. Al-Masoudi, Bahjat A. Saeed
Publikováno v:
Zeitschrift für Naturforschung B.
A new series of derivatives (compounds 8–20) of the breast antihormonal drug letrozole tagged with additional aryl groups were synthesized starting from the letrozole analog 7 via Suzuki cross-coupling reaction. Treatment of the ketone 9 with vario
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8083b2eeebb21e381e96176a085dc8f
https://doi.org/10.1515/znb-2022-0151
https://doi.org/10.1515/znb-2022-0151
Publikováno v:
World Journal of Biological and Pharmaceutical Research. 1:001-016
The possible effect of curcumin as a potential natural cancer treatment drug has been intensively discussed. In the present study the probabilities of a series of curcumin analogues to possess potential as antineoplastic, prostate cancer treatment an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a55726e54721938aef4b2df60ad7eaf
https://doi.org/10.53346/wjbpr.2021.1.2.0126
https://doi.org/10.53346/wjbpr.2021.1.2.0126
Publikováno v:
Anti-Cancer Agents in Medicinal Chemistry. 21:1671-1679
Background: Aromatase, a cytochrome P450 hemoprotein that is responsible for estrogen biosynthesis by conversion of androgens into estrogens, has been an attractive target in the treatment of hormonedependent breast cancer. Design of new steroidal ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76d60d9cab1f37e5e19d23c36c81d68e
https://doi.org/10.2174/1871520620999201124213655
https://doi.org/10.2174/1871520620999201124213655
Autor:
Yaseen A. Al-Soud, Ala’a H. Al-Ahmad, Raed A. Al-Qawasmeh, Hossam H. Al-Suod, Najim A. Al-Masoudi, Luay Abu-Qatouseh, Bahjat A. Saeed, Kafa’ A. S. Alhelal
Publikováno v:
Arkivoc. 2021:296-309
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fce45605d9af87524e2890aa7e7a7f3
https://doi.org/10.24820/ark.5550190.p011.479
https://doi.org/10.24820/ark.5550190.p011.479
Publikováno v:
Zeitschrift für Naturforschung B. 76:201-210
The development of new prostate cancer protein receptor cytochrome P450 17A1 inhibitors offers the possibility of generating structures of increased potency. To this end, the chalcone analogs 7 and 8 were prepared from treatment of methyl 3-oxo-3H-be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d074323842ac0912008226dc99c25a12
https://doi.org/10.1515/znb-2020-0204
https://doi.org/10.1515/znb-2020-0204
Publikováno v:
Magnetic Resonance in Chemistry. 58:750-762
1 J(15 N,H) coupling constants for enaminones and NH-forms of intramolecularly hydrogen-bonded Schiff bases as model compounds for sp2 -hybridized nitrogen atoms are evaluated using density functional theory (DFT) to find the optimal functionals and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e93e45ffcfaa6cf6b8f7ee248cc901a5
https://doi.org/10.1002/mrc.5052
https://doi.org/10.1002/mrc.5052
Autor:
Nabeel A. Abdul-Rida, Ali M. Farhan, Dannah R. Miller, Ming Fong Lin, Najim A. Al-Masoudi, Bahjat A. Saeed
Publikováno v:
Molecular Diversity. 25:661-671
New pregnene analogs of N-hydroxamic acid 6, imino-propane hydrazides 7 and 8 as well as the aryl amides 9–11, oxadiazole, pyrazole and sulfinyl analogs 13–15, via the hydrazide analog 5 of methyl ((5-pregnen-3β,17β-diol-15α-yl)thio)propanoate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79311f375dc72cea22ad7b1769ce4967
https://doi.org/10.1007/s11030-020-10038-w
https://doi.org/10.1007/s11030-020-10038-w