Zobrazeno 1 - 10
of 187
pro vyhledávání: '"NAJIM A. AL-MASOUDI"'
Publikováno v:
ARKIVOC, Vol 2010, Iss 11, Pp 242-253 (2010)
Externí odkaz:
https://doaj.org/article/d54abc37caac4a9c84cdeadc4edf33cf
Publikováno v:
ARKIVOC, Vol 2010, Iss 9, Pp 185-195 (2010)
Externí odkaz:
https://doaj.org/article/460c28c8cf104cc29c021e21c57b0a7d
Autor:
Yaseen A. Al-Soud, Haitham H. Al-Sa’doni, Bahjat Saeed, Ihsan H. Jaber, Mohammad O. Beni-Khalid, Najim A. Al-Masoudi, Tahsin Abdul-Kadir, Paolo La Colla, Bernardetta Busonera, Tiziana Sanna, Roberta Loddo
Publikováno v:
ARKIVOC, Vol 2008, Iss 15, Pp 225-238 (2008)
Externí odkaz:
https://doaj.org/article/2cdb9e5a182b43d7856bbb26b8ec0ba3
Publikováno v:
ARKIVOC, Vol 2008, Iss 13, Pp 255-265 (2008)
Externí odkaz:
https://doaj.org/article/133db68933a24a10b568c181a51c4af2
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
A new class of tamoxifen analogues, using McMurry reaction conditions, is described. The scheme involved the conversion of ketoprofen (6) into amide derivatives 7 and 8, by coupling with N1,N1-substituted propan-1,3-diamine derivatives in the presenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21ca5f0ab92466cd893f16f688578f1b
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
Autor:
Najim A. Al-Masoudi, Hamsa Hussein Al-Hujaj, Ahmed Majeed Jassem, Faeza Abdul Kareem Almashal
Publikováno v:
Russian Journal of Bioorganic Chemistry. 46:360-370
A new series of 1,4-disubstituted-1,2,3-triazolethymine derivatives (VIa–e) were synthesized and characterized by spectroscopic studies. The in vitro cytotoxic activities of selected compounds against human cancer cell line (MDA-MB 231) were evalua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ca367eb1cfaeb82a213750628454d2f
https://doi.org/10.1134/s1068162020030024
https://doi.org/10.1134/s1068162020030024