Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Omaima M. Aboulwafa"'
Autor:
Maha S. Almutairi, Areej N. Al Suwayyid, Amal Aldarwesh, Omaima M. Aboulwafa, Mohamed I. Attia
Publikováno v:
Molecules, Vol 25, Iss 7, p 1553 (2020)
The preparation of certain 2-(2-oxo-2H-chromen-4-yl)-N-substituted acetamides IIIa–h was planned as a step in the development of new modified nonsteroidal antiestrogens. The purity of target compounds IIIa–h was checked by thin-layer chromatograp
Externí odkaz:
https://doaj.org/article/c4f5f951394847829280d588bd270011
Publikováno v:
Acta Crystallographica Section E, Vol 70, Iss 6, Pp o672-o673 (2014)
In the title compound, C15H14N4O2, the triazolopyrimidine ring system is almost planar (r.m.s. deviation = 0.02 Å) and the phenyl ring is inclined to its mean plane by 42.45 (9)°. The carboxyl group is inclined to the triazolopyrimidine ring mean p
Externí odkaz:
https://doaj.org/article/ec9d4d573ae54c90a8901119058d1767
Publikováno v:
Bioorganic Chemistry. 134:106437
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d93c885f5c5372154e4b643babb3f4bf
https://doi.org/10.1016/j.bioorg.2023.106437
https://doi.org/10.1016/j.bioorg.2023.106437
Publikováno v:
Alexandria Dental Journal. 44:83-90
INTRODUCTION: Durability of the removable prostheses is dependent on strong adhesion between the metal framework and acrylic resin. Weak adhesion causes separation of the denture base from the metal framework. It was reported that Neodynium-doped ytt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9db85c1f6a59a9012746cba4ff7e76ff
https://doi.org/10.21608/adjalexu.2019.57369
https://doi.org/10.21608/adjalexu.2019.57369
Autor:
Samir M.Y. Sedra, Hoda H. Baghdadi, Marium M. Shamaa, Heba A. Abd El Razik, Omaima M. Aboulwafa, Ahmed M. Farghaly
Publikováno v:
Bioorganic chemistry. 115
An array of newly synthesized thieno[3,2-d]pyrimidine-based derivatives and thienotriazolopyrimidines hybridized with some pharmacophoric anticancer fragments were designed, synthesized and assessed for their in vitro antiproliferative activity again
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56fd48627d5093aa958633450d210079
https://pubmed.ncbi.nlm.nih.gov/34365057
https://pubmed.ncbi.nlm.nih.gov/34365057
Autor:
Yaseen A.M.M. Elshaier, Haridy H. Haridy, Omaima M. Aboulwafa, Heba A. E. Mubarak, Waleed A. Badawi, Ahmed M. Farghaly
Publikováno v:
Medicinal Chemistry Research. 28:360-379
A new series of achiral pyrimidine derivatives based on nifedipine-like structure was designed and synthesized. These pyrimidyl derivatives contained hydrazine, hydrazones, acetohydrazide, differently substituted benzylidene functionalities, benzosul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7ac7788b3cec10b17564cd0075b5929
https://doi.org/10.1007/s00044-019-02289-6
https://doi.org/10.1007/s00044-019-02289-6
Autor:
Areej N Al Suwayyid, Mohamed I. Attia, Amal Aldarwesh, Maha S. Almutairi, Omaima M. Aboulwafa
Publikováno v:
Molecules
Molecules, Vol 25, Iss 1553, p 1553 (2020)
Volume 25
Issue 7
Molecules, Vol 25, Iss 1553, p 1553 (2020)
Volume 25
Issue 7
The preparation of certain 2-(2-oxo-2H-chromen-4-yl)-N-substituted acetamides IIIa&ndash
h was planned as a step in the development of new modified nonsteroidal antiestrogens. The purity of target compounds IIIa&ndash
h was checked by thin-
h was planned as a step in the development of new modified nonsteroidal antiestrogens. The purity of target compounds IIIa&ndash
h was checked by thin-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f64cd79bb3d494502cd9c9d0e8924e4
https://pubmed.ncbi.nlm.nih.gov/32231072
https://pubmed.ncbi.nlm.nih.gov/32231072
Autor:
Mai S. El-Shoukrofy, Mohamed A Abdelsalam, El-Sayed A. M. Badawey, Noha Gouda, Omaima M. Aboulwafa, Mostafa M.M. El-Miligy
Publikováno v:
Future Medicinal Chemistry. 10:2791-2814
Aim: Some anticancer β-carbolines exhibited dual inhibition of topo-I and KSP. Methodology/Results: Novel β-carbolines were synthesized and screened for their anticancer activity according to the NCI protocol. Five dose assays results indicated tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b3a64d022e3d2f543ca30ea7cc21afa
https://doi.org/10.4155/fmc-2018-0226
https://doi.org/10.4155/fmc-2018-0226
Publikováno v:
Archiv der Pharmazie. 354:2100177
6-Thienylpyrimidine-5-carbonitrile derivatives were synthesized and screened for their in vitro antiproliferative activities against two human breast cancer cell lines in comparison to 5-fluorouracil as a reference. Compounds 2, 3a-c, and 6b evolved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b6bfafd9406e4a05a337fdb465a8eaa
https://doi.org/10.1002/ardp.202100177
https://doi.org/10.1002/ardp.202100177
Publikováno v:
Bioorganic Chemistry. 109:104752
New benzoxazole derivatives containing 1,3,4-oxadiazole, 1,2,4-triazole or triazolothiadiazine rings were synthesized and screened for their in vitro antiproliferative activities against MCF-7 and MDA-MB-231 breast cancer cell lines using MTT assay.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::628d6ded844658cd97426ec4e64bfc0c
https://doi.org/10.1016/j.bioorg.2021.104752
https://doi.org/10.1016/j.bioorg.2021.104752