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Showing results for amino haggar[Author]
Your search for Amina Haggar[Author] retrieved no results
Development of isatin-thiazolo[3,2-a]benzimidazole hybrids as novel CDK2 inhibitors with potent in vitro apoptotic anti-proliferative activity: Synthesis, biological and molecular dynamics investigations.
Eldehna WM, El Hassab MA, Abo-Ashour MF, Al-Warhi T, Elaasser MM, Safwat NA, Suliman H, Ahmed MF, Al-Rashood ST, Abdel-Aziz HA, El-Haggar R. Eldehna WM, et al. Among authors: el haggar r. Bioorg Chem. 2021 May;110:104748. doi: 10.1016/j.bioorg.2021.104748. Epub 2021 Feb 18. Bioorg Chem. 2021. PMID: 33684714
This could be attributed to an incorporation of the 5-OCH(3) group that was engaged in an extra hydrogen bonding with key THR14 amino acid residue. Finally, these results suggested hybrid 7d as a good candidate for further optimization as promising breast cancer antitumor …
This could be attributed to an incorporation of the 5-OCH(3) group that was engaged in an extra hydrogen bonding with key THR14 amino …
Anti-inflammatory screening and molecular modeling of some novel coumarin derivatives.
El-Haggar R, Al-Wabli RI. El-Haggar R, et al. Molecules. 2015 Mar 26;20(4):5374-91. doi: 10.3390/molecules20045374. Molecules. 2015. PMID: 25822078 Free PMC article.
Coumarin and their derivatives have drawn much attention in the pharmacological and pharmaceutical fields due to their broad range and diverse biological activities. In the present work, starting from the 6-amino-7-hydroxy-4-methyl-2H-chromen-2-one, a series of 6-(substitu …
Coumarin and their derivatives have drawn much attention in the pharmacological and pharmaceutical fields due to their broad range and diver …
Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature.
Al-Haggar M, Ahmad N, Yahia S, Shams A, Hasaneen B, Hassan Hassan R, Wahba Y, Salem NA, Abdel-Hady D. Al-Haggar M, et al. Case Rep Genet. 2013;2013:834605. doi: 10.1155/2013/834605. Epub 2013 Jan 23. Case Rep Genet. 2013. PMID: 23424689 Free PMC article.
Most of the isolated classic cases of FOP showed heterozygous mutation in the ACVR1 gene on chromosome 2q23 that encodes a bone morphogenetic protein BMP (ALK2). The most common mutation is (c.617G > A) leading to the amino acid substitution of arginine by histidine (p. …
Most of the isolated classic cases of FOP showed heterozygous mutation in the ACVR1 gene on chromosome 2q23 that encodes a bone morphogeneti …