Fatemah Ali Aryan

Dr. Fatemah Ali Aryan


Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 December 2020 in Scientific Reports
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HBHaider Behbehani
Haider Behbehani
FAFatemah Ali Aryan
Fatemah Ali Aryan
KDKamal M. Dawood
Kamal M. Dawood
HIHamada Ibrahim
Hamada Ibrahim
A novel, expedient and effective methodology for the synthesis of distinctly substituted 6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-b]pyridine and 5,6-dihydrobenzo[h]quinoline systems has been developed with a new synthetic platform. This process includes ammonium acetate-mediated cyclocondensation reactions of 3-oxo-2-arylhydrazonopropanals with benzosuberone and tetralone precursors, respectively, using the high-pressure Q-tube reactor, which has been found to be superior to both conventional heating and microwave irradiation. The novel protocol benefits from its high atom efficiency, economy, ease of workup, broad substrate scope and is also applicable to gram-scale synthesis. To identify and confirm the newly synthesized targeted compounds, the X-ray single-crystal as well as all possible spectroscopic methods were utilized. The cytotoxicity of the newly synthesized 6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-b]pyridine 4a–j and 5,6-dihydrobenzo-[h]quinolines derivatives 6a–e were preliminary examined toward three cell lines of human cancer; lung cancer (A549), breast cancer (MCF-7) and colon cancer (HCT-116), by applying the MTT colorimetric assay. The achieved results reflected the promising profile of the prepared compounds in this study against cancer cells and have shown that members from the synthesized 6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-b]pyridine 4a–j exhibited promising cytotoxicity’s against MCF-7, and A549 cancer cells respectively, while the HCT-116 (colon) cancer cells were inhibited by certain examples of 5,6-dihydrobenzo[h]quinoline derivatives 6c,d. These promising results could serve as a good primary base for further research into the design of anticancer drugs.

2 September 2025 in Animals
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FAFatemah Ali Aryan
Fatemah Ali Aryan
OAOsama Mohamed Elshfei El- Azazy
Osama Mohamed Elshfei El- Azazy
EJEvelina Juozaitytė-Ngugu
Evelina Juozaitytė-Ngugu
DSDonatas Sneideris
Donatas Sneideris
LTLaila M. A. Tahrani
Laila M. A. Tahrani
Petras PrakasPetras Prakas
Petras Prakas
Sarcocystis is a genus of heteroxenous, globally distributed coccidian parasites. Limited research has been conducted on the natural infection of Sarcocystis in rodents in the Middle East. In this study, the Libyan jird (Meriones libycus) was identified as the natural intermediate host of the new species Sarcocystis meriones, based on morphological and molecular data. Microscopic sarcocysts were detected in the thigh muscles of 8.5% (4/47) of Libyan jirds captured from a semi-desert area in Amghara, Eastern Kuwait. Under the light microscope, sarcocysts were filamentous with blunt ends and thin walls, measuring 1550 × 89 µm. Transmission electron microscopy analysis showed the densely packed protrusions measure 1.2 × 0.5 µm and resemble thuja or a cylinder and having lateral microvilli, while the ground substance layer was 0.5–0.6 µm thick and type 22-like. Based on four genetic loci (18S rRNA, 28S rRNA, ITS1, and cox1), S. meriones was genetically most similar to S. myodes and S. ratti, infecting voles and mice of the genus Apodemus and black rats (Rattus rattus), respectively. Phylogenetic results suggest predatory mammals as potential definitive hosts of S. meriones. Further studies are needed to reveal host specificity, geographical distribution, and the impact of the parasite on the host’s health of the newly described Sarcocystis species.