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Dive into the research topics where Ashraf N. E. Hamed is active.

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Featured researches published by Ashraf N. E. Hamed.


Natural Product Research | 2016

Officinalioside, a new lignan glucoside from Borago officinalis L.

Mamdouh Nabil Samy; Ashraf N. E. Hamed; Sachiko Sugimoto; Hideaki Otsuka; Mohamed S. Kamel; Katsuyoshi Matsunami

Abstract A new lignan glucoside, officinalioside (1), was isolated from n-BuOH fraction of the aerial parts of Borago officinalis L., together with four known compounds: actinidioionoside (2), roseoside (3), crotalionoside C (4) and kaempferol 3-O-β-D-galactopyranoside (5). The structure of the new compound was established by means of spectroscopic and chemical analyses. Compounds 1 and 2 showed a moderate DPPH radical scavenging activity (IC50: 52.6 ± 1.70 and 41.3 ± 0.25 μM, respectively) comparable with that of the standard trolox (16.6 ± 2.2 μM) without any significant cytotoxicity towards human cell line A549 (IC50 > 100 μM). Graphical abstract


Natural Product Research | 2018

Forsskamide, a new ceramide from aerial parts of Forsskaolea tenacissima Linn.

Hamdy K Assaf; Alaa M. Nafady; Ahmed E. Allam; Ashraf N. E. Hamed; Mohamed S. Kamel; Kuniyoshi Shimizu

Abstract Although the various folk medicine uses and the biological activity of Forsskaolea tenacissima L., few chemical constituents of this plant have been reported, this provoked us to make our study. Forsskamide, a new ceramide was isolated from aerial parts of F. tenacissima L. (Urticaceae). The chemical structure was established by different spectroscopic methods (1H, 13C-NMR, HMBC, HSQC, ROESY, FAB-MS and HR-FAB-MS). Forsskamide showed a moderate cytotoxic activity by (MTT) method against human colorectal carcinoma cell line (HCT-116) with IC50 33.25 μM in comparison with 5-fluorouracil IC50 26.42 μM. While, it did not show any activity against human hepatocarcinaoma cell line (HepG-2).


European journal of medicinal plants | 2015

Pharmacotherapeutic evaluation of Parmentiera cereifera Seem. (Family Bignoniaceae) cultivated in Egypt on albino rats.

Nada M. Abdel-Wahab; Ashraf N. E. Hamed; Hany E. Khalil; Mohamed S. Kamel

Aims: The current study evaluates different biological activities viz., anti-inflammatory, antihyperglycemic and gastroprotective of methanolic extracts (MEs) of different parts viz., [mixture of leaves & stems (1:3) (MLS13), flowers and stem barks] and different fractions of ME of MLS13 of Parmentiera cereifera Seem. Moreover, this study estimates LD50 of ME of MLS13. Place and Duration of Study: The study was carried out for nine months in 2012 in the Department of Pharmacology, Faculty of Medicine and Department of Pharmacognosy and Phytochemistry, Faculty of Pharmacy, Minia University, Minia, Egypt. Methodology: The different MEs of various parts such as MLS13, flowers and stem barks and the Original Research Article Abdel-Wahab et al.; EJMP, 8(1): 29-38, 2015; Article no.EJMP.2015.087 30 different fractions of ME of MLS13 of P. cereifera were used in the present study. The different pharmacological activities such as anti-inflammatory, anti-hyperglycemic, gastroprotective and LD50 were determined using animal models as described in standard methods. Results: In yeast-induced paw edema method, ME of MLS13 had the highest anti-inflammatory activity (***P<0.001). While, in carrageenan-induced paw edema method, the highest antiinflammatory activity (***P<0.001) was exhibited by ME of stem barks. Moreover, both ME of flowers (***P<0.001) and ethyl acetate (EtOAc) fraction (***P<0.01) exhibited significant antihyperglycemic activity in alloxan-induced diabetes method. Furthermore, in indomethacin-induced gastric ulcer method, the highest gastroprotective effect (***P<0.001) was demonstrated by the petroleum ether (pet. ether) fraction. Finally, there is no toxicity symptoms of ME of MLS13 of P. cereifera up to 5 gm/kg. Conclusion: The biological results revealed that P. cereifera may be used in the development of various pharmaceutical preparations viz., anti-infalammatory, anti-hypergycemic as well as gastroprotective drugs, due to its wide safety margin.


European Journal of Medicinal Chemistry | 2017

Antifungal potential of marine natural products

Ebaa M. El-Hossary; Cheng Cheng; Mostafa M. Hamed; Ashraf N. E. Hamed; Knut Ohlsen; Ute Hentschel; Usama Ramadan Abdelmohsen


Journal of Pharmacognosy and Phytochemistry | 2014

Evaluation of antimicrobial and cytotoxic activities of the mehanolic and petroleum ether extract of Blumea lacera Burm.f in Bangladesh

Ashraf N. E. Hamed; Marwa H. H. Muhammad; Hany E. Khalil; Mohamed S. Kamel


BMC Complementary and Alternative Medicine | 2016

Hepatoprotective activity of ethanolic extract of Salix subserrata against CCl4-induced chronic hepatotoxicity in rats

Ahmed Wahid; Ashraf N. E. Hamed; Heba M. Eltahir; Mekky Mohammed Abouzied


Journal of Pharmacognosy and Phytochemistry | 2015

Triterpenes and sterols of family Apocynaceae (2013-1955), A review

Dina F. El-Kashef; Ashraf N. E. Hamed; Hany E. Khalil; Mohamed S. Kamel


Journal of Pharmacognosy and Phytochemistry | 2014

Investigation of the Unsaponifiable and Saponifiable Matters of Pachypodium lamerei Drake Leaves and Stems by GC/MS

Dina F. El-Kashef; Ashraf N. E. Hamed; Hany E. Khalil; Mohamed S. Kamel


Journal of Pharmacognosy and Phytochemistry | 2015

Botanical studies of the leaf of Pachypodium lamerei Drake, family Apocynaceae, cultivated in Egypt

Dina F. El-Kashef; Ashraf N. E. Hamed; Hany E. Khalil; Mohamed S. Kamel


Phytochemistry Letters | 2014

Phenolic acid glycosides from Parmentiera cereifera Seem. (Candle tree)

Nada M. Abdel-Wahab; Ashraf N. E. Hamed; Hany E. Khalil; Mamdouh N. Samy; Amira S Wanas; Mostafa A. Fouad; Mohamed S. Kamel

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Ebaa M. El-Hossary

Egyptian Atomic Energy Authority

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