Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2005 1
2007 1
2011 1
2016 1
2017 1
2018 5
2019 2
2020 4
2021 4
2022 3
2023 4
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

24 results

Results by year

Filters applied: . Clear all
Page 1
Cladamide: a new ceramide from the endophytic fungus Cladosporium cladosporioides.
Sallam A, El-Metwally M, Sabry MA, Elsbaey M. Sallam A, et al. Nat Prod Res. 2023 Apr;37(7):1082-1091. doi: 10.1080/14786419.2021.1986709. Epub 2021 Oct 8. Nat Prod Res. 2023. PMID: 34622719
Compound 3 showed the highest acetylcholine esterase inhibitory activity (IC(50) = 0.057 0.003 M), followed by compound 4 (IC(50) = 0.068 0.003 M) and compound 1 (IC(50) = 0.099 0.005 M) compared to donepezil, the positive control, (IC(50) = 0.044 0.002 M
Compound 3 showed the highest acetylcholine esterase inhibitory activity (IC(50) = 0.057 0.003 M), followed by compound 4 (IC(50) = 0 …
Aurasperone A Inhibits SARS CoV-2 In Vitro: An Integrated In Vitro and In Silico Study.
ElNaggar MH, Abdelwahab GM, Kutkat O, GabAllah M, Ali MA, El-Metwally MEA, Sayed AM, Abdelmohsen UR, Khalil AT. ElNaggar MH, et al. Mar Drugs. 2022 Feb 28;20(3):179. doi: 10.3390/md20030179. Mar Drugs. 2022. PMID: 35323478 Free PMC article.
Aurasperone A (3) was found to inhibit SARS CoV-2 efficiently (IC(50) = 12.25 M) with comparable activity with the positive control remdesivir (IC(50) = 10.11 M). ...More potent anti-SARS CoV-2 M(pro) inhibitors can be developed according to our findings pres …
Aurasperone A (3) was found to inhibit SARS CoV-2 efficiently (IC(50) = 12.25 M) with comparable activity with the positive control r …
Terretonin O: a new meroterpenoid from Aspergillus terreus.
Hamed A, Abdel-Razek AS, Omran DA, El-Metwally MM, El-Hosari DG, Frese M, Soliman HSM, Sewald N, Shaaban M. Hamed A, et al. Nat Prod Res. 2020 Apr;34(7):965-974. doi: 10.1080/14786419.2018.1544977. Epub 2019 Jan 3. Nat Prod Res. 2020. PMID: 30602325
Terretonin O (1), a new meroterpenoid, was isolated individually from both methanolic extracts of thermophilic Aspergillus terreus TM8 and marine Aspergillus terreus LGO13. The recently reported terretonins M (2) and N (3) were further isolated from the fungus LGO13 along …
Terretonin O (1), a new meroterpenoid, was isolated individually from both methanolic extracts of thermophilic Aspergillus terreus TM8 and m …
New [1,2,4]triazolo[4,3-c]quinazolines as intercalative Topo II inhibitors: Design, synthesis, biological evaluation, and in silico studies.
Gaber AA, Sobhy M, Turky A, Eldehna WM, El-Sebaey SA, El-Metwally SA, El-Naggar AM, Ibrahim IM, Elkaeed EB, Metwaly AM, Eissa IH. Gaber AA, et al. PLoS One. 2023 Jan 30;18(1):e0274081. doi: 10.1371/journal.pone.0274081. eCollection 2023. PLoS One. 2023. PMID: 36716311 Free PMC article.
Further mechanistic investigations revealed the capability of compound 16 to induce apoptosis in HCT-116 cells and arrest the growth at the S and G2/M phases. Also, compound 16 showed a significant increase in the level of BAX (2.18-fold) and a marked decrease in the level …
Further mechanistic investigations revealed the capability of compound 16 to induce apoptosis in HCT-116 cells and arrest the growth at the …
Quality and accuracy of electronic pre-anesthesia evaluation forms.
Almeshari M, Khalifa M, El-Metwally A, Househ M, Alanazi A. Almeshari M, et al. Comput Methods Programs Biomed. 2018 Jul;160:51-56. doi: 10.1016/j.cmpb.2018.03.006. Epub 2018 Mar 15. Comput Methods Programs Biomed. 2018. PMID: 29728246
Design, synthesis, anti-proliferative evaluation, docking, and MD simulation studies of new thieno[2,3-d]pyrimidines targeting VEGFR-2.
El-Metwally SA, Elkady H, Hagras M, Husein DZ, Ibrahim IM, Taghour MS, El-Mahdy HA, Ismail A, Alsfouk BA, Elkaeed EB, Metwaly AM, Eissa IH. El-Metwally SA, et al. RSC Adv. 2023 Aug 4;13(33):23365-23385. doi: 10.1039/d3ra03128d. eCollection 2023 Jul 26. RSC Adv. 2023. PMID: 37545598 Free PMC article.
Further studies revealed that compound 18 induced cell cycle arrest in G2/M phase and promoted apoptosis in MCF-7 cancer cells. Apoptosis was stimulated by compound 18 by increasing BAX (3.6-fold) and decreasing Bcl-2 (3.1-fold). ...
Further studies revealed that compound 18 induced cell cycle arrest in G2/M phase and promoted apoptosis in MCF-7 cancer cells. Apopt …
Anti-cancer and immunomodulatory evaluation of new nicotinamide derivatives as potential VEGFR-2 inhibitors and apoptosis inducers: in vitro and in silico studies.
Yousef RG, Elwan A, Gobaara IMM, Mehany ABM, Eldehna WM, El-Metwally SA, A Alsfouk B, Elkaeed EB, Metwaly AM, Eissa IH. Yousef RG, et al. J Enzyme Inhib Med Chem. 2022 Dec;37(1):2206-2222. doi: 10.1080/14756366.2022.2110868. J Enzyme Inhib Med Chem. 2022. PMID: 35980113 Free PMC article.
Compound 10 revealed the highest anti-proliferative activities with IC(50) values of 15.4 and 9.8 M against HCT-116 and HepG2, respectively compared to sorafenib (IC(50) = 9.30 and 7.40 M). Compound 7 owned promising cytotoxic activities with IC(50) values of 15.7 a …
Compound 10 revealed the highest anti-proliferative activities with IC(50) values of 15.4 and 9.8 M against HCT-116 and HepG2, respec …
Discovery of thieno[2,3-d]pyrimidine-based derivatives as potent VEGFR-2 kinase inhibitors and anti-cancer agents.
El-Metwally SA, Abou-El-Regal MM, Eissa IH, Mehany ABM, Mahdy HA, Elkady H, Elwan A, Elkaeed EB. El-Metwally SA, et al. Bioorg Chem. 2021 Jul;112:104947. doi: 10.1016/j.bioorg.2021.104947. Epub 2021 Apr 27. Bioorg Chem. 2021. PMID: 33964580
Compound 17f exhibited the highest cytotoxic activities against the examined cell lines, HCT-116 and HepG2, with IC(50) values of 2.80 0.16 and 4.10 0.45 M, respectively. Aiming at exploring the mechanism of action of these compounds, the most active cytotoxic derivatives …
Compound 17f exhibited the highest cytotoxic activities against the examined cell lines, HCT-116 and HepG2, with IC(50) values of 2.80 0.16 …
Effect of sildenafil on the isolated rat aortic rings.
Sharabi FM, Daabees TT, El-Metwally MA, Senbel AM. Sharabi FM, et al. Fundam Clin Pharmacol. 2005 Aug;19(4):449-56. doi: 10.1111/j.1472-8206.2005.00345.x. Fundam Clin Pharmacol. 2005. PMID: 16011732
Sildenafil produced significant potentiation of acetylcholine (ACh, 2 x 10(-6) m)-induced relaxation at concentration > or =1 x 10(-8) m. Addition of sildenafil (1 x 10(-7) m) to aortic rings failed to alter the effect of N(G)-nitro-L-arginine (l-NNA, 3 x …
Sildenafil produced significant potentiation of acetylcholine (ACh, 2 x 10(-6) m)-induced relaxation at concentration > or =1 x 10 …
24 results