Nanogel-mediated drug delivery system for anticancer agent: pH stimuli responsive poly (ethylene glycol/acrylic acid) nanogel prepared by gamma irradiation

NEA Abd El-Sattar, SESA El-Hddad, MM Ghobashy… - Bioorganic …, 2022 - Elsevier
The popularity of nanogel as nano drug carrier lies in its adjustable physical properties, and
the ability to encapsulate drug particles with improved properties is being developed to meet …

Design, synthesis, in silico docking, ADMET and anticancer evaluations of thiazolidine-2, 4-diones bearing heterocyclic rings as dual VEGFR-2/EGFR T790M tyrosine …

NAAM Aziz, RF George, K El-Adl, WR Mahmoud - RSC advances, 2022 - pubs.rsc.org
Fourteen recent thiazolidine-2, 4-diones bearing furan and/or thiophene heterocyclic rings
have been designed, synthesized and assessed for their anticancer activities against four …

Chemistry and engineering of cyclodextrins for molecular imaging

WF Lai, AL Rogach, WT Wong - Chemical Society Reviews, 2017 - pubs.rsc.org
Cyclodextrins (CDs) are naturally occurring cyclic oligosaccharides bearing a basket-
shaped topology with an “inner–outer” amphiphilic character. The abundance of hydroxyl …

Design, synthesis, molecular docking and in silico ADMET profile of pyrano [2, 3-d] pyrimidine derivatives as antimicrobial and anticancer agents

NEA Abd El-Sattar, K El‐Adl, MA El-Hashash… - Bioorganic …, 2021 - Elsevier
Abstract Pyrano [2, 3-d] pyrimidine derivatives were synthesized by treating cyclic
compounds containing active methylene group with aldehyde and malononitrile in butanol …

Design, synthesis, molecular docking, anticancer evaluations, and in silico pharmacokinetic studies of novel 5‐[(4‐chloro/2, 4‐dichloro) benzylidene] thiazolidine‐2, 4 …

K El‐Adl, AGA El‐Helby, H Sakr, RR Ayyad… - Archiv der …, 2021 - Wiley Online Library
The anticancer activity of novel thiazolidine‐2, 4‐diones was evaluated against HepG2, HCT‐
116, and MCF‐7 cells. MCF‐7 was the most sensitive cell line to the cytotoxicity of the new …

Phthalazine‐based VEGFR‐2 inhibitors: Rationale, design, synthesis, in silico, ADMET profile, docking, and anticancer evaluations

F Khedr, MK Ibrahim, IH Eissa… - Archiv der …, 2021 - Wiley Online Library
In the designed compounds, a new linker was inserted in the form of fragments with verified
VEGFR‐2 inhibitory potential, including an α, β‐unsaturated ketonic fragment, pyrazole, and …

1, 2, 4-Triazolo [4, 3-c] quinazolines: a bioisosterism-guided approach towards the development of novel PCAF inhibitors with potential anticancer activity

MH El-Shershaby, A Ghiaty, AH Bayoumi… - New Journal of …, 2021 - pubs.rsc.org
Targeting PCAF with small inhibitor molecules has emerged as a potential therapeutic
strategy for the treatment of cancer. Recently, L-45 was identified as a potent …

Design, synthesis, molecular docking, in silico ADMET profile and anticancer evaluations of sulfonamide endowed with hydrazone-coupled derivatives as VEGFR-2 …

AM Sayed, FA Taher, MRK Abdel-Samad… - Bioorganic …, 2021 - Elsevier
A new series of sulfonamide endowed with hydrazone coupled to dimethyl and/or diethyl
malonates were prepared. Various sulfa drugs were diazotized and followed by coupling …

Unravelling the anticancer potency of 1,2,4-triazole-N-arylamide hybrids through inhibition of STAT3: synthesis and in silico mechanistic studies

A Turky, AH Bayoumi, FF Sherbiny, K El-Adl… - Molecular …, 2021 - Springer
The discovery of potent STAT3 inhibitors has gained noteworthy impetus in the last decade.
In line with this trend, considering the proven biological importance of 1, 2, 4-triazoles …

Microbiome-mediated bile acid modification: role in intestinal drug absorption and metabolism

EF Enright, BT Griffin, CGM Gahan, SA Joyce - Pharmacological Research, 2018 - Elsevier
Once regarded obscure and underappreciated, the gut microbiota (the microbial
communities colonizing the gastrointestinal tract) is gaining recognition as an influencer of …