Dexibuprofen therapeutic advances: Prodrugs and nanotechnological formulations

A Gliszczyńska, E Sánchez-López - Pharmaceutics, 2021 - mdpi.com
S-(+) enantiomer of ibuprofen (IBU) dexibuprofen (DXI) is known to be more potent than its R-
(−) form and exhibits many advantages over the racemic mixture of IBU such as lower …

Experimental models as refined translational tools for breast cancer research

E Costa, T Ferreira-Gonçalves, G Chasqueira… - Scientia …, 2018 - mdpi.com
Breast cancer is one of the most common cancers worldwide, which makes it a very
impactful malignancy in the society. Breast cancers can be classified through different …

[HTML][HTML] Synthesis, antiproliferative activity and molecular docking studies of novel doubly modified colchicine amides and sulfonamides as anticancer agents

J Krzywik, W Mozga, M Aminpour, J Janczak, E Maj… - Molecules, 2020 - mdpi.com
Colchicine is a well-known compound with strong antiproliferative activity that has had
limited use in chemotherapy because of its toxicity. In order to create more potent anticancer …

Network-based drug repurposing identifies small molecule drugs as immune checkpoint inhibitors for endometrial cancer

F Ahmed, A Samantasinghar, W Ali, KH Choi - Molecular Diversity, 2024 - Springer
Endometrial cancer (EC) is the 6th most common cancer in women around the world. Alone
in the United States (US), 66,200 new cases and 13,030 deaths are expected to occur in …

New quinoline/1, 2, 4-triazole hybrids as dual inhibitors of COX-2/5-LOX and inflammatory cytokines: Design, synthesis, and docking study

AM Mohassab, HA Hassan, D Abdelhamid… - Journal of Molecular …, 2021 - Elsevier
A novel series of 19 quinoline/1, 2, 4-triazole hybrid 6a-i and 7a-j was synthesized and
evaluated in vitro as dual COX-2/5-LOX inhibitors. Compounds 6e, 6i, and 7e displayed the …

Site-selective C (sp3)–H functionalizations mediated by hydrogen atom transfer reactions via α-amino/α-amido radicals

J Kaur, JP Barham - Synthesis, 2022 - thieme-connect.com
Amines and amides, as N-containing compounds, are ubiquitous in pharmaceutically-active
scaffolds, natural products, agrochemicals, and peptides. Amides in nature bear a key …

[HTML][HTML] Pharmacokinetic and molecular docking studies to design antimalarial compounds targeting Actin I

V Guleria, T Pal, B Sharma, S Chauhan… - International Journal of …, 2021 - ncbi.nlm.nih.gov
Objective: Malaria is an ancient disease that still causes more than 200 million of cases 7
with high mortality globally. Identification of new drug targets and development of novel …

Amide synthesis through the in situ generation of chloro-and imido-phosphonium salts

CD Irving, JT Floreancig, S Laulhé - ACS omega, 2020 - ACS Publications
We describe a methodology for the amidation of carboxylic acids by generating
phosphonium salts in situ from N-chlorophthalimide and triphenylphosphine. Aliphatic …

[HTML][HTML] Utilizing machine learning to identify nifuroxazide as an inhibitor of ubiquitin-specific protease 21 in a drug repositioning strategy

J Tak, TK Nguyen, K Lee, SG Kim, HC Ahn - Biomedicine & …, 2024 - Elsevier
Abstract Ubiquitin-specific protease (USP), an enzyme catalyzing protein deubiquitination, is
involved in biological processes related to metabolic disorders and cancer proliferation. We …

Synthesis of indole-tetrazole coupled aromatic amides; In vitro anticancer activity, in vitro tubulin polymerization inhibition assay and in silico studies

TS Reddy, S Rai, SK Koppula - Journal of Molecular Structure, 2022 - Elsevier
Herein, we described the synthesis of indole-tetrazole coupled aromatic amides (6a-o) and
evaluated their in vitro anticancer activity. Some of the compounds namely N-(4 …