Strategies towards the synthesis of anti-tuberculosis drugs

HB Rode, DM Lade, R Grée, PS Mainkar… - Organic & …, 2019 - pubs.rsc.org
Antituberculosis drugs have captured the attention of the scientific community due to the
emergence of drug resistance. Hence, the development of new analogs and new drugs …

[HTML][HTML] Dihydrotestosterone-based A-ring-fused pyridines: Microwave-assisted synthesis and biological evaluation in prostate cancer cells compared to structurally …

MA Kiss, M Peřina, L Bereczki, Á Baji, J Bělíček… - The Journal of Steroid …, 2023 - Elsevier
Dysfunction of the androgen receptor (AR) signalling axis plays a pivotal role in the
development and progression of prostate cancer (PCa). Steroidal and non-steroidal AR …

New arylethanolimidazole derivatives as HO-1 inhibitors with cytotoxicity against MCF-7 breast cancer cells

V Ciaffaglione, S Intagliata, V Pittalà… - International Journal of …, 2020 - mdpi.com
In this paper, a novel series of imidazole-based heme oxygenase-1 (HO-1) inhibitors is
reported. These compounds were obtained by modifications of previously described high …

Synthesis of Antifungal Heterocycle-Containing Mannich Bases: A Comprehensive Review

D Quiroga, E Coy-Barrera - Organics, 2023 - mdpi.com
Mannich bases are a class of organic compounds usually obtained by the condensation
reaction between an amine, a compound with active hydrogens, and an aldehyde. They are …

Synthesis and anti-tubercular activity of conformationally-constrained and bisquinoline analogs of TMC207

D Kalia, AK KS, G Meena, KP Sethi, R Sharma… - …, 2015 - pubs.rsc.org
One of the most significant breakthroughs in the battle against tuberculosis is the recent
approval of the quinoline compound, TMC207, for the treatment of drug-resistant …

1-Aryl-3-(1H-imidazol-1-yl)propan-1-ol esters: synthesis, anti-Candidapotential and molecular modeling studies

MI Attia, AA Radwan, AS Zakaria, MS Almutairi… - Chemistry Central …, 2013 - Springer
Background An increased incidence of fungal infections, both invasive and superficial, has
been witnessed over the last two decades. Candida species seem to be the main etiology of …

Synthesis, X-ray Single Crystal Structure, Molecular Docking and DFT Computations on N-[(1E)-1-(2H-1,3-Benzodioxol-5-yl)-3-(1H-imidazol-1-yl)propylidene] …

RI Al-Wabli, AR Al-Ghamdi, HA Ghabbour… - Molecules, 2017 - mdpi.com
Mycoses are serious health problem, especially in immunocompromised individuals. A new
imidazole-bearing compound containing an oxime functionality was synthesized and …

Ball mill and microwave assisted synthetic routes to Fluoxetine

R Solà, OB Sutcliffe, CE Banks, B Maciá - Sustainable Chemistry and …, 2017 - Elsevier
Remarkable advances have been made in the development of an environmentally-friendly
approach for the rapid and simple construction of the Active Pharmaceutical Ingredient (API) …

In Vitro Anti-Candida Activity of Certain New 3-(1H-Imidazol-1-yl)propan-1-one Oxime Esters

MI Attia, AS Zakaria, MS Almutairi, SW Ghoneim - Molecules, 2013 - mdpi.com
Anti-Candida activities of certain new oximes 4a–d and their respective aromatic esters 5a–l
are reported. The tested compounds 4a–d and 5a–l exhibited better anti-Candida profiles …

Anticonvulsant Potential of Certain New (2E)‐2‐[1‐Aryl‐3‐(1H‐imidazol‐1‐yl)propylidene]‐N‐(aryl/H)hydrazinecarboxamides

MI Attia, MN Aboul-Enein… - The Scientific World …, 2014 - Wiley Online Library
Anticonvulsant potential and neurotoxicity of certain new imidazole‐containing
arylsemicarbazones 6a–p are reported. The test compounds 6a–p exhibited anticonvulsant …