Molecular Genetics and Metabolism, Journal Year: 2024, Volume and Issue: 143(3), P. 108581 - 108581
Published: Sept. 28, 2024
Language: Английский
Molecular Genetics and Metabolism, Journal Year: 2024, Volume and Issue: 143(3), P. 108581 - 108581
Published: Sept. 28, 2024
Language: Английский
International Journal of Pharmaceutics, Journal Year: 2025, Volume and Issue: unknown, P. 125385 - 125385
Published: Feb. 1, 2025
Language: Английский
Citations
1International Journal of Molecular Sciences, Journal Year: 2024, Volume and Issue: 25(11), P. 5977 - 5977
Published: May 29, 2024
Human mycoses cover a diverse field of fungal diseases from skin disorders to systemic invasive infections and pose an increasing global health problem based on ineffective treatment options, the hampered development new efficient drugs, emergence resistant strains. Niclosamide is currently applied for worm infections. Its mechanisms action, which include suppression mitochondrial oxidative phosphorylation (also known as uncoupling), among others, has led repurposing this promising anthelmintic drug therapy further human such cancer, diabetes, microbial Given urgent need develop drugs against infections, considerable antifungal properties niclosamide are highlighted in review. chemical pharmacological relevant also briefly mentioned, described mitochondria-targeting action add current arsenal approved drugs. In addition, activities salicylanilide-based analogs pathogens, including agents veterinary medicine many years, discussed their feasibility antifungals humans. Preliminary structure-activity relationships determined discussed. Various salicylanilide derivatives with showed increased oral bioavailabilities when compared niclosamide. The simple synthesis vouchsafes broad cost-effective availability poorer patient groups. Pertinent literature covered until 2024.
Language: Английский
Citations
7Drug Design Development and Therapy, Journal Year: 2024, Volume and Issue: Volume 18, P. 4153 - 4182
Published: Sept. 1, 2024
Niclosamide (NIC), an anthelmintic drug, has garnered recent attention for its potential as antiviral, antibacterial, and chemotherapeutic agent, among other applications. Repurposing NIC presents a current trend, offering significant time cost savings compared to developing entirely new therapeutic chemical entities. However, drawback lies in poor solubility, resulting notably low oral bioavailability. This review consolidates efforts overcome this limitation by summarizing twelve categories of formulations, spanning derivatives, amorphous solid dispersions, co-crystals, nanocrystals, micelles, nanohybrids, lipid nanoparticles emulsions, cyclodextrins, polymeric nanoparticles, dry powders inhalation, 3D printlets, nanofibers. These formulations cover oral, injectable, inhalable potentially (trans)dermal routes administration. Additionally, we present comprehensive overview characteristics, including physico-chemical properties, metabolism, safety, pharmacokinetics. Moreover, identify gaps formulation administration pathways that warrant further investigation address
Language: Английский
Citations
4RSC Medicinal Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Niclosamide, an FDA-approved anthelmintic drug, known to uncouple the mitochondria induces cyclin D1 degradation via CRL4 AMBRA1 . We find a striking correlation between two processes and that it is observed amongst various compounds.
Language: Английский
Citations
0Molecular Genetics and Metabolism, Journal Year: 2024, Volume and Issue: 143(3), P. 108581 - 108581
Published: Sept. 28, 2024
Language: Английский
Citations
1