Unlabelled: Aims/Objective: Phosphonium salts are compounds whose structural characteristics enable them to cross the plasma and mitochondrial membrane with ease. Cancer cells have higher plasma membrane potentials than normal cells; phosphonium salts selectively accumulate in the mitochondria of neoplastic cells and inhibit mitochondrial function.
Method: In the present work, we investigated the cytotoxic activity of lipophilic phosphonium salt (11- methoxy11-oxo-undecyl) triphenylphosphonium bromide (MUTP) as well as of the two new phosphine oxide salts, 3,3'-(methylphosphoryl) dibenzenaminium chloride (SBAMPO) and 3,3' (phenylphosphoryl) dibenzenaminium chloride (SBAPPO) on the proliferation of breast cancer cell line (MCF-7) and human uterin cervix adenocarcinoma cells (HeLa).
Result: We showed that only MUTP exhibits antiproliferative effects on both cell lines, without affecting the normal breast epithelial cell proliferation. More specifically, we demonstrated that MUTP treatment of breast cancer cells is associated with impaired cell-cycle progression and metabolically induces mitochondrial damage and triggers apoptotic cell death in MCF-7 and HeLa cells. Taken together, these findings suggest that MUTP may be capable of selectively targeting neoplastic cell growth and therefore has potential applications as anticancer agent.
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http://dx.doi.org/10.2174/1871520617666170719154249 | DOI Listing |
Polymers (Basel)
November 2024
Faculty of Dental Medicine, "Apollonia" University of Iasi, 11 Pacurari Street, 700115 Iasi, Romania.
(1) Background: Since the discovery of antibiotics in the first half of the 20th century, humans have abused this privilege, giving rise to antibiotic-resistant pathogens. Recent research has brought to light the use of antimicrobial peptides in polymers, hydrogels, and nanoparticles (NPs) as a newer and safer alternative to traditional antibiotics. (2) Methods: This review article is a synthesis of the scientific works published in the last 15 years, focusing on the synthesis of polymers with proven antimicrobial properties.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Key Laboratory of Surface and Interface Science of Polymer Materials of Zhejiang Province, School of Chemistry and Chemical Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, Zhejiang, P. R. China.
Functional porous organic polymers (POPs) have been widely developed as heterogeneous catalysts for carbon dioxide (CO) conversion. However, the integration of multifunctional active sites into POPs remains a major challenge. Herein, a facile postsynthesis modification strategy was explored to fabricate metalloporphyrin- and phosphonium-bifunctionalized POPs (TAPPM-PTBAR) as the heterogeneous catalysts for CO conversion.
View Article and Find Full Text PDFChem Rec
December 2024
Department of Chemistry, Universidade Federal de Minas Gerais (UFMG), 31.270-901, Belo Horizonte, MG, Brazil.
Alkylation reactions and their products are considered crucial in various contexts. Synthetically, the alkylation of a nucleophile is usually promoted using hazardous alkyl halides. Here, we aim to highlight the potential of pnictogen (ammonium or phosphonium) and chalcogen salts (sulfonium, selenonium, and telluronium) to function as alkylating agents.
View Article and Find Full Text PDFDalton Trans
December 2024
Department of Chemistry, University of Toronto, 80 St George St, Toronto, ON, Canada, M5S3H6.
Phosphazenium cations were first characterized 60 years ago and yet little is known of their reactivity. The bidentate phosphonium dicationic salts [(CH)(PPhF)][B(CF)]2 and [(CH)(PPhCl)][Cl]3 were prepared. Reaction of 2 with (MeSi)NMe gave the phosphazenium dication [(CH)(PPh)(μ-NMe)][B(CF)]4, while reaction of 3 with two equivalents of MeN(SiMe) gave the related dication [(CH)(PPhNMe)][Cl]5.
View Article and Find Full Text PDFJ Org Chem
November 2024
Department of Chemistry, Indian Institute of Technology Delhi, New Delhi 110016, India.
A set of structurally analogous, albeit electronically distinct, phosphamides () is prepared, and the effect of the electronic amendment due to p-substitution has been tested for the conversion of alcohols to halides via the Appel reaction. The -OMe-substituted diphosphamide () remains the most active, providing ∼96% conversion of alcohols to halides with a TON of 11 in moderate reaction conditions with a large substrate scope. Halide formation follows a pseudo-first-order rate with a constant rate () of 7.
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