A new application about150-19-6

Name: m-Methoxyphenol. Welcome to talk about 150-19-6, If you have any questions, you can contact Schito, AM; Piatti, G; Caviglia, D; Zuccari, G; Alfei, S or send Email.

Name: m-Methoxyphenol. Schito, AM; Piatti, G; Caviglia, D; Zuccari, G; Alfei, S in [Schito, Anna Maria; Piatti, Gabriela; Caviglia, Debora] Univ Genoa, Dept Surg Sci & Integrated Diagnost DISC, Viale Benedetto 15,6, I-16132 Genoa, Italy; [Zuccari, Guendalina; Alfei, Silvana] Univ Genoa, Dept Pharm, Viale Cembrano, I-16148 Genoa, Italy published Broad-Spectrum Bactericidal Activity of a Synthetic Random Copolymer Based on 2-Methoxy-6-(4-Vinylbenzyloxy)-Benzylammonium Hydrochloride in 2021.0, Cited 50.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.

Low-molecular-weight organic ammonium salts exert excellent antimicrobial effects by interacting lethally with bacterial membranes. Unfortunately, short-term functionality and high toxicity limit their clinical application. On the contrary, the equivalent macromolecular ammonium salts, derived from the polymerization of monomeric ammonium salts, have demonstrated improved antibacterial potency, a lower tendency to develop resistance, higher stability, long-term activity, and reduced toxicity. A water-soluble non-quaternary copolymeric ammonium salt (P7) was herein synthetized by copolymerizing 2-methoxy-6-(4-vinylbenzyloxy)-benzylammonium hydrochloride monomer with N, N-di-methyl-acrylamide. The antibacterial activity of P7 was assessed against several multidrug-resistant (MDR) clinical isolates of both Gram-positive and Gram-negative species. Except for colistin-resistant Pseudomonas aeruginosa, most isolates were susceptible to P7, also including some Gram-negative bacteria with a modified charge in the external membrane. P7 showed remarkable antibacterial activity against isolates of Enterococcus, Staphylococcus, Acinetobacter, and Pseudomonas, and on different strains of Escherichia coli and Stenotrophomonas maltophylia, regardless of their antibiotic resistance. The lowest minimal inhibitory concentrations (MICs) observed were 0.6-1.2 mu M and the minimal bactericidal concentrations (MBC) were frequently overlapping with the MICs. In 24-h time-kill and turbidimetric studies, P7 displayed a rapid non-lytic bactericidal activity. P7 could therefore represent a novel and potent tool capable of counteracting infections sustained by several bacteria that are resistant to the presently available antibiotics.

Name: m-Methoxyphenol. Welcome to talk about 150-19-6, If you have any questions, you can contact Schito, AM; Piatti, G; Caviglia, D; Zuccari, G; Alfei, S or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles