White, Lisa J.; Boles, Jessica E.; Allen, Nyasha; Alesbrook, Luke S.; Sutton, J. Mark; Hind, Charlotte K.; Hilton, Kira L. F.; Blackholly, L. R.; Ellaby, Rebecca J.; Williams, George T.; Mulvihill, Daniel P.; Hiscock, Jennifer R. published an article in 2020, the title of the article was Controllable hydrogen bonded self-association for the formation of multifunctional antimicrobial materials.Recommanded Product: 92-36-4 And the article contains the following content:
SSAs are a class of supramol. self-associating amphiphilic salt, the anionic component of which contains a covalently bound hydrogen bond donor-acceptor motif. This results in a monomeric unit which can adopt multiple hydrogen bonding modes simultaneously. Previous investigations have shown examples of SSAs to act as antimicrobial agents against clin. relevant methicillin-resistant Staphylococcus aureus (MRSA). Herein, we report an intrinsically fluorescent SSA which can self-associate producing dimers, spherical aggregates and hydrogels dependent on solvent environment, while retaining antimicrobial activity against both model Gram-pos. (MRSA) and Gram-neg. (Escherichia coli) bacteria. Finally, we demonstrate the SSA supramol. hydrogel to tolerate the inclusion of the antibiotic ampicillin, leading to the enhanced inhibition of growth with both model bacteria, and derive initial mol. structure-physicochem. property-antimicrobial activity relationships. The experimental process involved the reaction of 2-(4-Aminophenyl)-6-methylbenzothiazole(cas: 92-36-4).Recommanded Product: 92-36-4
The Article related to antibacterial, Pharmaceuticals: Pharmaceutics and other aspects.Recommanded Product: 92-36-4
Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica