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Chapter 15: Cyclic peptides as privileged structures
Book PartAbstract:Palabras claves:Autores:Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Jad Y.E., Kruger H.G., Ramesh S.Fuentes:scopusAn efficient solid-phase strategy for total synthesis of naturally occurring amphiphilic marine siderophores: Amphibactin-T and moanachelin ala-B
ArticleAbstract: Microorganisms such as bacteria, fungi and some plants secrete an abundance of suites of low moleculPalabras claves:Autores:Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Kruger H.G., Ramesh S.Fuentes:scopusAn improved and efficient strategy for the total synthesis of a colistin-like peptide
ArticleAbstract: Polymyxins have re-emerged as the last-line therapy for treatment against extremely multi-drug resisPalabras claves:Antimicrobial peptide, colistin, Convergent method, SynthesisAutores:Alberício F., B. G. De la Torre, Govender T., Kruger H.G., Ramesh S.Fuentes:scopus2-Methyltetrahydrofuran and cyclopentyl methyl ether for green solid-phase peptide synthesis
ArticleAbstract: 2-MeTHF and CPME were evaluated as greener alternatives for the most employed solvents in peptide syPalabras claves:2-methyltetrahydrofuran, Cyclopentyl methyl ether, Green solvents, Peptide synthesis, Solid-phase peptide synthesisAutores:Acosta G.A., Alberício F., B. G. De la Torre, El-Faham A., Govender T., Jad Y.E., Khattab S.N., Kruger H.G.Fuentes:scopusA Facile Synthesis of NODASA-Functionalized Peptide
ArticleAbstract: Herein, we report a mild and efficient synthesis of a NODASA-functionalized peptide, which was initiPalabras claves:bifunctional chelators, NODASA, NOTA, peptide, PetAutores:Alberício F., Arvidsson P.I., B. G. De la Torre, Chinthakindi P.K., Dutta J., Govender T., Kruger H.G., Naicker T.Fuentes:scopusGreen Solid-Phase Peptide Synthesis (GSPPS) 3. Green Solvents for Fmoc Removal in Peptide Chemistry
ArticleAbstract: DMF (N,N-dimethylformamide) is the most widely used solvent for Fmoc-SPPS, which is the conventionalPalabras claves:Fmoc, Green solvents, Peptide aggregation, Protecting groups, Solid-phase peptide synthesis, valerolactoneAutores:Alberício F., B. G. De la Torre, El-Faham A., Govender T., Jad Y.E., Kruger H.G.Fuentes:scopusEDC·HCl and Potassium Salts of Oxyma and Oxyma-B as Superior Coupling Cocktails for Peptide Synthesis
ArticleAbstract: Nowadays, DIC is the most widely used carbodiimide for solid-phase peptide synthesis, while EDC·HClPalabras claves:peptide coupling, Peptides, solid-phase synthesis, Steric hindrance, synthetic methodsAutores:Alberício F., B. G. De la Torre, El-Faham A., Govender T., Jad Y.E., Khattab S.N., Kruger H.G.Fuentes:scopusHighly chemoselective ligation of thiol- and amino-peptides on a bromomaleimide core
ArticleAbstract: Application of a bromomaleimide core allows for the incorporation of three different peptides. The kPalabras claves:Autores:Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Kruger H.G., Ramesh S.Fuentes:scopusOptimized microwave assisted synthesis of LL37, a cathelicidin human antimicrobial peptide
ArticleAbstract: LL37, a human cathelecidin antimicrobial peptide comprising of 37 amino acids has emerged as one ofPalabras claves:DIC, LL37, MICROWAVE, OxymaPure, SPPS, THFAutores:Alberício F., B. G. De la Torre, Dutta J., Essack S.Y., Govender T., Kruger H.G., Radebe S.M., Ramesh S., Somboro A.M.Fuentes:scopusOxyma-B, an excellent racemization suppressor for peptide synthesis
ArticleAbstract: Peptide-bond formation is a key process in the synthesis of peptide oligomers. Among the many coupliPalabras claves:Autores:Alberício F., B. G. De la Torre, El-Faham A., Govender T., Jad Y.E., Khattab S.N., Kruger H.G.Fuentes:scopus