نتایج جستجو برای: Solution-phase peptide synthesis

تعداد نتایج: 1546114  

Ebrahim Safavi Mahboubeh Rabbani, Maryam Khosravi Rahmatollah Rahimi

Peptides have shown Promising effect as pharmaceutics with the potential to treat a widevariety of diseases. Peptides are mostly synthesized by biological technology or chemicalmethods. Solution phasepeptide synthesis (SPS) and solid phase peptide synthesis (SPPS) aretwo major chemical techniques for peptidesproduction.In this research, the synthesis ofdipeptde(β-alanine-L-histidine)wasexamined...

Journal: :iranian journal of pharmaceutical research 0
enayatollah sheikhhosseini islamic azad university, kerman branch saeed balalaie peptide chemistry research center, k. n. toosi university of technology mohammadali bigdeli kharazmi (tarbiat moallem) uinversity, 43 mofateh ave., tehran

a new biological active hexapeptide of c-terminal of nocistatin, contains glu-gln-lys-gln-leu-gln sequence was synthesized according to solid phase peptide synthesis on the surface of 2-chloro tritylchloride resin and using fmoc-protected amino acids in the presence of tbtu (o-(benzotriazol-1-yl)-n,n,n',n'-tetramethyl uranium tetrafluoroborate) as a coupling reagent. then, amidation o...

Journal: :Molecules 2013
Seong Jong Kim Shelli R McAlpine

Comparing a solution phase route to a solid phase route in the synthesis of the cytotoxic natural product urukthapelstatin A (Ustat A) confirmed that a solid phase method is superior. The solution phase approach was tedious and involved cyclization of a ridged heterocyclic precursor, while solid phase allowed the rapid generation of a flexible linear peptide. Cyclization of the linear peptide w...

Journal: :Chemical communications 2010
Sheung So Ludmila G Peeva Edward W Tate Robin J Leatherbarrow Andrew G Livingston

This communication reports a new technology platform that advantageously combines organic solvent nanofiltration (a newly emerging technology capable of molecular separations in organic solvents) with solution phase peptide synthesis-Membrane Enhanced Peptide Synthesis (MEPS).

2007
Fanny Guzmán Sonia Barberis Andrés Illanes

Abbreviations: CD: circular dichroism CLEC: cross linked enzyme crystals DDC: double dimer constructs ESI: electrospray ionization HOBT: hydroxybenzotriazole HPLC: high performance liquid hromatography KCS: kinetically controlled synthesis MALDI: matrix-assisted laser desorption ionization MAP: multiple antigen peptide system MS: mass spectrometry NMR: nuclear magnetic resonance SPS: solution p...

Journal: :Organic & biomolecular chemistry 2015
Yahya E Jad Gerardo A Acosta Sherine N Khattab Beatriz G de la Torre Thavendran Govender Hendrik G Kruger Ayman El-Faham Fernando Albericio

To date, DMF has been considered as the only solvent suitable for peptide synthesis. Here we demonstrate the capacity of THF and ACN, which are friendlier solvents than DMF, to yield the product in higher purity than DMF. Using various peptide models, both THF and ACN reduced racemization in solution-phase and solid-phase synthesis when compared with DMF. Moreover, the use of ACN and THF in the...

Journal: :Organic letters 2011
Paolo Bruno Stella Peña Xavier Just-Baringo Fernando Albericio Mercedes Álvarez

The first total synthesis of Aeruginazole A, prepared via a convergent strategy that involved both solid-phase peptide synthesis and solution phase chemistry and that enabled conservation of the stereochemistry of the intermediates, is reported.

Journal: :Organic & biomolecular chemistry 2013
Rosaria De Marco Mariagiovanna Spinella Anna De Lorenzo Antonella Leggio Angelo Liguori

In this paper we describe a solution phase peptide synthesis strategy using the 4-nitrobenzenesulfonamido/N-methyl-4-nitrobenzenesulfonamido group as a protecting/activating system of the carboxyl function. The 4-nitrobenzenesulfonamido group is stable during peptide chain elongation (Fmoc chemistry). The N-aminoacyl or N-dipeptidyl-4-nitrobenzensulfonamides, when activated by methylation, can ...

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