نتایج جستجو برای: solid phase peptide synthesis

تعداد نتایج: 1276997  

Journal: :Organic letters 2004
Mallesham Bejugam Sabine L Flitsch

[reaction: see text] Chemical glycopeptide synthesis requires access to gram quantities of glycosylated amino acid building blocks. Hence, the efficiency of synthesis of such building blocks is of great importance. Here, we report a fast and highly efficient synthetic route to Fmoc-protected asparaginyl glycosides from unprotected sugars in three steps with high yields. The glycosylated amino a...

Masoud Farahani Mohammad Ghannadi Maragheh Mohammad Shafiei Mostafa Erfani, Mostafa Goudarzi Seyed Pezhman Shirmardi

  Introduction: It has been shown that some primary human tumors and their metastases, including prostate and breast tumors, over-express gastrin-releasing peptide (GRP) receptors. Bombesin is a neuropeptide with a high affinity for these GRP receptors. The purpose of this study was to prepare and evaluate the characteristics of a new Freeze-dried kit, [6-hydrazinopyr...

Mohammad Mazidi Mohammad Shafiee Mostafa Gandomkar Mostafa Goudarzi Nourollah Sadeghzadeh Seyed Esamaeil Sadat Ebrahimi Seyed Hassan Mirfallah

  Introduction: Bombesin (BN), a 14-amino acid neuropeptide, shows high affinity for the human GRP (gastrin releasing peptide) receptors, which are overexpressed by a variety of cancers, including prostate, breast, pancreas, gastrointestinal, and small cell lung cancer. Aim was to prepare [6-hydrazinopyridine-3-carboxylic acid (HYNIC0), D-Tyr6, D...

Journal: :Journal of the American Chemical Society 2004
Kie-Moon Sung David W Mosley Beau R Peelle Shuguang Zhang Joseph M Jacobson

In this communication, solid-phase reactions for the synthesis of Lys-monofunctionalized gold nanoparticles are described. A controlled and selective fabrication of linear nanoparticle arrays can be achieved through peptide linkage systems, and therefore it is essential to prepare Fmoc amino acid nanoparticle building blocks susceptible to Fmoc solid-phase peptide synthesis. Gold nanoparticles ...

Journal: :PLoS Biology 2004
David R Halpin Juanghae A Lee S. Jarrett Wrenn Pehr B Harbury

DNA-directed synthesis represents a powerful new tool for molecular discovery. Its ultimate utility, however, hinges upon the diversity of chemical reactions that can be executed in the presence of unprotected DNA. We present a solid-phase reaction format that makes possible the use of standard organic reaction conditions and common reagents to facilitate chemical transformations on unprotected...

Journal: :Chemistry: A European Journal 2021

Despite the great advances in solid-phase peptide synthesis (SPPS), incorporation of certain functional groups into sequences is restricted by compatibility building blocks with conditions used during SPPS. In particular, introduction highly reactive modern bioorthogonal reactions peptides remains elusive. Here, we present an optimized synthetic protocol enabling installation two strained dieno...

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