Replace tBu with THP or Trt and give your amino acids a smarter protection, removable under milder acidic conditions to minimize side products. Learn more in our latest publication!
Recent years have seen major advances in greener peptide synthesis. To highlight such products, we introduced the category "Green Chemistry" on our website.
Hot off the press - Discover our new flyer about glycosylated Fmoc-Asparagines for SPPS! Explore detailed information and practical tips - simply download it for free from our website knowledge base.
Anchor your peptides: Unlock the secrets of defying protease attacks and extend the serum half-life of your next peptide medication. Our building blocks will help you to reach your goals.
From fragments to full peptides - ligases like e.g., Sortase, Omniligase, enable efficient ligation and cyclization. Read our blog and learn how enzymatic tools can enhance your peptide synthesis.
Optimize your drug delivery with non-immunogenic biodegradable PEG alternatives and discover strategies for synthesizing defined sarcosine oligomers for targeted drug conjugation.
A photolabile anchor for SPPS that facilitates the synthesis of thioesters for native chemical ligation and which can be used to generate peptide chains fragmenting by flash photolysis. To discover NIC, read on!
New azidobenzyl side-chain-protected aspartic and glutamic acid building blocks allowing, e.g., for selective reductive deprotection even in physiological systems.
What is the difference between net content and purity and why are both parameters so important for reliable experimental results? Read our blog for more details!
The example of Semaglutide: Improve the pharmacokinetics of your therapeutic peptides by increasing their resistance against proteases via binding to plasma proteins.