Pipecolic, nipecotic, and homonipecotic acid are the basic motifs that combine piperidine with carboxylic acids. And they are only the starting points for countless MedChem building blocks.
Fluorosulfate-tyrosine (OSF-Tyr) brings reactive docking sites into proteins and peptides. Discover this “click-type” and learn how proximity-activated SuFEx chemistry enables covalent modification.
Keep your peptide synthesis clean – prevent aspartimide formation by using our novel aspartic acid hydrazide building block Fmoc-L-Asp(NH-NMe-Boc)-OH. Read our blog for more information!
Backbone protecting groups provide peptides with temporary disguise: they mask backbone amides to control reactivity and suppress aggregation until synthesis is complete. Learn more!
Diyne-girder bridged stapled peptides in the ideal helical geometry are accessible through our new alkyne functionalized building block. They can be watched by Raman microscopy.
Pseudoprolines act as molecular hinges: introducing precise turns that disrupt early folding and reduce aggregation in challenging peptide sequences. Read on to learn how they work!
Struggling with aggregating peptides or poor solubility? Take the rescue route: introduce solubility tags with our removable linkers. Learn more about your linker choices in our blog.
Solvatochromic dyes of our building blocks provide a fluorescent color palette that enables the integration of sensitive optical sensors into peptides, proteins, and other organic systems.
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.