The Exciting World of Macrocycle Structures
In this post, we discuss the unique structure of macrocyclic peptide drugs (often 4 to 24 amino acids), which falls between small-molecule drugs and biologics (such as monoclonal antibodies).
In this post, we discuss the unique structure of macrocyclic peptide drugs (often 4 to 24 amino acids), which falls between small-molecule drugs and biologics (such as monoclonal antibodies).
The expansion of the drug discovery CRO market highlights the need to minimize costs and timelines in pharmaceutical drug development. Discover how SARomics Biostructures can help with this!
It was a year marked by the most significant changes in recent memory: a new home for the company, four new team members, new collaborations, new publications, a revamped homepage, and a greatly expanded list of off-the-shelf structures.
SARomics Biostructures AB and Vipergen ApS partner to offer hit and lead identification services based on Vipergen’s unique DNA-encoded library (DEL) screening technology.
In this article, we discuss weak affinity chromatography (WAC™), the proprietary fragment screening technique jointly owned by SARomics Biostructures and Red Glead Discovery.
In this article, we will discuss some significant publications and company activities in 2023. The publications showcase our expertise in the three main areas of our services: X-ray crystallography, NMR spectroscopy, and integrated drug discovery.
In the second part of our article series on antibody therapeutics, we discuss biosimilars and their structure comparability analysis.
Using an integrated drug discovery approach, first-in-class TAK1 kinase inhibitors were designed in a hit-to-lead program run in close cooperation between three partners, SARomics Biostructures, Red Glead Discovery, and Aqilion.
What makes a successful services company? What is our strength, and how to define our selling points? We arrive at a list of 8 essential selling points defining the success of SARomics Biostructures.
A pleasant surprise! A paper describing the interaction of the therapeutic peptide dusquetide with the ZZ domain of the autophagic receptor p62 was published around 12 years after the structure was solved!