Targeted Protein Degraders
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Our expertise includes
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  • At Chemveda, we are committed to advancing the field of PROTAC (Proteolysis Targeting Chimera) technology. Collaborating closely with leading researchers, we deliver high-quality, potent, and selective PROTACs engineered for specific therapeutic targets to accelerate your research in targeted protein degradation. (TPD)
  • Our extensive expertise in heterocyclic chemistry and asymmetric synthesis enables the efficient synthesis of novel warheads, inhibitors in milligram to gram scales supporting early-stage discovery
  • We utilize flash chromatography, prep-HPLC and chiral-SFC for purification, 1H-NMR and mass spectrometry for characterization and HPLC for purity assessment
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Our Experience and Expertise
  • Our team has extensive experience in the synthesis of anchoring ligands and bifunctional molecules essential for the development of novel targeted protein degraders, including PROTACs and molecular glues
  • We leverage our expertise in Staudinger ligation chemistry, solid-phase synthesis and click chemistry to enable the efficient and modular construction of PROTACs and other bifunctional degraders
  • Extensive experience in the synthesis of small molecules serving as ligands for proteins of interest, enabling their use in targeted protein degradation
  • Synthetic chemistry expertise in the synthesis (often multi-step) of heterobifunctional molecules with multiple functional handles
Custom PROTAC
Synthesis Services
  • Chemveda provides a comprehensive suite of PROTAC synthesis services, including the development of novel PROTACs, partial PROTACs, and ligands. Chemveda provides end-to-end custom synthesis services for bifunctional molecules
  • With a strong track record in synthesizing challenging compounds, we offer our PROTAC discovery synthesis from milligrams to grams with high purity
Heterobifunctional Degrader Synthesis Capabilities

Synthesis and purification of different types of PROTACs and partial PROTACs, novel degrader building blocks in milligram to gram quantities.

Synthesis and functionalization of various E3-ligase ligands such as CRBN, VHL, MDM2 and clAP1 (in multi-gram scale)

  • Synthesis of novel linkers-both flexible and rigid linkers, PEG based linkers of varying length, hydrophobicity and composition
  • Synthesis of tailored linkers or hybrid designs to suite your project needs
  • Synthesis support for the optimization of linker types and size, linker-anchor or linker-recruiter connection
  • Design and synthesis of ligands for the protein of interest (POI)
  • Optimization of functional groups on the ligands of interest for linker attachment (SAR support)

Synthesis of bifunctional molecules for other degradation technologies such as AUTACs, LYTACs, etc.

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