Promotional price valid on web orders only. Your contract pricing may differ. Interested in signing up for a dedicated account number?
Learn More
  1. Home
  2. Products
  3. 5000353519

Medchemexpress LLC Aeide-C1-NHS ester | 824426-32-6 | 98.0% | C6H6N4O4 | 100 MG
SDP

Catalog No. 5000353519
Encompass_Preferred

Aeide-C1-NHS ester is an alkyl/ether-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent, featuring an Azide group that can participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. It is also capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

  • Alkyl/ether-based PROTAC linker.
  • Used in the synthesis of PROTACs.
  • Click chemistry reagent.
  • Contains an Azide group for copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne groups.
  • Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups.
  • PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.

Catalog No. 50-003-53519 Supplier Medchemexpress LLC Supplier No. HY140755100MG
May include imposed supplier surcharges.
Add to Cart
Add to Cart

missing translation for 'validMainframeMsg'

Aeide-C1-NHS ester is an alkyl/ether-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent, featuring an Azide group that can participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. It is also capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

  • Alkyl/ether-based PROTAC linker.
  • Used in the synthesis of PROTACs.
  • Click chemistry reagent.
  • Contains an Azide group for copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne groups.
  • Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups.
  • PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.

Product Title
Select an issue

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.