| Catalogue number: | PA 27 0032945 |
| Chemical name: | (S,R,S)-AHPC-C6-PEG3-butyl-N3 |
CAS Number: |
2300155-90-0 |
| Category: | miscellaneous compounds,Antibody Drug Conjugate |
| Synonyms: | (2S,4R)-1-((S)-22-Azido-2-(tert-butyl)-4-oxo-10,13,16-trioxa-3-azadocosanoyl)-4-hydroxy-N-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide; |
| Molecular form: | C38H59N7O7S |
| Appearance: | NA |
| Mol. Weight: | 757.99 |
| Storage: | 2-8°C Refrigerator |
| Shipping Conditions: | Ambient |
| Applications: | (S,R,S)-AHPC-C6-PEG3-butyl-N3 is a click chemistry reagent containing an azide group. (S,R,S)-AHPC-C6-PEG3-butyl-N3 serves as crosslinker-E3 ligase ligand conjugate, Click reactive protein degrader building block for PROTAC research, Template for synthesis of targeted protein degrader, VH032 conjugate[1]. (S,R,S)-AHPC-C6-PEG3-butyl-N3 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. |
(S,R,S)-AHPC-C6-PEG3-butyl-N3
(S,R,S)-AHPC-C6-PEG3-butyl-N3
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