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Product Description
– (2R,4S)-Boc-D-Pro(4-N3)-OH is a click chemistry reagent containing an azide[1]. (2R,4S)-Boc-D-Pro(4-N3)-OH 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. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
Web ID
– HY-151677
Shipping
– Room temperature
Applications
– Cancer-programmed cell death
Molecular Formula
– C10H16N4O4
References
– [1]Gómez-Vidal JA, et al. Potent and selective conformationally restricted neuronal nitric oxide synthase inhibitors. J Med Chem. 2004 Jan 29;47(3):703-10.
CAS Number
– 132622-77-6
Molecular Weight
– 256.26
SMILES
– CC(C)(C)OC(N1[C@H](C[C@@H](C1)N=[N+]=[N-])C(O)=O)=O
Clinical Information
– No Development Reported
Research Area
– Others
Solubility
– 10 mM in DMSO
Target
– ADC Linker
Pathway
– Antibody-drug Conjugate/ADC Related
Product type
– Reference compound
Disclaimer: All products are for research use only unless clearly stated otherwise on the product datasheet. Datasheets provided on the website are drafts for reference purpose only and you are requested to always refer to the hard copy included in the kit for your experimentation.
