(2S,4R) -H-L-Pro (4-N3) -OH
(2S,4R) -H-L-Pro (4-N3) -OH is a click chemistry reagent containing an azide group. (2S,4R) -H-L-Pro (4-N3) -OH can be used for the research of various biochemical studies[1]. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.
Product Specifications
CAS Number
[1019849-13-8]
UNSPSC
12352005
Target
ADC Linker
Type
Reference compound
Related Pathways
Antibody-drug Conjugate/ADC Related
Applications
Cancer-programmed cell death
Field of Research
Others
Assay Protocol
https://www.medchemexpress.com/2s-4r-h-l-pro-4-n3-oh.html
Solubility
10 mM in DMSO
Smiles
OC([C@@H]1C[C@H](CN1)N=[N+]=[N-])=O
Molecular Formula
C5H8N4O2
Molecular Weight
156.14
References & Citations
[1]Nellie A K Ochs, et al. Oligoprolines guide the self-assembly of quaterthiophenes. Chem Sci. 2019 May 2;10 (20) :5391-5396.
Shipping Conditions
Room temperature
Scientific Category
Reference compound1
Clinical Information
No Development Reported
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