(2S,4R)-H-L-Pro(4-N3)-OH
Product Specifications
UNSPSC Description
(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.
Target Antigen
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 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
Product Datasheet
http://file.medchemexpress.com/batch_PDF/HY-151639/2S-4R-H-L-Pro-4-N3-OH-DataSheet-MedChemExpress.pdf
Product MSDS
http://file.medchemexpress.com/batch_PDF/HY-151639/
Clinical Information
No Development Reported
CAS Number
1019849-13-8
Curated Selection
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