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(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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