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(2R,4S) -Boc-D-Pro (4-N3) -OH (DCHA)

(2R,4S) -Boc-D-Pro (4-N3) -OH DCHA is a click chemistry reagent containing an azide[1]. (2R,4S) -Boc-D-Pro (4-N3) -OH (DCHA) 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.

Product Specifications

UNSPSC

12352005

Target

ADC Linker

Type

Reference compound

Related Pathways

Antibody-drug Conjugate/ADC Related

Field of Research

Others

Assay Protocol

https://www.medchemexpress.com/2r-4s-boc-d-pro-4-n3-oh-dcha.html

Solubility

10 mM in DMSO

Smiles

CC(C)(C)OC(N1[C@H](C[C@@H](C1)N=[N+]=[N-])C(O)=O)=O.C2(CCCCC2)NC3CCCCC3.C

Molecular Formula

C23H43N5O4

Molecular Weight

453.62

References & Citations

[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.

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Curated Selection

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