Z-L-Aha-OH (DCHA)
Product Specifications
UNSPSC Description
Z-L-Aha-OH (DCHA) is a click chemistry reagent containing azide group[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
Field of Research
Others
Assay Protocol
https://www.medchemexpress.com/z-l-aha-oh-dcha.html
Solubility
10 mM in DMSO
Smiles
O=C(OCC1=CC=CC=C1)N[C@H](C(O)=O)CCN=[N+]=[N-].C2(CCCCC2)NC3CCCCC3
Molecular Weight
459.58
References & Citations
[1]Jiang X, et al. Recent applications of click chemistry in drug discovery. Expert Opin Drug Discov. 2019 Aug;14(8):779-789.
Shipping Conditions
Room temperature
Product Datasheet
http://file.medchemexpress.com/batch_PDF/HY-151668A/Z-L-Aha-OH-DCHA-DataSheet-MedChemExpress.pdf
Product MSDS
http://file.medchemexpress.com/batch_PDF/HY-151668A/
Clinical Information
No Development Reported
CAS Number
1423018-09-0
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