2737202-65-0
Chemical Structure
N3-L-Cit-OH DCHA
- CAS No.: 2737202-65-0
- Formula:C18H34N6O3
- Molecular Weight:382.50
IUPAC Name: 1,8-dimethyl-9H-carbazole
InChIKey: PRCFSZNWPCQNEC-VWMHFEHESA-N
SMILES: NC(NCCC[C@@H](C(O)=O)N=[N+]=[N-])=O.C1(CCCCC1)NC2CCCCC2
Biological Activity: N3-L-Cit-OH DCHA is a click chemistry reagent containing an azide group. N3-L-Cit-OH DCHA can be used to construct peptidomimetic ADC linkers using Click-chemistry[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.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
N3-L-Cit-OH DCHA | N3-L-Cit-OH DCHA is a click chemistry reagent containing an azide group. N3-L-Cit-OH DCHA can be used to construct peptidomimetic ADC linkers using Click-chemistry. 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. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
