Lenalidomide-PEG1-azide
CAT:
HY-133139
HY-133139
804-HY-133139-01
Size:
5 mg
For Laboratory Research Only. Not for Clinical or Personal Use.
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- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


Lenalidomide-PEG1-azide
Description:
Lenalidomide-PEG1-azide is a E3 ligase lgand-linker conjugate. Lenalidomide-PEG1-azide incorporates the Lenalidomide based cereblon ligand and a linker. Lenalidomide-PEG1-azide can be used to design a PROTAC BRD4 Degrader-2 (HY-133136) [1]. Lenalidomide-PEG1-azide 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.UNSPSC:
12352005Hazard Statement:
H302, H315, H319, H335Target:
E3 Ligase Ligand-Linker ConjugatesType:
Reference compoundRelated Pathways:
PROTACApplications:
Cancer-programmed cell deathField of Research:
CancerAssay Protocol:
https://www.medchemexpress.com/lenalidomide-peg1-azide.htmlPurity:
95.84Solubility:
DMSO : 100 mg/mL (ultrasonic)Smiles:
O=C(NC1=CC=CC2=C1CN(C(CC3)C(NC3=O)=O)C2=O)COCCN=[N+]=[N-]Molecular Formula:
C17H18N6O5Molecular Weight:
386.36Precautions:
H302, H315, H319, H335References & Citations:
[1]Zhang F, et al. Discovery of a new class of PROTAC BRD4 degraders based on a dihydroquinazolinone derivative and lenalidomide/pomalidomide. Bioorg Med Chem. 2020 Jan 1;28 (1) :115228.Shipping Conditions:
Room TemperatureStorage Conditions:
-20°C, 3 years; 4°C, 2 years (Powder)Scientific Category:
Reference compound1Clinical Information:
No Development ReportedCAS Number:
[2185795-67-7]
