2489242-23-9
Chemical Structure
Lenalidomide-propargyl-C2-NH2 hydrochloride
- CAS No.: 2489242-23-9
- Formula:C18H20ClN3O3
- Molecular Weight:361.82
IUPAC Name: 3-(4-(5-aminopent-1-yn-1-yl)-1-oxoisoindolin-2-yl)piperidine-2,6-dione hydrochloride
InChIKey: QONOSTNDZFIDAF-UHFFFAOYSA-N
SMILES: O=C(C(N(CC1=C2C=CC=C1C#CCCCN)C2=O)CC3)NC3=O.Cl
Biological Activity: Lenalidomide-propargyl-C2-NH2 hydrochloride incorporates a cereblon (CRBN) ligand for the E3 ubiquitin ligase, and a linker. Lenalidomide-propargyl-C2-NH2 hydrochloride can be used to design the PROTAC MD-224 (HY-114312)[1]. Lenalidomide-propargyl-C2-NH2 (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Lenalidomide-propargyl-C2-NH2 hydrochloride | 98.01% | Lenalidomide-propargyl-C2-NH2 hydrochloride incorporates a cereblon (CRBN) ligand for the E3 ubiquitin ligase, and a linker. Lenalidomide-propargyl-C2-NH2 hydrochloride can be used to design the PROTAC MD-224 (HY-114312). Lenalidomide-propargyl-C2-NH2 (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. | ||||||||||||||||||||
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Similarity Score 0.98
HY-W591717EM-12-alkyne-C3-NH2 -
Similarity Score 0.91
HY-W998278Desamino lenalidomide-acetylene-C2-NH2 -
Similarity Score 0.91
HY-W9982813-(4-(5-Hydroxypent-1-yn-1-yl)-1-oxoisoindolin-2-yl)piperidine-2,6-dione -
Similarity Score 0.88
HY-W998277Desamino lenalidomide-acetylene-C2-OH -
Similarity Score 0.88
HY-172218Lenalidomide-hex-5-ynoic acid -
Similarity Score 0.88
HY-156700Lenalidomide-acetylene-Br -
Similarity Score 0.86
HY-169181Lenalidomide-7-bromohept-1-yne -
Similarity Score 0.84
HY-129608Lenalidomide-acetylene-C5-COOH -
Similarity Score 0.83
HY-159145Lenalidomide-acetylene-C3-MsO -
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