919969
C5 Lenalidomide-PEG2-Butyl NH2 hydrochloride
≥95%
Manufacturer: Sigma Aldrich
Synonym(S): 2-(2-((6-Aminohexyl)oxy)ethoxy)-N-(2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl)acetamide hydrochloride, C5 Lenalidomide conjugate, Crosslinker−E3 Ligase ligand conjugate, Protein degrader building block for PROTAC® research, Template for synthesis of targeted protein degrader
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 50 MG | 919969-50-MG | In Stock | ₹ 64,798.45 |
919969 - 50 MG
In Stock
Quantity
1
Base Price: ₹ 64,798.45
GST (18%): ₹ 11,663.721
Total Price: ₹ 76,462.171
ligand
C5 Lenalidomide
Quality Level
100
Assay
≥95%
form
powder or crystals
reaction suitability
reactivity: carboxyl reactivereagent type: ligand-linker conjugate
functional group
amine
storage temp.
2-8°C
SMILES string
O=C1N(C2CCC(NC2=O)=O)CC3=CC(NC(COCCOCCCCCCN)=O)=CC=C31.Cl
Related Products
Description
- Application: Protein degrader building block C5 Lenalidomide-PEG2-Butyl NH2 hydrochloride enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology. This conjugate contains a Cereblon (CRBN)-recruiting ligand with alternative exit vector, a linker with both hydrophobic and hydrophilic moieties, and a pendant amine for reactivity with an acid on the target warhead. Because even slight alterations in ligands and crosslinkers can affect ternary complex formation between the target, E3 ligase, and PROTAC, many analogs are prepared to screen for optimal target degradation. When used with other protein degrader building blocks with a terminal amine, parallel synthesis can be used to more quickly generate PROTAC libraries that feature variation in crosslinker length, composition, and E3 ligase ligand.
- Other Notes: Technology Spotlight: Degrader Building Blocks for Targeted Protein DegradationPortal: Building PROTAC® Degraders for Targeted Protein DegradationTargeted Protein Degradation by Small MoleculesSmall-Molecule PROTACS: New Approaches to Protein DegradationTargeted Protein Degradation: from Chemical Biology to Drug Discovery
- Legal Information: PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license
SAFETY INFORMATION
WGK
WGK 3
Compare Similar Items
Show Difference
ligand: C5 Lenalidomide
Quality Level: 100
Assay: ≥95%
form: powder or crystals
reaction suitability: reactivity: carboxyl reactivereagent type: ligand-linker conjugate
functional group: amine
storage temp.: 2-8°C
SMILES string: O=C1N(C2CCC(NC2=O)=O)CC3=CC(NC(COCCOCCCCCCN)=O)=CC=C31.Cl
ligand:
C5 Lenalidomide
Quality Level:
100
Assay:
≥95%
form:
powder or crystals
reaction suitability:
reactivity: carboxyl reactivereagent type: ligand-linker conjugate
functional group:
amine
storage temp.:
2-8°C
SMILES string:
O=C1N(C2CCC(NC2=O)=O)CC3=CC(NC(COCCOCCCCCCN)=O)=CC=C31.Cl
ligand: __
Quality Level: 200
Assay: 99.99% trace metals basis
form: __
reaction suitability: __
functional group: __
storage temp.: __
SMILES string: [Li]N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F
ligand:
__
Quality Level:
200
Assay:
99.99% trace metals basis
form:
__
reaction suitability:
__
functional group:
__
storage temp.:
__
SMILES string:
[Li]N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F
ligand: __
Quality Level: 200
Assay: 99.99% trace metals basis
form: __
reaction suitability: __
functional group: __
storage temp.: __
SMILES string: [Li]N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F
ligand:
__
Quality Level:
200
Assay:
99.99% trace metals basis
form:
__
reaction suitability:
__
functional group:
__
storage temp.:
__
SMILES string:
[Li]N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F
ligand: __
Quality Level: 200
Assay: 99.99% trace metals basis
form: __
reaction suitability: __
functional group: __
storage temp.: __
SMILES string: [Li]N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F
ligand:
__
Quality Level:
200
Assay:
99.99% trace metals basis
form:
__
reaction suitability:
__
functional group:
__
storage temp.:
__
SMILES string:
[Li]N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F