911704

C5 Lenalidomine-C3-NH2 hydrochloride

≥95%

Manufacturer: Sigma Aldrich

Synonym(S): 4-Amino-N-(2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl)butanamide 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 911704-50-MG In Stock ₹ 46,770.00

911704 - 50 MG

₹ 46,770.00

In Stock

Quantity

1

Base Price: ₹ 46,770.00

GST (18%): ₹ 8,418.60

Total Price: ₹ 55,188.60

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(CCCN)=O)=CC=C31.Cl

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Description

  • Application: Protein degrader builiding block C5 Lenalidomide-C3-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 and an alkyl-chain crosslinker with pendant amine for reactivity with an acid on the target warhead. Because even slight alterations in ligands, warheads, 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: Degrader Building Blocks for Targeted Protein DegradationBuilding 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

Pictograms

GHS08

Signal Word

Warning

Hazard Statements

H361d,H373

Precautionary Statements

P202 - P260 - P280 - P308 + P313 - P405 - P501

Hazard Classifications

Repr. 2 - STOT RE 2

Target Organs

Blood

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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2-8°C

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O=C1N(C2CCC(NC2=O)=O)CC3=CC(NC(CCCN)=O)=CC=C31.Cl

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amine

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O=C1N(C2CCC(NC2=O)=O)CC3=CC(NC(CCCCCCN)=O)=CC=C31.Cl

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amine

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2-8°C

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O=C1N(C2CCC(NC2=O)=O)CC3=CC(NC(CCCCCCCCCN)=O)=CC=C31.Cl

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≥95%

form:
powder

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(COCCN)=O)=CC=C31.Cl