920754

C5 Lenalidomide-benzyl-piperazine hydrochloride

Manufacturer: Sigma Aldrich

Synonym(S): N-(2-(2,6-Dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl)-4-(piperazin-1-ylmethyl)benzamide hydrochloride, 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 920754-50-MG In Stock ₹ 34,650.00

920754 - 50 MG

₹ 34,650.00

In Stock

Quantity

1

Base Price: ₹ 34,650.00

GST (18%): ₹ 6,237.00

Total Price: ₹ 40,887.00

ligand

C5 Lenalidomide

Quality Level

100

form

solid

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(C4=CC=C(CN5CCNCC5)C=C4)=O)=CC=C31.Cl

Related Products

Img

Sigma Aldrich

920746

--

Img

Sigma Aldrich

920797

≥95%...

Img

Sigma Aldrich

923877

--

Img

Sigma Aldrich

911739

≥95%...

Img

Sigma Aldrich

911720

≥95%...

Img

Sigma Aldrich

919896

--

Img

Sigma Aldrich

917729

≥95%...

Img

Sigma Aldrich

923885

--

Description

  • Application: Protein degrader building block C5 Lenalidomide-benzyl-piperazine hydrochloride enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology. This conjugate contains a Cereblon (CRBN)-recruiting ligand, a rigid linker, and a pendant amine for reactivity with a carboxylic acid on the target ligand. 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 pendant 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 DiscoveryImpact of linker length on the activity of PROTACs
  • Legal Information: PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Compare Similar Items

Show Difference

Img

Sigma Aldrich

920754

--


ligand:
C5 Lenalidomide

Quality Level:
100

form:
solid

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(C4=CC=C(CN5CCNCC5)C=C4)=O)=CC=C31.Cl

Img

Sigma Aldrich

920762

--


ligand:
VH032

Quality Level:
100

form:
solid

reaction suitability:
reactivity: carboxyl reactivereagent type: ligand-linker conjugate

functional group:
amine

storage temp.:
2-8°C

SMILES string:
CC(N=CS1)=C1C2=CC=C(CNC([C@@H]3C[C@@H](O)CN3C([C@@H](NC(C4=CC=C(CN5CC[ClH](CC5)=N)C=C4)=O)C(C)(C)C)=O)=O)C=C2

Img

Sigma Aldrich

920789

--


ligand:
pomalidomide

Quality Level:
100

form:
powder or crystals

reaction suitability:
reactivity: carboxyl reactivereagent type: ligand-linker conjugate

functional group:
amine

storage temp.:
2-8°C

SMILES string:
O=C(N(C1CCC(NC1=O)=O)C2=O)C3=C2C=CC=C3NC(CC4=CC=C(OCCCN5CCNCC5)N=C4)=O.Cl

Img

Sigma Aldrich

920797

≥95%...


ligand:
C5 Lenalidomide

Quality Level:
100

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(CC4=CC=C(OCCCN5CCNCC5)N=C4)=O)=CC=C31.Cl