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About This Item

Empirical Formula (Hill Notation):
C26H33F2N5O7 · xHCl
Molecular Weight:
565.57 (free base basis)
MDL number:
UNSPSC Code:
12352101
NACRES:
NA.21
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ligand

pomalidomide

Quality Level

Assay

≥95%

form

powder

storage temp.

2-8°C

SMILES string

O=C(C(CC1)N(C2=O)C(C3=C2C=CC=C3NC(COCC(F)(F)COCCCCN4CCNCC4)=O)=O)NC1=O.Cl

InChI

1S/C26H33F2N5O7.ClH/c27-26(28,15-39-13-2-1-10-32-11-8-29-9-12-32)16-40-14-21(35)30-18-5-3-4-17-22(18)25(38)33(24(17)37)19-6-7-20(34)31-23(19)36;/h3-5,19,29H,1-2,6-16H2,(H,30,35)(H,31,34,36);1H

InChI key

VNTZNMLSYIMLPL-UHFFFAOYSA-N

Application

Protein degrader building block Pomalidomide-difluoroPEG1-C4-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 fluorinated linker with both hydrophobic and hydrophilic moieties, 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.

Targeted Protein Degradation

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Repr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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