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915572

Pomalidomide-dipiperazine-NH2 hydrochloride

≥95%

Synonym(s):

4-(4-(4-(2-Aminoethyl)piperazine-1-carbonyl)piperazin-1-yl)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride, Crosslinker−E3 ligase ligand conjugate, Pomalidomide conjugate, Protein degrader building block for PROTAC® research, Template for synthesis of targeted protein degrader

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Size/SKUAvailabilityPrice
50 mg

Estimated to ship onSeptember 01, 2026fromMILWAUKEE

$474.00

About This Item

Empirical Formula (Hill Notation):
C24H31N7O5 · xHCl
Molecular Weight:
497.55 (free base basis)
UNSPSC Code:
12352101
NACRES:
NA.22

$474.00


Estimated to ship onSeptember 01, 2026Details


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ligand

pomalidomide

Quality Segment

assay

≥95%

form

powder

reaction suitability

reactivity: carboxyl reactive, reagent 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=C3N4CCN(C(N5CCN(CCN)CC5)=O)CC4

InChI key

KLJJLERZEMIGTG-UHFFFAOYSA-N

Application

Protein degrader building block Pomalidomide-dipiperazine-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, a rigid linker, 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.

Legal Information

PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license

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This Item
911666909394911658
functional group

amine

functional group

amine

functional group

azide

functional group

amine

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

reaction suitability

-

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

assay

≥95%

assay

≥95%

assay

≥95%

assay

≥95%

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

form

powder

form

powder

form

powder

form

powder


Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable



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Questions

  1. Can the mentioned number (12.9%) be considered as the percentage of HCl, given that the amount of HCl in general is typically determined by titration? Additionally, the only test listed is "Titration with AgNO3," but it does not specify what is being titrated.

    1 answer
    1. The AgNO3 titration is used to determine the HCl content in the molecule, and the mentioned 12.9% is indeed the HCl content.

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