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934410

Sigma-Aldrich

Carbamic acid, N-[2-(1-piperazinyl)ethyl]-, 1,1-dimethylethyl ester

≥95%

Sinônimo(s):

1,1-Dimethylethyl N-[2-(1-piperazinyl)ethyl]carbamate, 1-(2-((tert-Butoxycarbonyl)amino)ethyl)piperazine, tert-Butyl N-(2-(piperazin-1-yl)ethyl)carbamate, tert-Butyl [2-(piperazin-1-yl)ethyl]carbamate, Carbamic acid, [2-(1-piperazinyl)ethyl]-, 1,1-dimethylethyl ester

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About This Item

Fórmula empírica (Notação de Hill):
C11H23N3O2
Número CAS:
140447-78-5
Peso molecular:
229.32
Número MDL:
MFCD02683050
Código UNSPSC:
12352108
NACRES:
NA.21

Nível de qualidade

100

Ensaio

≥95%

Formulário

powder

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

N1(CCNCC1)CCNC(=O)OC(C)(C)C

InChI

1S/C11H23N3O2/c1-11(2,3)16-10(15)13-6-9-14-7-4-12-5-8-14/h12H,4-9H2,1-3H3,(H,13,15)

chave InChI

VPOIPCJBJNWHSJ-UHFFFAOYSA-N

Aplicação

A functionalized cereblon ligand for development of Thalidomide based PROTACs. Allows rapid conjugation with carboxyl linkers due to presence of amine group via peptide coupling reactions. Amenable for linker attachement via reductive amination, and a basic building block for making protein degrader library.

Technology Spotlight:

Degrader Building Blocks for Targeted Protein Degradation

Protein Degrader Building Blocks

Outras notas

Targeted Protein Degradation by Small Molecules
Destruction of DNA-Binding Proteins by Programmable Oligonucleotide PROTAC (O′PROTAC): Effective Targeting of LEF1 and ERG
Small-Molecule PROTACS: New Approaches to Protein Degradation
Targeted Protein Degradation: from Chemical Biology to Drug Discovery
Impact of linker length on the activity of PROTACs

Informações legais

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

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Certificados de análise (COA)

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Daniel P Bondeson et al.
Annual review of pharmacology and toxicology, 57, 107-123 (2016-10-13)
Protein homeostasis networks are highly regulated systems responsible for maintaining the health and productivity of cells. Whereas therapeutics have been developed to disrupt protein homeostasis, more recently identified techniques have been used to repurpose homeostatic networks to effect degradation of

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