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Merck
모든 사진(1)

Key Documents

930695

Sigma-Aldrich

4-Aminomethyl-2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione hydrochloride

≥95%

동의어(들):

1H-Isoindole-1,3(2H)-dione, 4-(aminomethyl)-2-(2,6-dioxo-3-piperidinyl) hydrochloride

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About This Item

실험식(Hill 표기법):
C14H13N3O4 · xHCl
CAS Number:
Molecular Weight:
287.27 (free base basis)
MDL number:
UNSPSC 코드:
12352101
NACRES:
NA.26

Quality Level

분석

≥95%

형태

powder

반응 적합성

reagent type: ligand

작용기

amine

저장 온도

2-8°C

SMILES string

NCC1=C(C(N(C2CCC(NC2=O)=O)C3=O)=O)C3=CC=C1

애플리케이션

4-Aminomethyl-2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione hydrochloride is a functionalized Cereblon ligand used for development of protein degrader building blocks. Contains a terminal amine group, allowing rapid conjugation of carboxyl containing linkers. A basic building block for development of a protein degrader library.

법적 정보

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

픽토그램

Health hazard

신호어

Danger

유해 및 위험 성명서

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


시험 성적서(COA)

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DNA-binding proteins, including transcription factors (TFs), play essential roles in various cellular processes and pathogenesis of diseases, deeming to be potential therapeutic targets. However, these proteins are generally considered undruggable as they lack an enzymatic catalytic site or a ligand-binding
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Annual review of pharmacology and toxicology, 57, 107-123 (2016-10-13)
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Conventional genetic approaches have provided a powerful tool in the study of proteins. However, these techniques often preclude selective manipulation of temporal and spatial protein functions, which is crucial for the investigation of dynamic cellular processes. To overcome these limitations
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Angewandte Chemie (International ed. in English), 55(6), 1966-1973 (2016-01-13)
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Traditional pharmaceutical drug discovery is almost exclusively focused on directly controlling protein activity to cure diseases. Modulators of protein activity, especially inhibitors, are developed and applied at high concentration to achieve maximal effects. Thereby, reduced bioavailability and off-target effects can

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