Ugrás a tartalomra
Merck

910007

Sigma-Aldrich

20-Azido-3,6,9,12,15,18-hexaoxaicosanoic acid

95%

Szinonimák:

Azido-PEG6-CH2CO2H, Azido-PEG6-acid, N3-PEG6-CH2COOH

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

Tapasztalati képlet (Hill-képlet):
C14H27N3O8
CAS-szám:
Molekulatömeg:
365.38
UNSPSC kód:
12352106

Teszt

95%

form

(Liquid or Semi-Solid or Paste or Solid)

reakcióalkalmasság

reaction type: click chemistry
reagent type: cross-linking reagent

funkcionális csoport

azide
carboxylic acid

tárolási hőmérséklet

2-8°C

SMILES string

OC(COCCOCCOCCOCCOCCOCCN=[N+]=[N-])=O

Alkalmazás

This heterobifunctional, PEGylated crosslinker 20-Azido-3,6,9,12,15,18-hexaoxaicosanoic acid features a carboxyl group at one end and azide at the other. The hydrophillic PEG linker facilitates solubility in biological applications. This azido-PEG6-acid linker can be used for bioconjugation or as a building block for synthesis of small molecules, conjugates of small molecules and/or biomolecules, or other tool compounds for chemical biology and medicinal chemistry that require ligation. Examples of applications include its synthetic incorporation into antibody-drug conjugates or proteolysis-targeting chimeras (PROTAC® molecules) for targeted protein degradation.

Jogi információk

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

kapcsolódó termék

Product No.
Leírás
Árazás

Tárolási osztály kódja

10 - Combustible liquids

WGK

WGK 3

Lobbanási pont (F)

Not applicable

Lobbanási pont (C)

Not applicable


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Dokumentumtár megtekintése

Joel Hwang et al.
Chemical communications (Cambridge, England), 50(24), 3159-3162 (2014-01-30)
Oligo(ethylene glycol)-linked light fluorous tags have been found to be optimal for conjugating to glycans for both high-yield enzymatic glycosylation reactions using one-pot multienzyme (OPME) systems and quick product purification using fluorous solid-phase extraction (FSPE) cartridges. The combination of OPME
Yong Ma et al.
Bioconjugate chemistry, 21(11), 1994-1999 (2010-10-14)
A surface-bound cytomimetic assembly based on chemically selective and biocompatible immobilization and further modification of intact liposome is described. Liposomes carrying PEG-triphenylphosphine were chemoselectively immobilized onto azide-modified glass slides through Staudinger ligation, followed by modification with azide-modified lactose as a
Ryota Sato et al.
Journal of the American Chemical Society, 139(48), 17397-17404 (2017-11-10)
Single-molecule imaging (SMI) has been widely utilized to investigate biomolecular dynamics and protein-protein interactions in living cells. However, multicolor SMI of intracellular proteins is challenging because of high background signals and other limitations of current fluorescence labeling approaches. To achieve
Souad Kachbi-Khelfallah et al.
Beilstein journal of organic chemistry, 12, 1366-1371 (2016-08-26)
The use of nanotechnologies for biomedical applications took a real development during these last years. To allow an effective targeting for biomedical imaging applications, the adsorption of plasmatic proteins on the surface of nanoparticles must be prevented to reduce the
Mingcheng Qian et al.
ChemMedChem, 13(9), 944-956 (2018-02-17)
Currently, there is mounting evidence that intermolecular receptor-receptor interactions may result in altered receptor recognition, pharmacology and signaling. Heterobivalent ligands have been proven useful as molecular probes for confirming and targeting heteromeric receptors. This report describes the design and synthesis

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