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P4902

Sigma-Aldrich

2-Phenylethyl β-D-thiogalactoside

≥98% (TLC)

Synonyme(s) :

PETG, Phenethyl β-D-thiogalactoside

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About This Item

Formule empirique (notation de Hill):
C14H20O5S
Numéro CAS:
63407-54-5
Poids moléculaire :
300.37
Numéro Beilstein :
20033
Numéro MDL:
MFCD00057554
Code UNSPSC :
12352201
ID de substance PubChem :
24898569
Nomenclature NACRES :
NA.25

Niveau de qualité

200

Pureté

≥98% (TLC)

Forme

powder

Activité optique

[α]/D -33.00 to -27.00°, c = 9.00-11.00 mg/mL in methanol

Technique(s)

thin layer chromatography (TLC): suitable

Couleur

white

Solubilité

methanol: 49.00-51.00 mg/mL, clear, colorless

Température de stockage

2-8°C

Chaîne SMILES 

OC[C@H]1O[C@@H](SCCc2ccccc2)[C@H](O)[C@@H](O)[C@H]1O

InChI

1S/C14H20O5S/c15-8-10-11(16)12(17)13(18)14(19-10)20-7-6-9-4-2-1-3-5-9/h1-5,10-18H,6-8H2/t10-,11+,12+,13-,14+/m1/s1

Clé InChI

ZNAMMSOYKPMPGC-HTOAHKCRSA-N

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Description générale

2-Phenylethyl β-D-thiogalactoside is a cell-permable inhibitor of the reporter enzyme β-galactosidase.

Application

2-Phenylethyl β-D-thiogalactoside has been used in a study to assess subnanoliter enzymatic assays on microarrays. It has also been used in a study that investigated the integration of on-column immobilized enzyme reactor in microchip electrophoresis.

Autres remarques

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Certificats d'analyse (COA)

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Todd Galbraith et al.
Biotechnology journal, 14(1), e1800306-e1800306 (2018-11-30)
There is a strong clinical need to develop small-caliber tissue-engineered blood vessels for arterial bypass surgeries. Such substitutes can be engineered using the self-assembly approach in which cells produce their own extracellular matrix (ECM), creating a robust vessel without exogenous
Pranav R H Joshi et al.
Molecular therapy. Methods & clinical development, 13, 279-289 (2019-03-20)
Despite numerous advancements in production protocols, manufacturing AAV to meet exceptionally high demand (1016-1017 viral genomes [VGs]) in late clinical stages and for eventual systemic delivery poses significant challenges. Here, we report an efficient, simple, scalable, robust AAV5 production process
Stefan Schwenk et al.
Nucleic acids research, 46(11), 5837-5849 (2018-04-05)
The success of Mycobacterium tuberculosis relies on the ability to switch between active growth and non-replicating persistence, associated with latent TB infection. Resuscitation promoting factors (Rpfs) are essential for the transition between these states. Rpf expression is tightly regulated as
Peter N Ciaccia et al.
Frontiers in microbiology, 9, 2103-2103 (2018-09-27)
The human pathogen, Vibrio cholerae, belongs to the 10% of bacteria in which the genome is divided. Each of its two chromosomes, like bacterial chromosomes in general, replicates from a unique origin at fixed times in the cell cycle. Chr1
Kyung-Han Lee et al.
European journal of nuclear medicine and molecular imaging, 31(3), 433-438 (2004-01-28)
There has recently been increasing interest in the development of radioprobes that specifically target proteins transcribed from expression of reporter genes of interest. The purpose of this study was to develop a radioprobe that targets one of the most widely
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