CAS 540729-08-6

(3S,4S,5S,6S)-3,4,5-trihydroxy-6-[3-methyl-4-[(1R)-3-(methylamino)-1-phenyl-propoxy]phenoxy]tetrahydropyran-2-carboxylic acid

Description:

The chemical substance with the name "(3S,4S,5S,6S)-3,4,5-trihydroxy-6-[3-methyl-4-[(1R)-3-(methylamino)-1-phenyl-propoxy]phenoxy]tetrahydropyran-2-carboxylic acid" and CAS number 540729-08-6 is a complex organic compound characterized by its multiple hydroxyl groups and a carboxylic acid functional group, which contribute to its hydrophilicity and potential biological activity. The presence of a tetrahydropyran ring indicates a cyclic structure that can influence its stereochemistry and reactivity. The compound also features a phenoxy group, which may enhance its interaction with biological targets, potentially making it relevant in medicinal chemistry. The methylamino and phenyl substituents suggest that it may exhibit specific pharmacological properties, possibly acting as a ligand or inhibitor in biochemical pathways. Overall, this compound's intricate structure and functional groups suggest it could have significant implications in drug design and development, particularly in targeting specific receptors or enzymes in biological systems.

Formula: C₂₃H₂₉NO₈

InChI: InChI=1/C23H29NO8/c1-13-12-15(30-23-20(27)18(25)19(26)21(32-23)22(28)29)8-9-16(13)31-17(10-11-24-2)14-6-4-3-5-7-14/h3-9,12,17-21,23-27H,10-11H2,1-2H3,(H,28,29)/t17-,18+,19+,20+,21?,23-/m1/s1

4''-Hydroxy atomoxetine b-D-glucuronide

CAS: 540729-08-6

Ref: 7W-GC0755

4’-Hydroxy Atomoxetine Glucuronide

CAS: 540729-08-6

Formula: C₂₃H₂₉NO₈

Color and Shape: Off-White Solid

Molecular weight: 447.48

Ref: 4Z-A-255

4’-Hydroxy Atomoxetine β-D-Glucuronide

Controlled Product

CAS: 540729-08-6

Applications A metabolite of Atomoxetine (A791400).
References Wong, D., et al.: J. Pharmacol. Exp. Ther., 222, 61 (1982), Steiner, E., et al.: Clin. Pharmacol. Ther., 44, 431 (1988), Gehlert, D., et al.: Neurosci. Lett., 157, 203 (1993), Kuczenski, R., et al.: J. Neurochem., 68, 2032 (1997), Sauer, J., et al.: Drug Metab. Dispos., 31, 98 (2003),

Formula: C₂₃H₂₉NO₈

Color and Shape: Light Brown

Molecular weight: 447.48

Ref: TR-H802510

4’-Hydroxy Atomoxetine β-D-Glucuronide-d3

Controlled Product

CAS: 540729-08-6

Formula: C₂₃D₃H₂₆NO₈

Color and Shape: Neat

Molecular weight: 450.497

Ref: TR-H802512

4'-Hydroxy atomoxetine b-D-glucuronide

CAS: 540729-08-6

4'-Hydroxy atomoxetine b-D-glucuronide is a synthetic compound that has been modified for use in the synthesis of saccharides and oligosaccharides. The modification is a high-yielding, efficient, and economical method for the preparation of complex carbohydrates. This compound is an intermediate in the synthesis of glycosylations. It can be used for the click modification of proteins or polysaccharides.br>br>
4'-Hydroxy atomoxetine b-D-glucuronide is an intermediate in the synthesis of glycosylations. It can be used for the click modification of proteins or polysaccharides. Click chemistry is a form of chemical reaction used to modify molecules by attaching them to other molecules with similar reactive groups, such as hydroxyl groups, through a process called "click" chemistry. The term was coined by K. Barry Sharpless at Stanford University in 2000 after he demonstrated that certain metal

Formula: C₂₃H₂₉NO₈

Purity: Min. 95%

Molecular weight: 447.49 g/mol

Ref: 3D-MH09752

4\'-Hydroxy Atomoxetine D-glucuronide

CAS: 540729-08-6

Formula: C₂₃H₂₉NO₈

Molecular weight: 447.48

Ref: ST-EA-CP-A30024