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Merck
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M-137

Supelco

Mycophenolic acid-d3 solution

100 μg/mL in acetonitrile, ampule of 1 mL, certified reference material, Cerilliant®

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About This Item

Formule empirique (notation de Hill):
C17H17O6D3
Numéro CAS:
Poids moléculaire :
323.36
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

certified reference material

Forme

liquid

Caractéristiques

Snap-N-Spike®/Snap-N-Shoot®

Conditionnement

ampule of 1 mL

Fabricant/nom de marque

Cerilliant®

Concentration

100 μg/mL in acetonitrile

Technique(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

Application(s)

clinical testing

Format

single component solution

Température de stockage

−20°C

Chaîne SMILES 

C/C(CCC(O)=O)=C\CC1=C(O)C2=C(COC2=O)C(C)=C1OC([2H])([2H])[2H]

InChI

1S/C17H20O6/c1-9(5-7-13(18)19)4-6-11-15(20)14-12(8-23-17(14)21)10(2)16(11)22-3/h4,20H,5-8H2,1-3H3,(H,18,19)/b9-4+/i3D3

Clé InChI

HPNSFSBZBAHARI-HZIIEIAOSA-N

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Description générale

A Certified Spiking Solution® and internal standard for use in the quantitation of mycophenolic acid levels in serum or whole blood by LCMS. Assayed in therapeutic drug monitoring to ensure patients remain within the drug′s therapeutic range, mycophenolic acid is an immunosuppressant drug and the active metabolite of the prodrug mycophenolate mofetil.

Application


  • Ultra Performance Liquid Chromatography in Pharmacokinetics: A study utilizes ultra-performance liquid chromatography tandem mass spectrometry (UPLC/MS/MS) to determine mycophenolic acid in human plasma, enhancing drug monitoring in clinical settings. This technique offers high sensitivity and specificity, critical for therapeutic drug monitoring of immunosuppressants used in transplant medicine (Upadhyay et al., 2014).

  • Comparative Methods for Immunosuppressant Monitoring: This research compares two rapid ultra-performance liquid chromatography/tandem mass spectrometry methods for therapeutic drug monitoring of immunosuppressants, including mycophenolic acid, against traditional immunoassay techniques. The study highlights the precision and faster turnaround times of UPLC/MS/MS methods, offering significant improvements in patient care management for those undergoing immunosuppressive therapy (Tszyrsznic et al., 2013).

Informations légales

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
CERTIFIED SPIKING SOLUTION is a registered trademark of Cerilliant Corporation
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

FlameExclamation mark

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

35.6 °F - closed cup

Point d'éclair (°C)

2 °C - closed cup


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

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Nature structural & molecular biology, 25(9), 787-796 (2018-08-22)
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L L Hernandez et al.
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Serotonin (5-HT), a neurotransmitter synthesized from tryptophan, has been proposed as a feedback inhibitor of lactation. We determined that the gene coding for tryptophan hydroxylase 1, the rate-limiting enzyme for 5-HT synthesis, is expressed in bovine mammary epithelial cells in
Lingyan Xing et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 35(44), 14794-14808 (2015-11-06)
Modulation of connectivity formation in the developing brain in response to external stimuli is poorly understood. Here, we show that the raphe nucleus and its serotonergic projections regulate pathfinding of commissural axons in zebrafish. We found that the raphe neurons

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