Labetalol-d5 (hydrochloride)

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Labetalol-d₅ (hydrochloride)

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Cat No: 31609

Biochemicals - Isotopically Labeled Standards

Labetalol-d5 is intended for use as an internal standard for the quantification of labetalol (Item No. 20249) by GC- or LC-MS. Labetalol is an adrenergic receptor (AR) antagonist.{54376} It inhibits agonist-induced contraction of rabbit aortic strips,...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

2-hydroxy-5-(1-hydroxy-2-((4-(phenyl-d5)butan-2-yl)amino)ethyl)benzamide, monohydrochloride

Correlated keywords:

36894-69-6 GCMS LCMS Deuturium deuterated SCH15719W AH5158A ?ARS ?1ARs ?2ARS vaso-relaxation

Product Overview:
Labetalol-d5 is intended for use as an internal standard for the quantification of labetalol (Item No. 20249) by GC- or LC-MS. Labetalol is an adrenergic receptor (AR) antagonist.{54376} It inhibits agonist-induced contraction of rabbit aortic strips, decreases in contractile force in isolated guinea pig atria, and vasorelaxation in isolated guinea pig tracheal strips (pA2s = 6.99, 7.68, and 7.54, respectively), tissues that endogenously express high levels of α-, β1-, and β2-ARs, respectively. Labetalol (2.5-25 mg/kg) reduces blood pressure in spontaneously hypertensive rats. It reduces blood pressure in DOC-salt rats, two-kidney Goldblatt rats, and one-kidney dogs. Labetalol (5 mg/kg) reduces infarct size in a dog model of myocardial infarction induced by occlusion of the left anterior descending artery. Topical administration of labetalol (0.25-1% v/v) reduces intraocular pressure in rabbits. Formulations containing labetalol have been used in the treatment of hypertension.

Size	1 mg
Shipping	dry ice
Molecular Formula	C₁₉H₁₉D₅N₂O₃ • HCl
SMILES	OC1=CC=C(C(CNC(C)CCC2=C([2H])C([2H])=C([2H])C([2H])=C2[2H])O)C=C1C(N)=O.Cl
Molecular Weight	369,9
Formulation	A solid
Purity	≥99% deuterated forms (d1-d5)
Custom Code	3822.19
UNSPSC code	12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.