Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-013988 |
CAS: 1309283-20-2 |
Molecular Formula: C14H15D7N2O3 |
Molecular Weight: 273.38 |
Chemical Structure |
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Description | (S)-Atenolol-[d7] is the labelled analogue of (S)-Atenolol, which is a selective β-adrenergic blocker and could be used as an antihypertensive agent. |
Synonyms | (S)-Atenolol-d7 (Iso-propyl-d7); 4-[(2S)-2-Hydroxy-3-[(1-methylethyl-d7)amino]propoxy]benzeneacetamide; (-)-Atenolol-d7; Esatenolol-d7; S-(-)-Atenolol-d7 |
IUPAC Name | 2-[4-[(2S)-3-(1,1,1,2,3,3,3-heptadeuteriopropan-2-ylamino)-2-hydroxypropoxy]phenyl]acetamide |
Related CAS | 93379-54-5 (unlabelled) |
Canonical SMILES | CC(C)NCC(COC1=CC=C(C=C1)CC(=O)N)O |
InChI | InChI=1S/C14H22N2O3/c1-10(2)16-8-12(17)9-19-13-5-3-11(4-6-13)7-14(15)18/h3-6,10,12,16-17H,7-9H2,1-2H3,(H2,15,18)/t12-/m0/s1/i1D3,2D3,10D |
InChI Key | METKIMKYRPQLGS-FAPHKGRVSA-N |
Melting Point | 151-153°C |
Purity | 95% by HPLC; 98% atom D |
Solubility | Soluble in DMSO, Methanol |
Appearance | White Solid |
Storage | Store at -20°C |
(S)-Atenolol-[d7], a deuterated version of the beta-blocker atenolol, finds extensive use in both research and preclinical environments. Here are the key applications of (S)-Atenolol-[d7]:
Pharmacokinetic Studies: Delving into the intricate realm of pharmacokinetics, (S)-Atenolol-[d7] serves as a vital tool for exploring the absorption, distribution, metabolism, and excretion (ADME) of atenolol. Through deuterium labeling, researchers can distinguish this variant from the non-labeled drug within the body, shedding light on the drug’s behavior and aiding in the optimization of dosing regimens.
Bioavailability Assessment: In the realm of bioavailability studies, (S)-Atenolol-[d7] takes center stage, offering insights into the efficiency of atenolol formulations. By scrutinizing the blood plasma levels of deuterated and non-deuterated atenolol, researchers can infer the performance of drug delivery systems, a crucial step in the development of novel formulations with enhanced therapeutic profiles.
Drug Interaction Studies: Unraveling the complexities of drug interactions, (S)-Atenolol-[d7] plays a pivotal role in evaluating potential interactions between atenolol and other compounds. By administering deuterated atenolol alongside other drugs, researchers can gauge how these compounds impact the pharmacokinetics of atenolol, ensuring the safety and efficacy of multi-drug therapeutic regimens.
Metabolic Pathway Analysis: Dive into the depths of metabolic pathways with (S)-Atenolol-[d7], leveraging its deuterium labeling to illuminate the biotransformation of atenolol within the body. By tracking the metabolic journey of atenolol, researchers can pinpoint the specific enzymes involved in its metabolism, offering valuable insights into metabolic profiles and the potential side effects of this drug.
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