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-011605 |
CAS: 1398065-63-8 |
Molecular Formula: C22H18D5ClN2O2 |
Molecular Weight: 387.92 |
Chemical Structure |
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Description | Loratadine-[d5] is the labelled analogue of Loratadine. Loratadine is a histamine H1 receptor antagonist, used to treat allergies. |
Synonyms | Loratadine D5; Loratadine-d5 (ethyl-d5); 4-(8-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinecarboxylic Acid-d5 Ethyl Estere; Claritine-d5; Alavert-d5; Clarityn-d5; Lisino-d5 |
IUPAC Name | 1,1,2,2,2-pentadeuterioethyl 4-(13-chloro-4-azatricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,12,14-hexaen-2-ylidene)piperidine-1-carboxylate |
Related CAS | 79794-75-5 (unlabelled) |
Canonical SMILES | CCOC(=O)N1CCC(=C2C3=C(CCC4=C2N=CC=C4)C=C(C=C3)Cl)CC1 |
InChI | InChI=1S/C22H23ClN2O2/c1-2-27-22(26)25-12-9-15(10-13-25)20-19-8-7-18(23)14-17(19)6-5-16-4-3-11-24-21(16)20/h3-4,7-8,11,14H,2,5-6,9-10,12-13H2,1H3/i1D3,2D2 |
InChI Key | JCCNYMKQOSZNPW-ZBJDZAJPSA-N |
Purity | 95% by HPLC; 99% atom D |
Solubility | Soluble in Chloroform (Slightly), Methanol (Slightly) |
Appearance | White to Off-white Solid |
Storage | Store at -20°C |
Loratadine-[d5], a deuterated iteration of the commonly prescribed antihistamine Loratadine, plays a multifaceted role in the pharmaceutical sphere. Here are the key applications of Loratadine-[d5]:
Pharmacokinetic Studies: Delving deep into the absorption, distribution, metabolism, and excretion (ADME) profiles of Loratadine, the deployment of Loratadine-[d5] in pharmacokinetic studies unveils a realm of possibilities. By harnessing the power of the deuterated variant, researchers embark on a meticulous journey to monitor and discern the drug amidst endogenous compounds in biological samples. This intricate process unravels a comprehensive understanding of drug behavior, paving the way for the optimization of dosage regimens.
Bioanalytical Method Development: Within the intricate landscape of bioanalytical assay development, Loratadine-[d5] emerges as a beacon of reliability. Serving as a crucial internal standard in the realm of mass spectrometry-based quantification of Loratadine, the incorporation of stable isotopic labeling elevates precision and accuracy to unprecedented levels. This meticulous approach enables the precise measurement of Loratadine levels across diverse biological matrices, bolstering the reliability and sensitivity of analytical methods in both clinical and research settings.
Drug-Drug Interaction Studies: At the heart of pharmacological exploration, Loratadine-[d5] takes center stage in the meticulous evaluation of potential drug-drug interactions. Shedding light on the intricate dance of concomitant medications impacting the pharmacokinetics of Loratadine, the deuterated drug serves as a vigilant sentinel. Through astute monitoring and differentiation of metabolic pathways, researchers navigate the labyrinth of interactions between Loratadine and co-administered drugs, ensuring the safe and efficacious use of medications.
Toxicology Research: Within the realm of toxicology inquiries, Loratadine-[d5] emerges as an indispensable tool for unraveling the mysteries of drug metabolism. Serving as a key instrument in tracing and characterizing the metabolites of Loratadine, the utilization of deuterated compounds offers a nuanced perspective on the drug's metabolic destiny and potential toxicity. This profound insight into the interplay between parent drugs and metabolites fuels an accurate assessment of the safety profile associated with Loratadine, safeguarding the well-being of patients and advancing the field of toxicology research.
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