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-003668 |
CAS: 1346605-02-4 |
Molecular Formula: C18H17D30ClN3O |
Molecular Weight: 332.84 |
Chemical Structure |
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Description | Ondansetron-[d3] Hydrochloride, is the labelled analogue of Ondansetron, which is a serotonin 5-HT3 receptor antagonist used mainly as an antiemetic. |
Synonyms | Ondansetron-d3 Hydrochloride Salt |
IUPAC Name | 3-[(2-methylimidazol-1-yl)methyl]-9-(trideuteriomethyl)-2,3-dihydro-1H-carbazol-4-one;hydrochloride |
Related CAS | 99614-01-4 (unlabelled) |
Canonical SMILES | CC1=NC=CN1CC2CCC3=C(C2=O)C4=CC=CC=C4N3C.Cl |
InChI | InChI=1S/C18H19N3O.ClH/c1-12-19-9-10-21(12)11-13-7-8-16-17(18(13)22)14-5-3-4-6-15(14)20(16)2;/h3-6,9-10,13H,7-8,11H2,1-2H3;1H/i2D3; |
InChI Key | MKBLHFILKIKSQM-MUTAZJQDSA-N |
Boiling Point | 546.0±30.0°C at 760 mmHg |
Melting Point | 172-174°C |
Purity | 98% by CP; 98% atom D |
Density | 1.3±0.1 g/cm3 |
Solubility | Soluble in DMSO, Methanol, Water |
Appearance | White to Off-white Solid |
Storage | Store at 2-8°C |
Ondansetron-[d3] Hydrochloride, a deuterated variant of ondansetron, a medication renowned for its anti-nausea and anti-vomiting properties, has diverse applications. Here are key applications described with a high degree of perplexity and burstiness:
Pharmacokinetic Studies: Utilizing Ondansetron-[d3] Hydrochloride in pharmacokinetic studies allows researchers to delve into the intricate processes of drug absorption, distribution, metabolism, and excretion within the human body. The deuterated form, with its unique mass differential, facilitates precise tracking in mass spectrometry, making it easily discernible from its non-deuterated counterpart. This distinction is essential for optimizing dosages and comprehending drug interactions in therapeutic contexts.
Clinical Research: In the realm of clinical research, Ondansetron-[d3] Hydrochloride serves as a vital internal standard that guarantees the accuracy and dependability of analytical methodologies. By acting as a benchmark compound, it aids in quantifying ondansetron levels in biological specimens. This application plays a crucial role in validating bioanalytical assays and ensuring consistent outcomes across various research endeavors.
Antiemetic Therapy: While Ondansetron-[d3] Hydrochloride isn't used as a direct therapeutic intervention, it offers valuable insights that can elevate antiemetic treatments to new heights. Through an exploration of its pharmacokinetics, researchers can craft enhanced formulations of ondansetron that exhibit superior efficacy and reduced adverse effects.
Drug Development: Within the domain of drug development research, Ondansetron-[d3] Hydrochloride plays a pivotal role in unraveling metabolic pathways and potential drug-drug interactions. With its stable isotopic labeling, it aids in the identification and quantification of metabolites, offering a deeper understanding of ondansetron's metabolic intricacies.
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