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-013938 |
Molecular Formula: C27H36D3ClN2O4 |
Molecular Weight: 494.09 |
Chemical Structure |
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Description | One of the isotopic labelled form of (±)-Verapamil, which is a calcium channel blocker and could be used as antiarrhythmic and antihypertensive agent. |
Synonyms | 5-((3,4-Dimethoxyphenethyl)(methyl-d3)amino)-2-(3,4-dimethoxyphenyl)-2-isopropylpentanenitrile monohydrochloride |
IUPAC Name | 2-(3,4-dimethoxyphenyl)-5-[2-(3,4-dimethoxyphenyl)ethyl-(trideuteriomethyl)amino]-2-propan-2-ylpentanenitrile;hydrochloride |
Related CAS | 152-11-4 (unlabelled) 1185032-80-7 (d6-labelled) |
Canonical SMILES | CC(C)C(CCCN(C)CCC1=CC(=C(C=C1)OC)OC)(C#N)C2=CC(=C(C=C2)OC)OC.Cl |
InChI | InChI=1S/C27H38N2O4.ClH/c1-20(2)27(19-28,22-10-12-24(31-5)26(18-22)33-7)14-8-15-29(3)16-13-21-9-11-23(30-4)25(17-21)32-6;/h9-12,17-18,20H,8,13-16H2,1-7H3;1H/i3D3; |
InChI Key | DOQPXTMNIUCOSY-FJCVKDQNSA-N |
Purity | 95% by HPLC; 98% atom D |
Storage | Store at -20°C |
(±)-Verapamil-[d3] HCl, a deuterated variant of verapamil hydrochloride, plays a pivotal role in research and preclinical pharmacology. Here are the key applications:
Pharmacokinetic Studies: Widely utilized in pharmacokinetic investigations, (±)-Verapamil-[d3] HCl sheds light on the absorption, distribution, metabolism, and excretion (ADME) dynamics of verapamil. The deuterium labeling enables precise tracking through mass spectrometry, facilitating the determination of the drug’s bioavailability and the optimization of dosing regimens.
Drug-Drug Interaction Studies: Delving into drug-drug interactions, researchers employ (±)-Verapamil-[d3] HCl to explore verapamil’s effects on the metabolism of other drugs. By scrutinizing how verapamil perturbs cytochrome P450 enzymes, scientists can anticipate potential adverse interactions, which is crucial for ensuring the safety and efficacy of combined drug therapies.
Cardiovascular Research: Within cardiovascular investigations, (±)-Verapamil-[d3] HCl serves as a key tool in examining the impact of verapamil on cardiac function and blood pressure. Its role as a calcium channel blocker is instrumental in deciphering the mechanisms underlying conditions like hypertension and arrhythmias. Through observing its effects in preclinical models, researchers embark on exploring novel therapeutic avenues.
Toxicological Studies: Employed in toxicological inquiries, (±)-Verapamil-[d3] HCl aids in assessing the safety profile of verapamil. The use of the deuterated form facilitates the differentiation between the parent compound and its metabolites, enhancing the identification of potential toxicities and the establishment of safe concentration thresholds for clinical applications.
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