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rac Felodipine-[d3]

General Information
Catalog: BLP-013030
CAS: 1189970-31-7
Molecular Formula: C18H16D3Cl2NO4
Molecular Weight: 387.28
Chemical Structure
rac Felodipine-[d3]
Description rac Felodipine-[d3] is the labelled analogue of rac Felodipine, which could be used as a dihydropyridine calcium channel blocker.
Synonyms Felodipine D3; 4-(2,3-Dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic Acid Ethyl Methyl Ester-d3; rac Felodipine-(Methoxy-d3); (±)-Felodipine-d3
IUPAC Name 3-O-ethyl 5-O-(trideuteriomethyl) 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
Related CAS 72509-76-3 (unlabelled)
Canonical SMILES CCOC(=O)C1=C(NC(=C(C1C2=C(C(=CC=C2)Cl)Cl)C(=O)OC)C)C
InChI InChI=1S/C18H19Cl2NO4/c1-5-25-18(23)14-10(3)21-9(2)13(17(22)24-4)15(14)11-7-6-8-12(19)16(11)20/h6-8,15,21H,5H2,1-4H3/i4D3
InChI Key RZTAMFZIAATZDJ-GKOSEXJESA-N
Melting Point >124°C (dec.)
Purity 95% by HPLC; 98% atom D
Solubility Soluble in Chloroform (Slightly), Methanol (Slightly, Heated)
Appearance Light Yellow Solid
Storage Store at -20°C

Rac Felodipine-[d3], a deuterated derivative of felodipine employed in the treatment of hypertension and angina pectoris, boasts a wide array of applications in the medical field. Here are the key applications of rac Felodipine-[d3]:

Pharmacokinetics Studies: Serving as a cornerstone in pharmacokinetic explorations, rac Felodipine-[d3] significantly enhances the understanding of drug absorption, distribution, metabolism, and excretion (ADME). Its deuterium labeling enables precise tracking and differentiation from the non-deuterated drug, ultimately facilitating the development of more efficacious and safer dosing regimens. This sophisticated methodology stands as indispensable in propelling pharmaceutical research forward and optimizing therapeutic interventions.

Metabolite Analysis: The deuterium-labeled rac Felodipine-[d3] emerges as a valuable asset in discerning drug metabolites amidst a sea of other compounds in biological samples. This capability proves particularly advantageous in identifying and quantifying metabolites within complex biological matrices such as blood or urine, elevating the precision and efficiency of metabolic profiling in both clinical and preclinical settings. The incorporation of deuterium atoms empowers researchers to unravel intricate metabolic pathways and unveil crucial insights for drug development.

Bioavailability Studies: Within the domain of bioavailability assessments, rac Felodipine-[d3] assumes a pivotal role in comparing the rate and extent of drug absorption across various formulations. By acting as a reliable internal standard, the deuterated version ensures consistent and accurate measurements, paving the way for evaluating generic drugs and alternative formulations. This application stands essential for optimizing drug delivery strategies and enhancing therapeutic outcomes through rigorous bioavailability studies.

Drug-Drug Interaction Studies: The utilization of rac Felodipine-[d3] facilitates comprehensive investigations into potential drug-drug interactions by establishing a clear differentiation between the administered drug and its deuterated analogue. These studies shed light on how concurrent medications may impact the metabolism or efficacy of felodipine, guiding the development of prescribing guidelines and safeguarding patient safety. The comprehensive insights gleaned from drug-drug interaction studies underscore the significance of precision medicine and individualized treatment approaches in modern healthcare practices.

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