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-013929 |
Molecular Formula: C20H18D4ClF3N4O |
Molecular Weight: 430.89 |
Chemical Structure |
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Description | Flibanserin-[d4] HCl is an isotope labelled derivative of Flibanserin. Flibanserin is used for the treatment of pre-menopausal women with hypoactive sexual desire disorder. |
Synonyms | 1-(2-(4-(3-(Trifluoromethyl)phenyl)piperazin-1-yl)ethyl)-1H-benzo[d]imidazol-2(3H)-one-d4 hydrochloride |
Related CAS | 147359-76-0 (unlabelled) |
Canonical SMILES | O=C1N(C([2H])([2H])C([2H])([2H])N2CCN(C3=CC(C(F)(F)F)=CC=C3)CC2)C4=CC=CC=C4N1.Cl |
InChI | InChI=1S/C20H21F3N4O.ClH/c21-20(22,23)15-4-3-5-16(14-15)26-11-8-25(9-12-26)10-13-27-18-7-2-1-6-17(18)24-19(27)28;/h1-7,14H,8-13H2,(H,24,28);1H/i10D2,13D2; |
InChI Key | XGAGFLQFMFCIHZ-BMJFOILFSA-N |
Purity | 95% by HPLC; 99% atom D |
Solubility | Soluble in DMSO (Slightly), Methanol (Slightly) |
Storage | Store at -20°C |
Flibanserin-[d4] hydrochloride, a deuterium-labeled analogue of flibanserin, exemplifies versatility with its primary applications spanning various research domains. Here are the key applications of Flibanserin-[d4] hydrochloride:
Pharmacokinetic Studies: Interwoven within the intricate fabric of pharmacokinetic inquiries, Flibanserin-[d4] hydrochloride assumes a pivotal role in unraveling the complexities of drug absorption, distribution, metabolism, and excretion (ADME) of flibanserin. Its deuterium labeling enables meticulous tracing within biological systems through mass spectrometry, facilitating the generation of precise and critical data on drug behavior crucial for safety and efficacy evaluations.
Drug Metabolism Research: By harnessing Flibanserin-[d4] hydrochloride, researchers embark on a voyage to explore the metabolic pathways of flibanserin, identifying its diverse metabolites and unraveling their potential pharmacological or toxicological impacts. The stable isotope labeling assists in discriminating between the parent compound and its metabolites, providing vital information for the development of safer and more efficient drug formulations.
Quality Control in Manufacturing: Positioned within the intricate tapestry of pharmaceutical manufacturing, Flibanserin-[d4] hydrochloride assumes the mantle of an internal standard for quality control and assurance purposes. It plays a critical role in maintaining consistency and precision in the analytical methods used to quantify flibanserin in both bulk drug substances and finished pharmaceutical products, ensuring adherence to purity and potency specifications.
Neuropharmacology Research: Nestled in the realm of neuropharmacology, Flibanserin-[d4] hydrochloride emerges as a prominent player in unraveling the mechanism of action of the drug within the brain and its influence on neurotransmitter systems. Through the utilization of the deuterium-labeled analogue, researchers can meticulously assess the interactions of flibanserin with diverse brain receptors and pathways, fostering a deeper understanding of its therapeutic capabilities and potential side effects.
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