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3-Amino-6-bromo-4-(2-chlorophenyl)-2(1H)-quinolinone-[d5]

General Information
Catalog: BLP-006395
CAS: 1794793-32-0
Molecular Formula: C15H5D5BrClN2O
Molecular Weight: 354.64
Chemical Structure
3-Amino-6-bromo-4-(2-chlorophenyl)-2(1H)-quinolinone-[d5]
Description 3-Amino-6-bromo-4-(2-chlorophenyl)-2(1H)-quinolinone-[d5] is the labelled analogue of 3-Amino-6-bromo-4-(2-chlorophenyl)-2(1H)-quinolinone, which is an impurity of Phenazepam.
Synonyms 3-Amino-6-bromo-4-(2-chlorophenyl)-2(1H)-quinolinone-d5
IUPAC Name 3-amino-6-bromo-4-(2-chloro-3,4,5,6-tetradeuteriophenyl)-8-deuterio-1H-quinolin-2-one
Related CAS 86636-71-7 (unlabelled)
Canonical SMILES C1=CC=C(C(=C1)C2=C(C(=O)NC3=C2C=C(C=C3)Br)N)Cl
InChI InChI=1S/C15H10BrClN2O/c16-8-5-6-12-10(7-8)13(14(18)15(20)19-12)9-3-1-2-4-11(9)17/h1-7H,18H2,(H,19,20)/i1D,2D,3D,4D,6D
InChI Key RXPHLIAWRAZJSH-SNOLXCFTSA-N
Melting Point >300°C (dec.)
Purity 98%
Solubility Soluble in DMSO, Ethyl Acetate, Methanol
Appearance White Solid
Storage Store at 2-8°C

3-Amino-6-bromo-4-(2-chlorophenyl)-2(1H)-quinolinone-[d5], a compound utilized in scientific research, particularly in the field of medicinal chemistry and pharmaceuticals, possesses diverse applications. Here are key applications presented with a high degree of perplexity and burstiness:

Pharmaceutical Research: Serving as a stable isotope-labeled analog, this compound aids in drug development and metabolic studies. It functions as a reference compound or internal standard in mass spectrometry analyses, facilitating accurate quantification of related drugs or metabolites. This critical application delves into drug absorption, distribution, metabolism, and excretion (ADME) properties, pivotal in both preclinical and clinical trials.

Drug Metabolism Studies: Playing a pivotal role in exploring the metabolic pathways of potential drug candidates, 3-Amino-6-bromo-4-(2-chlorophenyl)-2(1H)-quinolinone-[d5] assists researchers in tracing the conversion and breakdown of quinolinone derivatives in biological samples. This knowledge is instrumental in identifying active metabolites and investigating potential toxicological concerns, crucial for drug development and safety evaluations.

Protein Binding Studies: In the realm of pharmacology, this compound is harnessed to evaluate binding affinity and interactions with target proteins, such as receptors or enzymes. By unraveling binding dynamics, scientists can craft compounds with enhanced efficacy and safety profiles, revolutionizing the landscape of drug design. Such studies pave the way for the development of cutting-edge therapeutic agents with improved efficacy and safety profiles.

Chemical Biology: The labeled form of this quinolinone compound plays a pivotal role in elucidating biological processes at the molecular level. Researchers leverage it in cellular assays to monitor compound distribution, uptake, and localization within cells, providing a clear map of biological pathways. This precision aids in the understanding of cellular mechanisms critical for disease intervention, adding depth to our knowledge of intricate biological processes.

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