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N-Acetylamonafide-[d6]

General Information
Catalog: BLP-004884
CAS: 1217018-31-9
Molecular Formula: C18H13D6N3O3
Molecular Weight: 331.40
Chemical Structure
N-Acetylamonafide-[d6]
Description N-Acetylamonafide-[d6] is the labelled analogue of N-Acetylamonafide, which is a metabolite of Amonafide. Amonafide is a topoisomerase II inhibitor.
Synonyms N-Acetyl Amonafide-d6; N-[2-[2-(Dimethylamino-d6)ethyl]-2,3-dihydro-1,3-dioxo-1H-benz[de]isoquinolin-5-yl]acetamide; MADE-FA 4512-d6; N-Acetylamonafide-d6
IUPAC Name N-[2-[2-[bis(trideuteriomethyl)amino]ethyl]-1,3-dioxobenzo[de]isoquinolin-5-yl]acetamide
Related CAS 69409-02-5 (unlabelled)
Canonical SMILES CC(=O)NC1=CC2=C3C(=C1)C=CC=C3C(=O)N(C2=O)CCN(C)C
InChI InChI=1S/C18H19N3O3/c1-11(22)19-13-9-12-5-4-6-14-16(12)15(10-13)18(24)21(17(14)23)8-7-20(2)3/h4-6,9-10H,7-8H2,1-3H3,(H,19,22)/i2D3,3D3
InChI Key VQQUFGOEIGXAOM-XERRXZQWSA-N
Solubility Soluble in DMSO
Appearance Pale Yellow Solid
Storage Store at 2-8°C

N-Acetylamonafide-[d6], a nuanced deuterium-labeled derivative of N-acetylamonafide utilized in diverse pharmacological and biochemical investigations, showcases a myriad of applications. Here are key applications of N-Acetylamonafide-[d6] presented with heightened perplexity and burstiness:

Pharmacokinetic Studies: Nestled within the intricate tapestry of pharmacokinetics, N-Acetylamonafide-[d6] plays a pivotal role in meticulously scrutinizing the metabolism and distribution patterns of amonafide and its metabolites. The incorporation of deuterium imparts a heightened precision in tracking the compound within biological systems, facilitating an enriched analysis through mass spectrometry. This refined methodology serves as a compass leading to a deeper comprehension of drug absorption, distribution, metabolism, and elimination dynamics.

Drug Development Research: As a beacon at the forefront of drug development, N-Acetylamonafide-[d6] emerges as a vital instrument for delving into drug interactions and mechanisms of action. Through a detailed dissection of its behavior in cellular and animal models, researchers extract invaluable insights into the potential performance of amonafide derivatives in therapeutic settings. These insights serve as guiding stars for optimizing drug candidates, enhancing their efficacy, and finessing their safety profiles.

Metabolic Pathway Elucidation: Unraveling the labyrinthine pathways of metabolism, N-Acetylamonafide-[d6] is harnessed to probe the acetylation reactions at play. The strategic isotope labeling serves as a torchlight in identifying specific enzymes and transporters involved in amonafide metabolism, particularly under varied physiological conditions. This reservoir of information holds immense value in deciphering biochemical pathways and sculpting targeted interventions for heightened comprehension and precision.

Toxicological Assessments: Within the realm of toxicological scrutiny, N-Acetylamonafide-[d6] emerges as a potent tool for quantitatively appraising the potential toxic impacts of amonafide metabolites. Researchers wield this compound to gauge the potential accumulation of toxic metabolites across an array of tissue samples, aiding in ascertaining safety profiles and untangling potential risks linked to drug exposure. This comprehensive assessment framework stands as a cornerstone in ensuring the safety and efficacy of pharmaceutical interventions.

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