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Chlorambucil-[d8]

General Information
Catalog: BLP-013920
Molecular Formula: C14H11D8Cl2NO2
Molecular Weight: 312.26
Chemical Structure
Chlorambucil-[d8]
Description One of the isotopic labelled form of Chlorambucil, which is an alkylating agent and could be used in chronic lymphocytic leukemia therapy.
Synonyms 4-[Bis(2-chloroethyl)amino]benzenebutanoic Acid-d8; 4-[p-[Bis(2-chloroethyl)amino]phenyl]butyric Acid-d8; Ambochlorin-d8; Amboclorin-d8; Ecloril-d8; Leukeran-d8; Leukeran Tablets-d8; Linfolizin-d8
Related CAS 305-03-3 (unlabelled)
Purity 95% by HPLC; 98% atom D

Chlorambucil-[d8], a deuterium-labeled derivative of the renowned chemotherapeutic agent chlorambucil, finds diverse applications in various fields. Here are the key applications:

Pharmacokinetic Studies: Utilizing Chlorambucil-[d8] in pharmacokinetic studies offers comprehensive insights into the absorption, distribution, metabolism, and excretion of chlorambucil. The deuterium label enables precise tracking of the drug’s metabolic pathways through cutting-edge mass spectrometry. This detailed information plays a pivotal role in optimizing dosing regimens and enhancing therapeutic efficacy for improved patient outcomes.

Drug Metabolism Research: In the realm of drug metabolism research, Chlorambucil-[d8] serves as a stable isotope-labeled internal standard for quantifying chlorambucil and its metabolites in biological samples. This crucial tool assists scientists in evaluating the metabolic stability of the drug and potential drug interactions, paving the way for safer and more effective drug development. Accurate metabolic profiling contributes to enhanced understanding and precision in pharmaceutical research.

Bioanalytical Assays: Chlorambucil-[d8] stands as a reference standard in bioanalytical assays designed to measure the concentration of chlorambucil in plasma and other tissues. This foundational role is essential for monitoring therapeutic drug levels in patients undergoing treatment. By validating analytical methods with a labeled compound, the accuracy and reliability of clinical studies are assured, ensuring the efficacy and safety of therapeutic interventions.

Cancer Research: Chlorambucil-[d8] emerges as a valuable asset in cancer research, shedding light on the mechanisms of action and resistance associated with chlorambucil. Researchers leverage the comparison between labeled and unlabeled chlorambucil to probe deeper into its impact on cancer cell lines, enhancing the understanding of its efficacy in combating cancer. This profound knowledge serves as a cornerstone for designing innovative combination therapies and developing cutting-edge anticancer agents, driving forward the fight against cancer.

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