Description

5-Methyl-2'-Deoxyzebularine Cep is a high-purity nucleoside analog derivative, identified by CAS No. 125258-62-0, designed for advanced research and pharmaceutical development. This compound serves as a critical building block and reference standard in the synthesis of novel therapeutic agents, particularly in the field of oncology and epigenetics. It is essential for pharmaceutical R&D laboratories, biotechnology companies, and academic institutions focused on developing next-generation treatments targeting DNA methylation and cellular signaling pathways.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of novel nucleoside-based antiviral and anticancer drugs.
• Biochemical Research: Used as a reference standard and substrate in enzymatic studies, particularly those involving DNA methyltransferases and related epigenetic modifiers.
• Antiviral Agent Development: Investigated for its potential activity against a range of viral targets due to its modified nucleoside structure.
• Oncology Research: Employed in studies exploring epigenetic therapies and the role of DNA methylation in cancer progression and treatment.
• Chemical Biology Probes: Utilized in the design and synthesis of molecular probes to study nucleic acid metabolism and function within cells.
• Process Development: Serves as a critical raw material for process chemistry and scale-up activities in API (Active Pharmaceutical Ingredient) manufacturing.

Basic Information

Product Name	5-Methyl-2'-Deoxyzebularine Cep
CAS No.	125258-62-0
Molecular Formula	C11H15N3O4
Molecular Weight	253.25 g/mol
Synonyms	5-Methyl-2'-deoxyzebularine; 5-Methyldeoxyzebularine; 1-(2-Deoxy-β-D-ribofuranosyl)-5-methylpyrimidin-2(1H)-one; 5-Methyl-2'-deoxyzebularine C-ethylphosphonate; 5-Methyl-2'-deoxyzebularine CEP; 5-Methyl-2'-deoxyzebularine C-ethyl phosphonate; 5-Methyl-2'-deoxyzebularine cyclic ethyl phosphonate; 5-Methyl-2'-deoxyzebularine CEP intermediate.
EINECS	Contact for details

Quality Control

Our 5-Methyl-2'-Deoxyzebularine Cep is manufactured under strict quality control protocols to ensure high purity and batch-to-batch consistency suitable for research and development. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to cGMP guidelines where applicable, and our quality systems are designed to meet the stringent requirements of the pharmaceutical and biotechnology industries.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a desiccated environment to prevent degradation. For long-term storage, consider storing under an inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.