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3-Deoxy-D-glycero-D-galacto-2-nonulosonic acid (KDN) is a sialic acid derivative provided as a high-purity research reagent. Supplied as a white to off-white solid, it is intended for glycobiology, carbohydrate analysis, and biochemical assays. Documentation such as a certificate of analysis and safety data sheets are available; follow recommended storage to maintain stability.
High purity suitable for analytical and research use (99.9%).
Available in milligram-scale packages for small-scale experiments.
Molecular weight 268.22 g/mol and formula C9H16O9 for stoichiometric calculations.
White to off-white solid, easy to weigh and dissolve for assays.
Certificate of analysis and safety data sheets available from the supplier.
Recommended storage: powder at -20°C for long-term stability.
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Ethyl 2-deoxy-2-phthalimido-β-D-thioglucopyranoside is a specialized glycobiology reagent used in carbohydrate chemistry and oligosaccharide synthesis. It functions as an ethyl thio-glycoside donor and is supplied for laboratory research applications where glycosylation steps or mechanistic studies of carbohydrate reactions are required.
Used as a glycosyl donor in carbohydrate synthesis.
Suitable for glycobiology and carbohydrate chemistry research.
Molecular formula C16H19NO6S.
Molecular weight 353.39 g/mol.
Provided as a stable solid for laboratory-scale experiments.
Recommended storage maintains long-term stability under cooled conditions.
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2′-Deoxy-5-methylisocytidine is a deoxy nucleoside analog used as a research reagent in nucleoside chemistry and nucleic acid studies. It is provided as a solid powder intended for laboratory research use only and is typically stored at -20°C to preserve stability.
Purine nucleoside analog suitable for biochemical and nucleic acid research.
High reported purity (~99.6%) supports reproducible experimental results.
Supplied as a powder for flexible handling and dissolution in common solvents.
Suitable for synthesis, analytical characterization, and method development.
Long-term stability when stored at -20°C under recommended conditions.
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3′-Deoxy-3′-fluoroguanosine is a fluorinated guanosine nucleoside analog supplied for laboratory research. It is used in nucleic acid and antiviral studies where modified nucleosides are required to probe polymerase activity and viral replication. The material is provided as a solid or solution format for experimental assays.
Fluorinated guanosine nucleoside analog for biochemical research.
Exhibits antiviral activity against certain RNA viruses via RNA-dependent RNA polymerase interaction.
Purity greater than 98% as measured by supplier quality control.
Molecular formula C10H12FN5O4; molecular weight 285.24 g/mol.
Available in small-scale research formats including 10 mg and 100 mg, and 10 mM solution.
For research use only; not for human or animal therapeutic use.
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2-Deoxy-D-glucose 6-phosphate disodium is produced in mammalian cells by the action of hexokinase on 2-DG. It is a glucose analog that acts as a competitive inhibitor of glucose metabolism, inhibiting glycolysis via its actions on hexokinase.
Derivative of 2-Deoxy-D-glucose
Produced in mammalian cells by hexokinase action on 2-DG
Functions as a glucose analog
Acts as a competitive inhibitor of glucose metabolism
Inhibits glycolysis via hexokinase actions
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2'-Fluoro-2'-deoxy-ara-C(Bz)-3'-phosphoramidite is a cytidine analog. Cytidine analogs work by inhibiting DNA methyltransferases and show potential anti-metabolic and anti-tumor activities.
Cytidine analog
Inhibits DNA methyltransferases
Shows potential anti-metabolic activities
Shows potential anti-tumor activities
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2′-Deoxy-2′-fluoroadenosine is a fluorinated deoxyadenosine nucleoside analog used in biochemical research for its antiviral and antitumor activity. It can be incorporated into DNA to disrupt viral or cancer cell replication and is used as a building block for synthesis of 2′-fluoro-modified oligonucleotides. The compound can be enzymatically converted to 2-fluoroadenine, enabling enzyme-directed activation studies.
Fluorinated deoxyadenosine nucleoside analog.
Interferes with DNA replication in viral and tumor models.
Useful for synthesis of 2′-fluoro-modified oligonucleotides.
High purity suitable for research applications (≈99.7%).
Available in mg-scale pack sizes for laboratory use.
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1-O-Methyl-2-deoxy-D-ribose is a ribose derivative obtained through a one-step reaction by introducing a methoxy protective group at the anomeric carbon position under acidic conditions, which assists in the acquisition of 2-deoxy-D-ribose. It can be used in research for the synthesis of chemical materials.
Ribose derivative
One-step synthesis
Facilitates 2-deoxy-D-ribose acquisition
Research utility in chemical materials synthesis
Available documentation: Data sheet, SDS, and handling instructions
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2'-Deoxy-2'-fluoro-β-D-arabinocytidine is a fluorinated cytidine nucleoside analog provided for biochemical and cell-based research. It is supplied as solid material or as a ready-to-use 10 mM solution in DMSO, and is characterized by a molecular weight of 245.21 g/mol, CAS 56632-83-8, and high reported purity.
Ready-to-use 10 mM solution in DMSO for rapid assay setup.
Also available as solid in multiple mass sizes for custom preparation.
High purity suitable for analytical and biological experiments.
Fluorinated nucleoside analog useful for incorporation and enzymatic studies.
Documentation provided: datasheet, certificate of analysis, and safety data sheet.
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2'-Deoxy-2'-fluoro-β-D-arabinocytidine is a fluorinated nucleoside analogue used in biochemical and preclinical research. It functions as a modified cytidine analogue for studies of DNA synthesis inhibition, nucleic acid chemistry, and investigations of anticancer or antiviral activity. The compound is supplied as a solid for laboratory use and is documented with CAS and molecular formula identifiers.
Fluorinated cytidine analogue for studies of DNA synthesis and metabolism.
Applicable to cellular and biochemical assays investigating antitumor and antiviral effects.
Suitable for milligram-scale laboratory use as a solid reagent.
Serves as a building block in oligonucleotide and nucleic acid chemistry research.
Documented by CAS and molecular formula for compound traceability.
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2'-Deoxy-2'-fluoro-β-D-arabino-6-azauridine is a purine nucleoside analog that primarily targets DNA synthesis pathways. It exhibits broad antitumor activity and is particularly effective against indolent lymphoid malignancies. Its mechanisms of action include the inhibition of DNA replication and the induction of apoptosis, making it a valuable tool for cancer research and therapeutic development in oncology.
Primarily targets DNA synthesis pathways.
Exhibits broad antitumor activity.
Effective against indolent lymphoid malignancies.
Inhibits DNA replication.
Induces apoptosis.
Valuable tool for cancer research.
Useful for therapeutic development in oncology.
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2'-Fluoro-2'-deoxy-ara-A(Bz)-3'-phosphoramidite is an adenosine analog. Adenosine analogs primarily act as smooth muscle vasodilators and have also been shown to inhibit cancer progression.
Adenosine analog
Acts as a smooth muscle vasodilator
Inhibits cancer progression
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