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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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1-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)uracil is a fluorinated nucleoside analogue provided for research use. It exhibits reported antiviral activity and is characterized by defined physicochemical properties and batch-specific quality documentation for reliable use in in vitro and in vivo studies.
Fluorinated nucleoside analogue with reported antiviral activity.
Purity ≥98.0%.
Chemical formula C9H11FN2O5; molecular weight 246.19 g·mol⁻1.
White to off-white solid form, soluble in DMSO (100 mg/mL).
Storage stability: powder -20°C (long-term) or 4°C (short-term); solutions -80°C for extended storage.
Supplied with batch-specific certificate of analysis for quality verification.
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3'-Azido-3'-deoxy-5-methylcytidine is an azide-functionalized nucleoside derivative used as an antiviral research reagent and a click-chemistry building block. The compound has reported inhibitory activity in cell-based antiviral assays and is suitable for copper-catalyzed and strain-promoted azide-alkyne cycloaddition bioconjugation.
Azide-functionalized nucleoside for bioconjugation via CuAAC and SPAAC.
Reported antiviral activity in cell-based assays, including XMRV and HIV-1 reverse transcriptase inhibition.
Molecular formula C10H14N6O4 and molecular weight 282.26 g/mol.
High purity (99.9%) suitable for research applications.
Light yellow to yellow solid supplied in small-mass laboratory packs.
Storage: powder at -20°C (long term) or 4°C; in solvent at -80°C or -20°C.
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6A-azido-6A-deoxy-β-cyclodextrin is an azide-functionalized derivative of β-cyclodextrin used as a water-soluble click-chemistry reagent and bioconjugation building block. The azido group enables copper-catalyzed and strain-promoted azide-alkyne cycloaddition reactions for conjugation to alkyne-bearing molecules in chemical biology and drug-delivery research.
Azide-functionalized for copper-catalyzed and strain-promoted azide-alkyne cycloaddition.
Water-soluble β-cyclodextrin derivative for aqueous reactions.
Suitable for bioconjugation and drug delivery research.
Enables site-specific conjugation to alkyne-containing partners.
Solid form, suitable for standard handling and storage.
Compatible with common analytical methods such as HPLC and NMR.
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1-O-Methyl-2-deoxy-D-ribose is a ribose derivative formed by introducing a methoxy protective group at the anomeric carbon position under acidic conditions. This process facilitates the acquisition of 2-deoxy-D-ribose and can be utilized in research on the synthesis of chemical materials.
Ribose derivative obtained through a one-step reaction
Methoxy protective group introduced at anomeric carbon position
Facilitates the acquisition of 2-deoxy-D-ribose
Utilized in research on the synthesis of chemical materials
For research use only
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2'-Deoxy-2'-fluorocytidine is a nucleoside analog that acts as a potent inhibitor of Crimean-Congo hemorrhagic fever virus (CCHFV) replication. It can also synergistically enhance the antiviral effects of T705 against CCHFV replication.
Potent inhibitor of Crimean-Congo hemorrhagic fever virus (CCHFV) replication.
Acts synergistically with T705 to increase antiviral effects on CCHFV replication.
Available in various quantities and forms: solid, and solutions (e.g., 10 mM * 1 mL in Water).
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5'-Deoxy-5'-iodouridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.