Complex Aldehydes
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Filtered Search Results
eMolecules EMOLECULES INC
5000841240 2-DEOXY-2-FLUORO-L-FUCOSE 5MG
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Medchemexpress LLC 2-DEOXY-2-FLUORO-D-M 5 mg
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2-DEOXY-2-FLUORO-D-M 5MG
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Medchemexpress LLC 5 -DEOXY-5-FLUOROCYT 10 mg
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5 -DEOXY-5-FLUOROCYT 10MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000282756 2 -DEOXY-2 -FLUORO-B 5MG
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Medchemexpress LLC 14-Deoxy-11,12-didehydroandrographolide | 42895-58-9 | MFCD07778081 | 332.43 | 100 MG
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14-Deoxy-11,12-didehydroandrographolide is an analogue of Andrographolide. It inhibits NF-κB activation.
- An analogue of Andrographolide.
- Inhibits NF-κB activation.
- Reduces ovalbumin (OVA)-induced inflammatory cell recruitment into bronchoalveolar lavage (BAL) fluid, IL-4, IL-5, IL-13, eotaxin production, serum IgE synthesis, pulmonary eosinophilia, mucus hypersecretion, mast cell degranulation, and airway hyper-responsiveness (AHR) in a mouse asthma model.
- At 1 mg/kg, it dramatically reduces resistance (Rl) and restores Cdyn in OVA-challenged mice in response to methacholine.
- Appearance: Solid.
- Color: White to light yellow.
- Purity: 99.93%.
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Medchemexpress LLC 6-DEOXY-D-GLUCOSE 5 mg
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6-DEOXY-D-GLUCOSE 5MG
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eMolecules EMOLECULES INC
5000841698 N4-ACETYL-2-DEOXY-5- 2000MG
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Chemscene CHEMSCENE
5000579049 2-DEOXY-D-GLUCOSE 100G
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Medchemexpress LLC 2'-Deoxy-5'-O-DMT-2'-fluorouridine | 146954-74-7 | 98.6% | 548.56 | 5 G
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2'-Deoxy-5'-O-DMT-2'-fluorouridine is a nucleoside analogue and a 5'-O-DMTr-5-FUDR derivative with potent anti-yellow fever (YFV) activity. It shows 100% inhibition against YFV at 20 mM and is noncytotoxic at concentrations up to 20 mM. This product is for research use only.
- Nucleoside analogue
- Potent anti-yellow fever (YFV) activity
- Shows 100% inhibition against YFV at 20 mM
- Noncytotoxic at concentrations up to 20 mM
- Solid appearance, off-white to light yellow in color
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Medchemexpress LLC 2′-deoxy-2′-fluoroadenosine | 64183-27-3 | 99.7% | 269.24 g/mol | C10H12FN5O3 | 100 MG
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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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Medchemexpress LLC 2'-Fluoro-2'-deoxy-ara-C(Bz)-3'-phosphoramidite | 1404463-12-2 | 99.8% | 851.90 g·mol⁻¹ | C46H51FN5O8P | 10 MG
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2'-Fluoro-2'-deoxy-ara-C(Bz)-3'-phosphoramidite is a protected cytidine phosphoramidite monomer intended for use in automated solid-phase oligonucleotide synthesis. Its 2'-fluoro arabino configuration and benzoyl protection facilitate incorporation of modified cytidine residues into synthetic oligonucleotides for research applications in nucleic acid modification, therapeutic oligonucleotides, and epigenetic studies.
- Suitable for automated solid-phase oligonucleotide synthesis.
- Enables incorporation of 2'-fluoro arabino cytidine into oligonucleotides.
- Benzoyl-protected nucleobase improves stability during synthesis.
- High purity supports consistent coupling efficiency.
- Supplied in a small research pack for method development and optimization.
- White to off-white solid form, easy to handle and store.
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Medchemexpress LLC 3'-azido-3'-deoxy-5-fluorocytidine | 2095417-18-6 | 99.9% | 286.22 g/mol | C9H11FN6O4 | 5 MG
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3'-Azido-3'-deoxy-5-fluorocytidine is a cytidine derivative used as a click-chemistry reagent for bioorthogonal labeling and conjugation. It contains an azide group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAC) and strain-promoted azide-alkyne cycloaddition (SPAAC) reactions, and is supplied as a white to off-white solid with high reported purity.
- Contains an azide functional group for bioconjugation.
- Compatible with CuAAC and strain-promoted click reactions.
- Reported purity 99.9%.
- Soluble in DMSO (≈140 mg/mL).
- Stable as a powder at -20 °C for long-term storage.
- Available in small research quantities and solution formulations.
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Medchemexpress LLC 2′-deoxy-5-methylisocytidine | 19316-88-2 | 99.6% | 241.24 | C10H15N3O4 | 10 MG
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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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Medchemexpress LLC 2'-deoxy-2'-fluoro-5-iodouridine | 55612-21-0 | MFCD17214423 | 99.5% | 372.09 g/mol | C9H10FIN2O5 | 50 MG
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2'-Deoxy-2'-fluoro-5-iodouridine is a purine nucleoside analog used in research to study DNA synthesis inhibition and apoptosis in cell and biochemical assays. It is supplied as a solid and as a ready-to-use DMSO solution and is intended for laboratory research use only.
- High purity (99.46%) suitable for biochemical and cell-based studies.
- Molecular formula C9H10FIN2O5 and molecular weight 372.09 g/mol.
- Available as solid powders and 10 mM DMSO solutions for convenient use.
- Useful as a tool compound in studies of nucleoside metabolism and antitumor activity.
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Medchemexpress LLC 3'-azido-3'-deoxy-beta-L-uridine | 2095417-28-8 | MFCD30718534 | 98.8% | 269.21 g/mol | C9H11N5O5 | 5 MG
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3-Azido-3-deoxy-beta-L-uridine is an azide-containing nucleoside derivative used as a clickable building block for bioconjugation and nucleoside chemistry. It participates in copper-catalyzed azide-alkyne cycloaddition (CuAAC) and strain-promoted alkyne-azide cycloaddition (SPAAC), enabling conjugation to alkyne- or cyclooctyne-functionalized molecules.
- Azide functional group enabling CuAAC and SPAAC reactions.
- Suitable for bioconjugation and nucleoside analogue synthesis.
- High purity (98.8%) for reliable experimental use.
- Molecular weight 269.21 g/mol; formula C9H11N5O5.
- Available in small research pack sizes for laboratory use.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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