Carbonyl compounds
Medchemexpress LLC 3′-deoxy-3′-fluoroguanosine | 123402-21-1 | MFCD09263707 | >98.0% | 285.24 g/mol | C10H12FN5O4 | 10 MG
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.
Medchemexpress LLC 2-deoxy-2-fluoro-D-galactose | 51146-53-3 | MFCD00061625 | 95.0% | 182.15 g/mol | C6H11FO5 | 25mg
2-Deoxy-2-fluoro-D-galactose is a class of biochemical reagents used in glycobiology research Glycobiology studies the structure synthesis biology and evolution of sugars It involves carbohydrate chemistry enzymology of glycan formation and degradation protein-glycan recognition and the role of glycans in biological systems This field is closely related to basic research biomedicine and biotechnology[1]
Medchemexpress LLC 3'-azido-3'-deoxy-beta-L-uridine | 2095417-28-8 | MFCD30718534 | 98.8% | 269.21 g/mol | C9H11N5O5 | 5 MG
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.
Cayman Chemical 5-deoxy-D-RIbose 250mg
A building block; has been used in the synthesis of carcinolytic compounds
Medchemexpress LLC 2-Deoxy-D-glucose 6-phosphate disodium | 33068-19-8 | ≥98.0% | 288.10 | 25 MG
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
Medchemexpress LLC 2'-Fluoro-2'-deoxy-ara-C(Bz)-3'-phosphoramidite | 1404463-12-2 | C46H51FN5O8P | 1 ML
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
Ambeed 2'-Fluoro-2'-deoxyadenosine | 64183-27-3 | 269.23 g/mol | 1G
2'-Fluoro-2'-deoxyadenosine | 64183-27-3 | 269.23 g/mol | 1G
Medchemexpress LLC 2'-Deoxy-2'-fluoroinosine | 80049-87-2 | C10H11FN4O4 | 250 MG
2'-Deoxy-2'-fluoroinosine 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.
- Broad antitumor activity targeting indolent lymphoid malignancies.
- Inhibits DNA synthesis.
- Induces apoptosis.
Medchemexpress LLC 2′-deoxy-2′-fluoroadenosine | 64183-27-3 | 99.7% | 269.24 g/mol | C10H12FN5O3 | 100 MG
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.
Medchemexpress LLC 1-O-Methyl-2-2-deoxy-D-ribose | 60134-26-1 | C6H12O4 | 25 G
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
Medchemexpress LLC Deoxy-bigchap | MFCD20924625 | 99.9% | 862.06 | C42H75N3O15 | 100 MG
Deoxy-bigchap is a non-ionic detergent used as a biochemical reagent for solubilization and gentle extraction of membrane proteins and other biomolecules in life-science research. Supplied with analytical documentation, it is intended for research use only and supports reproducible experimental workflows.
- Non-ionic detergent for membrane solubilization.
- Improved solubility compared with related detergents.
- Suitable for gentle extraction of membrane proteins.
- Provided with analytical documents (SDS, COA, HNMR, RP-HPLC, MS).
- High purity to support reproducible results.
Medchemexpress LLC 2-Deoxy-D-glucose | 154-17-6 | 99.9% | 164.16 | 25 G
2-Deoxy-D-glucose is a glucose analog that acts as a competitive inhibitor of glucose metabolism, inhibiting glycolysis via its actions on hexokinase.
- Significantly reduces the level of ATP in MCF-7 cells in a dose- and time-dependent manner.
- Decreases phosphorylated Akt levels and increases phosphorylated AMPK and Sirt-1 levels in MCF-7 cells.
- Increases the levels of pentose phosphate pathway (PPP) metabolites and augments the generation of NADPH by glucose-6-phosphate dehydrogenase.
- Increases the reduced form of glutathione by 2-DG in NB4 cells.
- Causes a 7% decrease in final weight and delays the appearance of palpable mammary carcinomas in vivo.
- Decreased in a dose-dependent manner in rat muscle in vivo.
Medchemexpress LLC 3-Deoxy-D-glycero-D-galacto-2-nonulosonic acid sodium | 95.0% | C9H15NaO9 | 50 MG
3-Deoxy-D-glycero-D-galacto-2-nonulosonic acid (KDN) sodium is a sialic acid. It protects the oligo/(poly)sialyl chains from exosialidases at the nonreducing terminal and plays a role in egg activation of salmonid fish. This compound is abundant in fetal cord red blood cells and malignant human ovarian cancer cells.
- Sialic acid
- Protects oligo/(poly)sialyl chains from exosialidases
- Plays a role in egg activation of salmonid fish
- Abundant in fetal cord red blood cells
- Abundant in malignant human ovarian cancer cells
Medchemexpress LLC 3-Deoxy-D-glycero-D-galacto-2-nonulosonic acid (KDN) | 153666-19-4 | 99.9% | C9H16O9 | 25 MG
3-Deoxy-D-glycero-D-galacto-2-nonulosonic acid (KDN) is a type of sialic acid that can be hydrolyzed by sialidase from the loach (Misgurnus fossilis).
- Solid appearance
- White to off-white color
- Soluble in water at 100 mg/mL (372.83 mM), requires ultrasonic
- Purity of 99.9%
- Molecular weight of 268.22
- Chemical formula: C9H16O9
- CAS number: 153666-19-4
- Ships at room temperature in continental US; may vary elsewhere
- Powder storage: -20°C for 3 years, 4°C for 2 years
- In solvent storage: -80°C for 6 months, -20°C for 1 month
Cayman Chemical 5-deoxy-D-RIbose 50mg
A building block; has been used in the synthesis of carcinolytic compounds