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Organic compounds that contain one or more carbonyl (a carbon atom with a double bond to an oxygen atom) functional groups. Includes compounds with functional groups that contain a carbonyl in their structure such as ketones, aldehydes, and others.
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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]
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2-Deoxy-D-glucose-d (2-DG-d1) is a deuterium-labeled stable isotope of 2-deoxy-D-glucose used as a metabolic probe and analytical standard. It acts as a glucose analog and competitive inhibitor of glycolysis, suitable for tracer studies and mass spectrometry-based metabolomics. Molecular formula C6H11DO5; molecular weight 165.16; CAS 188004-07-1.
Deuterium-labeled internal standard for metabolic tracing.
Competitive inhibitor of glucose metabolism and glycolysis.
Suitable for mass spectrometry and metabolomics analyses.
High purity (98.0%) for research applications.
Available in small quantities for analytical workflows.
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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]
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2-Acetamido-2-deoxy-D-glucono-1,5-lactone (90%) is an N-acetylglucosamine 1,5-lactone supplied as a solid reagent for carbohydrate chemistry and biochemical assays. It is commonly used as a mechanistic inhibitor in glycosidase studies, and as an analytical reference for method development.
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2'-Deoxy-2'-fluoro-β-D-arabino-6-azauridine is a purine nucleoside analogue provided for laboratory research. It is reported to act via inhibition of DNA synthesis and induction of apoptosis and is supplied as a solid suitable for biochemical and cellular studies. Handle according to laboratory safety guidelines and the product safety data sheet.
Purity 96.9% suitable for research use.
Solid form, off-white to light yellow.
Molecular formula C8H10FN3O5.
Molecular weight 247.18 g·mol⁻¹.
Intended for in vitro research use only; not for human use.
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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]
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5 -Deoxy-2 3 -di-O-acetyl-5-fluorocytidine (2 3 -Di-O-acetyl-5 -deoxy-5-fluorocytidine) is an antiviral compound that inhibits HBV reverse transcriptase activity 5 -Deoxy-2 3 -di-O-acetyl-5-fluorocytidine shows potential to control HBV replication in vitro 5 -Deoxy-2 3 -di-O-acetyl-5-fluorocytidine as a nucleoside analog may provide a new option for the suppression of chronic hepatitis B[1]
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2'-Deoxy-2'-fluoroadenosine is a fluorinated deoxyadenosine nucleoside analog used in biochemical, antiviral, and antitumor research. It is supplied in both solid form and as a 10 mM solution in DMSO to support a range of laboratory applications, and has associated safety and technical documentation available.
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2'-Deoxy-2'-fluoro-5-iodouridine is a halogenated uridine nucleoside analog used as a research reagent in studies of nucleoside metabolism, nucleic acid incorporation, and preclinical antiviral or anticancer research. It is supplied as a solid laboratory reagent for biochemical and cellular experiments.
Halogenated uridine analog for nucleoside metabolism and incorporation studies.
Reported purity 99.5% by HPLC, suitable for analytical and preparative research.
White to off-white powder, supplied in small mass packages for laboratory use.
Molecular formula C9H10FIN2O5; molecular weight 372.09 g/mol.
Store refrigerated at 2-8 °C to preserve stability.
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5'-Deoxy-5-fluorocytidine is a cytidine analog and a metabolite of Capecitabine. It is converted by carboxylesterase in the liver and then deaminated by cytidine deaminase to generate 5'-deoxy-5-fluorouridine, which is finally converted into 5-fluorouracil by thymidine phosphorylase in tumor tissues, exerting anti-tumor effects.
Used in research for solid tumors such as colorectal cancer, non-small cell lung cancer, and breast cancer.
Significantly inhibits the proliferation of chemotherapy-resistant A549 paraclone cells in vitro (at 200 μM).
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