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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-Acetamido-2-deoxy-D-glucono-1,5-lactone (CAS 19026-22-3) is a carbohydrate-derived δ-lactone supplied as a research reagent at 90% purity. It is used in sugar chemistry and biochemical studies as a substrate or intermediate for enzyme assays, method development, and analytical testing. Handle and store under standard laboratory conditions to preserve stability.
90% purity suitable for research and analytical applications.
White crystalline solid with molecular formula C8H13NO6.
Useful as a substrate or intermediate in carbohydrate chemistry and enzyme assays.
Available in small laboratory pack sizes for method development.
Store as recommended to maintain compound stability.
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1-Deoxy-1-morpholino-D-fructose is a fructose-derived biochemical reagent used in sugar science research and biochemical assays. It is a solid carbohydrate derivative with chemical formula C10H19NO6 and molecular weight 249.26 g/mol, typically supplied at ≥97.0% purity.
Suitable for biochemical assays and sugar chemistry research.
High purity (≥97.0%) reduces analytical interference.
Available in 100 mg, 250 mg, 500 mg, 1 g, and larger pack sizes.
Powder stability: -20°C (3 years) or 4°C (2 years); in solvent stability is shorter.
Molecular formula C10H19NO6 and molecular weight 249.26 g/mol.
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6-Azido-6-deoxy-D-galactose 95% can be used as a substrate in enzymology to study the activity and specificity of galactosyltransferases and other glycosylation enzymes
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2'-Deoxy-2'-fluoroinosine is a purine nucleoside analog that demonstrates broad antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms include inhibition of DNA synthesis and induction of apoptosis.
Purine nucleoside analog
Demonstrates broad antitumor activity
Targets indolent lymphoid malignancies
Inhibits DNA synthesis
Induces apoptosis
Appears as a white to off-white solid
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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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6A-azido-6A-deoxy-β-cyclodextrin is a mono-substituted β-cyclodextrin bearing an azide functional group at the 6A position. It is a water-soluble derivative commonly used as a linker in click chemistry for bioconjugation and for host-guest complexation studies.
Contains an azide group for CuAAC and SPAAC click reactions.
High purity (98.0%).
Water-soluble mono-substituted β-cyclodextrin.
Suitable for bioconjugation and host-guest complexation studies.
Solid form for straightforward handling and weighing.
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A reducing sugar; increases levels of ROS in HL-60 human leukemia cells at 15 mM; induces tubulogenesis and migration of BAE cells at 10 µM; topical administration of 2-deoxy-D-ribose increases blood vessel formation and accelerates wound healing in a rat full-thickness cutaneous wound model
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9-(2-Deoxy-beta-D-ribofuranosyl)-6-methylpurine is a purine nucleoside analogue used as a research reagent and reference compound in biochemical and anticancer studies. It functions as a nucleoside antimetabolite that can inhibit DNA synthesis and induce apoptosis. The compound is supplied as an off-white to light yellow solid and is characterized by CAS number 16006-64-7, molecular formula C12H15N3O3, and molecular weight 249.27 g/mol.
Purity 95.0%.
Available in small quantities, including 5 mg, for screening and reference use.
Analytical documentation available: COA, 1H NMR, LCMS, and SDS.
Suitable for studies of nucleoside metabolism and anticancer mechanisms.
Solid form, easy to handle and store.
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3'-Deoxy-3'-fluoroadenosine is a purine nucleoside analogue used as a research nucleoside antimetabolite with reported antitumor activity. It acts via inhibition of DNA synthesis and induction of apoptosis, and is applied in studies of nucleoside metabolism and anticancer mechanisms. The material is supplied in multiple solid sizes and as a DMSO solution for laboratory use.
High reported purity (99.29%).
Molecular formula C10H12FN5O3 and molecular weight 269.24 Da.
Available as solid quantities and as a 10 mM solution in DMSO.
COA and SDS available for quality and safety information.
Suitable for biochemical and anticancer research applications.
Provided in small-scale quantities for research workflows.
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2'-Deoxy-GDP (dGDP) trisodium is a guanosine monophosphate (GMP) analogue and a hypoxanthine phosphoribosyltransferase (HGPRT) inhibitor with an IC50 of 12.5 μM. HGPRT is a central enzyme in the purine recycling pathway of all protozoan parasites. It is for research use only and not sold to patients.
HGPRT inhibitor
Guanosine monophosphate (GMP) analogue
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2-Deoxycytidine 5-monophosphate (CAS 1032-65-1) is a deoxycytosine nucleotide with a phosphate group linked to the 5 position of the deoxyribose sugar It serves as a fundamental building block in DNA synthesis participating in enzymatic processes involving DNA polymerases and repair enzymes This compound is widely utilized in studies of nucleic acid metabolism DNA replication and repair mechanisms Its incorporation into oligonucleotides and use in in vitro assays make it valuable for elucidating DNA-protein interactions and the dynamics of nucleic acid biochemistry
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3-Deoxy-D-glycero-D-galacto-2-nonulosonic acid (sodium), commonly called KDN sodium, is the sodium salt of a deoxy sialic acid used as a research reagent in glycobiology and metabolic studies. It is supplied in small-mass vials for laboratory use and intended for research applications; supporting documentation is provided by the supplier.
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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 is intended for research use only.
Nucleoside analog
Potent inhibitor of CCHFV replication
Can synergistically increase antiviral potency when combined with another antiviral compound
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