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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-2,2-difluoro-D-erythro-pentonic acid γ-lactone 3,5-dibenzoate is a chemically synthesized fluorinated carbohydrate derivative used in glycobiology and carbohydrate chemistry research. It is supplied as a white to off-white solid with high reported purity suitable for laboratory applications.
Chemical class: Fluorinated carbohydrate γ-lactone.
Cas number: 122111-01-7.
Chemical formula: C19H14F2O6.
Molecular weight: 376.31 g/mol.
Purity: ≥97.0%.
Appearance: White to off-white solid.
Storage: Store at room temperature (solid); in solvent, store at -80°C (2 years) or -20°C (1 year).
Available pack sizes: 5 g, 10 g, 25 g, 50 g, 100 g.
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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-5'-O-DMT-2'-fluorouridine is a nucleoside analogue and a 5'-O-DMTr-5-FUDR derivative. It demonstrates potent activity against yellow fever virus (YFV).
Potent anti-yellow fever (YFV) activity
Shows 100% inhibition against YFV at 20 mM
Noncytotoxic at concentrations up to 20 mM
For research use only
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6-Amino-6-deoxy-β-cyclodextrin is an amino-functionalized derivative of β-cyclodextrin supplied as a solid reagent for research and synthesis. It is commonly used to prepare other cyclodextrin derivatives and as a chiral selector in analytical separations.
Amino-functionalized β-cyclodextrin for derivatization and host-guest chemistry.
Useful as a chiral selector for capillary electrophoresis separations.
Supplied as a solid reagent suitable for laboratory synthesis.
Typical purity 95.0% (HPLC).
Molecular weight 1,134.00 g/mol.
Store at 4°C under nitrogen and protect from moisture.
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2'-Deoxy-2'-fluoroarabino inosine is a purine nucleoside analog. These analogs possess broad antitumor activity, specifically targeting indolent lymphoid malignancies. Their anticancer mechanisms involve inhibiting DNA synthesis and inducing apoptosis.
Purine nucleoside analog
Exhibits broad antitumor activity
Targets indolent lymphoid malignancies
Inhibits DNA synthesis
Induces apoptosis
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5′-Deoxy-5-fluoro-N4-(isopentyloxycarbonyl)cytidine is a small-molecule impurity formed during the synthesis of the anticancer prodrug capecitabine. It is provided as a research and analytical reference for laboratories performing impurity profiling, method development, and quality-control testing of synthetic processes.
Provided as an analytical reference standard for impurity profiling.
Suitable for HPLC, LC-MS, and method validation.
Supplied in small milligram quantities for laboratory use.
Molecular formula C15H22FN3O6 and molecular weight 359.35 g·mol-1.
Intended for research use only; not for human therapeutic use.
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18-Hydroxy-11-deoxy corticosterone (18-OH-DOC) is a mineralocorticoid whose synthesis is regulated by adrenocorticotropic hormone (ACTH) and angiotensin II 18-Hydroxy-11-deoxy corticosterone is an intermediate in the metabolism of progesterone and plays an important role in regulating blood pressure and water-salt balance Continuous infusion of 18-Hydroxy-11-deoxy corticosterone can increase systolic blood pressure in rats and plasma levels of 18-Hydroxy-11-deoxy corticosterone are significantly elevated in the db/db mouse model of type 2 diabetes suggesting its potential involvement in metabolic dysregulation and diabetes-related regulation 18-Hydroxy-11-deoxy corticosterone holds promise for research in areas such as hypertension diabetes and other related fields[1]
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2′-Deoxy-β-L-uridine is a nucleoside analogue for biochemical and antiviral research. It functions as a substrate for certain viral enzymes and, through its 5'-triphosphates, interacts with viral DNA polymerase, making it useful for enzymatic and polymerase assays. The compound is provided as a high-purity research chemical.
Nucleoside analogue for biochemical and antiviral research.
Specific substrate for viral enzymes and polymerase assay applications.
High reported purity: 99.96%.
Chemical formula C9H11N2O5; molecular weight 227.195 g·mol^-1.
Available in research-scale quantities (500 mg).
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2′-Deoxy-β-L-uridine is the L-enantiomer of 2′-deoxyuridine, a nucleoside analogue used in biochemical and virology research as a substrate for viral enzymes and for studies of nucleoside metabolism. Supplied as a high-purity solid for analytical and research applications.
High purity: 99.96%.
Molecular weight: 228.20 g/mol.
Chemical formula: C9H12N2O5.
CAS number: 31501-19-6.
Stable as a powder at -20°C for up to 3 years and at 4°C for up to 2 years.
In solvent, store at -80°C for up to 6 months or at -20°C for up to 1 month.
Suitable as a substrate for viral enzyme assays and studies of nucleoside metabolism.
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1-(2-Deoxy-β-D-threo-pentofuranosyl)thymine is a thymidine analog with a purity of 99.68% and a molecular weight of 242.23. This compound exhibits insertional activity towards replicated DNA, making it suitable for labeling cells and tracking DNA synthesis. It also demonstrates antiviral activity against HBV in human 2.2.15 cells with an EC50 of 10 μg/mL and against DHBV in duck hepatocytes with an EC50 of 4.13 μM. Cytotoxicity against human HuH7 cells is observed with a CC50 of > 200 μg/mL.
Thymidine analog
Exhibits insertional activity towards replicated DNA
Used for labeling cells and tracking DNA synthesis
Demonstrates antiviral activity against HBV and DHBV
High purity of 99.68%
Appears as a white to off-white solid
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2'-Deoxy-2'-fluoroarabino inosine is a purine nucleoside analog that exhibits broad antitumor activity. It specifically targets indolent lymphoid malignancies by inhibiting DNA synthesis and inducing apoptosis.
Molecular weight: 270.22
Appearance: Solid
Color: White to off-white
Purity: 95.0%
Targets indolent lymphoid malignancies
Inhibits DNA synthesis
Induces apoptosis
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