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Filtered Search Results
Medchemexpress LLC 3-deoxy-galactosone | 4134-97-8 | MFCD18643020 | 162.14 g/mol | C6H10O5 | 5 MG
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3-Deoxy-galactosone (CAS 4134-97-8) is an endogenous 1,2-dicarbonyl compound produced by degradation of galactose and formed in foods during Maillard and caramelization reactions. It can be generated from 3-deoxyglucosone (3-DG) via the intermediate 3,4-dideoxyglucosone-3-ene (3,4-DGE). Molecular formula C6H10O5; molecular weight 162.14 g/mol. Purity and appearance are on the product page - consult the Certificate of Analysis for lot-specific data.
- Endogenous 1,2-dicarbonyl metabolite relevant to food chemistry and metabolic studies.
- Provided in small research pack sizes suitable for analytical and reference use.
- Molecular formula C6H10O5 and molecular weight 162.14 g/mol support identification and calculations.
- Consult Certificate of Analysis for lot-specific purity and storage instructions.
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Medchemexpress LLC 3'-Azido-3'-deoxy-beta-L-uridine | 2095417-28-8 | 98.8% | 269.21 | 1 ML
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3'-Azido-3'-deoxy-beta-L-uridine (Compound 25) is a nucleoside derivative. It is a click chemistry reagent that contains an Azide group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- Nucleoside derivative
- Click chemistry reagent
- Contains an Azide group
- Can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc)
- Can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
- Appearance: Solid
- Color: White to off-white
- For research use only
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Medchemexpress LLC 2'-Deoxy-2'-fluorocytidine | 10212-20-1 | 99.98% | 245.21 | 10 G
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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 can work synergistically with T705 to enhance the antiviral effects of both compounds on CCHFV replication. It has demonstrated antiviral activities with EC50 values of 61 nM and 31 nM against CCHFV and CCHFV/ZsG in Huh7 cells, respectively, and a CC50 of >50.0 μM in Huh7 cells.
- Potent inhibitor of Crimean-Congo hemorrhagic fever virus (CCHFV) replication.
- Acts synergistically with T705 to increase antiviral potency.
- Antiviral activities observed in various cell lines (HEp-2, Huh-7, Vero 76).
- Available in solid and solution forms.
- For research use only.
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Medchemexpress LLC Guanosine 5'-(trihydrogen diphosphate), 2'-deoxy-, sodium salt (1:3) | 102783-74-4 | 98.8% | 493.15 | 25 MG
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2′-Deoxy-GDP (dGDP) trisodium is an analog of guanosine monophosphate (GMP) that acts as an inhibitor of hypoxanthine phosphoribosyltransferase (HGPRT). This enzyme is crucial for the purine recycling pathway in all protozoan parasites. It has an IC50 of 12.5 μM.
- Guanosine monophosphate (GMP) analogue.
- Hypoxanthine phosphoribosyltransferase (HGPRT) inhibitor.
- IC50 of 12.5 μM for HGPRT.
- Useful for research purposes.
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Medchemexpress LLC 5'-Deoxy-5-fluorocytidine (Standard) | 66335-38-4 | 99.9% | 245.21 | 1 ML
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5'-Deoxy-5-fluorocytidine is a cytidine analog and a metabolite of Capecitabine. It is converted from Capecitabine by carboxylesterase in the liver. This compound is deaminated by cytidine deaminase to generate 5'-deoxy-5-fluorouridine, which is then converted into 5-fluorouracil by thymidine phosphorylase in tumor tissues to exert anti-tumor effects. It is 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.
- Used in research for solid tumors such as colorectal cancer, non-small cell lung cancer, and breast cancer.
- Cytidine analog and metabolite of capecitabine.
- Converted to 5-fluorouracil by thymidine phosphorylase in tumor tissues.
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Medchemexpress LLC 2′-Deoxy-N-methylguanosine | 19916-77-9 | C11H15N5O4 | 25 MG
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2′-Deoxy-N-methylguanosine is a DNA adduct and a purine nucleoside analog known for its broad antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms involve the inhibition of DNA synthesis and the induction of apoptosis.
- DNA adduct
- Purine nucleoside analog
- Exhibits broad antitumor activity
- Targets indolent lymphoid malignancies
- Inhibits DNA synthesis
- Induces apoptosis
- Classified under nucleoside analogs
- Relevant to cancer research including leukemia and lymphoma
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Medchemexpress LLC 1-deoxy-1-(octylamino)-d-glucitol | 23323-37-7 | 293.40 | 100 G
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1-Deoxy-1-(octylamino)-D-glucitol is a biochemical reagent used in glycobiology research. Glycobiology is the study of the structure, synthesis, biology, and evolution of sugars, encompassing carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is relevant to basic research, biomedicine, and biotechnology.
- Used as a biochemical reagent in glycobiology research.
- Supports studies on the structure, synthesis, biology, and evolution of sugars.
- Applicable in carbohydrate chemistry and enzymology of glycan formation and degradation.
- Facilitates protein-glycan recognition and understanding the role of glycans in biological systems.
- Relevant for basic research, biomedicine, and biotechnology.
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Medchemexpress LLC 1-Deoxy-1-(octylamino)-D-glucitol | 23323-37-7 | 293.40 | 500 G
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1-Deoxy-1-(octylamino)-D-glucitol is a biochemical reagent used in glycobiology research. Glycobiology focuses on the structure, synthesis, biology, and evolution of sugars, encompassing carbohydrate chemistry, the enzymology of glycan formation and degradation, protein-glycan recognition, and the biological roles of glycans. This field is relevant to basic research, biomedicine, and biotechnology.
- Application: Biochemical reagent for glycobiology research
- Research area: Studies of sugar structure, synthesis, biology, and evolution
- Related fields: Carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition
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Medchemexpress LLC 5 -Deoxy-2 3 -di-O- 25g
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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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Medchemexpress LLC 2'-deoxy-2'-fluoroarabino inosine | 98983-40-5 | 95.0% | 270.22 g·mol⁻¹ | C10H11FN4O4 | 10 MG
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2'-Deoxy-2'-fluoroarabino inosine is a purine nucleoside analog provided as a white to off-white solid for research use. It is used as a nucleoside antimetabolite in biochemical and medicinal chemistry studies and is supplied with a supplier certificate of analysis.
- White to off-white solid appearance.
- Molecular formula C10H11FN4O4.
- Molecular weight 270.22 g·mol⁻¹.
- Purity 95.0% (NMR).
- Storage: 4°C under nitrogen; in solvent, -80°C up to 6 months or -20°C up to 1 month.
- Intended for research applications as a nucleoside analog.
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Medchemexpress LLC 5 -Deoxy-2 3 -di-O- 10g
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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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Medchemexpress LLC Guanosine, 2′-deoxy-N-methyl | 19916-77-9 | 99.8% | 281.27 | C11H15N5O4 | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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2′-Deoxy-N-methylguanosine is a purine nucleoside analog supplied as a solid for research use. It is a 2′-deoxy derivative of N-methylguanosine and is used in studies of modified nucleosides, DNA adducts, enzymatic assays, and nucleic acid chemistry.
- Purity 99.8% for reliable experimental results.
- Molecular weight 281.27 and formula C11H15N5O4 for precise molecular characterization.
- Available in multiple milligram quantities to support small-scale experiments.
- Solid form for stable storage and accurate weighing.
- SMILES provided for computational chemistry and database indexing.
- Suitable for biochemical and nucleic acid research applications.
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[C@@H](O)[C@@H](O)[C@H](F)C=O | 25mg | 801686164](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000190419.jpg-250.jpg)
eMolecules 70763-62-1 | 2-Deoxy-2-fluoro-L-fucose | Ambeed166.148 | C6H11FO4 | 98.000 | C[C@H](O)[C@@H](O)[C@@H](O)[C@H](F)C=O | 25mg | 801686164
2-Deoxy-2-fluoro-L-fucose | Ambeed | 70763-62-1166.148 | C6H11FO4 | 98.000 | C[C@H](O)[C@@H](O)[C@@H](O)[C@H](F)C=O | 25mg | 801686164
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![eMolecules 97614-44-3 | 3,5-Di-O-benzoyl-2-deoxy-2-fluoro-?-D-arabinofuranosyl bromide | Apollo Scientific | MFCD15144963 | 423.234 | C19H16BrFO5 | 0.000 | F[C@@H]1[C@@H](Br)O[C@H](COC(=O)c2ccccc2)[C@H]1OC(=O)c1ccccc1 | 500mg | 603092322](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000191653.jpg-250.jpg)
eMolecules 97614-44-3 | 3,5-Di-O-benzoyl-2-deoxy-2-fluoro-?-D-arabinofuranosyl bromide | Apollo Scientific | MFCD15144963 | 423.234 | C19H16BrFO5 | 0.000 | F[C@@H]1[C@@H](Br)O[C@H](COC(=O)c2ccccc2)[C@H]1OC(=O)c1ccccc1 | 500mg | 603092322
3,5-Di-O-benzoyl-2-deoxy-2-fluoro-?-D-arabinofuranosyl bromide | Apollo Scientific | 97614-44-3 | MFCD15144963 | 423.234 | C19H16BrFO5 | 0.000 | F[C@@H]1[C@@H](Br)O[C@H](COC(=O)c2ccccc2)[C@H]1OC(=O)c1ccccc1 | 500mg | 603092322
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Medchemexpress LLC 2'-Deoxy-2'-fluoroinosine | 80049-87-2 | C10H11FN4O4 | 1 G
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2'-Deoxy-2'-fluoroinosine is a purine nucleoside analog. These analogs exhibit broad antitumor activity, particularly against indolent lymphoid malignancies, and their anticancer mechanisms involve inhibiting DNA synthesis and inducing apoptosis.
- Purine nucleoside analog
- Has broad antitumor activity targeting indolent lymphoid malignancies
- Anticancer mechanisms include inhibition of DNA synthesis and induction of apoptosis
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