Purine nucleosides
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Filtered Search Results
Medchemexpress LLC Cyanidin-3-O-arabinoside | 111613-04-8 | MFCD27952825 | 95.7% | 454.81 g/mol | C20H19ClO10 | 5 MG
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Cyanidin-3-O-arabinoside is an anthocyanin pigment isolated from the flowers of Rhododendron cv. Lems Stormcloud. Supplied as a research-grade material, the compound is provided as a 5 mg sample with manufacturer-reported purity and supporting documentation for laboratory use.
- Anthocyanin pigment with antioxidant activity.
- Molecular formula C20H19ClO10 and molecular weight 454.81 g/mol.
- Supplied as a 5 mg sample with reported purity 95.7%.
- Manufacturer datasheet, COA, and SDS available for quality and handling information.
- Intended for biochemical assays and antioxidant research applications.
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Medchemexpress LLC Adenosine, 8-bromo-2'-deoxy- | 14985-44-5 | ≥98.0% | 330.14 | 10 MM 1 ML
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8-Bromo-2'-deoxyadenosine 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.
- Exhibits broad antitumor activity
- Targets indolent lymphoid malignancies
- Inhibits DNA synthesis
- Induces apoptosis
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Meridian Life Science HUMAN CA15-3 LCR CALIB. GRADE
Cancer Antigen CA15-3 (Breast Cancer) Calibrator Grade (Low Cross Reactivity)
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Medchemexpress LLC Peonidin-3-O-arabinoside chloride | 524943-91-7 | 98.5% | 468.84 | 10 MG
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Peonidin-3-O-arabinoside chloride is an anthocyanin that can be isolated from Vaccinium myrtillus L. This product is for research use only.
- For research use only
- Store at 4°C, sealed, away from moisture
- Stable in solvent for 6 months at -80°C or 1 month at -20°C
- Appearance: Solid, brown to black
- Molecular formula: C21H21ClO10
- Structure classification: Phenols, polyphenols
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Cayman Chemical N6-Methyl-2-deoxyadenosIn 50mg
A nucleoside and inducer of EPC proliferation; stimulates the proliferation of EPCs isolated from mouse fetal livers and colony formation of isolated mouse bone marrow cell-derived progenitor cells at 10 and 100 µM; accumulates along promoters and gene coding sequences in activated mouse prefrontal cortical neurons; is associated with activation at the Bdnf promoter
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Medchemexpress LLC 2'-Deoxyadenosine-5'-triphosphate-13C10 dilithium | 1927-31-7 | 95.0% | 512.97 | 1 MG
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2'-Deoxyadenosine-5'-triphosphate-13C10 dilithium (dATP-13C10 dilithium) is a 13C-labeled version of 2'-Deoxyadenosine-5'-triphosphate (dATP). dATP is a nucleotide crucial for DNA synthesis or replication in cells, serving as a substrate for DNA polymerase.
- Used as a tracer
- Used as an internal standard for quantitative analysis
- Suitable for analysis by NMR
- Suitable for analysis by GC-MS
- Suitable for analysis by LC-MS
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eMolecules 892-48-8 | 5'-CHLORO-5'-DEOXYADENOSINE | AstaTech | MFCD00049038 | 285.690 | C10H12ClN5O3 | 95.000 | Nc1ncnc2n(cnc12)[C@@H]1O[C@H](CCl)[C@@H](O)[C@H]1O | 5g | 296380143
5'-CHLORO-5'-DEOXYADENOSINE | AstaTech | 892-48-8 | MFCD00049038 | 285.690 | C10H12ClN5O3 | 95.000 | Nc1ncnc2n(cnc12)[C@@H]1O[C@H](CCl)[C@@H](O)[C@H]1O | 5g | 296380143
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Medchemexpress LLC 2'-Deoxyadenosine monohydrate-13C10,15N5 hydrate | 2483830-27-7 | 99.7% | 284.15 | 1 MG
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2'-Deoxyadenosine monohydrate-13C10,15N5 hydrate | 2483830-27-7 | 99.7% | 284.15 | 1 MG
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Medchemexpress LLC NBI-961 25 mg
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NBI-961 25MG
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Medchemexpress LLC 6-Thio-2'-deoxyguanosine | 789-61-7 | 99.7% | 283.31 | 10 MG
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6-Thio-2'-Deoxyguanosine is a nucleoside analogue that can be incorporated into de novo-synthesized telomeres by telomerase. This compound has shown rapid cell death in various cancer cell lines with IC50 values between 0.7-2.9 μM. In A549 lung cancer cell-based mouse xenograft studies, it decreased tumor growth rate, outperforming 6-thioguanine treatment, and increased telomere dysfunction in tumor cells in vivo. It is for research use only.
- Nucleoside analogue
- Incorporated into de novo-synthesized telomeres by telomerase
- Induces rapid cell death in various cancer cell lines
- Decreases tumor growth rate in mouse xenograft studies
- Increases telomere dysfunction in tumor cells in vivo
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Apexbio Technology LLC 6-O-Propynyl-2-deoxyguanosine 25mg
6-O-Propynyl-2-deoxyguanosine (CAS 1640051-47-3) is a modified nucleoside featuring an alkyne functional group at the 6-position of deoxyguanosine This structural modification enables its use in bioorthogonal click chemistry reactions facilitating site-specific labeling and conjugation in nucleic acid research The alkynyl group serves as a chemical handle for copper-catalyzed azide-alkyne cycloaddition allowing researchers to attach probes or other functional molecules 6-O-Propynyl-2-deoxyguanosine is utilized for studying DNA structure dynamics and for the development of modified oligonucleotides in biochemical and molecular biology assays
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Cayman Chemical 2-DeoxyadenosIn-5-monphos 1g
A derivative of AMP that has been used in the synthesis of novel photoaffinity labels for incorporation into DNA and to study adenosine-based interactions during DNA synthesis and DNA damage
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Medchemexpress LLC 3′-Deoxyguanosine | 3608-58-0 | 97.0% | 267.25 | 25 MG
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3′-Deoxyguanosine is a derivative of Guanosine. It interacts with human purine nucleoside phosphorylase through hydrogen bonding with residues like Glu201 and Asn243. This compound demonstrates moderate displacement activity for [3H]-guanosine in rat meninges and is useful for studying the mechanism of guanosine receptors and purine metabolism.
- Derivative of guanosine.
- Interacts with human purine nucleoside phosphorylase via hydrogen bonding.
- Exhibits moderate displacement activity for [3H]-guanosine in rat meninges.
- Useful for studying guanosine receptor mechanisms.
- Useful for studying purine metabolism.
- Displaces 50 nM [3H]-guanosine binding to rat brain membranes.
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Cambridge Isotope Laboratories 8-Hydroxy-2-deoxyguanosine (15N5 98%) CP 95% 1 mg
8-Hydroxy-2-deoxyguanosine (15N5 98%) CP 95% 1 mg
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Apexbio Technology LLC 2-Deoxyadenosine-monoH2O
2 -Deoxyadenosine monohydrate (CAS No 16373-93-6) is widely used in biomedical research particularly in molecular biology and pharmacology studies This compound originates from the deoxyribonucleic acid (DNA) and acts by integrating into DNA strands impacting replication and cellular processes It targets pathways involved in nucleoside metabolism and DNA synthesis In vitro it demonstrates activity typically in the nanomolar to low micromolar range making it valuable for studying DNA replication and repair mechanisms Common applications include cell-based assays animal studies and drug screening to investigate its effects on cellular proliferation and apoptosis Experimental concentrations typically depend on the specific research design
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