Purine nucleosides
Medchemexpress LLC 2'-deoxyadenosine-5'-monophosphate | 653-63-4 | MFCD00005753 | 99.6% | 331.22 g/mol | C10H14N5O6P | 1 ML
2'-Deoxyadenosine-5'-monophosphate (dAMP) is a deoxynucleotide used in biochemical and molecular biology research as an adenine-containing monophosphate component of DNA. It is used to study DNA synthesis, nucleotide interactions, and DNA damage/repair. The compound is supplied as a solid and as a ready-to-use 10 mM solution in DMSO for assay use.
- Adenine nucleoside monophosphate for DNA research.
- Available as solid or 10 mM solution in DMSO for immediate use.
- High purity suitable for biochemical assays.
- Compatible with DNA synthesis and damage/repair studies.
- Formula C10H14N5O6P and molecular weight 331.22 g/mol; CAS 653-63-4 for identification.
Medchemexpress LLC 2'-Deoxyadenosine-5'-triphosphate-d14 (dilithium) (dATP-d14 (dilithium)) | 2687960-68-3 | 97.10% | 517.13 | 1 MG
2'-Deoxyadenosine-5'-triphosphate-d14 (dATP-d14) dilithium is deuterium labeled 2'-Deoxyadenosine-5'-triphosphate. It is a nucleotide used in cells for DNA synthesis (or replication), as a substrate of DNA polymerase. This product is for research use only.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Medchemexpress LLC 3′-Deoxyguanosine | 3608-58-0 | 97.0% | 267.25 | 10 MG
3′-Deoxyguanosine is a derivative of Guanosine that interacts with human purine nucleoside phosphorylase through hydrogen bonding. It demonstrates moderate displacement activity for [3H]-guanosine in rat meninges. This product is for research use only and not sold to patients.
- Derivative of guanosine
- Interacts with human purine nucleoside phosphorylase
- Useful for studying guanosine receptors
- Useful for studying purine metabolism
- Exhibits moderate displacement activity for [3H]-guanosine in rat meninges
Medchemexpress LLC 3′-Deoxyguanosine | 3608-58-0 | MFCD28041154 | 97.0% | 267.25 | 100 MG
3′-Deoxyguanosine is a derivative of Guanosine. It interacts with human purine nucleoside phosphorylase via hydrogen bonding with residues such as Glu201 and Asn243. It exhibits moderate displacement activity for [3H]-guanosine in rat meninges and is useful for studying the mechanism of guanosine receptors and purine metabolism.
- Useful for studying guanosine receptors
- Used in research on purine metabolism
- Interacts via hydrogen bonding with human purine nucleoside phosphorylase
Medchemexpress LLC 2'-deoxyadenosine-5'-monophosphate-d12 dilithium | 97.7% | 355.16 | C10D12Li2N5O6P | 1 MG
2'-Deoxyadenosine-5'-monophosphate-d12 (dilithium) is a deuterium-labeled form of 2'-deoxyadenosine-5'-monophosphate used as a research reagent to study DNA synthesis, nucleotide interactions, and isotope tracing by mass spectrometry or NMR. Supplied as the dilithium salt, it is intended for laboratory research use only.
- Isotopically labeled d12 for accurate mass-shift studies.
- Suitable for mass spectrometry and NMR applications.
- Dilithium salt form for improved solubility in selected buffers.
- High purity (97.7%) for reproducible experimental results.
- Compatible with nucleotide chemistry and DNA interaction studies.
Cambridge Isotope Laboratories 2-Deoxyadenosine 5-triphosphate ammonium salt (13C10 98% 15N5 96-98%) CP 90% (in solution) 20 umol
2-Deoxyadenosine 5-triphosphate ammonium salt (13C10 98% 15N5 96-98%) CP 90% (in solution) 20 umol
Apexbio Technology LLC 6-O-Propynyl-2-deoxyguanosine 1mg
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
Cayman Chemical N6-Methyl-2-deoxyadenosIn 25mg
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
Medchemexpress LLC Malvidin-3-O-arabinoside chloride | 28500-04-1 | 97.1% | 498.86 | 5 MG
Malvidin-3-O-arabinoside chloride (M3A chloride) is a research chemical that ameliorates ethyl carbamate-induced oxidative damage by stimulating AMPK-mediated autophagy. It is used in studies to understand cellular processes related to oxidative stress and autophagy.
- Stimulates phosphorylation of AMP-activated protein kinase (AMPK)
- Upregulates LAMP-1 expression
- Restores lysosomal acidity and strengthens lysosomal functions
- Inhibits excess reactive oxygen species (ROS) generation
- Enhances glutathione (GSH) levels and autophagy flux
- Upregulates LC3-II/LC3-I ratio
Medchemexpress LLC 2'-Deoxyguanosine 5'-monophosphate disodium hydrate | 146877-98-7 | 99.0% | C10H14N5O7.H2O.2Na | 100 MG
2'-Deoxyguanosine 5'-monophosphate disodium hydrate (dGMP) is an oxidizable target of the photosensitizer pterin. It can be used to evaluate the photosensitizing properties of biopterins. Pterin causes a photosensitive reaction of dGMP under UV-A radiation, leading to DNA damage. This process involves two main mechanisms in vitro for the photosensitive oxidation of purine nucleotides by pterin.
- A hydrogen abstraction reaction of electron transfer from dGMP to the triplet excited state of pterin (type I mechanism).
- Interaction between dGMP and pterin produces singlet molecular oxygen (1O2) (type II mechanism).
Medchemexpress LLC 2'-Deoxyguanosine (standard) | 961-07-9 | MFCD00080300 | 99.2% | 267.24 | 50 MG
2'-Deoxyguanosine (Standard) is the analytical standard for 2'-Deoxyguanosine. It is intended for research and analytical applications. This purine nucleoside exhibits diverse biological activities, including inducing DNA division in mouse thymus cells and acting as a potent cell division inhibitor in plant cells. In vitro, it inhibits the clonal growth of HL-60 and K562 leukemia cells with IC50 values of 50 and 80 μM, respectively.
- Analytical standard for 2'-deoxyguanosine
- Intended for research and analytical applications
- Induces DNA division in mouse thymus cells
- Potent cell division inhibitor in plant cells
- Inhibits clonal growth of HL-60 and K562 leukemia cells
- Used in qualitative, quantitative, and methodological research experiments
- Suitable for HPLC, GC, and MS applications
eMolecules 312693-72-4 | 2'-Deoxyguanosine monohydrate | 1g
Ambeed | 1-(2-Methoxyphenyl)-1H-imidazole-5-carboxylic acid | 100mg | 600849156 | A866307 | 762240-23-3 | MFCD25368751 | 218.212 | C11H10N2O3
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Medchemexpress LLC N6-cyclopentyladenosine | 41552-82-3 | MFCD00036845 | 100.0% | 335.36 g/mol | C15H21N5O4 | 1 ML
N6-Cyclopentyladenosine is a selective adenosine A1 receptor agonist used as a research reagent in pharmacology and receptor signaling studies. Supplied as a 10 mM solution in a 1 mL vial, it is intended for in vitro experiments and receptor-binding assays.
- Selective adenosine A1 receptor agonist for pharmacological studies.
- Provided as a 10 mM solution for ready-to-use experiments.
- High chemical purity suitable for research applications.
- Compact 1 mL vial format for small-scale assays.
- Molecular weight 335.36 g/mol; molecular formula C15H21N5O4.