Purine nucleosides
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.
Medchemexpress LLC 2'-Deoxyguanosine | 961-07-9 | 99.9% | 267.25 | 10 G
2'-Deoxyguanosine is a purine nucleoside with diverse biological activities, known to induce DNA division in mouse thymus cells and act as a potent cell division inhibitor in plant cells. It also demonstrates inhibitory effects on the clonal growth of HL-60 and K562 leukemia cells, with observed IC50 values of 50 and 80 μM, respectively. This compound typically appears as a solid, ranging from white to off-white in color.
- Endogenous metabolite
- Harmful if swallowed
- Causes skin irritation
- Causes serious eye irritation
- May cause respiratory irritation
Medchemexpress LLC 2'-Deoxyadenosine-5'-triphosphate-13C10 dilithium | 1927-31-7 | 95.0% | 512.97 | 1 MG
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
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.
Medchemexpress LLC 2'-Deoxyguanosine-13C10,15N5 monohydrate | 2483830-26-6 | 99.8% | 1 MG
2'-Deoxyguanosine-13C10,15N5 (monohydrate) is the 13C and 15N labeled 2'-Deoxyguanosine monohydrate, which is an endogenous metabolite. It is for research use only and not sold to patients.
- Used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules for quantitation during the drug development process.
- Deuteration has potential to affect pharmacokinetic and metabolic profiles of drugs.
Medchemexpress LLC Deoxyguanosine triphosphate trisodium solution | 93919-41-6 | 99.95% | 573.13 | 28.66 MG
Deoxyguanosine triphosphate (dGTP) trisodium solution (100mM) is a nucleotide precursor in cells for DNA synthesis. It is used in reverse transcription-polymerase chain reaction (RT-PCR) for DNA amplification. Deoxyguanosine triphosphate is abnormally elevated in the red blood cells of individuals with immunodeficiency related to purine nucleoside phosphorylase deficiency, and it can be regarded as a potential toxic metabolite.
- Nucleotide precursor for DNA synthesis.
- Used in reverse transcription-polymerase chain reaction (RT-PCR) for DNA amplification.
Cambridge Isotope Laboratories 2-Deoxyguanosine 5-triphosphate ammonium salt (13C10 98% 15N5 96-98%) CP 90% (in solution) 20 umol
2-Deoxyguanosine 5-triphosphate ammonium salt (13C10 98% 15N5 96-98%) CP 90% (in solution) 20 umol
Cambridge Isotope Laboratories 8-Hydroxy-2-deoxyguanosine (15N5 98%) CP 95% 1 mg
8-Hydroxy-2-deoxyguanosine (15N5 98%) CP 95% 1 mg
Cambridge Isotope Laboratories 2-Deoxyadenosine monohydrate (13C10 98% 15N5 96-98%) 10 mg
2-Deoxyadenosine monohydrate (13C10 98% 15N5 96-98%) 10 mg
Sigma Aldrich Fine Chemicals Biosciences 2'-Deoxyguanosine monohydrate 99-100% | 312693-72-4 | MFCD00150760 | 5G
2'-Deoxyguanosine monohydrate 99-100% | Purity: 99-100% | Mol Wt: 285.26 | 312693-72-4 | MFCD00150760 | 5G
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
Cayman Chemical N6-benzoyl-2'-Deoxyadenosine, Purity: ≥95%, CAS: 4546-72-9, 1 g
A nucleoside building block; has been used in the synthesis of various oligonucleotides
Apexbio Technology LLC 2-Deoxyadenosine 958-09-8 100mg
2-Deoxyadenosine (CAS 958-09-8) is a synthetic purine nucleoside analog that functions as a demethylated nucleoside in biological systems Structurally similar to adenosine but lacking a hydroxyl group at the 2 position it selectively pairs with deoxythymidine during DNA synthesis 2-Deoxyadenosine influences regulatory pathways associated with DNA replication and repair serving as a molecular probe to study these processes It is extensively utilized in molecular biology and genomics for investigating DNA synthesis repair mechanisms and the dynamics of nucleic acid metabolism