Sucres du squelette et nucléobases

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Applications Pyrimidine with the ability to form complexes with heavy metal ions. References Iltzsch, M., et al.: Biochem. Pharmacol., 48, 781 (1994),

2-Iodo-9H-purine is a synthetic molecule that is used for labeling dna duplexes. It binds to the ATP binding site on the enzyme and can be detected by magnetic resonance imaging. 2-Iodo-9H-purine has shown to be effective in synthesizing cross-coupling products, which are used in the synthesis of purines and polyhydroxylated compounds. The compound was also synthesized using a solid phase synthesis method and has shown to have antituberculosis activity.

Please enquire for more information about 6-Amino-1-benzyl-3-methyl-5-(N-formyl-N-methyl)uracil including the price, delivery time and more detailed product information at the technical inquiry form on this page

8-Methylxanthine is a metabolite of caffeine and theophylline. It has been shown to be a pro-inflammatory cytokine that stimulates the production of other pro-inflammatory cytokines such as interleukin (IL)-1β, IL-6, and tumor necrosis factor alpha (TNFα). 8-Methylxanthine is also a substrate for cytochrome P450 enzyme activity, which is responsible for metabolizing many drugs and other chemicals in the body. This compound has been detected in human liver and urine samples. 8-Methylxanthine has cytotoxic properties and may serve as an antioxidant. Mass spectrometric detection methods are used to identify this compound in biological fluids.

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Lambda DNA is a double stranded linear DNA of 48,502 base pairs in length. It is isolated from bacteriophage Lambda. The Lambda Phage is a bacterial virus (bacteriophage), that infects the bacterial species E. coli. The phage is isolated from the heat inducible lysogen E. coli strain.

Stability Hygroscopic Applications Adenine Hemisulfate can be one of the factors that influence in vitro growth and shoot multiplication of pomegranate. It can be used in biological study along with varied levels of sucrose, light intensity, and MS medium hydrogen ion concentration where those factors can all significantly influence multiplication and growth of Punica granatum shoots. References Singh, P., & Patel, R., M.: Bioscan, 9, 1031-1035 (2014)

1-Allyl-3,7-dimethyl-8-sulfophenylxanthine sodium salt is a chemical compound that is a competitive antagonist at the adenosine A1 receptor. It has been shown to be proconvulsant in mice and antagonizes the effects of caffeine. This drug also has an effect on neurotransmitter receptors and neurotransmitters, such as adenosine, which may be due to its ability to inhibit the breakdown of adenosine by methylxanthines.

Sulfo-Cy5.5 Trifluoroacetate: a cyano dye for low-background, non-invasive near-infrared in vivo imaging.

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2-Fluoro-9-benzylpurine is a stable and halogenated analog of purine. It is hydrolyzed by the enzyme in the body and converted to fluorodeoxyglucose, which is then used for labeling of cells. 2-Fluoro-9-benzylpurine has been used for positron emission tomography (PET) imaging studies as a radiolabeling agent and for diagnosis of malignant tumors. Its specific activity is high enough to allow it to be used in preparations with low concentrations of active ingredient. 2-Fluoro-9-benzylpurine's uptake has been shown to be influenced by chloride ions and glutathione levels in the blood, which can be beneficial when using it as a tracer.

2-Thiothymine is a nucleotide that can be synthesized by the polymerase chain reaction. It is used as a probe for determining the sequence of DNA duplexes. 2-Thiothymine binds to dna and forms hydrogen bonds with the nitrogen atoms in dna bases, which prevents them from being able to bind with other dna bases, thereby disrupting the binding of dna strands. This leads to chain reactions that result in high temperatures and could cause damage to the cells. 2-Thiothymine has been shown to be toxic to both bacteria and human cells. It was found to inhibit HIV infection by binding to viral RNA and preventing it from being translated into protein, leading to cell death.

2'-Deoxy-2'-Fluoroguanylyl-(3'-5')Uridine is a ribose analog that has been shown to inhibit catalytic activity. This compound binds to the active site of ribonucleotide reductase, which is an enzyme that catalyzes the reduction of ribonucleotides to deoxyribonucleotides. The 2'-deoxy-2'-fluoroguanylyl-(3'-5')uridine analogs have been shown to bind at different positions on the enzyme than the natural substrate and have been used as inhibitors in studies of ribonucleotide reductase. These compounds have also been shown to interact with other enzymes such as DNA polymerase and protein kinases, which are involved in signal transduction pathways.

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3,7-Dimethyl-1-propargylxanthine is a cyclase inhibitor that has been shown to have pharmacological effects. It has been shown to be effective in vivo models of Parkinson's disease and has reduced locomotor activity. This drug also inhibits the production of adenosine and dopamine, leading to neuronal death. The 3,7-dimethyl-1-propargylxanthine shows high selectivity for adenosine A3 receptors and is an antagonist at these receptors. It prevents mitochondrial membrane potential from decreasing, which may be due to inhibition of the production of reactive oxygen species by mitochondria. 3,7-Dimethyl-1-propargylxanthine also inhibits platelet aggregation by blocking the activation of phospholipase C and enhances platelet aggregation by inhibiting phosphodiesterase activity.