Nucleósidos

<p>Thymidine 3′-monophosphate disodium is a chemotherapeutic agent that has been shown to have antiviral and anticancer properties. It is a nucleoside analogue, which mimics the structure of thymidine and inhibits DNA synthesis by interfering with the DNA replication process. Thymidine 3′-monophosphate disodium is also used as an activator in the synthesis of deoxyribonucleosides and ribonucleosides. This product is synthetic, high quality, and not chemically modified. It has CAS number 68698-19-1 and molecular weight of 242.06 g/mol.</p>

<p>IMP + GMP is a DNA synthesis activator that can be used to synthesize DNA, RNA, and oligonucleotides. It is modified to have antiviral and anticancer properties. IMP + GMP has been shown to have antiviral activity against HIV-1 and inhibits the replication of the virus in human cells. The drug also has anticancer effects against certain types of cancerous cells. IMP + GMP is synthesized by modifying natural nucleosides with phosphoramidite chemistry, which allows it to be easily incorporated into many diverse synthetic pathways. IMP + GMP is highly purified and can be purchased at high quality for research purposes.</p>

<p>N2-Isobutyrylguanosine is a synthetic nucleoside analog. It is activated by the enzyme thymidine kinase and inhibits the synthesis of RNA and DNA, which leads to cell death. N2-Isobutyrylguanosine has been shown to be an effective inhibitor of epidermal growth factor receptor (EGFR) in mammalian cells. This drug has also been shown to inhibit insulin-like growth factor I and phosphorothioate monomers. N2-Isobutyrylguanosine inhibits the synthesis of fatty acids, leading to a decrease in lipid content in cells.</p>

<p>2'-Deoxy-5'-O-DMT-uridine is a bifunctional drug that has both antibacterial and anticancer activity. This drug is used to treat leishmania infections, which are caused by protozoan parasites. 2'-Deoxy-5'-O-DMT-uridine suppresses the growth of these organisms by inhibiting RNA synthesis and protein synthesis. It also inhibits proliferation of cancer cells in vivo by targeting cancer cells with high levels of primary amines. 2'-Deoxy-5'-O-DMT-uridine is an effective chemotherapeutic agent that can be used to treat pancreatic cancers with high rates of primary amines (e.g., insulinoma).</p>

<p>Thymidine-5'-diphosphate-4-keto-6-deoxy-D-glucose disodium salt is a precursor in the synthesis of nucleoside sugars in pathways such as rhamnose biosynthesis.</p>

<p>Xanthosine 5'-triphosphate disodium salt is a nucleotide that is an intermediate in the synthesis of DNA and RNA. It has a hydroxyl group at the 5' carbon atom and two carboxylic acid groups on the 3' carbon atom. Xanthosine 5'-triphosphate disodium salt can be found in many compounds, such as d-glucose, which contains six hydroxyl groups. <br>Xanthosine 5'-triphosphate disodium salt is also used as a building block for other molecules, such as ATP, which contains adenosine with one hydroxyl group on the 2' carbon atom and three phosphate groups.</p>

<p>3'-Amino-2',3'-dideoxy-5-methylcytidine is an antiviral agent that has been shown to inhibit the replication of viruses in cell culture. It also inhibits the synthesis of DNA, RNA, and proteins. This drug has been used in vivo studies on animals and humans. 3'-Amino-2',3'-dideoxy-5-methylcytidine has not been tested as a treatment for hepatitis B virus infections, but some evidence suggests it may be effective against hepatitis C virus infections.</p>

<p>Cytidine is a nucleoside that belongs to the group of pyrimidine nucleosides. It can be absorbed from the intestine and hydrolyzed to uridine by intestinal enzymes. Cytidine has been shown to inhibit angiogenesis in animal model systems and transfection experiments, as well as being genotoxic in vitro. Cytidine has also been shown to inhibit polymerase chain reactions (PCR) and enzyme activities, such as cytidine deaminase, which converts cytidine into uracil.</p>

<p>5-Hydroxyduridine is a nucleoside that is naturally found in the human body. It can be synthesized from uridine by oxidation of the 5-hydroxyl group to the corresponding aldehyde. It has been shown to have genotoxic effects in vitro and in prostate cancer cells. 5-Hydroxyduridine has also been shown to inhibit sugar transport, which may be due to its ability to form hydrogen bonds with glycosidic bonds. It has been reported that 5-hydroxyduridine causes acid formation and hydroxylation of cardiac lipids.</p>

<p>N4-Acetyl-2'-deoxy-5'-O-DMT-cytidine 3'-CE phosphoramidite is a novel nucleoside that belongs to the group of deoxyribonucleosides. It is a modified nucleotide with a phosphate at the 5' position and an acetyl group in place of the hydroxyl group at the 2' position. N4-Acetyl-2'-deoxy-5'-O-DMT-cytidine 3'-CE phosphoramidite has antiviral, anticancer, and activator properties. This compound is also known as 5′N4 acetyldeoxythymidine 3′Ce, or 5′N4 acetyldeoxythymidine 3′Ce phosphoramidite.</p>

<p>2'-O-Methylcytidine-5'-monophosphate triethylammonium salt is a synthetic nucleoside that has been shown to be a substrate for DNA polymerase and an inhibitor of RNA synthesis. It has been used in the laboratory as a primer and as a biochemical tool to study viruses. 2'-O-Methylcytidine-5'-monophosphate triethylammonium salt is active against murine leukemia virus, but not against ciliated protozoan parasites such as Tetrahymena pyriformis. This compound has also been shown to inhibit the enzyme form of HIV reverse transcriptase and to be cytotoxic at high concentrations.</p>

<p>Beta-nicotinamide adenine dinucleotide phosphate sodium salt (NADPH) is a coenzyme that mediates various biological processes. It’s a regenerating electron donor in cellular antioxidation systems and a regulator of energy metabolism and mitochondrial functions. It mediates calcium homeostasis via the generation of cyclic ADP-ribose and modulates several key factors in cell death such as mitochondrial permeability transition and poly(ADP-ribose) polymerase-1 (PARP1).</p>

<p>2,2’-Anhydro-5-methyluridine-3’-CE phosphoramidite is a monophosphate nucleotide that is used as a building block for DNA synthesis. It can be modified to form a novel 2,2’-anhydro-5-methyluridine analogue with anti-cancer properties. This product also has antiviral and activator activities.</p>

<p>S4-2-Cyanoethyl-4-thiothymidine is a novel nucleoside with high quality and high purity. It is a diphosphate that is an activator of DNA synthesis and has been shown to have anticancer properties. This product is suitable for use in the synthesis of oligonucleotides, phosphoramidites, and nucleosides.</p>

<p>Adenosine is a nucleoside that interacts with adenosine receptors in the central nervous system. It is found in most body tissues and fluids, including blood, cerebrospinal fluid, and synovial fluid. Adenosine has been shown to inhibit uptake of glucose and other substances in the brain. The uptake of adenosine by neurons is inhibited by solute transport inhibitors such as nevirapine, which prevents the accumulation of toxic levels of adenosine during excitotoxic injury. Adenosine also has thermodynamic properties that promote its removal from solution by binding to water molecules and forming crystals or precipitates. This property may be useful in the treatment of cerebral edema following traumatic brain injury.</p>

<p>2'-Deoxy-5-hydroxycytidine is a nucleoside analog that is used to treat human immunodeficiency virus (HIV). It inhibits the synthesis of HIV by inhibiting the enzyme reverse transcriptase. This drug binds to DNA duplexes, and has been shown to be reactive with damaged DNA. The compound has been shown to inhibit viral replication in a model system, and also inhibits the polymerase chain reaction. 2'-Deoxy-5-hydroxycytidine may also have thermodynamic properties that are related to its potential for reactivity with oxidative DNA.<br>2'-Deoxy-5-hydroxycytidine is an analog of cytidine. It can be synthesized using solid phase synthesis on a resin support.</p>

<p>Universal sulfonate donor for in vivo sulfonation by sulfotransferases</p>

<p>N6-Benzoyladenosine is a purine nucleoside that is synthesized from uridine and has a high resistance to phosphorylation. It is found in the mitochondrial matrix of rat hepatocytes and can be used as a specific agent for the treatment of symptoms related to Parkinson's disease. N6-Benzoyladenosine inhibits protein synthesis by inhibiting the catalytic subunit of guanine nucleotide-binding proteins, which are involved in cellular energy production. It also inhibits camp levels and camp concentrations in mitochondria, which may be due to its effects on the trimethylbenzodiazepine receptor.</p>

<p>2-Chloroinosine is a synthetic nucleoside analog derived from inosine, in which a chlorine atom is substituted at the 2-position of the purine base (hypoxanthine). This modifcation causes altered reactivity and can be used in research applications</p>

<p>5'-O-DMT-2'-O-(2-methoxyethyl)-5-methylcytidine is a phosphoramidite that is used in the synthesis of DNA and RNA. It has been shown to have antiviral and anticancer properties, as well as being a potential candidate for treating HIV infections. 5'-O-DMT-2'-O-(2-methoxyethyl)-5-methylcytidine has high quality and purity and is not hazardous to the environment.</p>

<p>5-Methoxymethyl-2'-deoxyuridine is an antiviral agent that inhibits viral replication by reacting with the glycosidic bond in the viral enzyme, which prevents the enzyme from functioning and so prevents virus replication. 5-Methoxymethyl-2'-deoxyuridine has been shown to be active against herpes simplex virus, although it is not active against wild-type viruses. This drug has toxic effects on animals, which may be due to its ability to inhibit amino transferase activity, which leads to systemic diseases. It has also been shown that 5-Methoxymethyl-2'-deoxyuridine can be used as a marker for autoimmune diseases.</p>

<p>Thymidine-5'-monophosphate disodium salt is a nucleoside that is synthesized by reductive phosphorylation of thymidine. It is a substrate for nucleotide synthesis and can be used as a reagent in the synthesis of oligonucleotides. Thymidine-5'-monophosphate disodium salt can be reduced to form thymidine, which can then be converted to 5-thio-2'-deoxyuridylate or 5-thio-2'-deoxycytidylate. This conversion takes place through the cleavage reaction of the thymidine residue from the disodium salt.</p>

<p>2-Thiothymidine is a hydrogen bond donor and acceptor that can be used as a substitute for thymine in the synthesis of DNA. 2-Thiothymidine has been shown to have successful in vivo treatment against bladder cancer and skin cells, as well as photochemical properties. It has been shown to inhibit the growth of prostate cancer cells by inhibiting DNA synthesis. 2-Thiothymidine binds to dna duplexes and polymerase chain reactions, which are important for replication of DNA. This drug also inhibits replication by preventing intramolecular hydrogen bonds from forming.<br>2-Thiothymidine is a nucleoside analog that is substituted for thymine during DNA synthesis. It inhibits the growth of prostate cancer cells by inhibiting DNA synthesis. It binds to dna duplexes and polymerase chain reactions, which are important for replication of DNA. This drug also inhibits replication by preventing intramolecular hydrogen bonds from forming.</p>

<p>7-Deaza-2’-C-methylinosine is an antiviral agent that inhibits the replication of DNA or RNA. It is a nucleoside analog that can be phosphorylated to form a diphosphate or monophosphate. 7-Deaza-2’-C-methylinosine has been shown to have anticancer effects in vitro and in vivo, as well as inhibit the proliferation of cancer cells. This agent also has novel properties due to the presence of the methyl group at position 2’ on the deoxyribose ring.</p>

<p>2’-Deoxy-8-methoxyadenosine is a synthetic nucleoside that is structurally similar to the natural nucleosides adenosine and cytidine. It can be used for antiviral and anticancer purposes, as well as in the treatment of HIV/AIDS by inhibiting viral replication. This compound has been shown to activate the immune system, stimulate the production of cytokines, and inhibit tumor cell growth. 2’-Deoxy-8-methoxyadenosine is also capable of inducing apoptosis in cancer cells, which may be due to its ability to inhibit DNA synthesis and protein synthesis.</p>

<p>2-Methyladenosine-5'-triphosphate (2-MeATP) is an inhibitor of the purinergic receptor P2X. It is a competitive antagonist of ATP at the P2X receptor, blocking ATP binding and inhibiting ATP-mediated signal transduction. 2-MeATP has been shown to inhibit angiotensin-mediated hyperpolarization in wild type and mutant strains of M. smegmatis, as well as m. tuberculosis perfusion in mesenteric lymph nodes and vasoconstriction in wildtype and mutant strains of AT1 receptors.</p>

<p>8-Azidoadenosine 3',5'-cyclic monophosphosphate is used for nucleotide labelling via a click reaction involving the azide moiety and a terminal alkyne conjugated to a label. The reaction generates a stable nucleotide labelled adduct containing a triazole link.</p>

<p>Anti-HCV agent; inhibitor of viral RNA polymerases</p>

<p>p-Topolin riboside is a potent antibacterial agent that binds to the receptor binding site of wild-type mice. This hydrogen bond inhibits the activity of cellular p-topolin riboside, which is required for the synthesis of carotenoids and nitro compounds in mitochondria. p-Topolin riboside has been shown to have anti-aging properties and can inhibit locomotor activity in vivo. It has also been shown to have potent antibacterial effects against bacteria such as MRSA, Pseudomonas aeruginosa, and Enterococcus faecalis.</p>

<p>2',3'-Dideoxy-5-iodocytidine is a modified nucleoside analog based on cytidine, one of the four standard nucleosides found in DNA and RNA. It has been chemically altered to interfere with DNA or RNA synthesis, making it potentially useful as an antiviral or anticancer agent.</p>

<p>2’-Deoxy-N3-methylcytidine is a novel nucleoside with antiviral and anticancer properties. It has been shown to inhibit the replication of HIV, Hepatitis C, and HSV. This drug can be used in the treatment of cancer, such as leukemia and lymphoma. 2’-Deoxy-N3-methylcytidine is also an effective inhibitor of DNA synthesis in cells that are resistant to other drugs. In addition, this drug also has a high purity level and a CAS number 5040-21-1.</p>

<p>2,4-Dithiouridine is a nucleoside for use in a variety of applications</p>

<p>5-Bromo-2-fluoronicotinic acid is a crystalline compound with an orthorhombic crystal system. The crystal structure of 5-bromo-2-fluoronicotinic acid monohydrate was determined by X-ray diffraction and refined to 2.5 Å resolution. The space group was found to be P212121 and the unit cell dimensions are a = 9.716 Å, b = 10.867 Å, c = 12.242 Å and β = 106.9°. The molecular weight of 5-bromo-2-fluoronicotinic acid monohydrate was found to be 277.3 g/mol with an elemental analysis of C: 67% H: 7% F: 16%.</p>

<p>N6-Benzoyl-5'-O-DMT-2'-O-(2-ethoxy-2-oxoethyl)adenosine 3'-CE phosphoramidite is a novel nucleoside analog which is a potent activator of the immune system. It is synthesized by reacting adenosine with N,N'-diisopropylcarbodiimide and 2,4,6-trichlorobenzoyl chloride in dichloromethane at room temperature. This product has antiviral and anticancer properties.</p>

<p>Please enquire for more information about p-Coumaryl-coenzyme A including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2'-O-Methyl-5-methyluridine is a nucleoside that is involved in the synthesis of RNA. It is a component of the 5-methyluridine (5MU) and 2'-O-methyl-5-hydroxymethyluridine (2'OMMU) families of nucleotides. This compound has been shown to be effective against organisms such as E. coli, S. typhimurium, and C. parapsilosis, which are amide sensitive. The amide group of 2'-O-methyl-5-methyluridine can be cleaved by reagents such as hydrazine or tris(2,4,6,-trimethlyphenyl)phosphonium bromide to form 5MU and 2'OMMU respectively. The modifications to the ribose ring are important for its activity and function in cells. The modification of the ribose ring is catalyzed by enzymes called</p>

<p>2',3'-O-Isopropylideneadenosine is a nucleoside that has a possible usage as an organic chemical synthesis intermediate</p>

<p>Cytidine is a nucleotide molecule formed through the attachment of cytosine to a ribose ring</p>

<p>1-Deaza-2'-deoxyadenosine is a modified nucleoside that is used as an anticancer agent. It inhibits DNA and RNA synthesis, which are required for cell division. 1-Deaza-2'-deoxyadenosine is also a novel activator of the enzyme ribonucleotide reductase, which converts ribonucleotides to deoxyribonucleotides. Ribonucleotides are needed for the production of DNA and RNA. 1-Deaza-2'-deoxyadenosine has been shown to kill cells by inhibiting the synthesis of DNA and RNA, which are needed for cell division.</p>

<p>4-Amino-1-(2-deoxy-α-D-erythro-pentofuranosyl)-5-methyl-2(1H)-pyrimidinone is a novel phosphate derivative of ribonucleosides, including 2'-deoxyadenosine and 2'-deoxycytidine. 4ADP has antiviral and anticancer activities, and can be used as a substrate for the synthesis of phosphoramidites. These derivatives are modified by the introduction of substituents at the 5' position of the pentose sugar. The monophosphate form is synthesized by reacting with sodium hydroxide followed by hydrolysis with dilute acid. The diphosphate form is synthesized by reacting with phosphorus oxychloride in presence of pyridine.</p>

<p>6-(2-Pyridylmethylthio)-9-(b-D-ribofuranosyl)purine is a nucleoside that has antiviral activity and is a potent activator of the immune system. It also has anticancer effects, which may be due to its ability to inhibit DNA synthesis. This nucleoside is synthesized from 2-pyridylethyl methyl sulfide and b-D-ribofuranose. 6-(2-Pyridylmethylthio)-9-(b-D-ribofuranosyl)purine is novel because it contains a modified sugar moiety, phosphoramidites, and monophosphate groups. This product has high purity and quality because it's been purified through high performance liquid chromatography (HPLC).</p>

<p>Toyocamycin is a macrolide antibiotic that inhibits protein synthesis by binding to the 50S ribosomal subunit. Toyocamycin monohydrate (TM) has been shown to have significant cytotoxicity against HL-60 cells, which may be due to its ability to inhibit mitochondrial membrane potential and induce apoptosis. The drug also has inhibitory properties against wild-type strains of bacteria, such as diastatochromogenes, and is active against high-resistant strains of bacteria, such as E. coli. Toyocamycin monohydrate has been shown to inhibit transcriptional regulation in hl-60 cells and k562 cells by binding to RNA polymerase II and blocking RNA synthesis.</p>

<p>Adenosine 5'-diphosphate (ADP) is a nucleoside that is an important component of the cell's energy pathways. ADP plays a role in platelet activation and nitrate reductase, which are enzymes that maintain the integrity of bacterial DNA. Adenosine 5'-diphosphate also has been shown to inhibit neural cell injury and protein oxidation.</p>

<p>N1-Methyladenosine-5’-monophosphate is a RNA modified nucleotide.</p>

<p>5-(Methoxycarbonyl)methyl-2’-O-methyluridine is a nucleoside that is a precursor of cytidine. It is synthesized by the enzyme UMP synthase, which converts 5-methoxycarbonylmethyl-2-thiouridine to uridine and 2′-O-methyluridine. The synthesis of 5-(Methoxycarbonyl)methyl-2’-O-methyluridine occurs in both mammalian cells and Xenopus oocytes. This compound has been shown to be a potential biomarker for cancer and may be useful as an indicator of detoxification enzymes activity.</p>

<p>1-(2`-Chloro-2`-deoxy-beta-L-arabinofuranosyl)thymine is a thymine molecule attached to a modified arabinose sugar. Scientists create and study these nucleoside analogs because they can have antiviral or anticancer properties. The changes in the sugar can affect how the molecule interacts with enzymes and other biological components.</p>

<p>Riboflavin 5'-(trihydrogen diphosphate) P'5'-ester with N-(2-Aminoethyl)adenosine is a nucleoside that is an active form of riboflavin. It is a monophosphate that is synthesized from riboflavin and adenosine. Riboflavin 5'-(trihydrogen diphosphate) P'5'-ester with N-(2-Aminoethyl)adenosine has been shown to have anticancer, antiviral, and antitumor properties in vitro and in vivo. In addition, this compound has been shown to inhibit the growth of various tumor cells by inhibiting DNA synthesis.</p>

<p>N2-Isobutyryl-O6-cyanoethyl-7’-OH-N-trityl-morpholino guanine is a nucleoside, ribonucleoside, and anti-cancer drug. It is modified with two acyl groups at the 2′ position of the sugar moiety and contains a phosphoramidite group in the 5′ position. N2-Isobutyryl-O6-cyanoethyl-7’-OH-N-trityl -morpholino guanine is an activator of DNA synthesis in vitro. In vivo studies have shown that N2-Isobutyryl O6 cyanoethyl 7' OH N trityl morpholino guanine can be used as an anticancer agent against human breast cancer cells.</p>

<p>2'-Deoxyguanosine-5'-triphosphate or dGTP, is a nucleotide used by the cell to synthesize DNA molecules. 2'-Deoxyguanosine-5'-triphosphate is used in molecular biology techniques and assays as a substrate of the enzyme DNA polymerase, e.g. polymerase chain reaction (PCR), DNA sequencing, pyrosequencing reactions.</p>

<p>Uridine 5'-triphosphate disodium salt is a supramolecular complex that binds to gold nanoparticles. The binding of uridine 5'-triphosphate disodium salt to gold nanoparticles can be used for the detection of metal ions through the photometric method. Uridine 5'-triphosphate disodium salt has been shown to inhibit the glutathione-dependent reduction of vitamin B12, which is a key step in methionine synthesis and folate metabolism. This inhibition may lead to a decrease in protein synthesis, ATP production, and cell division.</p>