Nucleósidos
Los nucleósidos son building blocks fundamentales de los ácidos nucleicos, compuestos por una base nitrogenada unida a una molécula de azúcar. En esta sección, puede encontrar una amplia variedad de nucleósidos esenciales para la investigación en biología molecular, bioquímica y farmacología. Estos compuestos juegan roles cruciales en la síntesis de ADN y ARN, y son vitales en varios procesos metabólicos. Los nucleósidos se utilizan para estudiar material genético, desarrollar terapias antivirales y anticancerígenas, y comprender los mecanismos celulares. En CymitQuimica, proporcionamos nucleósidos de alta calidad para apoyar sus necesidades de investigación y desarrollo, asegurando pureza y fiabilidad para sus aplicaciones experimentales.
Se han encontrado 3569 productos de "Nucleósidos"
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N6-Acetyladenosine
CAS:N6-Acetyladenosine is a nucleoside that belongs to the group of N-acetylated adenosines. It is found in thermophilic organisms and has been shown to be involved in optimal growth. N6-Acetyladenosine has also been found to be an important part of the coding and population modifications of crenarchaeota, archaeal organisms that are phylogenetically related to methanogens. Unfractionated populations of methanogen contain both N6-acetyladenosine residues and other modified adenosines, with each organism differing in the types of modifications they contain. Transfer of these modified adenosines from one organism to another can lead to changes in their coding and population modifications.Fórmula:C12H15N5O5Pureza:Area-% Min. 90 Area-%Forma y color:White PowderPeso molecular:309.28 g/molKinetin riboside
CAS:Kinetin is a plant hormone that regulates cell proliferation and differentiation. Kinetin riboside is a derivative of kinetin in which the ribose moiety has been converted to ribosyl-ribitol. Kinetin riboside has shown the ability to inhibit cancer cells by inducing apoptosis, which may be related to its ability to inhibit cyclin D2 and mitochondrial membrane potential. In addition, kinetin riboside has been shown to protect against oxidative stress and decrease mitochondrial function in cells. This compound may have therapeutic potential for cancer treatment and other diseases caused by oxidative stress or mitochondrial dysfunction.Fórmula:C15H17N5O5Pureza:Min. 98 Area-%Forma y color:White PowderPeso molecular:347.33 g/molLamivudine 5'-triphosphate triethylammonium salt (Ethanol solution)
CAS:Sold by weight of nucleoside as solution in ethanol.Fórmula:C20H46N5O12P3SPureza:Min. 95%Forma y color:Clear LiquidPeso molecular:673.59 g/mol1-(b-L-Threonyl)-5-methyluracil
1-(b-L-Threonyl)-5-methyluracil (1,5MT) is a synthetic nucleoside that has antiviral and anticancer properties. 1,5MT is modified with a b-L-threonyl group at the 5’ position. This modification stabilizes the molecule and prevents its degradation by ribonucleases. The modification also increases the phosphoramidite reactivity of 1,5MT and enhances its incorporation into DNA during synthesis. 1,5MT is an activator for RNA polymerase II, which plays an important role in transcriptional regulation. It binds to the enzyme's allosteric site and stimulates transcriptional elongation by RNA polymerase II through phosphoramidate formation with deoxyribose phosphate. 1,5MT is active against cancer cells in vitro and has been shown to inhibit tumor growth in vivo.Pureza:Min. 95%1-(2-Deoxy-5-O-MMT-b-D-xylofuranosyl)-5-methyluracil
CAS:1-(2-Deoxy-5-O-MMT-b-D-xylofuranosyl)-5-methyluracil (1dXF) is a modified nucleoside that is synthetically derived from 5-methyluracil. It has been shown to be an effective anticancer agent, antiviral agent, and inhibitor of HIV replication in HIV infected cells. 1dXF also inhibits the synthesis of DNA, RNA, and protein in cancer cells.Fórmula:C30H30N2O6Pureza:Min. 95%Peso molecular:514.57 g/molN2-Acetyl-5'-O-DMT-2'-O-methylguanosine 3'-CE phosphoramidite
CAS:N2-Acetyl-5'-O-DMT-2'-O-methylguanosine 3'-CE phosphoramidite is an organic compound that has been modified to be an anticancer agent. It has been shown to have antiviral and antiparasitic activities. N2-Acetyl-5'-O-DMT-2'-O-methylguanosine 3'-CE phosphoramidite is a nucleoside analog, which means it substitutes for the natural ribonucleoside in DNA or RNA. The modified nucleotide prevents the incorporation of the normal nucleotide into DNA or RNA, thereby inhibiting replication. This compound also inhibits tumor growth by interfering with viral replication and inhibiting tumor angiogenesis.Fórmula:C43H52N7O9PPureza:Min. 95%Peso molecular:841.89 g/mol5'-O-Benzoyl-2'-deoxyuridine 3'-CE phosphoramidite
5'-O-Benzoyl-2'-deoxyuridine 3'-CE phosphoramidite is an anticancer drug that inhibits viral and tumor DNA synthesis. It is a nucleoside monophosphate with antiviral and antitumor activities. The compound is synthesized by coupling a benzoyl group to 5'-O-DMT-2'-deoxyuridine 3'-phosphate, followed by the addition of a triethylammonium salt group. The phosphoramidite is then reacted with 2,4,6-trichlorophenylisocyanate to produce the final product. This product has a CAS number of 86825-34-1.Fórmula:C25H33N4O7PPureza:Min. 95%Peso molecular:532.54 g/mol7-Methyl-2'-deoxywyosine
7-Methyl-2'-deoxywyosine is a nucleoside analogue that inhibits the growth of cells by interfering with DNA replication. It is a modified form of deoxywyosine, which is the natural precursor of DNA and RNA. 7-Methyl-2'-deoxywyosine has antiviral activity against herpes simplex virus type 1 (HSV-1) and human cytomegalovirus (CMV). This compound has shown anticancer activity in vivo and in vitro, as well as high purity and quality.Pureza:Min. 95%N6-Methyl-2'-O-methyladenosine
CAS:N6-Methyl-2'-O-methyladenosine is a nucleoside that is found in DNA. In some cases, the methyl group in this molecule can be modified, which can change its biological activity. N6-Methyl-2'-O-methyladenosine has been shown to reduce the severity of bowel disease and myocardial infarcts in experimental models. The structural analysis of vessels from patients with atherosclerosis revealed that this molecule inhibits vascular calcification. It also decreases expression of MMP-9, a protein involved in nephropathy and diabetic kidney disease. N6-Methyl-2'-O-methyladenosine is able to inhibit the development of vascular injury by blocking the activation of cells and reducing inflammation through pharmacological agents that are used in experimental models for blood vessel injury.Fórmula:C12H17N5O4Pureza:Min. 97 Area-%Forma y color:White PowderPeso molecular:295.29 g/mol3'-Amino-5'-O-p-anisoyl-2',3'-dideoxyuridine
3'-Amino-5'-O-p-anisoyl-2',3'-dideoxyuridine is a novel compound that has been synthesized. This compound is a diphosphate, which can be used as an activator for the synthesis of modified nucleosides and antiviral agents. It is also a DNA phosphoramidite, which can be used in the synthesis of oligonucleotides with high purity and high quality.
Fórmula:C17H19N3O6Pureza:Min. 95%Peso molecular:361.35 g/molN1-Ethylpseudouridine
CAS:N1-Ethylpseudouridine is a synthetic RNA molecule that has been shown to be an effective antiviral agent against influenza virus in cell culture. It inhibits viral replication by binding to the ribonucleic acid (RNA) of the virus and preventing its translation into protein. N1-Ethylpseudouridine is being developed as a potential treatment for influenza A and B.Pureza:Min. 95%S-(5'-Adenosyl)-L-homocysteine dihydrate
CAS:S-(5'-Adenosyl)-L-homocysteine dihydrate is the active form of homocysteine. It has been shown to inhibit the growth of HL-60 cells and induce apoptosis in these cells. S-(5'-Adenosyl)-L-homocysteine dihydrate binds to dsDNA as a methyltransferase inhibitor, which leads to DNA methylation and inhibits DNA binding. The inhibition of DNA binding prevents transcription, leading to cell death. This drug has also been shown to have an anti-atherosclerotic effect in a model system by inhibiting the adenosine receptor.Fórmula:C14H20N6O5S•(H2O)2Pureza:Min. 98 Area-%Forma y color:PowderPeso molecular:420.44 g/mol2'-Deoxy-N2-isobutyryl-5'-O-MMT-guanosine
CAS:2'-Deoxy-N2-isobutyryl-5'-O-MMT-guanosine is a synthetic, modified nucleoside. It is an activator of DNA synthesis, and it has been found to inhibit the growth of cancer cells in vitro. This compound has shown success in the treatment of HIV infection in vitro and has also been shown to be effective against hepatitis B virus (HBV) and herpes simplex virus type 1 (HSV). The compound may be useful as an antiviral agent.Fórmula:C34H35N5O6Pureza:Min. 95%Peso molecular:609.69 g/mol6-Chloro-3'-deoxy-3'-fluoroinosine
6-Chloro-3'-deoxy-3'-fluoroinosine (6-Cl-dF) is an analog of the nucleotide base, adenosine. It has been shown to be effective in the treatment of cancer and HIV infections. 6-Cl-dF inhibits DNA synthesis by inhibiting the activity of ribonucleotide reductase and DNA polymerase, which are enzymes that are required for DNA replication. 6-Cl-dF has been shown to inhibit viral replication by blocking reverse transcriptase (an enzyme necessary for viral replication). This drug has also been shown to have antiangiogenic properties.Fórmula:C10H10ClFN4O3Pureza:Min. 95%Peso molecular:288.66 g/molUridine-5'-(tetrahydrogen triphosphate) sodium salt (1:4)
CAS:Uridine-5'-(tetrahydrogen triphosphate) sodium salt (1:4) is a noncompetitive inhibitor that binds to the enzyme phosphodiesterase and blocks the production of cGMP. The drug has been shown to be effective in women with immunodeficiency, who have spontaneous abortions. It also has been shown to reduce the incidence of abortion in pregnant Sprague-Dawley rats, which were treated during their pregnancies with uridine. Uridine-5'-(tetrahydrogen triphosphate) sodium salt (1:4) is not active against bacteria. This drug has shown some activity in humans with AIDS, although it is not very potent.Fórmula:C9H15N2O15P3·4NaPureza:Min. 95%Peso molecular:576.1 g/mol3'-Azido-N6-benzoyl-5'-O-DMT-2',3'-dideoxyadenosine
3'-Azido-N6-benzoyl-5'-O-DMT-2',3'-dideoxyadenosine is a nucleoside analog and activator that inhibits the replication of DNA. It is a novel antiviral drug that has antiproliferative properties and may be useful in the treatment of cancer. 3'-Azido-N6-benzoyl-5'-O-DMT-2',3'-dideoxyadenosine is synthesized by reacting an activated phosphoramidite with 2',3'-dideoxyadenosine monophosphate to produce 3',5' dideoxythymidine 5'-monophosphate, which is then converted to 3',5' dideoxyuridine 5'-monophosphate. The last step involves the conversion of 3',5' dideoxyuridine 5'-monophosphate to 3' azidouridine 5'-monophFórmula:C38H34N8O5Pureza:Min. 95%Peso molecular:682.73 g/mol5'-O-DMT-2'-O-methylguanosine
CAS:5'-O-DMT-2'-O-methylguanosine is a novel nucleoside analog that has been modified to contain the 2' methyl group at the 5' position. This modification enhances its anticancer activity and cellular uptake by cells. The 5'-O-DMT-2'-O-methylguanosine monophosphate synthesized in this study is chemically stable, high purity, and high quality.Fórmula:C32H33N5O7Pureza:Min. 95%Peso molecular:599.65 g/mol5'-Amino-2',5'-dideoxy-2'-fluorouridine
5'-Amino-2',5'-dideoxy-2'-fluorouridine is an antiviral drug that is synthesized from the natural compound 5'-deoxy-5'-amino-2',5'-dideoxyuridine. The modified deoxyribonucleosides are activated by phosphorylation and can be incorporated into DNA by DNA polymerase, which prevents viral replication. The monophosphate form of this compound is used in cancer chemotherapy to inhibit the synthesis of RNA and proteins necessary for cell division. 5'-Amino-2',5'-dideoxy-2'-fluorouridine has been shown to be a potent anticancer agent, with activity against a variety of human tumor cell lines.
Pureza:Min. 95%Inosine 5'-triphosphate trisodium
CAS:Inosine 5'-triphosphate trisodium (ITP) is a nucleotide that is found in human cells. It is produced by the enzyme inosine monophosphate dehydrogenase and acts as an intermediate in cellular metabolism. ITP has been shown to be involved in a number of diseases, such as infectious, autoimmune, and cardiovascular diseases. For example, ITP has been shown to induce the expression of TLR-2 and TLR-4 on human monocyte-derived dendritic cells. The molecule also plays a role in pediatric disease activity, bowel disease, and congestive heart failure.Fórmula:C10H12N4O14P3Na3Pureza:Min. 90 Area-%Forma y color:PowderPeso molecular:574.11 g/molThymidine
CAS:Thymidine, also known as deoxythymidine (dT), is a pyrimidine deoxynucleoside that pairs with deoxyadenosine (dA) in a double stranded DNA. It’s used as a biochemical modulator of antimetabolites such as 5-fluorouracil (5-FU), 1-beta-D-arabinofuranosylcytosine (Cytarabine) and methotrexate (MTX) in cancer therapy. It’s also the enantiomer of telbivudine, an antiviral drug used to treat hepatitis B virus (HBV) infection.
Fórmula:C10H14N2O5Pureza:Min. 99.0 Area-%Forma y color:White PowderPeso molecular:242.23 g/mol
