Nucleosídeos
Os nucleosídeos são building blocks fundamentais dos ácidos nucleicos, compostos por uma base nitrogenada ligada a uma molécula de açúcar. Nesta seção, você encontrará uma ampla variedade de nucleosídeos essenciais para pesquisas em biologia molecular, bioquímica e farmacologia. Esses compostos desempenham papéis cruciais na síntese de DNA e RNA, e também são vitais em vários processos metabólicos. Os nucleosídeos são usados para estudar material genético, desenvolver terapias antivirais e anticancerígenas, e entender os mecanismos celulares. Na CymitQuimica, fornecemos nucleosídeos de alta qualidade para apoiar suas necessidades de pesquisa e desenvolvimento, garantindo pureza e confiabilidade para suas aplicações experimentais.
Foram encontrados 3567 produtos de "Nucleosídeos"
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2,2'-Anhydro-L-uridine
CAS:<p>2,2'-Anhydro-L-uridine is a nucleoside used in for research purposes. It is of particular interest due to it being an L-isomer which is different from the D-form sugars used by the human body. It is useful to study these kinds of molecules for their use in medicine, especially as antivirals</p>Fórmula:C9H10N2O5Pureza:Min. 95%Cor e Forma:PowderPeso molecular:226.19 g/molN4-Acetyl-2'-deoxycytidine
CAS:<p>N4-Acetyl-2'-deoxycytidine is a nucleoside analogue that acts as an inhibitor of DNA synthesis. It binds to the active site of the enzyme ribonucleotide reductase, blocking the conversion of ribonucleotides to deoxyribonucleotides. This prevents DNA synthesis and replication, which leads to cell death. N4-Acetyl-2'-deoxycytidine has been shown to be more efficient than other analogues in terms of energy efficiency, control levels, and constant linear model. This compound is reactive and can cause low yields when isolated from solutions with high concentrations. A diode can be used for analytical purposes, while calcium binding may be used as a mathematical model in order to analyze this drug.</p>Fórmula:C11H15N3O5Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:269.25 g/mol5'-Amino-5'-deoxyadenosine hydrochloride
CAS:<p>5'-Amino-5'-deoxyadenosine hydrochloride (5'-ADeA) is a nucleotide that is synthesized from ribose 5-phosphate and adenosine monophosphate. It has been shown to have potential as a biomarker for skin cancer. The synthesis of 5'-ADeA is catalyzed by the enzyme caffeic acid 4-monooxygenase, which converts caffeic acid into 5'-ADeA. This reaction requires molecular oxygen, NADPH, and iron ions. The activity of this enzyme can be inhibited by sodium carbonate or basic fibroblast growth factor (bFGF). This drug has been shown to have anti-inflammatory effects in vivo.</p>Fórmula:C10H14N6O3Pureza:Min. 95 Area-%Cor e Forma:PowderPeso molecular:266.26 g/molN6-Benzoyl-5'-O-benzyl-2'-O-tert-butyldimethylsilyladenosine 3'-CE phosphoramidite
<p>N6-Benzoyl-5'-O-benzyl-2'-O-tert-butyldimethylsilyladenosine 3'-CE phosphoramidite is an activator of ribonucleosides and deoxyribonucleosides. It is a novel synthetic nucleoside, which has high quality and purity. The chemical modification of the base allows for the synthesis of DNA with modified bases. This product has been shown to have anticancer effects in vitro and in vivo, as well as antiviral activities against HIV.</p>Fórmula:C39H54N7O6PSiPureza:Min. 95%Peso molecular:775.97 g/molO2-3'-anhydro-β-D-fructofuranosyluracil
<p>O2-3'-anhydro-beta-D-fructofuranosyluracil is a novel nucleoside analogue that has antiviral and anticancer properties. It is synthesized by the reaction of beta-D-fructofuranosyluracil with phosphoramidites. The product is purified by HPLC and characterized by IR spectroscopy, UV spectroscopy, and mass spectrometry.</p>Pureza:Min. 95%Furano-dt cep
CAS:<p>Furano-dt cep is a novel antiviral drug that has been shown to inhibit the production of viral nucleic acid and to activate the immune system. Furano-dt cep is a phosphoramidite compound that is synthesized from ribonucleosides and deoxyribonucleosides, which are modified with 2,2-dithiobis(propionitrile). Furano-dt cep binds to the 5'-terminal phosphate group on the DNA strand, preventing RNA synthesis. Furano-dt cep also inhibits tumor growth by causing cell death through apoptosis.</p>Fórmula:C42H49N4O8PPureza:Min. 95%Peso molecular:768.8 g/mol9-(2’-Deoxy-2’-fluoro-arabinofuranosyl)adenine 5’-triphosphate triethyl ammonium salt
<p>Ai Product Descriptions 50 Creative</p>Pureza:Min. 95%Stavudine 5'-triphosphate sodium salt - 100 mM aqueous solution
<p>Stavudine 5'-triphosphate sodium salt is a modified nucleoside analog with antiviral and anticancer properties. It is a phosphoramidate of stavudine, which has been modified by the replacement of the L-cysteine moiety with a 2-thiophenecarboxamide group. The novel chemical structure of stavudine 5'-triphosphate sodium salt leads to higher solubility in water than other analogues and improved pharmacokinetics. Stavudine 5'-triphosphate sodium salt is an activator for the synthesis of DNA, RNA, and protein. It also inhibits viral replication by interfering with viral DNA polymerase and ribonucleotide reductase, which are essential enzymes for viral replication.</p>Fórmula:C10H17N2O13P3·xNaPureza:Min. 95 Area-%Cor e Forma:Clear LiquidPeso molecular:466.17 g/molN4-Benzoyl-2'-deoxy-5'-O-DMT-cytidine 3'-thiophosphoramidite
<p>N4-Benzoyl-2'-deoxy-5'-O-DMT-cytidine 3'-thiophosphoramidite is a novel nucleoside that has been shown to inhibit the growth of cancer cells in vitro. It is an analogue of cytidine and inhibits DNA synthesis by inhibiting the enzyme ribonucleotide reductase, which converts ribonucleotides to deoxyribonucleotides. This drug also inhibits the synthesis of viral RNA in cells infected with human immunodeficiency virus (HIV) and herpes simplex virus type 1 (HSV-1). N4-Benzoyl-2'-deoxy-5'-O-DMT-cytidine 3'-thiophosphoramidite is a phosphoramidite that is synthesized from 2,4,6-trichlorobenzoyl chloride, 5'-O-[(N,N-diisoprop</p>Fórmula:C50H51N4O8PS2Pureza:Min. 95%Peso molecular:931.07 g/molDiquafosol Impurity 2
CAS:<p>Diquafosol Impurity 2 is a high-purity phosphoramidite that can be used for the synthesis of DNA, RNA, and deoxyribonucleosides. This product is also a novel activator for phosphoramidites. Diquafosol Impurity 2 has CAS No. 63785-59-1 and a molecular weight of 228.24 g/mol. It is insoluble in water, but soluble in most organic solvents.</p>Fórmula:C18H25N4O20P3Pureza:Min. 95%Peso molecular:710.33 g/molN6-Benzoyl-5'-O-2'-deoxyadenosine
<p>N6-Benzoyl-5'-O-2'-deoxyadenosine is a modified nucleoside that contains a benzoyl group. This nucleoside has been shown to be an antiviral and anticancer agent, and is also active against herpes simplex virus type 1 (HSV1). N6-Benzoyl-5'-O-2'-deoxyadenosine may be a potential therapeutic for the treatment of HSV1 infection. It is also believed to have anti-inflammatory properties. The synthesis of this compound can be achieved by reacting 5'-O-tetraisopropyldiphenylphosphoramidite with benzoyl chloride in the presence of triethylamine.</p>Fórmula:C36H31N5O4Pureza:Min. 95%Peso molecular:597.66 g/molMorpholino T monomer
CAS:<p>Morpholino T is a modified nucleoside amidite used to prepare morpholino oligomers</p>Fórmula:C31H34ClN4O5PPureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:609.05 g/molN4-Benzoyl-5'-O-DMT-2'-O-methylcytidine 3'-CE phosphoramidite
CAS:<p>N4-Benzoyl-5'-O-DMT-2'-O-methylcytidine 3'-CE phosphoramidite is a diploid DNA molecule that is synthesized by the enzyme diploid. The clone was obtained from a yeast strain, and it has been shown to catalyze the conversion of isoprene to isopentenyl diphosphate. The optical spectra of this compound have been characterized in detail, and it has been found to have an absorption maximum at 243 nm. This compound has also been used in the disruption of yeast chromosomes, and its spectrum has been used as a reference for other compounds with similar chemical structures.</p>Fórmula:C47H54N5O9PPureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:863.96 g/mol5-(2-Fluorovinyl)-2'-Deoxyuridine
CAS:<p>5-(2-Fluorovinyl)-2'-Deoxyuridine is a hydrophobic analogue of acyclovir that has potent activity against herpes simplex virus type 1. It inhibits the synthesis of viral DNA, and thus prevents the formation of plaques in tissue culture. This drug also inhibits cell proliferation and viral production by l1210 cells as well as lung fibroblasts. 5-(2-Fluorovinyl)-2'-Deoxyuridine has shown inhibitory effects against uninfected cells, but not against cells infected with herpes simplex virus type 2.</p>Fórmula:C11H13FN2O5Pureza:Min. 95%Peso molecular:272.23 g/mol8-Bromoguanosine
CAS:<p>8-Bromoguanosine (8BrG) is a potent inhibitor of cyclase enzymes that lead to the formation of cyclic guanosine monophosphate (cGMP). It has been shown to inhibit signal pathways, such as those regulated by the G protein-coupled receptor (GPCR), which are activated by the 2-adrenergic receptor. 8BrG has been shown to be effective against C. glabrata and other fungi and has been used in experimental models for infectious diseases.</p>Fórmula:C10H12BrN5O5Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:362.14 g/mol2'-Deoxy-2',2'-difluorocytidine 5'-triphosphate triethylammonium salt - Aqueous solution
CAS:<p>2'-Deoxy-2',2'-difluorocytidine 5'-triphosphate triethylammonium salt - Aqueous solution is a nucleoside analog for research purposes</p>Fórmula:C9H14F2N3O13P3·C24H60N4Cor e Forma:Colorless PowderPeso molecular:907.9 g/mol2-Amino-6-chloro-9-(2'-deoxy-b-D-ribofuranosyl)purine
CAS:<p>2-Amino-6-chloro-9-(2'-deoxy-b-D-ribofuranosyl)purine is a purine nucleoside where the purine base has a 2-amino group at position 2 and a chlorine at position 6. The sugar is 2'-deoxy, meaning it is like the sugar found in DNA, lacking the 2'-hydroxyl group that is present in RNA. The amino and chloro groups on the purine base modify how this molecule behaves in biological systems making it useful in research applications.</p>Fórmula:C10H12ClN5O3Pureza:Min. 97 Area-%Cor e Forma:White PowderPeso molecular:285.69 g/mol7-Deaza-2'-deoxy-7-iodoadenosine
CAS:<p>7-Deaza-2'-deoxy-7-iodoadenosine (7DADI) is a modified nucleoside that has antiviral and anticancer properties. It is synthesized by the reaction of 2'-deoxyadenosine with iodine in the presence of an activator such as sodium hypochlorite. 7DADI binds to ribonucleosides, forming a phosphoramidate bond at the 3' position, which leads to inhibition of viral RNA synthesis and DNA replication. This drug also inhibits the growth of cancer cells by inhibiting DNA synthesis and protein synthesis. 7DADI is novel because it is not found in nature or produced by any other organism.</p>Fórmula:C11H13IN4O3Pureza:Min. 98 Area-%Peso molecular:376.16 g/mol8-Bromoguanosine hydrate
CAS:<p>8-Bromoguanosine hydrate is a brominated form of guanosine. It is used as a marker for colorectal cancer in urine samples. 8-Bromoguanosine hydrate can be used to calibrate the results of chromatographic analyses and to identify metabolic disorders, such as fatty acid oxidation defects. The compound is also an endogenous ligand that interacts with adenosine receptors and may have pro-apoptotic effects on cancer cells by triggering their death. 8-Bromoguanosine hydrate has been shown to be more effective than other brominated nucleosides in inducing apoptosis in malignant cells, including colorectal carcinoma cells.</p>Fórmula:C10H12BrN5O5·xH2OPureza:Min. 95%Cor e Forma:PowderPeso molecular:362.14 g/mol
