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Nucleoside 5’-triphospates Kit (A, G, U, C) BOC Sciences 2
nucleoside deoxyribosyltransferase Base1 and base2 represent various purines and pyrimidines. Group: Enzymes. Synonyms: purine(pyrimidine) nucleoside:purine(pyrimidine) deoxyribosyl transferase; deoxyribose transferase; nucleoside trans-N-deoxyribosylase; trans-deoxyribosylase; trans-N-deoxyribosylase; trans-N-glycosidase; nucleoside deoxyribosyltransferase I (purine nucleoside:purine deoxyribosyltransferase: strictly specific for transfer between purine bases); nucleoside deoxyribosyltransferase II [purine(pyrimidine) nucleoside:purine(pyrimidine) deoxyribosyltransferase]. Enzyme Commission Number: EC 2.4.2.6. CAS No. 9026-86-2. NDT. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2689; nucleoside deoxyribosyltransferase; EC 2.4.2.6; 9026-86-2; purine(pyrimidine) nucleoside:purine(pyrimidine) deoxyribosyl transferase; deoxyribose transferase; nucleoside trans-N-deoxyribosylase; trans-deoxyribosylase; trans-N-deoxyribosylase; trans-N-glycosidase; nucleoside deoxyribosyltransferase I (purine nucleoside:purine deoxyribosyltransferase: strictly specific for transfer between purine bases); nucleoside deoxyribosyltransferase II [purine(pyrimidine) nucleoside:purine(pyrimidine) deoxyribosyltransferase]. Cat No: EXWM-2689. Creative Enzymes
Nucleoside Deoxyribosyltransferase II from Lactobacillus leichmanii, Recombinant Class II N-Deoxyribosyltranferases, DRTases, catalyze the transfer of a 2'-deoxyribosyl group between purines or pyrimidines. In the absence of an acceptor nucleobase, these enzymes display hydrolase activity, converting the nucleoside to its base and a deoxyribose. In lactobacilli species, Nucleoside Deoxyribosyltransferase enzymes are part of the nucleoside salvage pathway for DNA synthesis. Applications: Nucleoside deoxyribosyltransferase ii has been used in a study that assessed its enzymatic synthesis with 2?-deoxyguanosine. nucleoside deoxyribosyltransferase ii has also been used in studies to investigate its molecular cloning, expression and spe... 2.4.2.6. CAS No. 9026-86-2. NDT. Storage: -20°C. Form: lyophilized powder. Source: E. coli. Species: Lactobacillus leichmanii. EC 2.4.2.6; purine (pyrimidine) nucleoside:purine (pyrimidine) deoxyribosyl transferase; deoxyribose transferase; nucleoside trans-N-deoxyribosylase; trans-deoxyribosylase; trans-N-deoxyribosylase; trans-N-glycosidase; nucleoside deoxyribosyltransferase I (purine nucleoside:purine deoxyribosyltransferase:strictly specific for transfer between purine bases); nucleoside deoxyribosyltransferase II [purine (pyrimidine) nucleoside:purine (pyrimidine) deoxyribosyltransferase]; DRTase; Deoxyribose transferase; NDT. Cat No: NATE-0478. Creative Enzymes
nucleoside-diphosphate kinase Many nucleoside diphosphates can act as acceptors, while many ribo- and deoxyribonucleoside triphosphates can act as donors. Group: Enzymes. Synonyms: nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase. Enzyme Commission Number: EC 2.7.4.6. CAS No. 9026-51-1. NDPK. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3216; nucleoside-diphosphate kinase; EC 2.7.4.6; 9026-51-1; nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase. Cat No: EXWM-3216. Creative Enzymes
Nucleoside-Diphosphate Kinase (Crude Enzyme) Nucleoside-diphosphate kinases (NDPKs, also NDP Kinase, (poly)nucleotide kinases and nucleoside diphosphokinases) are enzymesthat catalyze the exchange of terminal phosphate between different nucleoside diphosphates (NDP) and triphosphates (NTP) in a reversible manner to produce nucleotide triphosphates. Many NDP serve as acceptor while NTP are donors of phosphate group. The general reaction via ping-pong mechanism is as follows: XDP + YTP ?? XTP + YDP (X and Y each represent different nitrogenous base). NDPK activities maintain an equilibrium between the concentrations of different nucleoside triphosphates such as, for example, when guanosine triphosphate (GTP) produce... activity was briefly purified from engineered E. coli. Applications: Medicine. Group: Enzymes. Synonyms: nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase. Enzyme Commission Number: EC 2.7.4.6. CAS No. 9026-51-1. NDPK. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase. Pack: 100ml. Cat No: NATE-1829. Creative Enzymes
nucleoside diphosphate phosphatase The enzyme, which appears to be limited to metazoa, acts on multiple nucleoside diphosphates as well as on D-ribose 5-diphosphate. Specificity depends on species and isoform. Group: Enzymes. Synonyms: nucleoside-diphosphatase; thiaminpyrophosphatase; UDPase; inosine diphosphatase; adenosine diphosphatase; IDPase; ADPase; adenosinepyrophosphatase; guanosine diphosphatase; guanosine 5'-diphosphatase; inosine 5'-diphosphatase; uridine diphosphatase; uridine 5'-diphosphatase; type B nucleoside diphosphatase; GDPase; CDPase; nucleoside 5'-diphosphatase; type L nucleoside diphosphatase; NDPase; nucleoside diphosphate phosphohydrolase. Enzyme Commission Number: EC 3.6.1.6. CAS No. 9027-69-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4632; nucleoside diphosphate phosphatase; EC 3.6.1.6; 9027-69-4; nucleoside-diphosphatase; thiaminpyrophosphatase; UDPase; inosine diphosphatase; adenosine diphosphatase; IDPase; ADPase; adenosinepyrophosphatase; guanosine diphosphatase; guanosine 5'-diphosphatase; inosine 5'-diphosphatase; uridine diphosphatase; uridine 5'-diphosphatase; type B nucleoside diphosphatase; GDPase; CDPase; nucleoside 5'-diphosphatase; type L nucleoside diphosphatase; NDPase; nucleoside diphosphate phosphohydrolase. Cat No: EXWM-4632. Creative Enzymes
nucleoside oxidase Other purine and pyrimidine nucleosides (as well as 2'-deoxyribonucleosides) are substrates, but ribose and nucleotides are not substrates. The overall reaction takes place in two separate steps, with the 5'-dehydro nucleoside being released from the enzyme to serve as substrate for the second reaction. This enzyme differs from EC 1.1.3.39, nucleoside oxidase (H2O2-forming), as it produces water rather than hydrogen peroxide. Group: Enzymes. Enzyme Commission Number: EC 1.1.3.28. CAS No. 82599-71-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0406; nucleoside oxidase; EC 1.1.3.28; 82599-71-1. Cat No: EXWM-0406. Creative Enzymes
nucleoside oxidase (H2O2-forming) A heme-containing flavoprotein (FAD). Other purine and pyrimidine nucleosides (as well as 2'-deoxyribonucleosides and arabinosides) are substrates, but ribose and nucleotides are not substrates. The overall reaction takes place in two separate steps, with the 5'-dehydro nucleoside being released from the enzyme to serve as substrate for the second reaction. This enzyme differs from EC 1.1.3.28, nucleoside oxidase, as it produces hydrogen peroxide rather than water. Group: Enzymes. Enzyme Commission Number: EC 1.1.3.39. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0411; nucleoside oxidase (H2O2-forming); EC 1.1.3.39. Cat No: EXWM-0411. Creative Enzymes
nucleoside-phosphate kinase Many nucleotides can act as acceptors; other nucleoside triphosphates can act instead of ATP. Group: Enzymes. Synonyms: NMP-kinase. Enzyme Commission Number: EC 2.7.4.4. CAS No. 9026-50-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3215; nucleoside-phosphate kinase; EC 2.7.4.4; 9026-50-0; NMP-kinase. Cat No: EXWM-3215. Creative Enzymes
nucleoside phosphoacylhydrolase Attacks ribonucleoside 5'-nitrophenylphosphates, but is inactive against phosphodiesters. Group: Enzymes. Enzyme Commission Number: EC 3.6.1.24. CAS No. 37289-35-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4608; nucleoside phosphoacylhydrolase; EC 3.6.1.24; 37289-35-3. Cat No: EXWM-4608. Creative Enzymes
NUCLEOSIDE PHOSPHORYLASE NUCLEOSIDE PHOSPHORYLASE. Synonyms: Nucleoside Phosphorylase bacterial,PNP, Purine nucleoside phosphorylase, Purine nucleoside:orthophosphate ribosyltransferase;Purine nucleoside phosphorylase [ >=200 units/mg];Deoxyribonucleoside phosphorylase;Purine deoxynucleoside phosphorylase;Purine deoxyribonucleoside phosphorylase;Purine ribonucleoside phosphorylase;PNP/Purine-nucleoside phosphorylase;Nucleoside Phosphorylase from microorganisms. CAS No. 9030-21-1. Pack Sizes: 1 kg. Product ID: CDF4-0059. Molecular formula: C10H12N4O4. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; NUCLEOSIDE PHOSPHORYLASE; CDF4-0059; 9030-21-1; C10H12N4O4; 232-857-3; 9030-21-1. Purity: 0.98. EC Number: 232-857-3. Physical State: lyophilized Powder. Storage: -20°C. CD Formulation
Nucleoside Phosphorylase from bacterial, Recombinant In enzymology, a purine-nucleoside phosphorylase (EC 2.4.2.1) is an enzyme that catalyzes the chemical reaction:purine nucleoside + phosphate<-> purine + alpha-D-ribose 1-phosphate. Thus, the two substrates of this enzyme are purine nucleoside and phosphate, whereas its two products are purine and alpha-D-ribose 1-phosphate. This enzyme belongs to the family of glycosyltransferases, specifically the pentosyltransferases. This enzyme participates in 3 metabolic pathways:purine metabolism, pyrimidine metabolism, and nicotinate and nicotinamide metabolism. Applications: Nucleoside phosphorylase is used in coupled enzyme systems to measure protein dephosphorylation. bac...eoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; 9030-21-1; EC 2.4.2.1. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Activity: > 10 units/mg protein. Storage: -20°C. Form: lyophilized powder. Source: E. coli. Species: Bacterial. purine-nucleoside phosphorylase; inosine phosphorylase; PNP; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; 9030-21-1; EC 2.4.2.1. Cat No: NATE-0607. Creative Enzymes
nucleoside phosphotransferase Phenyl phosphate and nucleoside 3'-phosphates can act as donors, although not so well as nucleoside 5'-phosphates. Nucleosides as well as 2'-deoxyribonucleosides can act as acceptors. Group: Enzymes. Synonyms: nonspecific nucleoside phosphotransferase; nucleotide:3'-deoxynucleoside 5'-phosphotransferase. Enzyme Commission Number: EC 2.7.1.77. CAS No. 9055-37-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3106; nucleoside phosphotransferase; EC 2.7.1.77; 9055-37-2; nonspecific nucleoside phosphotransferase; nucleotide:3'-deoxynucleoside 5'-phosphotransferase. Cat No: EXWM-3106. Creative Enzymes
nucleoside ribosyltransferase Base1 and base2 represent various purines and pyrimidines. Group: Enzymes. Synonyms: nucleoside N-ribosyltransferase. Enzyme Commission Number: EC 2.4.2.5. CAS No. 9030-31-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2679; nucleoside ribosyltransferase; EC 2.4.2.5; 9030-31-3; nucleoside N-ribosyltransferase. Cat No: EXWM-2679. Creative Enzymes
nucleoside-triphosphate-adenylate kinase Many nucleoside triphosphates can act as donors. Group: Enzymes. Synonyms: guanosine triphosphate-adenylate kinase; nucleoside triphosphate-adenosine monophosphate transphosphorylase; GTP:AMP phosphotransferase; isozyme 3 of adenylate kinase. Enzyme Commission Number: EC 2.7.4.10. CAS No. 9026-74-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3191; nucleoside-triphosphate-adenylate kinase; EC 2.7.4.10; 9026-74-8; guanosine triphosphate-adenylate kinase; nucleoside triphosphate-adenosine monophosphate transphosphorylase; GTP:AMP phosphotransferase; isozyme 3 of adenylate kinase. Cat No: EXWM-3191. Creative Enzymes
nucleoside-triphosphate-aldose-1-phosphate nucleotidyltransferase In decreasing order of activity, guanosine, inosine and adenosine diphosphate hexoses are substrates in the reverse reaction, with either glucose or mannose as the sugar. Group: Enzymes. Synonyms: NDP hexose pyrophosphorylase; hexose 1-phosphate nucleotidyltransferase; hexose nucleotidylating enzyme; nucleoside diphosphohexose pyrophosphorylase; hexose-1-phosphate guanylyltransferase; GTP:α-D-hexose-1-phosphate guanylyltransferase; GDP hexose pyrophosphorylase; guanosine diphosphohexose pyrophosphorylase; nucleoside-triphosphate-hexose-1-phosphate nucleotidyltransferase; NTP:he. Enzyme Commission Number: EC 2.7.7.28. CAS No. 37278-26-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3239; nucleoside-triphosphate-aldose-1-phosphate nucleotidyltransferase; EC 2.7.7.28; 37278-26-5; NDP hexose pyrophosphorylase; hexose 1-phosphate nucleotidyltransferase; hexose nucleotidylating enzyme; nucleoside diphosphohexose pyrophosphorylase; hexose-1-phosphate guanylyltransferase; GTP:α-D-hexose-1-phosphate guanylyltransferase; GDP hexose pyrophosphorylase; guanosine diphosphohexose pyrophosphorylase; nucleoside-triphosphate-hexose-1-phosphate nucleotidyltransferase; NTP:hexose-1-phosphate nucleotidyltransferase. Cat No: EXWM-3239. Creative Enzymes
nucleoside-triphosphate phosphatase The enzyme is found in eukaryotes and thermophilic bacteria, but appears to be absent from mesophilic bacteria. Also hydrolyses nucleoside diphosphates, thiamine diphosphate and FAD. The enzyme from the plant Pisum sativum (garden pea) is regulated by calmodulin. Group: Enzymes. Synonyms: nucleoside-triphosphatase; nucleoside triphosphate phosphohydrolase; nucleoside-5-triphosphate phosphohydrolase; nucleoside 5-triphosphatase; unspecific diphosphate phosphohydrolase. Enzyme Commission Number: EC 3.6.1.15. CAS No. 9075-51-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4599; nucleoside-triphosphate phosphatase; EC 3.6.1.15; 9075-51-8; nucleoside-triphosphatase; nucleoside triphosphate phosphohydrolase; nucleoside-5-triphosphate phosphohydrolase; nucleoside 5-triphosphatase; unspecific diphosphate phosphohydrolase. Cat No: EXWM-4599. Creative Enzymes
1,2,3-Triazole-4-carboxamide, 5-b-D-ribofuranosyl-5'-triphosphate-nucleoside triethyl ammonium salt 1,2,3-Triazole-4-carboxamide, 5-b-D-ribofuranosyl-5'-triphosphate-nucleoside triethyl ammonium salt, an indispensable substance in the realm of biomedical research, assumes paramount importance. It acts as an integral constituent facilitating the synthesis of antiviral agents and nucleoside analogs deployed for tackling diverse viral afflictions like HIV and hepatitis. Moreover, this exceptional product assumes a pivotal role in comprehending the intricate intricacies of viral replication mechanisms, subsequently propelling the design and development of novel therapeutic interventions against pernicious viral disorders. Molecular formula: C8H12N4O14P3. Mole weight: 481.12. BOC Sciences 3
3',5'-nucleoside bisphosphate phosphatase The enzyme, characterized from the bacterium Chromobacterium violaceum, has similar catalytic efficiencies with all the bases. The enzyme has similar activity with ribonucleoside and 2'-deoxyribonucleoside 3',5'-bisphosphates, but shows no activity with nucleoside 2',5'-bisphosphates (cf. EC 3.1.3.7, 3'(2'),5'-bisphosphate nucleotidase). Group: Enzymes. Enzyme Commission Number: EC 3.1.3.97. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3704; 3',5'-nucleoside bisphosphate phosphatase; EC 3.1.3.97. Cat No: EXWM-3704. Creative Enzymes
5' to 3' exodeoxyribonuclease (nucleoside 3'-phosphate-forming) Preference for single-stranded DNA. The enzyme from the archaeon Sulfolobus solfataricus contains a [4Fe-4S] cluster and requires a divalent metal cation, such as Mg2+ or Mn2+, for activity. Group: Enzymes. Synonyms: Cas4; 5' to 3' single stranded DNA exonuclease. Enzyme Commission Number: EC 3.1.12.1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3535; 5' to 3' exodeoxyribonuclease (nucleoside 3'-phosphate-forming); EC 3.1.12.1; Cas4; 5' to 3' single stranded DNA exonuclease. Cat No: EXWM-3535. Creative Enzymes
(deoxy)nucleoside-phosphate kinase dATP can substitute for ATP. Group: Enzymes. Synonyms: deoxynucleoside monophosphate kinase; deoxyribonucleoside monophosphokinase; deoxynucleoside-5'-monophosphate kinase; ATP:deoxynucleoside-phosphate phosphotransferase. Enzyme Commission Number: EC 2.7.4.13. CAS No. 37278-20-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3194; (deoxy)nucleoside-phosphate kinase; EC 2.7.4.13; 37278-20-9; deoxynucleoside monophosphate kinase; deoxyribonucleoside monophosphokinase; deoxynucleoside-5'-monophosphate kinase; ATP:deoxynucleoside-phosphate phosphotransferase. Cat No: EXWM-3194. Creative Enzymes
Diaminopyrazine-C-nucleoside CEP Acknowledged as an indispensable entity within the biomedical industry, diaminopyrazine-C-nucleoside CEP stands tall as a profound compound. Its offering extends far beyond its mere presence, encompassing an unparalleled influence in the realm of novel pharmaceutical interventions. A vast array of afflictions, including the notorious cancers and viral infections, succumb to its far-reaching medicinal dominion. Molecular formula: C57H82ClN8O6P. Mole weight: 1041.74. BOC Sciences 3
diphosphate-purine nucleoside kinase The enzyme from the Acholeplasma class of Mollicutes catalyses the conversion of adenosine, guanosine and inosine to AMP, GMP and IMP. ATP cannot substitute for diphosphate as a substrate. Group: Enzymes. Synonyms: pyrophosphate-purine nucleoside kinase. Enzyme Commission Number: EC 2.7.1.143. CAS No. 70356-41-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2973; diphosphate-purine nucleoside kinase; EC 2.7.1.143; 70356-41-1; pyrophosphate-purine nucleoside kinase. Cat No: EXWM-2973. Creative Enzymes
Native Bacillus sp. Purine Nucleoside Phosphorylase Purine nucleoside phosphorylase (also known as PNPase) is an enzyme (EC 2.4.2.1) involved in purine metabolism. PNP metabolizes adenosine into adenine, inosine into hypoxanthine, and guanosine into guanine, in each case creating ribose phosphate. NP encodes the enzyme purine nucleoside phosphorylase that together with adenosine deaminase (ADA) serves a key role in purine catabolism, referred to as the salvage pathway. Mutations in either enzyme result in a severe combined immunodeficiency (SCID). Confusingly, the same abbreviation (PNPase), is also used for another, otherwise unrelated, enzyme, namely Polynucleotide Phosphorylase. Purine nucleoside phosphorylase produced in microorganism has a molecular mass of 32 kda. Applications: Useful for enzymatic determination of inorganic phosphate. Group: Enzymes. Synonyms: inos. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Activity: > 500U/mL. Appearance: Colourless to light brown solution. Storage: -20°C. Form: Liquid. Source: Bacillus sp. inosine phosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; purine-nucleoside: phosphate ribosyltransferase; EC 2.4.2.1. Cat No: DIA-164. Creative Enzymes
Native Baker's yeast (S. cerevisiae) Nucleoside 5'-Diphosphate Kinase Nucleoside 5'-diphosphate kinase is a cytosolic enzyme. Nucleoside 5'-diphosphate kinase from Saccharomyces cerevisiae is found highly expressed in the cytoplasm. It affects DNA synthesis, in part, by binding to Cdc8p. Nucleoside 5?-diphosphate kinase is a cytosolic enzyme. Applications: Nucleoside 5?-diphosphate kinase has been used in a study to examine a possible intracellular activity of the drug disodium cromoglycate in mast cells. it has also been used in a study to investigate protein synthesis in rabbit reticul ocytes. Group: Enzymes. Synonyms: nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase; nucleoside-diphosphate kinase; EC 2.7.4.6; 9026-51-1; NDPK. Enzyme Commission Number: EC 2.7.4.6. CAS No. 9026-51-1. NDPK. Storage: -20°C. Form: lyophilized powder; essentially sulfate-free powder. Contains sodium Citrate with a trace of magnesium and EDTA salts. Source: Baker's yeast (S. cerevisiae). nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase; nucleoside-diphosphate kinase; EC 2.7.4.6; 9026-51-1; NDPK. Cat No: NATE-0476. Creative Enzymes
Native Bovine Nucleoside 5'-Diphosphate Kinase Nucleoside-diphosphate kinases are enzymes that catalyze the exchange of phosphate groups between different nucleoside diphosphates. NDK activities maintain an equilibrium between the concentrations of different nucleoside triphosphates such as, for example, when GTP produced in the citric acid (Krebs) cycle is converted to ATP. Nucleoside Diphosphate Kinase exists in two isoforms in eukaryotic cells, NDK-A and NDK-B. These enzymes are found expressed both in the mitochondria and the cytoplasm. Nucleoside diphosphate kinase exists in two isoforms in eukaryotic cells, ndk-a and ndk-b. these enzymes are found expressed both in the mit ochondria and the cytoplasm. Applica...cleotide phosphate kinase; UDP kinase; uridine diphosphate kinase; ATP:nucleoside diphosphate phosphotransferase; NDPK; NDKs; NDP Kinase; EC 2.7.4.6; 9026-51-1. Enzyme Commission Number: EC 2.7.4.6. CAS No. 9026-51-1. NDPK. Activity: > 1,000 units/mg protein (biuret). Storage: 2-8°C. Form: buffered aqueous glycerol solution. Source: Bovine liver. Species: Bovine. nucleoside-diphosphate kinase; nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase; ATP:nucleoside diphosphate phosphotransferase; NDPK; NDKs; NDP Kinase; EC 2.7.4.6; 9026-51-1. Cat No: NATE-0477. Creative Enzymes
Native Bovine Nucleoside monophosphate kinase This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with a phosphate group as acceptor. Group: Enzymes. Synonyms: ATP : nucleoside-monophosphate phosphotransferase; NMP-kinase; EC 2.7.4.4; 9026-50-0; nucleoside-phosphate kinase. Enzyme Commission Number: EC 2.7.4.4. CAS No. 9026-50-0. Activity: Approximately 0.5 units per mg protein. Appearance: White to slightly beige lyophillized powder. Form: Lyophilized powder containing approximately 80% sacharose. Source: Bovine liver. Species: Bovine. ATP : nucleoside-monophosphate phosphotransferase; NMP-kinase; EC 2.7.4.4; 9026-50-0; nucleoside-phosphate kinase. Cat No: NATE-1722. Creative Enzymes
Native Microorganism Purine-nucleoside phosphorylase In enzymology, a purine-nucleoside phosphorylase (EC 2.4.2.1) is an enzyme that catalyzes the chemical reaction: purine nucleoside + phosphate <-> purine + alpha-D-ribose 1-phosphate. Thus, the two substrates of this enzyme are purine nucleoside and phosphate, whereas its two products are purine and alpha-D-ribose 1-phosphate. This enzyme belongs to the family of glycosyltransferases, specifically the pentosyltransferases. Applications: This enzyme is useful for enzymatic determination of inorganic phosphorus, 5'-nucleotidase and adenosine deaminase when coupled with xanthine oxidase and uricase. Group: Enzymes. Synonyms: EC 2.4.2.1; inosine phosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynuc. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Mole weight: approx. 120 kDa. Activity: Grade? 15U/mg-solid or more. Stability: Stable at-20°C for at least 12 months. Appearance: White amorphous powder, lyophilized. Source: Microorganism. EC 2.4.2.1; inosine phosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; purine-nucleoside: phosphate ribosyltransferase. Cat No: DIA-216. Creative Enzymes
Native Microorganisms Nucleoside Phosphorylase In enzymology, a purine-nucleoside phosphorylase (EC 2.4.2.1) is an enzyme that catalyzes the chemical reaction:purine nucleoside + phosphate<-> purine + alpha-D-ribose 1-phosphate. Thus, the two substrates of this enzyme are purine nucleoside and phosphate, whereas its two products are purine and alpha-D-ribose 1-phosphate. This enzyme belongs to the family of glycosyltransferases, specifically the pentosyltransferases. This enzyme participates in 3 metabolic pathways:purine metabolism, pyrimidine metabolism, and nicotinate and nicotinamide metabolism. Applications: Nucleoside phosphorylase is used in coupled enzyme systems to measure protein dephosphorylation. this e...osphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; 9030-21-1; EC 2.4.2.1. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Mole weight: mol wt ~120 kDa. Activity: > 10 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing potassium gluconate, mannitol and EDTA. Source: Microorganisms. purine-nucleoside phosphorylase; inosine phosphorylase; PNP; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; pu Creative Enzymes
purine-nucleoside phosphorylase Specificity not completely determined. Can also catalyse ribosyltransferase reactions of the type catalysed by EC 2.4.2.5, nucleoside ribosyltransferase. Group: Enzymes. Synonyms: inosine phosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2638; purine-nucleoside phosphorylase; EC 2.4.2.1; 9030-21-1; inosine phosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase. Cat No: EXWM-2638. Creative Enzymes
Purine nucleoside phosphorylase, Microorganism Purine nucleoside phosphorylase, Microorganism (PNP) is a key enzyme in purine metabolism, which is involved in the purine rescue pathway. The deficiency of Purine nucleoside phosphorylase resulted in impaired T cell function. In the presence of inorganic orthophosphate as the second substrate, Purine nucleoside phosphorylase catalyzes the breaking of the glycosidic bond between ribose and deoxyribonucleoside to generate purine base and ribose (deoxyribose) -1-phosphate [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PNP. CAS No. 9030-21-1. Pack Sizes: 100 U. Product ID: HY-P2724. MedChemExpress MCE
Purine nucleoside phosphorylase, Recombinant Purine nucleoside phosphorylase is an enzyme involved in purine metabolism. PNP metabolizes adenosine into adenine, inosine into hypoxanthine, and guanosine into guanine. Mutations in the PNP gene are responsible for purine nucleoside phosphorylase deficiency. Applications: Purine nucleoside phosphorylase is used to study nucleotide salvage pathways and purine metabolism. it is used to study purine nucleoside phosphorylase deficiency and responsible pnp genetic mutations. this product is recombinant and expressed in e. coli. Group: Enzymes. Synonyms: purine-nucleoside phosphorylase; inosine phosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosp. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. PNPase. Activity: > 120 U/mL. Storage: -20°C. Form: buffered aqueous solution (100 mM phosphate buffer with 1 mM MgCl2. Source: E. coli. purine-nucleoside phosphorylase; inosine phosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; EC 2.4.2.1; 9030-21-1. Cat No: NATE-0644. Creative Enzymes
pyrimidine-nucleoside phosphorylase Unlike EC 2.4.2.3, uridine phosphorylase, and EC 2.4.2.4, thymidine phosphorylase, this enzyme can accept both the ribonucleoside uridine and the 2'-deoxyribonucleosides 2'-deoxyuridine and thymidine. The reaction is reversible, and the enzyme does not distinguish between α-D-ribose 1-phosphate and 2-deoxy-α-D-ribose 1-phosphate in the synthetic direction. Group: Enzymes. Synonyms: Py-NPase; pdp (gene name). Enzyme Commission Number: EC 2.4.2.2. CAS No. 9055-35-0. PyNPase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2647; pyrimidine-nucleoside phosphorylase; EC 2.4.2.2; 9055-35-0; Py-NPase; pdp (gene name). Cat No: EXWM-2647. Creative Enzymes
Pyrimidine nucleoside phosphorylase, Recombinant Pyrimidine nucleoside phosphorylase (PyNPase) is a glycosyltransferase that catalyzes the conversion of pyrimidine nucleoside and phosphate to a pyrimidine base and α-D-ribose 1-phosphate. PyNPase plays a significant role in breast cancer angiogenesis. Applications: Pyrimidine nucleoside phosphorylase (pynpase) may be used as a marker to predict the malignant potential of breast cancer, especially lymph node metastasis. pynpase is used to study breast cancer, specifically its role in angiogenesis. Group: Enzymes. Synonyms: Pyrimidine nucleoside phosphorylase; EC 2.4.2.2; Py-NPase; 9055-35-0; pdp (gene name); PyNPase. Enzyme Commission Number: EC 2.4.2.2. CAS No. 9055-35-0. PyNPase. Activity: > 1300 U/mL. Storage: -20°C. Source: E. coli. Pyrimidine nucleoside phosphorylase; EC 2.4.2.2; Py-NPase; 9055-35-0; pdp (gene name); PyNPase. Cat No: NATE-0646. Creative Enzymes
Recombinant mutant (Met62Val) purine nucleoside phosphorylase from E. coli Purine nucleoside phosphorylase is an enzyme involved in purine metabolism. PNP metabolizes adenosine into adenine, inosine into hypoxanthine, and guanosine into guanine. Mutations in the PNP gene are responsible for purine nucleoside phosphorylase deficiency. Applications: These enzymes are widely used for the synthesis of modified nucleotides (virasol, cladribine, fludarabine) which are efficient antiviral and antitumor drugs. Group: Enzymes. Synonyms: purine-nucleoside phosphorylase; inosine phosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase;. Enzyme Commission Number: EC 2.4.2.1. CAS No. 9030-21-1. Purity: > 95 %. PNPase. Mole weight: 156 kDa. Activity: 27 U/mg. Appearance: Colourless clear liquid. Storage: Store at -20 degree C, for extended storage, conserve at -20 degree C or -80 degree C. Source: E. coli. Species: E. coli. purine-nucleoside phosphorylase; inosine phosphorylase; PNPase; PUNPI; PUNPII; inosine-guanosine phosphorylase; nucleotide phosphatase; purine deoxynucleoside phosphorylase; purine deoxyribonucleoside phosphorylase; purine nucleoside phosphorylase; purine ribonucleoside phosphorylase; EC 2.4.2.1; 9030-21-1. Cat No: NATE-1000. Creative Enzymes
ribonucleoside-diphosphate reductase This enzyme is responsible for the de novo conversion of ribonucleoside diphosphates into deoxyribonucleoside diphosphates, which are essential for DNA synthesis and repair. An iron protein. While the enzyme is activated by ATP, it is inhibited by dATP. Group: Enzymes. Synonyms: ribonucleotide reductase; CDP reductase; ribonucleoside diphosphate reductase; UDP reductase; ADP reductase; nucleoside diphosphate reductase; ribonucleoside 5'-diphosphate reductase; ribonucleotide diphosphate reductase; 2'-deoxyribonucleoside-diphosphate:oxidized-thioredoxin 2'-oxidoreductase; RR. Enzyme Commission Number: EC 1.17.4.1. CAS No. 9047-64-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1090; ribonucleoside-diphosphate reductase; EC 1.17.4.1; 9047-64-7; ribonucleotide reductase; CDP reductase; ribonucleoside diphosphate reductase; UDP reductase; ADP reductase; nucleoside diphosphate reductase; ribonucleoside 5'-diphosphate reductase; ribonucleotide diphosphate reductase; 2'-deoxyribonucleoside-diphosphate:oxidized-thioredoxin 2'-oxidoreductase; RR. Cat No: EXWM-1090. Creative Enzymes
tC Nucleoside tC Nucleoside, an exceptional fluorescent analogue of thymidine intended for DNA synthesis and detection, has proven to be instrumental in numerous DNA studies. Its use in DNA hybridization, polymerase chain reaction (PCR), and DNA sequencing is scientifically deemed significant. Additionally, its exclusive fluorescent properties have contributed significantly to drug discovery research as it enables accurate detection of interactions with DNA. Grades: ≥ 97%. CAS No. 162902-04-7. Molecular formula: C15H15N3O4S. Mole weight: 333.36. BOC Sciences 2
Xanthine nucleoside dihydrate Xanthine nucleoside dihydrate. Uses: For analytical and research use. Group: Impurity standards. CAS No. 146-80-5. Molecular Formula: C10H12N4O6. Mole Weight: 284.23. Catalog: APB146805. Alfa Chemistry Analytical Products 2
10-O-[1-Propyl-3-N-carbamoylcholesteryl]-TEG-CE phosphoramidite Activator nucleoside for viral RNA replication. Synonyms: 5'-Cholesterol-TEG-CE Phosphoramidite; 10-O-[1-Propyl-3-N-carbamoylcholesteryl]-triethyleneglycol-1-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite. Grades: 95%. CAS No. 1325147-19-0. Molecular formula: C46H82N3O7P. Mole weight: 820.13. BOC Sciences 2
11-Cyclopropyl-5,11-dihydro-4-(hydroxymethyl)-6H-dipyrido[3,2-b:2',3'-e][1,4]. diazepin-6-one 11-Cyclopropyl-5,11-dihydro-4-(hydroxymethyl)-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one, is a metabolite of Nevirapine (N391275), which is a potent (IC50=84nM) and selective non-nucleoside inhibitor of HIV-1 reverse transcriptase. It is also an antiviral. Group: Biochemicals. Alternative Names: 12-Hydroxy Nevirapine. Grades: Highly Purified. CAS No. 133627-24-4. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 3
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11-Cyclopropyl-5, 11-dihydro-4-[[ (methylsulfonyl) oxy]methyl]-6H-dipyrido[3, 2-b: 2', 3'-e][1, 4]diazepin-6-one 11-Cyclopropyl-5, 11-dihydro-4-[[ (methylsulfonyl) oxy]methyl]-6H-dipyrido[3, 2-b: 2', 3'-e][1, 4]diazepin-6-one is an intermediate in synthesizing Nevirapine-d1 (N391279), an isotope labelled Nevirapine (N391275), which acts as a potent (IC50=84nM) and selective non-nucleoside inhibitor of HIV-1 reverse transcriptase. Antiviral. Group: Biochemicals. Grades: Highly Purified. CAS No. 1046462-02-5. Pack Sizes: 5mg, 10mg. Molecular Formula: C16H16N4O4S. US Biological Life Sciences. USBiological 9
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11-Cyclopropyl-5, 11-dihydro-4-[[ (methylsulfonyl) oxy]methyl]-6H-dipyrido[3, 2-b: 2', 3'-e][1, 4]diazepin-6-one-d2 11-Cyclopropyl-5, 11-dihydro-4-[[ (methylsulfonyl) oxy]methyl]-6H-dipyrido[3, 2-b: 2', 3'-e][1, 4]diazepin-6-one is an intermediate in synthesizing Nevirapine-d2 (N391276), an isotope labelled Nevirapine (N391275), which acts as a potent (IC50=84nM) and selective non-nucleoside inhibitor of HIV-1 reverse transcriptase. Antiviral. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. Molecular Formula: C16H14D2N4O4S. US Biological Life Sciences. USBiological 9
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1-((1R,3R,4R,6S,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-7-hydroxy-6-methyl-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-5-methylpyrimidine-2,4(1H,3H)-dione 1-((1R,3R,4R,6S,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-7-hydroxy-6-methyl-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-5-methylpyrimidine-2,4(1H,3H)-dione. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-(2,5-Anhydro-4-{[bis(4-methoxyphenyl)(phenyl)methoxy]methyl}-6-deoxy-alpha-L-mannofuranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione. Product Category: Nucleosides. CAS No. 1197033-21-8. Molecular formula: C33H34N2O8. Mole weight: 586.64. Purity: 0.98. IUPACName: 1-[(1R,3R,4R,6S,7S)-1-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-7-hydroxy-6-methyl-2,5-dioxabicyclo[2.2.1]heptan-3-yl]-5-methylpyrimidine-2,4-dione. Product ID: PR1197033218. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
1-((1R,3R,4R,6S,7S)-7-hydroxy-1-(hydroxymethyl)-6-methyl-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-5-methylpyrimidine-2,4(1H,3H)-dione 1-((1R,3R,4R,6S,7S)-7-hydroxy-1-(hydroxymethyl)-6-methyl-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-5-methylpyrimidine-2,4(1H,3H)-dione. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2'-o,4'-C-((1S)-Ethane-1,1-diyl)beta-D-ribose 5-methyl uridine; 1-(2,5-Anhydro-6-deoxy-4-C-(hydroxymethyl)-alpha-L-mannofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione. Product Category: Nucleosides. CAS No. 1197032-96-4. Molecular formula: C12H16N2O6. Mole weight: 284.27. Purity: 0.98. IUPACName: 1-[(1R,3R,4R,6S,7S)-7-hydroxy-1-(hydroxymethyl)-6-methyl-2,5-dioxabicyclo[2.2.1]heptan-3-yl]-5-methylpyrimidine-2,4-dione. Product ID: PR1197032964. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
1-((1R,3R,4R,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-5-methylpyrimidine-2,4(1H,3H)-dione 1-((1R,3R,4R,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-5-methylpyrimidine-2,4(1H,3H)-dione. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5'-O-DMT-2'-O,4'-C-methylene-5-methyluridine. Product Category: Nucleosides. CAS No. 206055-71-2. Molecular formula: C32H32N2O8. Mole weight: 572.61. Purity: 0.98. Product ID: PR206055712. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
1-((1R,3R,4R,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl)pyrimidine-2,4(1H,3H)-dione 1-((1R,3R,4R,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl)pyrimidine-2,4(1H,3H)-dione. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5'-o-(4,4'-dimethoxytrityl)-2'-o,4'-c-methyleneuridine. Product Category: Nucleosides. CAS No. 195705-32-9. Molecular formula: C31H30N2O8. Mole weight: 558.59. Purity: >99%. IUPACName: 1-[(1R,3R,4R,7S)-1-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl]pyrimidine-2,4-dione. Product ID: PR195705329. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
1-((1R,5R,7R,8S)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-8-hydroxy-2,6-dioxabicyclo[3.2.1]octan-7-yl)-5-methylpyrimidine-2,4(1H,3H)-dione 1-((1R,5R,7R,8S)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-8-hydroxy-2,6-dioxabicyclo[3.2.1]octan-7-yl)-5-methylpyrimidine-2,4(1H,3H)-dione. Uses: Designed for use in research and industrial production. Product Category: Nucleosides. CAS No. 287737-39-7. Molecular formula: C33H34N2O8. Mole weight: 586.64. Purity: 0.98. Product ID: PR287737397. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
1-((1S,3R,4R,7S)-7-hydroxy-1-(hydroxymethyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-5-methylpyrimidine-2,4(1H,3H)-dione 1-((1S,3R,4R,7S)-7-hydroxy-1-(hydroxymethyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-5-methylpyrimidine-2,4(1H,3H)-dione. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-(2'-O,4-C-Methylene-beta-D-ribofuranosyl)thymine. Product Category: Nucleosides. CAS No. 206055-67-6. Molecular formula: C11H14N2O6. Mole weight: 270.24. Purity: 0.98. IUPACName: 1-[(1S,3R,4R,7S)-7-hydroxy-1-(hydroxymethyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl]-5-methylpyrimidine-2,4-dione. Product ID: PR206055676. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
1-((1S,3R,4R,7S)-7-hydroxy-1-(hydroxymethyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl)pyrimidine-2,4(1H,3H)-dione 1-((1S,3R,4R,7S)-7-hydroxy-1-(hydroxymethyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl)pyrimidine-2,4(1H,3H)-dione. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2'-o,4'-c-methyleneuridine; 1-(2'-O,4-C-Methylene-beta-D-ribofuranosyl)uridine. Product Category: Nucleosides. CAS No. 200435-92-3. Molecular formula: C10H12N2O6. Mole weight: 256.21. Purity: 0.98. IUPACName: 1-[(1S,3R,4R,7S)-7-hydroxy-1-(hydroxymethyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl]pyrimidine-2,4-dione. Product ID: PR200435923. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
1,2,3,4,6-Penta-O-trimethylsilyl-D-glucopyranose The chemical compound, 1,2,3,4,6-Penta-O-trimethylsilyl-D-glucopyranose, plays a pivotal role as a chemical reagent in the pharmaceutical and biotech industries. Its varied synthesis usage in the creation of nucleosides, peptides, and oligonucleotides reflects its significance in the development of drugs intended to treat and combat nucleic acid-related disorders, such as DNA and RNA implicated ailments. Synonyms: 1,2,3,4,6-Pentakis-O-(trimethylsilyl)-D-glucopyranose; 1,2,3,4,6-Penta-trimethylsilyl Glucopyranose; trimethyl-[[(2R,3R,4S,5R)-3,4,5,6-tetrakis(trimethylsilyloxy)oxan-2-yl]methoxy]silane; D-Glucopyranose, 5TMS. CAS No. 19126-99-9. Molecular formula: C21H52O6Si5. Mole weight: 541.07. BOC Sciences 11
1,2:3,4-Di-O-isopropylidene-L-arabinopyranose 1,2:3,4-Di-O-isopropylidene-L-arabinopyranose, a chemical compound, presents immense possibilities in the pharmaceutical and biotechnology domains, given its significant contribution towards the synthesis of diversified drug and molecular structures. Remarkably, this compound emerges as a crucial ingredient in the creation of nucleoside derivatives and a perfect precursor to the production of anti-viral drugs. Molecular formula: C11H18O5. Mole weight: 230.26. BOC Sciences 11
1,2,3,5-Tetra-O-acetyl β-L-Ribofuranose 1,2,3,5-Tetra-O-acetyl β-L-Ribofuranose is an isomer of 1,2,3,5-Tetra-O-acetyl β-D-Ribofuranose (T283100) which is used in the synthesis of 3-( β-D-ribofuranosyl)-2,3-dihydro-6H-1,3-oxazine-2,6-dione, a new pyrimidine nucleoside analog related to uridine. Group: Biochemicals. Grades: Highly Purified. CAS No. 144490-03-9. Pack Sizes: 500mg, 1g. Molecular Formula: C13H18O9. US Biological Life Sciences. USBiological 9
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1,2,3,5-Tetra-O-acetyl-b-L-ribofuranose 1,2,3,5-Tetra-O-acetyl-b-L-ribofuranose, a chemical compound of extraordinary molecular complexity, has found a valuable place in the biomedical industry. Acting as a precursor in the synthesis of an array of nucleoside analogs, this compound has demonstrated promising remedial implications in the treatment of viral infections including HIV and cancer. Moreover, it has shown great promise as a fundamental building block in the formulation of enzyme inhibitors and other pharmaceuticals, underscoring its indispensability in an increasingly diversified field of study. Synonyms: β-L-Ribofuranose Tetraacetate; (2R,3S,4S,5S)-5-(Acetoxymethyl)tetrahydrofuran-2,3,4-triyl triacetate; beta-L-Ribofuranose 1,2,3,5-tetraacetate. Grades: ≥95%. CAS No. 144490-03-9. Molecular formula: C13H18O9. Mole weight: 318.28. BOC Sciences 12
1-?(2, ?3, ?5-?Tri-?O-?acetyl-?β -?D-?ribofuranosyl)?-?1, ?2, ?4-?triazole-?3-?carboxylic Acid Methyl Ester As an IMP dehydrogenase inhibitor, 1-(2,?3,?5-Tri-O-acetyl-β-D-ribofuranosyl)?-1,?2,?4-triazole-3-carboxylic Acid Methyl Ester is a reactant used in the synthesis of azole nucleoside 5'-MP mimics (P1Ms). Synonyms: Methyl 1-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)?-1,2,4-triazole-3-carboxylate; 1-(2,3,5-Tri-O-acetyl-β-D-ribofuranosyl)-1H-1,2,4-triazole-3-carboxylic Acid Methyl Ester. Grades: 96%. CAS No. 39925-10-5. Molecular formula: C15H19N3O9. Mole weight: 385.33. BOC Sciences 2
1-?(2,?3,?5-?Tri-?O-?acetyl-? β-?D-?ribofuranosyl)?-?1,?2,?4-?triazole-?3-?carboxylic Acid Methyl Ester 1-?(2,?3,?5-?Tri-?O-?acetyl-? β-?D-?ribofuranosyl)?-?1,?2,?4-?triazole-?3-?carboxylic Acid Methyl Ester is a reactant used in the synthesis of azole nucleoside 5'-?MP mimics (P1Ms) as IMP dehydrogenase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 39925-10-5. Pack Sizes: 10mg, 100mg. Molecular Formula: C15H19N3O9, Molecular Weight: 385.33. US Biological Life Sciences. USBiological 9
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1-?(2,?3,?5-?Tri-?O-?acetyl-? β-?D-?ribofuranosyl)?-?1,?2,?4-?triazole-?3-?carboxylic Acid Methyl Ester-13C2 1-?(2,?3,?5-?Tri-?O-?acetyl-? β-?D-?ribofuranosyl)?-?1,?2,?4-?triazole-?3-?carboxylic Acid Methyl Ester-13C2 is the labeled analogue of 1-?(2,?3,?5-?Tri-?O-?acetyl-? β-?D-?ribofuranosyl)?-?1,?2,?4-?triazole-?3-?carboxylic Acid Methyl Ester (T767035), a reactant used in the synthesis of azole nucleoside 5'-?MP mimics (P1Ms) as IMP dehydrogenase inhibitors. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C1313C2H19N3O9, Molecular Weight: 387.31. US Biological Life Sciences. USBiological 9
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1-(2,3-Dideoxy-2-fluoropentofuranosyl)cytosine 1-(2,3-Dideoxy-2-fluoropentofuranosyl)cytosine is a fabricated analogue of nucleosides, manifesting potential antineoplastic characteristics, illustrating efficacy particularly in combating specific leukemia and lymphoma types. Regulating DNA synthesis inhibition, this molecule effectively impedes neoplastic cell proliferation. Synonyms: 2'-Fluoro-2',3'-dideoxyarabinosylcytosine. CAS No. 119555-47-4. Molecular formula: C9H12FN3O3. Mole weight: 229.21. BOC Sciences 3
1,2:5,6-di-O-isopropylidene-3-deoxy-α-D-ribo-hexofuranose 1,2:5,6-di-O-isopropylidene-3-deoxy-α-D-ribo-hexofuranose - a molecule with tremendous significance, playing a pivotal role as a key intermediate in the synthesis of numerous nucleoside-based drugs for therapeutic interventions against viral diseases, such as hepatitis and HIV. Additionally, this compound finds applications in the production of cancer-fighting agents and as a primary building block for the development of glycoconjugates, essential for the construction of successful vaccines. Synonyms: 3-Deoxy-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose; 3-Deoxy-1,2:5,6-di-O-isopropyliden-α-D-ribo Hexafuranose. Grades: 98%. CAS No. 81097-00-9. Molecular formula: C12H20O5. Mole weight: 244.29. BOC Sciences 11
1,2,5-Tri-O-acetyl-3-deoxy-3-fluoro-D-ribofuranose 1,2,5-Tri-O-acetyl-3-deoxy-3-fluoro-D-ribofuranose occupies a pivotal role in the creation of numerous fluorine-laden nucleosides, which possess the potential to act as antitumor and antiviral agents. Additionally, it serves as a substrate for the enzymatic generation of various distinct nucleoside derivatives. CAS No. 1556020-32-6. Molecular formula: C11H15FO7. Mole weight: 278.23. BOC Sciences 11
1-(2'-Chloro-2'-deoxy-b-D-arabinofuranosyl)cytosine 1-(2'-Chloro-2'-deoxy-b-D-arabinofuranosyl)cytosine is an antineoplastic biomolecule used in cancer research. It's an analog of the nucleoside cytosine, inhibiting DNA synthesis to stop tumor cells replication. Synonyms: 2(1H)-Pyrimidinone, 4-amino-1-(2-chloro-2-deoxy-beta-D-arabinofuranosyl)-; 4-Amino-1-(2-chloro-2-deoxy-.beta.-D-arabinofuranosyl)pyrimidin-2(1H)-one; 4-amino-1-[(2R,3S,4R,5R)-3-chloro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]pyrimidin-2-one. CAS No. 58461-30-6. Molecular formula: C9H12ClN3O4. Mole weight: 261.66. BOC Sciences 3
1-(2-C-Methyl-b-D-ribofuranosyl)-1H-1,2,4-triazole-3-carboxamide 1-(2-C-Methyl-b-D-ribofuranosyl)-1H-1,2,4-triazole-3-carboxamide is a nucleoside analogue, prominently targeting Hepatitis C therapeutics research. Synonyms: 1-((2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)-1H-1,2,4-triazole-3-carboxamide. CAS No. 847651-91-6. Molecular formula: C9H14N4O5. Mole weight: 258.23. BOC Sciences 2
1-(2-Deoxy-2,2-difluoro-b-D-xylofuranosyl)cytosine 1-(2-Deoxy-2,2-difluoro-b-D-xylofuranosyl)cytosine, known for its powerful antiviral properties, emerges as a vital nucleoside analogue. Primarily employed in the therapeutic interventions against viral infections like hepatitis B and C, this compound effectively thwarts viral DNA synthesis, thereby impeding virus replication. Synonyms: 4-Amino-1-(2-deoxy-2,?2-difluoro-b-D-threo-pentofuranosyl)?-2(1H)?-pyrimidinone. CAS No. 103828-86-0. Molecular formula: C9H11F2N3O4. Mole weight: 263.20. BOC Sciences 3
1-(2'-Deoxy-2'-chloro-b-L-arabinofuranosyl)-thymine 1-(2'-Deoxy-2'-chloro-b-L-arabinofuranosyl)-thymine, also known as 2'-C-C-AraT, is a nucleoside analog utilized in biomedical research particularly in antiviral and anticancer therapy studies. It has demonstrated inhibitory effects against Hepatitis B viral replication. Synonyms: 1-(2'-Deoxy-2'-chloro-β-L-arabinofuranosyl)-thymine; 1-[(2S,3R,4S,5S)-3-chloro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione; 1-(2-Chloro-2-deoxy-β-L-arabinofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione. Molecular formula: C10H13ClN2O5. Mole weight: 276.67. BOC Sciences 3
1-(2'-deoxy-2'-fluoro-3',5'-di-O-benzoyl-b-L-arabinofuranosyl)-uracil 1-(2'-deoxy-2'-fluoro-3',5'-di-O-benzoyl-b-L-arabinofuranosyl)-uracil is a nucleoside analogue useful in cancer treatment research. This nucleoside analogue selectively interacts with a thymidylate synthase, inhibiting DNA synthesis thereby disrupting tumor cell growth. Synonyms: 1-(3,5-Di-O-benzoyl-2-deoxy-2-fluoro-beta-L-arabinofuranosyl)-2,4(1H,3H)-pyrimidinedione; 2,4(1H,3H)-Pyrimidinedione, 1-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-L-arabinofuranosyl)-; 3,5-di-O-benzoyl-1,2-dideoxy-2-fluoro-1-uracil-1-yl-beta-L-arabino-pentofuranose. CAS No. 1312300-53-0. Molecular formula: C23H19FN2O7. Mole weight: 454.40. BOC Sciences 3
1-(2'-Deoxy-2'-fluoro-3'-O-mesyl-5'-O-trityl-β-L-arabinofuranosyl)-uracil 1-(2'-Deoxy-2'-fluoro-3'-O-mesyl-5'-O-trityl-β-L-arabinofuranosyl)-uracil, a potent nucleoside analogue, has found extensive application as a crucial precursor in drug discovery and therapy for various life-threatening ailments like viral infections and cancer. This arabinose-substituted compound is known to serve as a substantial scaffold for synthesizing a versatile range of potent nucleoside analogues with remarkable efficacy and specificity towards target cells. Molecular formula: C29H27FN2O7S. Mole weight: 566.60. BOC Sciences 3
1-(2'-Deoxy-5'-O-DMT-2'-fluoro-b-D-arabinofuranosyl)thymine 1-(2'-Deoxy-5'-O-DMT-2'-fluoro-b-D-arabinofuranosyl)thymine is a nucleoside analogue used in antiviral research. It's primarily used in research of antiretroviral therapies, specifically combating HIV due to its ability to inhibit reverse transcriptase, a key enzyme in HIV replication. Synonyms: 5'-O-(4,4'-Dimethoxytrityl)-2'-deoxy-2'-fluoro-5-methyl-b-D-arabinouridine; 1-{5-O-[Bis-(4-Methoxyphenyl)phenylmethyl]-2-deoxy-2-fluoro-D-arabinofuranosyl}-5-methyl-2,4(1H,3H)-pyrimidinedione; 5'-O-(dimethoxytrityl)-2'-β-fluorothymidine. Grades: ≥98% by HPLC. CAS No. 144822-48-0. Molecular formula: C31H31FN2O7. Mole weight: 562.59. BOC Sciences 2
1-(2'-Deoxy-5'-O-DMT-2'-fluoro-b-D-arabinofuranosyl)thymine 3'-CE phosphoramidite 1-(2'-Deoxy-5'-O-DMT-2'-fluoro-b-D-arabinofuranosyl)thymine 3'-CE phosphoramidite is an ingenious nucleoside analogue, finding its utility in concocting antiretroviral pharmaceutical substances. It has a strong inhibitory effect on various viruses (such as HIV), preventing the replication of the viral genome. Grades: 97%. CAS No. 208193-48-0. Molecular formula: C40H48FN4O8P. Mole weight: 762.82. BOC Sciences 3
1,2-Dideoxy-3,5-di-O-toluoyl-D-ribose 1,2-Dideoxy-3,5-di-O-toluoyl-D-ribose, a crucial component in the realm of antiviral nucleoside analog synthesis, finds extensive application as a safeguarding unit. It aids in the production of nucleoside analogs, which are essential in combating viral infections such as HIV and hepatitis B. Its role in the synthesis of these effective antiviral agents remains highly significant. BOC Sciences 11
1,2-Di-O-acetyl-3-O-benzyl-4-C-mesylmethyl-5-O-mesyl-D-ribofuranose Used as an adenosine receptor antagonist in the preparation of locked nucleosides. Synonyms: 1,2-Di-O-acetyl-3-O-benzyl-4-C-methanesulfonoxymethyl-5-O-methanesulfonyl-D-ribofuranose; 1,2-Diacetate-4-C-[[(methylsulfonyl)oxy]methyl]-3-O-(phenylmethyl)-D-erythro-pentofuranose 5-Methanesulfonate. CAS No. 1638766-68-3. Molecular formula: C19H26O12S2. Mole weight: 510.53. BOC Sciences 12
1',2'-Di-O-acetyl-5'-O-benzoyl-3'-deoxy-3'-fluoro-D-ribofuranose 1',2'-Di-O-acetyl-5'-O-benzoyl-3'-deoxy-3'-fluoro-D-ribofuranose, a compound of immense importance in the biomedical sector, finds diverse applications. Its utility spans extensive usage in research and development to unravel the intricate mechanisms behind nucleosides and nucleotides' synthesis and biological functions. Molecular formula: C16H17FO7. Mole weight: 340.30. BOC Sciences 12

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