Nucleic Acids, Nucleotides and Nucleosides
Items 141 to 150 of 156 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5′-O-Acetyl Adenosine | 2140-25-2 | sc-210413 | 100 mg | $340.00 | ||
5'-O-Acetyl Adenosine is a modified nucleoside that plays a crucial role in cellular energy transfer and signaling. The acetyl group enhances its hydrophobic character, influencing membrane permeability and interactions with various proteins. This modification can alter the kinetics of phosphorylation reactions, affecting ATP synthesis and utilization. Additionally, 5'-O-Acetyl Adenosine can participate in unique molecular interactions, impacting RNA stability and influencing post-transcriptional modifications. | ||||||
2-Aminopurine Riboside | 4546-54-7 | sc-220703 sc-220703A sc-220703B sc-220703C sc-220703D sc-220703E | 25 mg 50 mg 100 mg 250 mg 500 mg 1 g | $100.00 $158.00 $265.00 $490.00 $850.00 $1503.00 | ||
2-Aminopurine Riboside is an important nucleoside analog that plays a significant role in nucleic acid dynamics. Its amino group enhances base pairing interactions, promoting unique hydrogen bonding patterns that can alter the stability of nucleic acid duplexes. This compound can also influence the kinetics of polymerase enzymes, potentially affecting replication and transcription processes. Its structural features allow for distinct interactions with ribonucleic acid, impacting overall nucleic acid functionality. | ||||||
2′-Deoxy-5-hydroxyuridine | 5168-36-5 | sc-283473 sc-283473A sc-283473B sc-283473C | 25 mg 50 mg 500 mg 1 g | $475.00 $840.00 $1976.00 $2900.00 | ||
2'-Deoxy-5-hydroxyuridine is a unique nucleoside that features a hydroxyl group at the 5-position, which can engage in specific hydrogen bonding interactions, potentially influencing the conformation of nucleic acids. This modification may alter the stability and flexibility of DNA structures, affecting their interactions with proteins and other biomolecules. Additionally, its presence can impact the kinetics of nucleic acid synthesis, providing insights into the regulation of genetic processes. | ||||||
Guanosine 5′-monophosphate Disodium Salt | 5550-12-9 | sc-215108 sc-215108A | 5 g 25 g | $115.00 $415.00 | ||
Guanosine 5'-monophosphate Disodium Salt is a pivotal nucleotide that plays a crucial role in cellular signaling and energy transfer. Its unique phosphate group facilitates interactions with various enzymes, influencing reaction kinetics in metabolic pathways. The disodium salt form enhances solubility, promoting efficient incorporation into RNA during transcription. Additionally, its ability to form stable complexes with metal ions can modulate enzymatic activity, impacting nucleic acid dynamics and cellular processes. | ||||||
S-(p-Nitrobenzyl)-6-thioguanosine | 13153-27-0 | sc-296284 sc-296284A | 10 mg 25 mg | $148.00 $362.00 | ||
S-(p-Nitrobenzyl)-6-thioguanosine is a notable nucleoside analog characterized by its thiol group, which enhances its reactivity in nucleophilic substitution reactions. The presence of the p-nitrobenzyl moiety allows for specific interactions with nucleic acid components, potentially modulating enzyme activity and influencing the stability of RNA structures. Its unique electronic properties may also facilitate distinct pathways in nucleotide metabolism, affecting overall cellular dynamics. | ||||||
Guanosine 5′-diphospho-β-L-fucose sodium salt | 15839-70-0 | sc-221696 sc-221696A | 1 mg 2 mg | $210.00 $355.00 | 1 | |
Guanosine 5'-diphospho-β-L-fucose sodium salt is a unique nucleotide that plays a crucial role in glycosylation processes. Its β-L-fucose component allows for specific interactions with glycoproteins, influencing cellular signaling and adhesion. The diphosphate group enhances its reactivity, facilitating the transfer of fucose residues in various biosynthetic pathways. This compound's structural features contribute to its role in modulating enzymatic activities and cellular communication. | ||||||
Enoximone | 77671-31-9 | sc-252775 sc-252775A | 10 mg 50 mg | $181.00 $728.00 | 1 | |
Enoximone is a potent compound that interacts with nucleic acids by modulating their structural integrity and dynamics. It exhibits unique binding characteristics, influencing the conformation of nucleotides and nucleosides. This interaction can alter the kinetics of nucleic acid reactions, potentially affecting processes such as replication and transcription. Enoximone's distinct molecular interactions may also impact the stability of nucleic acid complexes, providing a deeper understanding of nucleic acid behavior. | ||||||
2′-Deoxyguanosine 5′-monophosphate sodium salt | 52558-16-4 | sc-298683 sc-298683A | 100 mg 500 mg | $57.00 $101.00 | ||
2'-Deoxyguanosine 5'-monophosphate sodium salt is a pivotal nucleotide in nucleic acid metabolism, characterized by its deoxyribose sugar and phosphate group. This compound participates in DNA synthesis, where it serves as a building block for polymerization reactions. Its unique hydrogen bonding capabilities enable specific base pairing, influencing the stability and structure of DNA. Additionally, its role in energy transfer and signaling pathways highlights its importance in cellular processes. | ||||||
Cordycepin 5′-triphosphate lithium salt | 71997-32-5 | sc-396725 | 1 µmol | $127.00 | 1 | |
Cordycepin 5'-triphosphate lithium salt is a unique nucleotide analog that plays a critical role in RNA metabolism. Its triphosphate structure facilitates high-energy interactions, making it a key player in various enzymatic reactions. The presence of the 3'-deoxy group alters its reactivity, influencing RNA polymerase activity and affecting transcription dynamics. This compound's distinct molecular interactions can modulate RNA stability and folding, impacting gene expression regulation. | ||||||
Adenosine 5′-triphosphate, periodate oxidized sodium salt | 71997-40-5 | sc-214508 sc-214508A | 25 mg 100 mg | $229.00 $739.00 | ||
Adenosine 5'-triphosphate, periodate oxidized sodium salt, is a modified nucleotide that exhibits unique reactivity due to its oxidized phosphate groups. This alteration enhances its ability to participate in phosphorylation reactions, influencing energy transfer processes. The compound's structural changes can affect enzyme binding affinities and alter metabolic pathways, leading to distinct kinetic profiles in nucleic acid synthesis and degradation. Its interactions with nucleic acids can also impact their structural conformation and stability. | ||||||