Nucleic Acids, Nucleotides and Nucleosides
Items 81 to 90 of 156 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Guanosine 5′-Triphosphate, Disodium Salt | 56001-37-7 | sc-295030 sc-295030A | 50 mg 250 mg | $163.00 $321.00 | ||
Guanosine 5′-Triphosphate, Disodium Salt is a crucial nucleotide that plays a pivotal role in cellular energy transfer and signaling. Its triphosphate structure allows for high-energy phosphate bonds, facilitating rapid phosphorylation reactions. This compound is integral in the synthesis of RNA and acts as a substrate for various enzymes, influencing metabolic pathways. Its interactions with ribozymes and protein kinases highlight its versatility in regulating biochemical processes. | ||||||
Uridine 5′-diphosphoglucuronic acid trisodium salt | 63700-19-6 | sc-216043C sc-216043 sc-216043D sc-216043A sc-216043B | 5 mg 25 mg 100 mg 250 mg 1 g | $56.00 $106.00 $388.00 $899.00 $2958.00 | 5 | |
Uridine 5'-diphosphoglucuronic acid trisodium salt serves as a vital nucleotide in cellular metabolism, particularly in glycosylation reactions. Its unique diphosphate structure enables efficient transfer of glucuronic acid moieties, influencing the conjugation of various substrates. This compound participates in the regulation of carbohydrate metabolism and is involved in the synthesis of glycosaminoglycans. Its interactions with specific enzymes underscore its role in modulating biochemical pathways. | ||||||
Adenosine 3′,5′-diphosphate disodium salt | 75431-54-8 | sc-210760 sc-210760A sc-210760B | 10 mg 25 mg 100 mg | $325.00 $620.00 $1945.00 | 2 | |
Adenosine 3',5'-diphosphate disodium salt is a key nucleotide that plays a crucial role in cellular signaling and energy transfer. Its unique structure allows it to participate in the regulation of cyclic nucleotide pathways, influencing various physiological processes. The compound acts as a substrate for specific kinases, facilitating phosphorylation reactions that modulate enzyme activity. Additionally, its interactions with proteins highlight its importance in signal transduction and metabolic regulation. | ||||||
3-Deazaneplanocin, HCl salt | 120964-45-6 | sc-351856 sc-351856A sc-351856B | 1 mg 5 mg 10 mg | $251.00 $600.00 $918.00 | 2 | |
3-Deazaneplanocin, HCl salt is a potent nucleoside analog that exhibits unique interactions with nucleic acid synthesis pathways. Its structural modifications enable it to inhibit key enzymes involved in RNA and DNA metabolism, thereby altering nucleic acid dynamics. The compound's ability to mimic natural nucleosides allows it to engage in specific binding interactions, influencing reaction kinetics and modulating cellular processes related to nucleic acid turnover and stability. | ||||||
cADP-Ribose (cADPR) | 119340-53-3 | sc-201512 | 500 µg | $322.00 | 2 | |
cADP-Ribose (cADPR) is a cyclic nucleotide that plays a pivotal role in calcium signaling and cellular processes. It acts as a second messenger, facilitating the release of calcium from intracellular stores. Its unique cyclic structure allows for rapid hydrolysis, influencing reaction kinetics and enabling swift cellular responses. cADPR interacts with various proteins, modulating their activity and impacting pathways such as apoptosis and muscle contraction, showcasing its versatility in cellular signaling. | ||||||
5-Chloro-2′-deoxyuridine | 50-90-8 | sc-221018 | 100 mg | $102.00 | ||
5-Chloro-2'-deoxyuridine is a modified nucleoside that incorporates a chlorine atom at the 5-position, influencing its hydrogen bonding and base pairing properties. This alteration can affect the stability of nucleic acid structures and their interactions with polymerases during DNA synthesis. Its unique substitution may also impact the kinetics of incorporation into DNA strands, potentially altering replication fidelity and influencing cellular responses to DNA damage. | ||||||
Trifluorothymidine | 70-00-8 | sc-222370 sc-222370A | 100 mg 1 g | $179.00 $500.00 | 1 | |
Trifluorothymidine is a fluorinated nucleoside that features three fluorine atoms, which significantly enhance its hydrophobic character and alter its hydrogen bonding capabilities. This modification can lead to unique interactions with nucleic acid polymerases, potentially affecting the kinetics of nucleotide incorporation. The presence of fluorine may also influence the stability of nucleic acid duplexes, impacting their structural dynamics and reactivity in various biochemical pathways. | ||||||
N6-Methyladenine | 443-72-1 | sc-236150 | 250 mg | $178.00 | 1 | |
N6-Methyladenine is a modified nucleobase that plays a crucial role in regulating gene expression and cellular processes. Its methyl group can influence base pairing and hydrogen bonding, potentially altering the stability of nucleic acid structures. This modification can affect the recognition by specific enzymes, such as methyltransferases, and may impact the kinetics of DNA replication and repair. Additionally, N6-methylation can modulate chromatin structure, influencing transcriptional activity. | ||||||
7-Methylxanthine | 552-62-5 | sc-233694 sc-233694A | 250 mg 2.5 g | $191.00 $877.00 | 5 | |
7-Methylxanthine is a purine derivative that exhibits unique interactions within nucleic acid metabolism. Its structural modifications can influence hydrogen bonding patterns, affecting the stability and conformation of RNA and DNA. This compound participates in various biochemical pathways, potentially altering the kinetics of nucleotide synthesis and degradation. Its presence can also impact the activity of ribonucleases, thereby influencing RNA turnover and cellular signaling processes. | ||||||
5-Bromo-2′-deoxycytidine | 1022-79-3 | sc-284555 sc-284555A sc-284555B sc-284555C sc-284555D | 500 mg 1 g 2 g 5 g 10 g | $204.00 $245.00 $306.00 $561.00 $1020.00 | 1 | |
5-Bromo-2'-deoxycytidine is a modified nucleoside that plays a significant role in nucleic acid dynamics. Its bromine substitution enhances base pairing properties, potentially altering the hydrogen bonding landscape in DNA. This compound can influence the replication and repair mechanisms by integrating into DNA strands, affecting polymerase activity and fidelity. Additionally, it may modulate epigenetic modifications, impacting gene expression and chromatin structure. | ||||||