Nucleic Acids, Nucleotides and Nucleosides
Items 71 to 80 of 156 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
NADH disodium salt | 606-68-8 | sc-205762 sc-205762A | 500 mg 1 g | $89.00 $127.00 | 3 | |
NADH disodium salt serves as a crucial cofactor in cellular metabolism, participating in redox reactions that facilitate energy transfer. Its unique ability to donate electrons allows it to engage in specific interactions with enzymes, influencing reaction kinetics and metabolic pathways. Additionally, NADH's role in nucleotide synthesis highlights its importance in maintaining cellular redox balance, impacting nucleic acid synthesis and repair processes through intricate biochemical networks. | ||||||
Pseudouridine 5′-Triphosphate Aqueous Solution | 1175-34-4 (non-salt) | sc-358858 sc-358858A | 1 µmol 5 µmol | $168.00 $764.00 | ||
Pseudouridine 5'-Triphosphate Aqueous Solution is a modified nucleotide that plays a pivotal role in RNA biology. Its unique structure enhances base pairing and stability, influencing RNA folding and function. This compound participates in various enzymatic reactions, acting as a substrate for RNA polymerases and impacting transcriptional regulation. The triphosphate moiety facilitates energy transfer, making it integral to RNA synthesis and processing pathways, thereby affecting gene expression dynamics. | ||||||
6-Mercapto-9-(b-D-arabinofuranosyl)purine | 892-49-9 | sc-284769 sc-284769A | 500 mg 1 g | $300.00 $500.00 | ||
6-Mercapto-9-(b-D-arabinofuranosyl)purine is a nucleoside analog characterized by its thiol group, which enhances its reactivity in biochemical pathways. This compound can engage in unique hydrogen bonding interactions, influencing nucleic acid structure and stability. Its arabinofuranosyl configuration alters the conformational dynamics of nucleic acids, potentially affecting enzyme recognition and substrate specificity. Additionally, it may modulate the kinetics of nucleoside phosphorylation, impacting metabolic pathways. | ||||||
NADP monosodium salt | 1184-16-3 | sc-202724 sc-202724A sc-202724B sc-202724C | 50 mg 250 mg 1 g 5 g | $71.00 $168.00 $510.00 $969.00 | 8 | |
NADP monosodium salt serves as a crucial cofactor in various biochemical reactions, particularly in redox processes. Its unique phosphate group facilitates the transfer of electrons, enhancing the efficiency of enzymatic reactions. The compound's ability to form stable complexes with enzymes influences metabolic pathways, while its role in nucleotide synthesis underscores its importance in cellular energy transfer. Additionally, NADP's interactions with metal ions can modulate reaction kinetics, impacting overall metabolic flux. | ||||||
5-Methyluridine | 1463-10-1 | sc-221037 | 25 g | $70.00 | 2 | |
5-Methyluridine is a modified nucleoside that plays a significant role in RNA metabolism and stability. Its methyl group enhances base pairing fidelity and influences RNA secondary structure, promoting efficient translation. This modification can affect the binding affinity of RNA-binding proteins, thereby regulating gene expression. Additionally, 5-Methyluridine participates in unique metabolic pathways, contributing to the dynamic balance of nucleoside pools within the cell. Its presence can also impact the kinetics of RNA synthesis and degradation, highlighting its importance in cellular processes. | ||||||
3′-Azido-2′,3′-dideoxyuridine | 84472-85-5 | sc-216614 | 10 mg | $300.00 | ||
3'-Azido-2',3'-dideoxyuridine is a nucleoside analog characterized by its azido group, which alters its interaction with nucleic acid polymerases. This modification can hinder the incorporation of the nucleoside into growing DNA strands, affecting replication dynamics. The presence of the azido group also influences hydrogen bonding patterns, potentially leading to unique structural conformations in nucleic acids. Its distinct reactivity can facilitate specific biochemical pathways, impacting nucleic acid stability and metabolism. | ||||||
N2-Methylguanosine | 2140-77-4 | sc-215517 | 1 mg | $215.00 | 2 | |
N2-Methylguanosine is a modified nucleoside that features a methyl group at the nitrogen-2 position of guanosine, influencing its hydrogen bonding capabilities and base pairing properties. This modification can enhance the stability of RNA structures, particularly in ribozymes and ribosomal RNA, by promoting unique tertiary interactions. Additionally, N2-methylation can affect the kinetics of RNA processing and splicing, altering the dynamics of gene expression and regulation. | ||||||
Nicotinamide guanine dinucleotide sodium salt | 5624-35-1 | sc-215563 sc-215563C | 5 mg 25 mg | $220.00 $980.00 | 1 | |
Nicotinamide guanine dinucleotide sodium salt serves as a crucial cofactor in various enzymatic reactions, facilitating electron transfer and redox processes. Its unique structure allows for specific interactions with enzymes, influencing metabolic pathways and energy production. The compound plays a pivotal role in cellular signaling, impacting the regulation of gene expression and protein synthesis. Its presence can modulate the activity of key enzymes, thereby affecting reaction kinetics and metabolic flux. | ||||||
Riboflavin 5′-monophosphate sodium salt dihydrate | 6184-17-4 | sc-215812 sc-215812A sc-215812B sc-215812C sc-215812D sc-215812E | 5 g 25 g 100 g 250 g 1 kg 5 kg | $58.00 $116.00 $240.00 $314.00 $840.00 $3000.00 | 1 | |
Riboflavin 5'-monophosphate sodium salt dihydrate is a vital nucleotide that participates in essential biochemical pathways, particularly in the synthesis of flavocoenzymes. Its phosphate group enhances solubility and reactivity, allowing for efficient phosphorylation reactions. This compound is integral in energy metabolism, influencing the electron transport chain and ATP production. Additionally, it plays a role in cellular signaling, impacting various metabolic processes through its interactions with specific enzymes and substrates. | ||||||
3′-Deoxycytidine | 7057-33-2 | sc-283942 sc-283942A | 10 mg 25 mg | $226.00 $425.00 | ||
3'-Deoxycytidine is a nucleoside that serves as a building block for DNA synthesis, lacking a hydroxyl group at the 3' position, which influences its incorporation into nucleic acids. This structural modification affects its reactivity and stability, making it resistant to hydrolysis. Its unique interactions with DNA polymerases can alter replication fidelity and influence repair mechanisms, thereby impacting genetic stability and cellular processes. | ||||||