Nucleic Acids, Nucleotides and Nucleosides
Items 111 to 120 of 157 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
4-Thiothymidine | 7236-57-9 | sc-284446 sc-284446A | 10 mg 25 mg | $66.00 $178.00 | ||
4-Thiothymidine is a modified nucleoside that features a sulfur atom in its structure, which enhances its reactivity and interaction with nucleic acids. This substitution can influence hydrogen bonding patterns, potentially altering base pairing and stability of nucleic acid duplexes. The presence of the thiol group may also facilitate unique redox reactions, impacting the kinetics of nucleic acid synthesis and degradation. Additionally, its distinct electronic properties can affect the absorption spectra, providing insights into molecular interactions in biochemical systems. | ||||||
5′-N-Ethylcarboxamidoadenosine | 35920-39-9 | sc-291071 sc-291071A sc-291071B | 10 mg 15 mg 50 mg | $82.00 $158.00 $226.00 | ||
5'-N-Ethylcarboxamidoadenosine is a modified nucleoside that exhibits unique interactions with nucleic acids due to its ethylcarboxamide group. This modification can enhance solubility and alter the conformational dynamics of nucleic acid structures, influencing their stability and reactivity. The compound may also participate in specific hydrogen bonding patterns, affecting the kinetics of enzymatic reactions and the overall thermodynamics of nucleic acid hybridization processes. | ||||||
2′,3′,5′-Tri-O-acetylinosine | 3181-38-2 | sc-220834 | 1 g | $90.00 | ||
2',3',5'-Tri-O-acetylinosine is a modified nucleoside characterized by its acetyl groups, which enhance its lipophilicity and stability against nucleolytic degradation. This compound can engage in unique stacking interactions with nucleic acids, potentially influencing their structural conformations. The presence of acetyl groups may also modulate the kinetics of phosphorylation reactions, impacting the overall dynamics of nucleotide incorporation during nucleic acid synthesis. | ||||||
2-Chloro-2′-deoxyadenosine | 4291-63-8 | sc-202399 | 10 mg | $144.00 | 1 | |
2-Chloro-2′-deoxyadenosine is a halogenated nucleoside that exhibits unique interactions with nucleic acids due to its chlorine substituent. This modification can alter hydrogen bonding patterns, potentially affecting base pairing and stability of nucleic acid structures. Its presence may influence the kinetics of enzymatic reactions, such as those involving polymerases, by modifying the binding affinity and catalytic efficiency during nucleotide incorporation. Additionally, the compound's structural features can impact its solubility and reactivity in biochemical pathways. | ||||||
Ethyl 2-thiouracil-5-carboxylate | 38026-46-9 | sc-280691 | 5 g | $45.00 | ||
Ethyl 2-thiouracil-5-carboxylate is a versatile compound that interacts with nucleic acids through its thiol and carboxyl functional groups. These groups can form hydrogen bonds and participate in nucleophilic attacks, influencing the stability and reactivity of nucleotides. The compound's unique structure allows it to modulate enzymatic activity, potentially altering reaction rates in nucleic acid metabolism. Its distinct electronic properties may also affect molecular recognition processes, enhancing specificity in biochemical pathways. | ||||||
6-Benzylaminopurine 9-(α-D-glucoside) | 4294-17-1 | sc-221084 | 10 mg | $280.00 | ||
6-Benzylaminopurine 9-(β-D-glucoside) is a modified purine nucleoside that showcases distinctive interactions with nucleic acids through its benzylamine moiety. This structural modification can enhance stacking interactions and alter the conformational dynamics of nucleic acid structures. Its glucoside linkage may influence solubility and cellular uptake, while also affecting the kinetics of enzymatic processes, such as phosphorylation and glycosylation, thereby modulating nucleic acid metabolism. | ||||||
Adenosine 5′-Monophosphate, Disodium Salt | 4578-31-8 | sc-202444 sc-202444A sc-202444B sc-202444C | 5 g 25 g 100 g 1 kg | $59.00 $158.00 $260.00 $908.00 | ||
Adenosine 5′-Monophosphate, Disodium Salt is a key nucleotide that plays a pivotal role in cellular energy transfer and signaling. Its disodium form enhances solubility, facilitating rapid diffusion across membranes. The molecule participates in crucial biochemical pathways, including ATP synthesis and cyclic AMP formation, influencing various enzymatic reactions. Its ability to form hydrogen bonds and ionic interactions with proteins and nucleic acids underscores its importance in cellular regulation and metabolic processes. | ||||||
5′-Deoxyadenosine | 4754-39-6 | sc-221057 sc-221057A | 25 mg 100 mg | $260.00 $765.00 | ||
5'-Deoxyadenosine is a unique nucleoside that serves as a precursor in the synthesis of various nucleotides. It exhibits distinct molecular interactions, particularly through its ability to form stable hydrogen bonds with complementary bases in nucleic acids. This property enhances its role in DNA synthesis and repair mechanisms. Additionally, its structural features allow for specific enzyme recognition, influencing reaction kinetics in metabolic pathways. Its hydrophobic regions contribute to its interactions within cellular membranes, impacting nucleic acid stability and function. | ||||||
3′-O-Methylguanosine | 10300-27-3 | sc-283951 sc-283951A | 10 mg 25 mg | $113.00 $300.00 | ||
3'-O-Methylguanosine is a modified nucleoside that plays a crucial role in RNA metabolism. Its unique 3'-O-methylation alters hydrogen bonding patterns, influencing RNA structure and stability. This modification can affect the binding affinity of RNA-binding proteins, thereby modulating gene expression and splicing processes. Additionally, its presence in RNA can impact the kinetics of transcription and translation, contributing to the regulation of various cellular pathways. | ||||||
5′-Amino-5′-deoxyadenosine hydrochloride | 14365-44-7 | sc-284702 sc-284702A | 1 mg 5 mg | $204.00 $816.00 | ||
5'-Amino-5'-deoxyadenosine hydrochloride is a nucleoside analog characterized by its amino group at the 5' position, which enhances its hydrogen bonding capabilities. This modification can influence the stability and conformation of nucleic acid structures, potentially affecting enzyme interactions and substrate recognition. Its unique properties may alter the kinetics of nucleic acid synthesis and degradation, thereby impacting various biochemical pathways and cellular processes. | ||||||