Nucleic Acids, Nucleotides and Nucleosides
Items 151 to 156 of 156 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5′-(4-Fluorosulfonylbenzoyl)adenosine hydrochloride | 78859-42-4 | sc-221051 sc-221051A | 25 mg 100 mg | $394.00 $1179.00 | ||
5'-(4-Fluorosulfonylbenzoyl)adenosine hydrochloride is a modified nucleoside that features a sulfonyl group, which enhances its electrophilic character. This unique modification facilitates specific interactions with nucleophiles, potentially influencing the kinetics of nucleic acid reactions. The compound's ability to form stable adducts can alter the dynamics of enzyme-substrate interactions, impacting nucleic acid stability and conformation. Its distinct reactivity profile may also affect the regulation of biochemical pathways involving nucleotides. | ||||||
5-Bromo-2′-deoxyuridine 5′-triphosphate sodium salt | 102212-99-7 | sc-214311 sc-214311A sc-214311B | 1 mg 5 mg 25 mg | $182.00 $502.00 $1986.00 | ||
5-Bromo-2'-deoxyuridine 5'-triphosphate sodium salt is a halogenated nucleotide that exhibits unique properties due to the presence of a bromine atom. This modification can influence base pairing and hydrogen bonding, potentially enhancing the stability of nucleic acid structures. Its triphosphate form allows for efficient incorporation into DNA during replication and repair processes, while its distinct electronic characteristics may affect the kinetics of polymerase activity and substrate affinity. | ||||||
P1,P3-Di(adenosine-5′) triphosphate ammonium salt | 102783-40-4 | sc-215654 sc-215654A | 10 mg 25 mg | $255.00 $533.00 | ||
P1,P3-Di(adenosine-5') triphosphate ammonium salt is a unique nucleotide that features dual adenosine moieties, enhancing its ability to participate in energy transfer and signaling pathways. The presence of two triphosphate groups facilitates rapid phosphorylation reactions, making it a key player in cellular energy metabolism. Its structural configuration allows for specific interactions with enzymes, influencing reaction kinetics and substrate specificity in nucleic acid synthesis and regulation. | ||||||
5-Fluoro-2′-deoxyuridine 5′-monophosphate sodium salt | 103226-10-4 | sc-214324 sc-214324A | 5 mg 25 mg | $224.00 $871.00 | ||
5-Fluoro-2'-deoxyuridine 5'-monophosphate sodium salt is a modified nucleotide that incorporates a fluorine atom, which alters its hydrogen bonding capabilities and enhances its stability in nucleic acid structures. This modification can influence base pairing and affect the kinetics of polymerization reactions. Its unique structure allows for distinct interactions with nucleic acid polymerases, potentially altering the fidelity and efficiency of DNA synthesis and repair processes. | ||||||
7-Methylguanosine 5′-triphosphate sodium salt | 104809-18-9 | sc-214409 sc-214409A sc-214409B | 5 mg 10 mg 25 mg | $194.00 $326.00 $643.00 | ||
7-Methylguanosine 5'-triphosphate sodium salt is a modified nucleotide featuring a methyl group that enhances its role in RNA metabolism. This modification influences its binding affinity to RNA polymerases and other nucleic acid-binding proteins, potentially affecting transcriptional regulation. The triphosphate moiety facilitates energy transfer in RNA synthesis, while its unique structure may impact the stability and conformation of RNA molecules, influencing their interactions in cellular processes. | ||||||
Adenosine 2′,5′-diphosphate sodium salt | 154146-84-6 | sc-214495 sc-214495A | 5 mg 25 mg | $143.00 $469.00 | 2 | |
Adenosine 2',5'-diphosphate sodium salt is a nucleotide that plays a crucial role in cellular energy transfer and signaling pathways. Its unique 2',5'-phosphate linkage distinguishes it from other nucleotides, influencing its reactivity and interactions with enzymes involved in RNA processing. This compound can participate in various phosphorylation reactions, impacting metabolic pathways and cellular communication. Its distinct structure also affects its binding dynamics with proteins, modulating enzymatic activities and regulatory mechanisms. | ||||||