Items 21 to 30 of 157 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Gemcitabine Monophosphate Formate Salt | 116371-67-6 | sc-211556 | 1 mg | $500.00 | ||
Gemcitabine Monophosphate Formate Salt serves as a key nucleotide analog, exhibiting unique interactions with nucleic acid synthesis pathways. Its structure allows for competitive inhibition of DNA polymerases, disrupting nucleotide incorporation during replication. This compound's distinct kinetic properties facilitate its rapid phosphorylation, enhancing its affinity for cellular uptake. Additionally, its ability to form stable complexes with nucleotides can influence cellular signaling and metabolic regulation, impacting overall nucleic acid dynamics. | ||||||
Inosine-5′-monophosphate disodium salt octahydrate | 20813-76-7 | sc-215181 sc-215181A sc-215181B | 5 g 50 g 500 g | $53.00 $418.00 $3682.00 | ||
Inosine-5'-monophosphate disodium salt octahydrate is a pivotal nucleotide that plays a crucial role in cellular energy transfer and metabolism. Its unique structure allows for effective participation in the synthesis of purine nucleotides, influencing the balance of nucleotide pools. The compound exhibits distinct solubility characteristics, enhancing its bioavailability in aqueous environments. Furthermore, it can engage in specific interactions with ribonucleotide reductase, modulating the conversion of ribonucleotides to deoxyribonucleotides, thereby impacting DNA synthesis and repair pathways. | ||||||
Uridine-3′-monophosphate Disodium Salt | 35170-03-7 | sc-222404 | 10 mg | $148.00 | ||
Uridine-3'-monophosphate disodium salt is a key nucleotide that serves as a precursor in RNA synthesis and metabolism. Its unique ribose structure facilitates interactions with RNA polymerases, enhancing transcription efficiency. The compound exhibits high solubility, promoting rapid cellular uptake and effective participation in metabolic pathways. Additionally, it plays a role in the regulation of nucleotide synthesis, influencing cellular signaling and energy transfer mechanisms. | ||||||
R,S-(5′-Adenosyl)-L-methionine p-toluenesulfonate salt | 52248-03-0 | sc-215827 sc-215827A sc-215827B | 25 mg 100 mg 500 mg | $72.00 $136.00 $622.00 | ||
R,S-(5'-Adenosyl)-L-methionine p-toluenesulfonate salt is a pivotal compound in cellular methylation processes, acting as a universal methyl donor. Its unique adenosyl moiety enables specific interactions with various enzymes, influencing gene expression and protein function. The compound's solubility enhances its bioavailability, facilitating rapid incorporation into metabolic pathways. Additionally, it plays a crucial role in the regulation of homocysteine levels, impacting overall cellular metabolism. | ||||||
Fludarabine | 21679-14-1 | sc-204755 sc-204755A | 5 mg 25 mg | $57.00 $200.00 | 15 | |
Fludarabine is a synthetic nucleoside analog that mimics natural nucleotides, featuring a distinct ribose sugar structure. Its unique configuration allows for selective incorporation into DNA, disrupting normal replication and transcription processes. The compound exhibits strong affinity for DNA polymerases, leading to altered reaction kinetics and inhibition of cellular proliferation. Additionally, its stability in aqueous solutions enhances its interaction with nucleic acids, influencing cellular signaling pathways. | ||||||
5′-Deoxy-5′-methylthioadenosine | 2457-80-9 | sc-202427 | 50 mg | $120.00 | 1 | |
5′-Deoxy-5′-methylthioadenosine is a naturally occurring nucleoside that plays a pivotal role in cellular metabolism. It serves as a key intermediate in the methionine salvage pathway, facilitating the regeneration of essential methyl groups. Its unique methylthio group enhances its reactivity, allowing for specific interactions with enzymes involved in nucleotide metabolism. This compound also participates in various biochemical pathways, influencing cellular energy dynamics and methylation processes. | ||||||
8-pCPT-2′-O-Me-cAMP | 634207-53-7 | sc-257020 | 1 mg | $300.00 | 5 | |
8-pCPT-2′-O-Me-cAMP is a synthetic cyclic nucleotide that acts as a potent modulator of intracellular signaling pathways. Its unique 2′-O-methyl modification enhances stability against phosphodiesterase degradation, prolonging its biological activity. This compound selectively activates protein kinase A, influencing downstream effects on gene expression and cellular responses. Its distinct structural features allow for specific interactions with target proteins, making it a valuable tool in studying cellular signaling mechanisms. | ||||||
Kinetin riboside | 4338-47-0 | sc-221789 sc-221789A | 500 mg 5 g | $138.00 $680.00 | ||
Kinetin riboside is a naturally occurring nucleoside that plays a pivotal role in plant growth regulation. Its unique ribosyl moiety facilitates specific interactions with adenosine receptors, influencing cellular signaling pathways. Kinetin riboside exhibits distinct reaction kinetics, promoting the stabilization of RNA structures and enhancing ribosomal function. This compound's ability to modulate gene expression through epigenetic mechanisms highlights its significance in cellular processes. | ||||||
Cytidine 5′-triphosphate disodium salt | 36051-68-0 | sc-217995 sc-217995A sc-217995B | 500 mg 1 g 10 g | $112.00 $214.00 $459.00 | ||
Cytidine 5'-triphosphate disodium salt is a crucial nucleotide that serves as a key energy donor in various biochemical reactions. Its triphosphate group enables high-energy phosphate transfer, essential for RNA synthesis and cellular signaling. The compound participates in unique molecular interactions, particularly in the formation of RNA structures, influencing enzymatic activity and metabolic pathways. Its role in nucleotide metabolism underscores its importance in cellular energy dynamics and regulatory mechanisms. | ||||||
Dynasore monohydrate | 304448-55-3 (anhydrous) | sc-214953 sc-214953A | 5 mg 25 mg | $79.00 $315.00 | 2 | |
Dynasore monohydrate is a unique compound that interacts with nucleic acids by modulating the dynamics of molecular assemblies. It exhibits distinct binding affinities that influence the stability of nucleic acid structures, impacting their conformational states. The compound's ability to disrupt specific protein-nucleic acid interactions highlights its role in regulating nucleic acid metabolism. Its kinetic properties facilitate rapid changes in molecular interactions, making it a significant player in cellular processes. |