Items 41 to 50 of 157 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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8-Bromoadenosine 3′,5′-cyclic monophosphate | 23583-48-4 | sc-217493B sc-217493 sc-217493A sc-217493C sc-217493D | 25 mg 50 mg 100 mg 250 mg 500 mg | $106.00 $166.00 $289.00 $550.00 $819.00 | 2 | |
8-Bromoadenosine 3',5'-cyclic monophosphate is a halogenated derivative of cyclic AMP, characterized by the presence of a bromine atom at the 8-position. This modification can significantly influence its interaction with protein kinases and phosphodiesterases, potentially altering signal transduction pathways. The bromine atom may enhance hydrophobic interactions, affecting the compound's stability and reactivity in biochemical assays, while also modulating its role in cellular signaling cascades. | ||||||
5′-Deoxy-5-fluorocytidine | 66335-38-4 | sc-221055 | 10 mg | $100.00 | ||
5'-Deoxy-5-fluorocytidine is a modified nucleoside featuring a fluorine atom at the 5-position, which alters its hydrogen bonding capabilities and steric properties. This substitution can impact its incorporation into nucleic acids, influencing base pairing and stability. The presence of fluorine may enhance resistance to enzymatic degradation, affecting reaction kinetics and the overall dynamics of nucleic acid synthesis. Its unique interactions can lead to distinct conformational changes in nucleic acid structures. | ||||||
Emtricitabine | 143491-57-0 | sc-207617 | 10 mg | $149.00 | 1 | |
Emtricitabine is a synthetic nucleoside analog characterized by its unique structural modifications that enhance its interaction with nucleic acids. The presence of a thiol group influences hydrogen bonding and base pairing, potentially altering the stability of nucleic acid duplexes. Its distinct molecular conformation can affect the kinetics of polymerase enzymes, leading to variations in replication fidelity. Additionally, the compound's hydrophilic nature may impact solubility and cellular uptake, influencing its behavior in nucleic acid environments. | ||||||
4-Thiouridine | 13957-31-8 | sc-204628 sc-204628A | 5 mg 25 mg | $66.00 $150.00 | 3 | |
4-Thiouridine is a modified nucleoside that features a sulfur atom in place of the oxygen at the 4-position of uridine. This substitution enhances its ability to participate in unique base pairing interactions, potentially stabilizing RNA structures. The presence of sulfur can also influence the reactivity of the nucleoside in various biochemical pathways, affecting the kinetics of RNA synthesis and degradation. Its distinct electronic properties may alter the overall charge distribution, impacting molecular interactions within nucleic acid frameworks. | ||||||
5-Ethynyl-2′-deoxyuridine | 61135-33-9 | sc-284628 sc-284628A sc-284628B | 250 mg 1 g 10 g | $216.00 $571.00 $3570.00 | 57 | |
5-Ethynyl-2'-deoxyuridine is a synthetic nucleoside characterized by an ethynyl group at the 5-position, which introduces unique steric and electronic properties. This modification can enhance its incorporation into DNA, influencing replication and repair mechanisms. The presence of the ethynyl moiety may also alter hydrogen bonding patterns, potentially affecting the stability of DNA duplexes. Its distinct structure can modulate interactions with polymerases, impacting reaction kinetics and fidelity during nucleic acid synthesis. | ||||||
Ganglioside GD3 disodium salt | 62010-37-1 | sc-202623 sc-202623A sc-202623B sc-202623C | 500 µg 1 mg 10 mg 50 mg | $270.00 $390.00 $2900.00 $13500.00 | ||
Ganglioside GD3 disodium salt is a complex glycosphingolipid that plays a pivotal role in cellular signaling and membrane dynamics. Its unique structure, featuring sialic acid residues, facilitates specific interactions with receptors, influencing cell adhesion and communication. The presence of multiple hydroxyl groups enhances its solubility and reactivity, allowing it to participate in lipid bilayer formation and modulate membrane fluidity. These properties can significantly affect cellular pathways and molecular interactions within the lipid environment. | ||||||
8-Bromo-cADP-Ribose (8-Br-cADPR) | 151898-26-9 | sc-201514 sc-201514B | 100 µg 1 mg | $130.00 $550.00 | 12 | |
8-Bromo-cADP-Ribose (8-Br-cADPR) is a potent analog of cyclic ADP-ribose, known for its role in calcium signaling and cellular processes. Its brominated structure enhances its reactivity, allowing for specific interactions with target proteins and enzymes involved in signaling pathways. This compound can modulate the activity of ADP-ribosyltransferases, influencing the dynamics of post-translational modifications. Additionally, its unique conformation can affect binding affinities, altering cellular responses to stimuli. | ||||||
Thymidine | 50-89-5 | sc-296542 sc-296542A sc-296542C sc-296542D sc-296542E sc-296542B | 1 g 5 g 100 g 250 g 1 kg 25 g | $48.00 $72.00 $265.00 $449.00 $1724.00 $112.00 | 16 | |
Thymidine is a nucleoside composed of a thymine base linked to a deoxyribose sugar, playing a crucial role in DNA synthesis. Its unique structure allows for specific hydrogen bonding interactions with complementary bases, facilitating accurate base pairing during replication. Thymidine's phosphorylation to thymidine monophosphate is a key step in nucleotide metabolism, influencing the balance of nucleotides available for DNA polymerization. Its presence is essential for maintaining genomic stability and integrity. | ||||||
7,8-Dihydro-L-biopterin | 6779-87-9 | sc-202895 sc-202895A | 10 mg 50 mg | $220.00 $414.00 | 1 | |
7,8-Dihydro-L-biopterin is a pivotal cofactor in various enzymatic reactions, particularly in the biosynthesis of neurotransmitters. Its unique dihydro form allows for specific redox interactions, enhancing electron transfer processes. This compound participates in critical metabolic pathways, influencing the kinetics of enzymatic reactions. Its structural features enable it to stabilize transition states, thereby modulating reaction rates and contributing to cellular homeostasis. | ||||||
Polyadenylic acid potassium salt | 26763-19-9 | sc-215725 sc-215725A sc-215725B sc-215725D | 25 mg 100 mg 250 mg 1 g | $124.00 $343.00 $669.00 $1573.00 | ||
Polyadenylic acid potassium salt is a polymeric nucleotide that plays a crucial role in cellular processes, particularly in RNA synthesis and regulation. Its unique polyadenylation structure facilitates interactions with RNA-binding proteins, influencing mRNA stability and translation efficiency. The compound exhibits distinct binding affinities, which can modulate gene expression. Additionally, its high molecular weight contributes to its physical properties, affecting solubility and viscosity in biological systems. |