Nucleic Acids, Nucleotides and Nucleosides
Items 31 to 40 of 157 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
NAD+, Free Acid | 53-84-9 | sc-208084B sc-208084 sc-208084A sc-208084C sc-208084D sc-208084E sc-208084F | 1 g 5 g 10 g 25 g 100 g 1 kg 5 kg | $56.00 $186.00 $296.00 $655.00 $2550.00 $3500.00 $10500.00 | 4 | |
NAD+, Free Acid is a pivotal coenzyme that plays a crucial role in redox reactions within cellular metabolism. It participates in electron transfer processes, facilitating the conversion of substrates in metabolic pathways. Its unique ability to form transient complexes with enzymes enhances reaction kinetics, promoting efficient energy production. Additionally, NAD+ influences the structural dynamics of nucleic acids, impacting their interactions and stability during various biochemical processes. | ||||||
1,3,7-Trimethyluric acid | 5415-44-1 | sc-224927 | 100 mg | $300.00 | 3 | |
1,3,7-Trimethyluric acid is a unique nucleic acid derivative characterized by its distinct methylation pattern, which influences its solubility and interaction with nucleotides. This compound exhibits specific binding affinities that can modulate enzyme activity in nucleotide metabolism. Its structural conformation allows for unique hydrogen bonding interactions, potentially affecting the stability of nucleic acid structures and influencing the kinetics of nucleic acid synthesis and degradation pathways. | ||||||
Puromycin Aminonucleoside | 58-60-6 | sc-200112 sc-200112A sc-200112B sc-200112C sc-200112D | 10 mg 50 mg 100 mg 500 mg 1 g | $102.00 $306.00 $502.00 $1607.00 $3004.00 | 7 | |
Puromycin Aminonucleoside is a unique nucleoside analog that mimics natural nucleotides, influencing RNA synthesis and cellular signaling pathways. Its structural similarity allows it to integrate into RNA chains, disrupting normal transcription processes. This incorporation can lead to altered gene expression and cellular responses. Furthermore, its interactions with ribosomes can inhibit protein synthesis, showcasing its role in modulating cellular functions through competitive inhibition. | ||||||
Cytosine β-D-arabinofuranoside hydrochloride | 69-74-9 | sc-221454 sc-221454A | 25 mg 1 g | $38.00 $160.00 | 2 | |
Cytosine β-D-arabinofuranoside hydrochloride is a nucleoside analog characterized by its unique β-D-arabinofuranosyl configuration, which enhances its stability against nucleases. This structural modification allows it to effectively compete with natural nucleosides for incorporation into nucleic acids, leading to altered polymerization kinetics. Its distinct interactions with DNA and RNA polymerases can result in modified replication and transcription dynamics, influencing cellular processes at the molecular level. | ||||||
2′,3′-Isopropylidene Adenosine | 362-75-4 | sc-220829 | 5 g | $260.00 | ||
2',3'-Isopropylidene Adenosine is a modified nucleoside featuring a protective isopropylidene group that enhances its stability and solubility in aqueous environments. This modification facilitates selective interactions with enzymes involved in nucleic acid synthesis, potentially altering substrate affinity and reaction rates. Its unique structure allows for distinct hydrogen bonding patterns, influencing the formation of nucleic acid duplexes and impacting overall nucleic acid metabolism. | ||||||
β-Nicotinamide mononucleotide | 1094-61-7 | sc-212376 sc-212376A sc-212376B sc-212376C sc-212376D | 25 mg 100 mg 1 g 2 g 5 g | $92.00 $269.00 $337.00 $510.00 $969.00 | 4 | |
β-Nicotinamide mononucleotide is a pivotal nucleotide that plays a crucial role in cellular energy metabolism and signaling pathways. Its unique structure allows for efficient phosphorylation, enhancing its reactivity in enzymatic processes. The compound participates in redox reactions, influencing the activity of NAD+ and NADH, which are vital for various metabolic pathways. Additionally, its interactions with specific enzymes can modulate the kinetics of nucleotide synthesis, impacting cellular homeostasis. | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $214.00 $316.00 $418.00 | 7 | |
5-Aza-2′-Deoxycytidine is a modified nucleoside that incorporates a nitrogen atom in place of a carbon in the pyrimidine ring, altering its hydrogen bonding capabilities and base pairing properties. This modification can influence DNA methylation patterns, affecting gene expression and chromatin structure. Its unique interactions with DNA polymerases can lead to altered replication dynamics, while its incorporation into DNA can induce structural changes that affect stability and accessibility for transcription factors. | ||||||
9-Methylguanine | 5502-78-3 | sc-233736 | 250 mg | $315.00 | 3 | |
9-Methylguanine is a modified nucleobase that exhibits unique hydrogen bonding patterns, which can influence the stability and structure of nucleic acid complexes. Its methyl group enhances base stacking interactions, potentially affecting the overall conformation of DNA and RNA. This modification can alter the kinetics of enzymatic reactions, such as those involving polymerases, by impacting substrate recognition and binding affinity. Additionally, its hydrophobic characteristics may influence its incorporation into nucleic acid strands, affecting molecular dynamics. | ||||||
Vidarabine | 5536-17-4 | sc-205881 sc-205881A | 100 mg 500 mg | $52.00 $137.00 | 1 | |
Vidarabine is a purine nucleoside analog that features a unique ribofuranosyl structure, enhancing its interaction with nucleic acid polymerases. Its distinct configuration allows for competitive inhibition of viral DNA synthesis, altering the kinetics of nucleotide incorporation. The compound's ability to form stable hydrogen bonds with complementary bases can influence the overall stability of nucleic acid duplexes, impacting replication and transcription processes. | ||||||
2′-C-Methyladenosine | 15397-12-3 | sc-283467 sc-283467A sc-283467B | 50 mg 100 mg 1 g | $200.00 $373.00 $649.00 | 14 | |
2'-C-Methyladenosine is a modified nucleoside that exhibits unique structural properties, particularly in its 2'-methyl group, which enhances its stability against enzymatic degradation. This modification influences its binding affinity to RNA and can alter the dynamics of RNA-protein interactions. The presence of the methyl group can also affect the conformational flexibility of RNA, potentially impacting secondary structure formation and the efficiency of ribosomal translation processes. | ||||||