Antivirals 02
Items 301 to 305 of 305 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Abacavir 5′-β-D-Glucuronide | 384329-76-4 | sc-207236 | 1 mg | $430.00 | ||
Abacavir 5'-β-D-Glucuronide is a glucuronide conjugate that showcases unique solubility properties due to its β-D-glucuronic acid moiety. This modification enhances its hydrophilicity, promoting efficient excretion via renal pathways. The compound engages in specific interactions with UDP-glucuronosyltransferases, influencing its metabolic clearance. Its structural configuration allows for distinct hydrogen bonding patterns, impacting its reactivity and stability in biological systems. | ||||||
ent-Abacavir | 136470-79-6 | sc-479383 | 5 mg | $430.00 | ||
Ent-Abacavir is an intriguing compound that exhibits unique reactivity as an acid halide, particularly in its ability to form stable acyl derivatives through nucleophilic acyl substitution. Its electrophilic nature allows for selective interactions with amines and alcohols, leading to the formation of diverse esters and amides. The compound's steric configuration influences reaction kinetics, promoting rapid acylation under mild conditions, which can be pivotal in synthetic applications. | ||||||
O2,2′-Cyclouridine | 3736-77-4 | sc-257938 | 1 g | $129.00 | ||
O2,2'-Cyclouridine exhibits intriguing properties as a nucleoside analog, influencing RNA synthesis and stability. Its unique bicyclic structure allows for specific hydrogen bonding interactions, enhancing base pairing fidelity. This compound can modulate enzymatic activity, impacting transcriptional regulation pathways. The presence of functional groups contributes to its solubility and reactivity, facilitating diverse interactions in biochemical systems, which can lead to altered metabolic pathways. | ||||||
OG-L002 | 1357302-64-7 | sc-478221 | 5 mg | $270.00 | ||
OG-L002 is an acid halide distinguished by its reactivity with nucleophiles, facilitating acylation reactions that are pivotal in organic synthesis. Its electrophilic carbonyl group exhibits a strong tendency to undergo nucleophilic attack, leading to the formation of stable acyl derivatives. The compound's unique steric and electronic properties enhance its selectivity in reactions, allowing for precise modifications of substrates. Furthermore, its ability to form transient intermediates contributes to its efficiency in various synthetic pathways. | ||||||
Clevudine | 163252-36-6 | sc-500848 | 250 mg | $535.00 | ||
Clevudine is a nucleoside analog characterized by its unique structural modifications that enhance its interaction with viral polymerases. Its specific conformation allows for selective incorporation into nucleic acid chains, disrupting normal replication processes. The compound exhibits distinct kinetic properties, influencing its rate of phosphorylation and subsequent activation. Additionally, its solubility profile and stability under physiological conditions contribute to its behavior in various biochemical environments. | ||||||