R1 and R2 Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Gemcitabine Hydrochloride | 122111-03-9 | sc-204763 sc-204763A | 25 mg 100 mg | $96.00 $289.00 | 13 | |
Gemcitabine Hydrochloride acts as a potent nucleoside analog, exhibiting unique interactions with DNA polymerases. Its structural conformation allows for effective incorporation into DNA strands, leading to chain termination during replication. The compound's affinity for nucleotide binding sites influences reaction kinetics, promoting a competitive inhibition mechanism. Furthermore, its solubility in polar solvents enhances its reactivity, enabling detailed exploration of its biochemical pathways and interactions. | ||||||
Hydroxyurea | 127-07-1 | sc-29061 sc-29061A | 5 g 25 g | $78.00 $260.00 | 18 | |
Hydroxyurea is a versatile compound that functions as a radical scavenger, engaging in unique interactions with reactive oxygen species. Its ability to form hydrogen bonds facilitates stabilization of various intermediates in biochemical pathways. The compound exhibits distinct kinetic properties, influencing the rate of reactions involving nitric oxide synthase. Additionally, its polar nature enhances solubility in aqueous environments, promoting diverse chemical interactions and reactivity profiles. | ||||||
2′-Deoxy-2′,2′-difluorocytidine | 95058-81-4 | sc-275523 sc-275523A | 1 g 5 g | $56.00 $128.00 | ||
2'-Deoxy-2',2'-difluorocytidine is a nucleoside analog characterized by its unique fluorinated structure, which alters hydrogen bonding patterns and enhances molecular stability. This compound exhibits distinct reactivity due to the presence of fluorine atoms, influencing its interaction with nucleophiles and electrophiles. Its modified base pairing properties can lead to altered kinetics in DNA synthesis, impacting the fidelity of replication and repair processes. The compound's hydrophobic characteristics also affect its solubility and partitioning behavior in biological systems. | ||||||
Trimidox | 95933-74-7 | sc-222372 sc-222372A | 5 mg 10 mg | $98.00 $187.00 | ||
Trimidox is an acid halide distinguished by its ability to engage in selective acylation reactions, facilitating the formation of stable intermediates. Its unique electronic configuration enhances electrophilic reactivity, allowing for rapid interactions with nucleophiles. The compound's steric properties influence reaction pathways, promoting regioselectivity in synthetic applications. Additionally, Trimidox exhibits notable solubility in organic solvents, which can affect its reactivity and interaction dynamics in various chemical environments. | ||||||
Gemcitabine Monophosphate Formate Salt | 116371-67-6 | sc-211556 | 1 mg | $510.00 | ||
Gemcitabine Monophosphate Formate Salt is characterized by its capacity to form robust hydrogen bonds, enhancing its solubility in polar solvents. This compound exhibits unique reactivity patterns due to its phosphate group, which can participate in nucleophilic substitution reactions. Its distinct steric hindrance influences the kinetics of these reactions, allowing for selective targeting of specific functional groups. Additionally, the compound's ionic nature contributes to its stability in various pH environments, affecting its overall reactivity. | ||||||