AR Inhibitors
Items 1 to 10 of 59 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
ICI 89406 | 53671-71-9 | sc-361212 sc-361212A | 10 mg 50 mg | $91.00 $520.00 | 1 | |
ICI 89406 (CAS 53671-71-9) is a chemical compound that functions as an inhibitor of AR, a key molecular pathway involved in various physiological processes. | ||||||
Propranolol hydrochloride | 3506-09-0 | sc-3580 sc-3580B | 1 g 5 g | $38.00 $124.00 | 9 | |
Propranolol hydrochloride exhibits intriguing behavior as an acid halide, characterized by its capacity to engage in nucleophilic acyl substitution reactions. The hydrochloride moiety enhances its ionic character, facilitating solvation in aqueous environments. Its unique steric arrangement allows for specific orientation during reactions, influencing the rate and outcome of chemical processes. Additionally, the compound's ability to stabilize transition states contributes to its reactivity profile, enabling diverse synthetic applications. | ||||||
Verapamil hydrochloride | 152-11-4 | sc-3590 sc-3590A sc-3590B | 100 mg 1 g 5 g | $50.00 $75.00 $150.00 | 22 | |
Verapamil hydrochloride functions as an acid halide, showcasing distinctive reactivity through its electrophilic carbonyl group, which readily participates in nucleophilic attacks. The presence of the hydrochloride enhances its solubility, promoting interactions with polar solvents. Its unique stereochemistry influences the selectivity of reactions, while the compound's ability to form stable intermediates can modulate reaction kinetics, allowing for controlled synthetic pathways. | ||||||
Oxprenolol hydrochloride | 6452-73-9 | sc-204152 sc-204152B sc-204152C sc-204152D | 100 mg 2.5 g 10 g 50 g | $133.00 $1938.00 $6630.00 $13260.00 | 2 | |
Oxprenolol hydrochloride exhibits unique reactivity as an acid halide, characterized by its ability to engage in nucleophilic substitution reactions due to its electrophilic nature. The hydrochloride form increases its solubility in aqueous environments, facilitating interactions with various nucleophiles. Its distinct molecular structure allows for specific conformational changes, influencing reaction pathways and enhancing the formation of transient intermediates, which can affect overall reaction dynamics. | ||||||
Alfuzosin hydrochloride | 81403-68-1 | sc-203812 sc-203812A | 10 mg 50 mg | $81.00 $301.00 | ||
Alfuzosin hydrochloride functions as an acid halide, showcasing notable reactivity through its electrophilic carbon center, which readily participates in nucleophilic attack. The presence of the hydrochloride moiety enhances its solubility, promoting interactions with polar solvents. Its unique steric configuration allows for selective binding with nucleophiles, leading to distinct reaction kinetics. Additionally, the compound's ability to stabilize transition states contributes to its reactivity profile, influencing the efficiency of subsequent reactions. | ||||||
S(−)-Propranolol hydrochloride | 4199-10-4 | sc-200153 | 100 mg | $102.00 | 4 | |
S(-)-Propranolol hydrochloride exhibits unique characteristics as an acid halide, primarily through its chiral center, which influences its interaction with nucleophiles. The compound's hydrophilic hydrochloride group enhances its solubility in aqueous environments, facilitating rapid diffusion and interaction with various substrates. Its specific steric arrangement allows for tailored reactivity, promoting selective pathways in chemical transformations. The compound's ability to form stable intermediates further impacts its kinetic behavior, leading to distinct reaction profiles. | ||||||
2-PMDQ | 139047-55-5 | sc-203771 sc-203771A | 10 mg 50 mg | $135.00 $560.00 | ||
2-PMDQ, functioning as an acid halide, exhibits remarkable reactivity attributed to its unique carbonyl group, which enhances its electrophilic nature. This compound engages in rapid acylation reactions, demonstrating distinct selectivity towards nucleophiles based on steric and electronic factors. Its high reactivity is further influenced by the presence of halogen substituents, which modulate the stability of intermediates, leading to diverse synthetic routes and efficient transformation processes. | ||||||
Doxazosin Mesylate | 77883-43-3 | sc-205656 sc-205656A | 50 mg 250 mg | $108.00 $403.00 | 3 | |
Doxazosin Mesylate, as an acid halide, showcases intriguing reactivity due to its sulfonate ester moiety, which enhances electrophilicity and facilitates nucleophilic attack. The compound's unique steric configuration allows for selective interactions with various nucleophiles, influencing reaction kinetics. Its solubility characteristics, driven by the mesylate group, promote efficient diffusion in polar solvents, enabling diverse chemical pathways and enhancing its reactivity in synthetic applications. | ||||||
Bicalutamide | 90357-06-5 | sc-202976 sc-202976A | 100 mg 500 mg | $41.00 $143.00 | 27 | |
Bicalutamide is an androgen receptor inhibitor useful in prostate cancer research | ||||||
Spironolactone | 52-01-7 | sc-204294 | 50 mg | $107.00 | 3 | |
Spironolactone, as an acid halide, showcases intriguing reactivity due to its unique structural features, particularly the presence of a lactone ring that influences its electrophilic character. This compound participates in nucleophilic acyl substitution reactions, where the halide group enhances its reactivity by stabilizing transition states. The compound's distinct steric hindrance and electronic distribution allow for selective interactions with various nucleophiles, facilitating complex synthetic pathways. | ||||||