CA II Inhibitors
Items 1 to 10 of 15 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Topiramate | 97240-79-4 | sc-204350 sc-204350A | 10 mg 50 mg | $105.00 $362.00 | ||
Topiramate, as a carbonic anhydrase inhibitor, showcases unique interactions with enzyme active sites, leading to altered bicarbonate ion dynamics. Its distinct molecular structure allows for competitive inhibition, impacting pH regulation in various biological systems. The compound's lipophilic characteristics enhance membrane permeability, promoting efficient cellular uptake. Furthermore, its reaction kinetics reveal a multi-faceted engagement with metabolic pathways, influencing overall stability and reactivity in diverse environments. | ||||||
Verapamil | 52-53-9 | sc-507373 | 1 g | $367.00 | ||
Blocks L-type calcium channels, reducing Ca^2+ influx. | ||||||
Dorzolamide Hydrochloride | 130693-82-2 | sc-207596 | 10 mg | $186.00 | ||
Dorzolamide Hydrochloride functions as a potent inhibitor of carbonic anhydrase, exhibiting specific binding affinity to the enzyme's active site. This interaction disrupts the equilibrium of carbon dioxide and bicarbonate, influencing acid-base balance. Its unique molecular configuration facilitates strong hydrogen bonding and hydrophilic interactions, enhancing solubility in aqueous environments. The compound's kinetic profile indicates rapid onset of action, reflecting its dynamic engagement in biochemical processes. | ||||||
Benzenesulfonamide | 98-10-2 | sc-239295 sc-239295A | 5 g 100 g | $22.00 $23.00 | ||
Benzenesulfonamide acts as a versatile sulfonamide compound, characterized by its ability to form strong hydrogen bonds and engage in dipole-dipole interactions due to its sulfonamide group. This enhances its solubility in polar solvents and facilitates its participation in various nucleophilic substitution reactions. The compound's electronic structure allows for resonance stabilization, influencing its reactivity and making it a key player in diverse chemical pathways. Its unique properties contribute to its role in various synthetic applications. | ||||||
Methocarbamol | 532-03-6 | sc-211809 sc-211809-CW | 1 g 1 g | $205.00 $390.00 | ||
Methocarbamol is a unique compound that exhibits intriguing molecular interactions, particularly through its ability to form transient dipole moments. This characteristic enhances its solubility in various organic solvents, facilitating its participation in complex reaction mechanisms. The compound's steric configuration allows for selective reactivity, influencing its kinetic behavior in nucleophilic attack scenarios. Additionally, its conformational flexibility contributes to its diverse chemical behavior, making it an interesting subject for further study in synthetic chemistry. | ||||||
Nifedipine | 21829-25-4 | sc-3589 sc-3589A | 1 g 5 g | $58.00 $170.00 | 15 | |
Selective L-type calcium channel blocker. | ||||||
Brinzolamide-d5 | 1217651-02-9 | sc-217790 sc-217790A | 1 mg 2.5 mg | $925.00 $1331.00 | ||
Brinzolamide-d5 is a distinctive compound characterized by its ability to modulate carbonic anhydrase activity through specific binding interactions. Its isotopic labeling enhances tracking in metabolic studies, providing insights into reaction pathways. The compound's unique stereochemistry influences its affinity for enzyme active sites, affecting reaction kinetics. Furthermore, its solubility profile in polar solvents allows for versatile applications in various chemical environments, making it a subject of interest in mechanistic research. | ||||||
Diltiazem | 42399-41-7 | sc-204726 sc-204726A | 1 g 5 g | $209.00 $464.00 | 4 | |
Blocks L-type calcium channels, slowing heart rate. | ||||||
Amlodipine | 88150-42-9 | sc-200195 sc-200195A | 100 mg 1 g | $73.00 $163.00 | 2 | |
Inhibits L-type calcium channels in vascular smooth muscle. | ||||||
Nimodipine | 66085-59-4 | sc-201464 sc-201464A | 100 mg 1 g | $60.00 $301.00 | 2 | |
Selective for cerebral blood vessels to prevent spasms. | ||||||