GCS Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
ODQ | 41443-28-1 | sc-200325 sc-200325A | 10 mg 50 mg | $78.00 $222.00 | 13 | |
ODQ is a selective guanylate cyclase stimulator that uniquely interacts with heme-containing enzymes, enhancing their catalytic activity. Its structure facilitates specific coordination with the heme group, promoting conformational changes that optimize enzyme function. The compound exhibits distinct reaction kinetics, characterized by rapid binding and prolonged effects on cyclic GMP levels. Additionally, its lipophilic nature influences membrane permeability, affecting cellular uptake and distribution. | ||||||
Zinc Protoporphyrin-9 | 15442-64-5 | sc-200329 sc-200329A | 25 mg 100 mg | $78.00 $213.00 | 31 | |
Zinc Protoporphyrin-9 acts as a guanylate cyclase stimulator through its unique ability to bind to heme sites, influencing the electronic environment of adjacent catalytic residues. This interaction alters the redox potential, enhancing the enzyme's activity. Its stability in various pH conditions allows for consistent performance in biochemical pathways. The compound's distinct spectroscopic properties enable real-time monitoring of enzyme dynamics, providing insights into reaction mechanisms. | ||||||
Methylene blue trihydrate | 7220-79-3 | sc-203744 sc-203744A | 5 g 25 g | $32.00 $62.00 | 3 | |
Methylene blue trihydrate exhibits unique redox properties, facilitating electron transfer processes in various chemical environments. Its ability to form stable complexes with metal ions enhances its role in catalysis, influencing reaction kinetics. The compound's distinct chromophoric structure allows for effective light absorption, making it useful in photochemical applications. Additionally, its solubility in polar solvents contributes to its versatility in diverse chemical reactions, promoting efficient molecular interactions. | ||||||
LY 83583 | 91300-60-6 | sc-200314 sc-200314A | 5 mg 25 mg | $82.00 $230.00 | 3 | |
LY 83583 is characterized by its reactivity as an acid halide, engaging in nucleophilic acyl substitution reactions that are pivotal in organic synthesis. Its electrophilic carbonyl group enhances its ability to form acyl derivatives with amines and alcohols, leading to diverse product formation. The compound's unique steric and electronic properties influence reaction rates and selectivity, making it a valuable intermediate in various synthetic pathways. Its stability under specific conditions further facilitates controlled reactions. | ||||||
BAY 41-2272 | 256376-24-6 | sc-202491 sc-202491A | 5 mg 25 mg | $238.00 $728.00 | 4 | |
BAY 41-2272 exhibits notable reactivity as a GCS, primarily through its ability to form stable complexes with nucleophiles. The compound's unique electronic configuration allows for selective interactions with various functional groups, promoting efficient acylation processes. Its distinct steric hindrance influences the kinetics of reactions, enabling precise control over product formation. Additionally, BAY 41-2272's solubility characteristics enhance its compatibility in diverse reaction environments, facilitating innovative synthetic strategies. | ||||||
AMP-Deoxynojirimycin | 216758-20-2 | sc-223780 sc-223780A | 500 µg 1 mg | $111.00 $208.00 | ||
AMP-Deoxynojirimycin functions as a GCS by engaging in specific hydrogen bonding interactions that stabilize enzyme-substrate complexes. Its unique stereochemistry allows for selective inhibition of glycosidases, altering reaction pathways and enhancing substrate specificity. The compound's dynamic solubility profile enables it to navigate various polar and non-polar environments, influencing reaction rates and product distribution. This versatility in molecular interactions contributes to its distinct reactivity in biochemical systems. | ||||||