LO Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Anacardic Acid | 16611-84-0 | sc-202463 sc-202463A | 5 mg 25 mg | $102.00 $204.00 | 13 | |
Anacardic acid exhibits unique properties as a natural phenolic compound, characterized by its ability to form hydrogen bonds and engage in π-π stacking interactions. These molecular features enhance its reactivity, particularly in electrophilic substitution reactions. Its hydrophobic tail contributes to membrane permeability, influencing cellular interactions. Additionally, the compound's antioxidant capacity stems from its ability to scavenge free radicals, impacting oxidative stress pathways. | ||||||
Phenidone | 92-43-3 | sc-200508 | 5 g | $32.00 | ||
Phenidone is a notable reducing agent, distinguished by its ability to facilitate electron transfer through its unique molecular structure. It exhibits strong interactions with metal ions, enhancing its reactivity in redox processes. The compound's low solubility in water, coupled with its high affinity for organic solvents, influences its behavior in various chemical environments. Its kinetic properties allow for rapid reaction rates, making it effective in specific photochemical applications. | ||||||
Terameprocol | 24150-24-1 | sc-224304 sc-224304A sc-224304B sc-224304C | 50 mg 100 mg 500 mg 1 g | $28.00 $44.00 $184.00 $321.00 | ||
Terameprocol is characterized by its unique ability to form stable complexes with various metal ions, which enhances its reactivity in diverse chemical reactions. Its distinct molecular architecture allows for selective interactions with nucleophiles, facilitating unique pathways in synthetic processes. Additionally, Terameprocol exhibits notable solubility in organic solvents, influencing its distribution and reactivity in non-aqueous environments, while its kinetic profile supports efficient reaction dynamics. | ||||||
Avarol | 55303-98-5 | sc-202480 | 1 mg | $136.00 | ||
Avarol is distinguished by its capacity to engage in specific molecular interactions with electrophiles, leading to unique reaction pathways. Its structural features promote selective reactivity, allowing for the formation of intermediates that can undergo further transformations. The compound's high reactivity is also influenced by its ability to stabilize transition states, enhancing reaction kinetics. Furthermore, Avarol's solubility in various solvents affects its behavior in different chemical environments, impacting its overall reactivity. | ||||||
(±)-Jasmonic Acid | 77026-92-7 | sc-205355 sc-205355A sc-205355B sc-205355C sc-205355D sc-205355E | 100 mg 250 mg 1 g 5 g 10 g 50 g | $96.00 $126.00 $198.00 $1675.00 $3339.00 $14056.00 | ||
(±)-Jasmonic Acid is notable for its role in plant signaling, where it interacts with specific receptors to initiate complex biochemical pathways. Its unique structure allows for the formation of reactive intermediates that can participate in diverse chemical reactions. The compound exhibits distinct stereochemical properties, influencing its reactivity and interaction with other biomolecules. Additionally, its ability to modulate gene expression highlights its significance in regulatory processes within biological systems. | ||||||
Phenylethyl 3-methylcaffeate | 71835-85-3 | sc-205804 sc-205804A | 50 mg 100 mg | $100.00 $145.00 | ||
Phenylethyl 3-methylcaffeate is characterized by its unique ability to engage in hydrogen bonding and π-π stacking interactions, which enhance its stability in various environments. This compound exhibits distinct solubility properties, allowing it to interact favorably with both polar and non-polar solvents. Its kinetic behavior in reactions is influenced by steric hindrance, affecting the rate of esterification and hydrolysis processes. The compound's structural features contribute to its reactivity, making it a subject of interest in various chemical studies. | ||||||