The chemical substance known as (2S,4S)-4-(4-Aminophenylsulfanylmethyl)-2-[2-(4-chlorophenyl)ethyl]-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolane dihydrochloride, with CAS number 143484-82-6, is a complex organic compound characterized by its multi-functional structure. It features a dioxolane ring, which contributes to its stability and solubility, and contains various functional groups, including an amine, a chlorophenyl moiety, and an imidazole ring, which may impart biological activity. The presence of the sulfonyl group suggests potential interactions with biological targets, making it of interest in medicinal chemistry. The dihydrochloride form indicates that the compound is a salt, enhancing its solubility in aqueous environments, which is crucial for pharmacological applications. Its stereochemistry, denoted by the (2S,4S) configuration, implies specific spatial arrangements that can influence its biological interactions and efficacy. Overall, this compound's unique structural features suggest potential utility in therapeutic contexts, particularly in drug development targeting specific biological pathways.

(2S,4S)-4-(4-Aminophenylsulfanylmethyl)-2-[2-(4-chlorophenyl)ethyl]-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolane dihydrochloride

143484-82-6: The chemical substance known as (2S,4S)-4-(4-Aminophenylsulfanylmethyl)-2-[2-(4-chlorophenyl)ethyl]-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolane dihydrochloride, with CAS number 143484-82-6, is a complex organic compound characterized by its multi-functional structure. It features a dioxolane ring, which contributes to its stability and solubility, and contains various functional groups, including an amine, a chlorophenyl moiety, and an imidazole ring, which may impart biological activity. The presence of the sulfonyl group suggests potential interactions with biological targets, making it of interest in medicinal chemistry. The dihydrochloride form indicates that the compound is a salt, enhancing its solubility in aqueous environments, which is crucial for pharmacological applications. Its stereochemistry, denoted by the (2S,4S) configuration, implies specific spatial arrangements that can influence its biological interactions and efficacy. Overall, this compound's unique structural features suggest potential utility in therapeutic contexts, particularly in drug development targeting specific biological pathways.

<p>Azalanstat: anti-obesity drug, inhibits cholesterol synthesis by blocking lanosterol 14α-demethylase, reduces LDL cholesterol in hamsters.</p>

CAS 143484-82-6

(2S,4S)-4-(4-Aminophenylsulfanylmethyl)-2-[2-(4-chlorophenyl)ethyl]-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolane dihydrochloride

Azalanstat HCl

Ref: TM-T70660