The chemical substance with the name "(3S,3aS,6S,6aR)-3,3a,6-trihydroxy-3-(5-methylfuran-2-yl)tetrahydrofuro[3,2-b]furan-2(3H)-one" and CAS number 93135-89-8 is a complex organic compound characterized by its unique stereochemistry and functional groups. It features multiple hydroxyl (-OH) groups, which contribute to its potential solubility in polar solvents and its reactivity in various chemical reactions. The presence of a furan ring indicates that it may exhibit aromatic properties, while the tetrahydrofurofuran structure suggests a cyclic ether component. This compound's specific stereochemistry, denoted by the (3S,3aS,6S,6aR) configuration, implies that it has distinct spatial arrangements that can influence its biological activity and interactions with other molecules. Such compounds are often of interest in medicinal chemistry and natural product synthesis due to their potential therapeutic properties. Overall, the combination of functional groups and stereochemistry makes this substance a candidate for further study in various chemical and biological applications.

(3S,3aS,6S,6aR)-3,3a,6-trihydroxy-3-(5-methylfuran-2-yl)tetrahydrofuro[3,2-b]furan-2(3H)-one (non-preferred name)

93135-89-8: The chemical substance with the name "(3S,3aS,6S,6aR)-3,3a,6-trihydroxy-3-(5-methylfuran-2-yl)tetrahydrofuro[3,2-b]furan-2(3H)-one" and CAS number 93135-89-8 is a complex organic compound characterized by its unique stereochemistry and functional groups. It features multiple hydroxyl (-OH) groups, which contribute to its potential solubility in polar solvents and its reactivity in various chemical reactions. The presence of a furan ring indicates that it may exhibit aromatic properties, while the tetrahydrofurofuran structure suggests a cyclic ether component. This compound's specific stereochemistry, denoted by the (3S,3aS,6S,6aR) configuration, implies that it has distinct spatial arrangements that can influence its biological activity and interactions with other molecules. Such compounds are often of interest in medicinal chemistry and natural product synthesis due to their potential therapeutic properties. Overall, the combination of functional groups and stereochemistry makes this substance a candidate for further study in various chemical and biological applications.

Nafocare B1 is a modifier of synthetic immune biological response.

CAS 93135-89-8

(3S,3aS,6S,6aR)-3,3a,6-trihydroxy-3-(5-methylfuran-2-yl)tetrahydrofuro[3,2-b]furan-2(3H)-one (non-preferred name)

Nafocare B1

Ref: TM-T19468