The chemical substance with the name "(2S,3S,4R)-8-[[3-[2,6-dimethyl-4-(3-methylsulfonylpropoxy)phenyl]phenyl]methoxy]-9-azatricyclo[4.4.0.02,4]deca-1(10),6,8-triene-3-carboxylate" and CAS number "2056254-98-7" is a complex organic compound characterized by its intricate molecular structure, which includes multiple chiral centers and functional groups. This compound features a tricyclic framework, specifically a 9-azatricyclo structure, which contributes to its unique stereochemistry and potential biological activity. The presence of a methoxy group and a carboxylate moiety suggests that it may exhibit polar characteristics, influencing its solubility and reactivity. Additionally, the incorporation of a sulfonyl group indicates potential interactions with biological targets, making it of interest in medicinal chemistry. The specific stereochemistry (2S,3S,4R) is crucial for its biological activity, as the spatial arrangement of atoms can significantly affect how the molecule interacts with enzymes or receptors. Overall, this compound's complexity and functional diversity may render it valuable for research in pharmacology or material science.

(2S,3S,4R)-8-[[3-[2,6-dimethyl-4-(3-methylsulfonylpropoxy)phenyl]phenyl]methoxy]-9-azatricyclo[4.4.0.02,4]deca-1(10),6,8-triene-3-carboxylate

2056254-98-7: The chemical substance with the name "(2S,3S,4R)-8-[[3-[2,6-dimethyl-4-(3-methylsulfonylpropoxy)phenyl]phenyl]methoxy]-9-azatricyclo[4.4.0.02,4]deca-1(10),6,8-triene-3-carboxylate" and CAS number "2056254-98-7" is a complex organic compound characterized by its intricate molecular structure, which includes multiple chiral centers and functional groups. This compound features a tricyclic framework, specifically a 9-azatricyclo structure, which contributes to its unique stereochemistry and potential biological activity. The presence of a methoxy group and a carboxylate moiety suggests that it may exhibit polar characteristics, influencing its solubility and reactivity. Additionally, the incorporation of a sulfonyl group indicates potential interactions with biological targets, making it of interest in medicinal chemistry. The specific stereochemistry (2S,3S,4R) is crucial for its biological activity, as the spatial arrangement of atoms can significantly affect how the molecule interacts with enzymes or receptors. Overall, this compound's complexity and functional diversity may render it valuable for research in pharmacology or material science.

MK-8666, a partial GPCR agonist, targets GPR40 to enhance insulin secretion, potentially treating type 2 diabetes without adverse effects.

CAS 2056254-98-7

(2S,3S,4R)-8-[[3-[2,6-dimethyl-4-(3-methylsulfonylpropoxy)phenyl]phenyl]methoxy]-9-azatricyclo[4.4.0.02,4]deca-1(10),6,8-triene-3-carboxylate

MK-8666 Tris

Ref: TM-T69953