The chemical substance known as (1R,2R,3R,5R,6R)-2-Amino-3-[(3,4-dichlorophenyl)methoxy]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid, with the CAS number 569686-87-9, is a bicyclic compound characterized by its complex structure, which includes multiple functional groups such as amino, carboxylic acid, and methoxy groups. This compound features a bicyclo[3.1.0]hexane core, which contributes to its unique three-dimensional conformation. The presence of fluorine and dichlorophenyl substituents indicates potential biological activity, possibly influencing its pharmacological properties. The stereochemistry, denoted by the (1R,2R,3R,5R,6R) configuration, suggests that the compound may exhibit specific interactions with biological targets, making it of interest in medicinal chemistry. Its dicarboxylic acid functionality may enhance solubility and reactivity, while the amino group could facilitate interactions with receptors or enzymes. Overall, this compound's structural features suggest potential applications in drug development, particularly in areas targeting specific biological pathways.

(1R,2R,3R,5R,6R)-2-Amino-3-[(3,4-dichlorophenyl)methoxy]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid

569686-87-9: The chemical substance known as (1R,2R,3R,5R,6R)-2-Amino-3-[(3,4-dichlorophenyl)methoxy]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid, with the CAS number 569686-87-9, is a bicyclic compound characterized by its complex structure, which includes multiple functional groups such as amino, carboxylic acid, and methoxy groups. This compound features a bicyclo[3.1.0]hexane core, which contributes to its unique three-dimensional conformation. The presence of fluorine and dichlorophenyl substituents indicates potential biological activity, possibly influencing its pharmacological properties. The stereochemistry, denoted by the (1R,2R,3R,5R,6R) configuration, suggests that the compound may exhibit specific interactions with biological targets, making it of interest in medicinal chemistry. Its dicarboxylic acid functionality may enhance solubility and reactivity, while the amino group could facilitate interactions with receptors or enzymes. Overall, this compound's structural features suggest potential applications in drug development, particularly in areas targeting specific biological pathways.

MGS-0039: Group II mGluR2/3 antagonist, non-serotonergic antidepressant-like effect, AMPA involvement, regulates dopamine in NAc.

CAS 569686-87-9

(1R,2R,3R,5R,6R)-2-Amino-3-[(3,4-dichlorophenyl)methoxy]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid

MGS-0039

Ref: TM-T28034