The chemical substance known as "(±)-1-[5,6-(Methylenedioxy)-1,2,3,4-tetrahydronaphth-1(R*)-ylmethyl]-3(R*)-phenylpyrrolidine methanesulfonate" with CAS number 149189-73-1 is a complex organic compound characterized by its unique structural features. It contains a tetrahydronaphthalene moiety fused with a methylenedioxy group, which contributes to its potential biological activity. The presence of a pyrrolidine ring and a phenyl group indicates that it may exhibit interesting pharmacological properties, possibly interacting with various biological targets. The methanesulfonate group suggests that it may be soluble in polar solvents, enhancing its bioavailability. This compound is likely to be of interest in medicinal chemistry and pharmacology, particularly in the development of new therapeutic agents. Its stereochemistry, indicated by the (R*) designations, may play a crucial role in its biological activity and interaction with receptors. Overall, this substance represents a class of compounds that could have significant implications in drug discovery and development.

(±)-1-[5,6-(Methylenedioxy)-1,2,3,4-tetrahydronaphth-1(R*)-ylmethyl]-3(R*)-phenylpyrrolidine methanesulfonate

149189-73-1: The chemical substance known as "(±)-1-[5,6-(Methylenedioxy)-1,2,3,4-tetrahydronaphth-1(R*)-ylmethyl]-3(R*)-phenylpyrrolidine methanesulfonate" with CAS number 149189-73-1 is a complex organic compound characterized by its unique structural features. It contains a tetrahydronaphthalene moiety fused with a methylenedioxy group, which contributes to its potential biological activity. The presence of a pyrrolidine ring and a phenyl group indicates that it may exhibit interesting pharmacological properties, possibly interacting with various biological targets. The methanesulfonate group suggests that it may be soluble in polar solvents, enhancing its bioavailability. This compound is likely to be of interest in medicinal chemistry and pharmacology, particularly in the development of new therapeutic agents. Its stereochemistry, indicated by the (R*) designations, may play a crucial role in its biological activity and interaction with receptors. Overall, this substance represents a class of compounds that could have significant implications in drug discovery and development.

<p>Napitane Mesylate inhibits norepinephrine transporter and blocks CNS CA uptake as an alpha 2-adrenoceptor antagonist.</p>

CAS 149189-73-1

(±)-1-[5,6-(Methylenedioxy)-1,2,3,4-tetrahydronaphth-1(R)-ylmethyl]-3(R)-phenylpyrrolidine methanesulfonate

Napitane Mesylate

Ref: TM-T26363