CAS 389572-70-7

Pyrrolidine, 1-[(2E)-3-(4-methoxyphenyl)-1-oxo-2-propenyl]-

Description:

Pyrrolidine, 1-[(2E)-3-(4-methoxyphenyl)-1-oxo-2-propenyl]- is a chemical compound characterized by its pyrrolidine ring structure, which is a five-membered saturated nitrogen-containing heterocycle. This compound features a substituent that includes a 4-methoxyphenyl group and an α,β-unsaturated carbonyl moiety, contributing to its potential reactivity and biological activity. The presence of the methoxy group enhances its lipophilicity, which may influence its interaction with biological targets. The compound's structure suggests it may exhibit properties typical of both pyrrolidine derivatives and α,β-unsaturated carbonyl compounds, such as potential for nucleophilic attack or participation in Michael addition reactions. Its specific applications or biological activities would depend on further studies, but compounds of this nature are often explored in medicinal chemistry for their potential therapeutic effects. As with any chemical substance, safety and handling precautions should be observed, particularly due to the presence of reactive functional groups.

Formula: C₁₄H₁₇NO₂

Piperlotine A

CAS: 389572-70-7

Formula: C₁₄H₁₇NO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 231.2903

Ref: IN-DA00CHMF

Piperlotine A

CAS: 389572-70-7

Piperlotine A

Purity: ≥98%

Molecular weight: 231.29g/mol

Ref: 54-BUP00370

Piperlotine A

CAS: 389572-70-7

Piperlotine A, from Piperonyssinus rolfsii, inhibits platelet aggregation and Mycobacterium tuberculosis (MIC 50 ug/mL).

Formula: C₁₄H₁₇NO₂

Purity: 99.27%

Color and Shape: Solid

Molecular weight: 231.29

Ref: TM-TN2086

Piperlotine A

CAS: 389572-70-7

Formula: C₁₄H₁₇NO₂

Molecular weight: 231.30

Ref: 7W-GY2039

Piperlotine A

CAS: 389572-70-7

Formula: C₁₄H₁₇NO₂

Purity: 95%~99%

Molecular weight: 231.295

Ref: BP-SBP03048

Piperlotine A

CAS: 389572-70-7

Piperlotine A is a bioactive compound, which is a selective dopamine receptor agonist. This compound is a product of meticulous chemical synthesis, developed through a series of organic reactions tailored to optimize receptor binding affinity and selectivity. Piperlotine A interacts primarily with D2-like dopamine receptors, modulating neurological functions by mimicking endogenous dopamine pathways.

Formula: C₁₄H₁₇NO₂

Purity: Min. 95%

Molecular weight: 231.29 g/mol

Ref: 3D-PQA57270