CAS 2314-80-9

1-(4-Methoxyphenyl)-2,5-pyrrolidinedione

Description:

1-(4-Methoxyphenyl)-2,5-pyrrolidinedione, also known as methoxyphenylpyrrolidinedione, is an organic compound characterized by its pyrrolidine ring structure substituted with a methoxyphenyl group. This compound features a five-membered cyclic structure containing two carbonyl groups, which contribute to its reactivity and potential biological activity. The methoxy group enhances its lipophilicity, potentially influencing its solubility and interaction with biological membranes. It is often studied for its pharmacological properties, including potential applications in medicinal chemistry. The compound may exhibit various chemical behaviors, such as undergoing nucleophilic addition reactions due to the electrophilic nature of the carbonyl groups. Additionally, its structural features may allow for interactions with specific biological targets, making it of interest in drug development. Safety and handling precautions should be observed, as with many organic compounds, due to potential toxicity or reactivity. Overall, 1-(4-Methoxyphenyl)-2,5-pyrrolidinedione represents a class of compounds that bridge organic chemistry and pharmacology.

Formula: C₁₁H₁₁NO₃

InChI: InChI=1S/C11H11NO3/c1-15-9-4-2-8(3-5-9)12-10(13)6-7-11(12)14/h2-5H,6-7H2,1H3

InChI key: InChIKey=MHZVVJBHJQRDQI-UHFFFAOYSA-N

SMILES: O=C1N(C2=CC=C(OC)C=C2)C(=O)CC1

Synonyms:

• 1-(4-Methoxyphenyl)-2,5-pyrrolidinedione
• 1-p-Methoxyphenylsuccinimide
• 2,5-Pyrrolidinedione, 1-(4-Methoxyphenyl)-
• N-(4-Methoxyphenyl)succinimide
• N-p-Anisylsuccinimide
• NSC 403637
• Succinimide, N-(p-methoxyphenyl)-

1-(4-Methoxyphenyl)pyrrolidine-2,5-dione

CAS: 2314-80-9

1-(4-Methoxyphenyl)pyrrolidine-2,5-dione is a potent inhibitor of p2y receptors. It has been shown to inhibit the generation of monoclonal antibodies and cytosolic Ca2+ in T cells, which are both important for the activation of immune cells. 1-(4-Methoxyphenyl)pyrrolidine-2,5-dione also inhibits the polymerase chain reaction (PCR), which is a DNA replication technique used in molecular biology. The molecule interacts with hydrogen bond and gamma-aminobutyric acid (GABA), but does not interact with glutamate or carbaryl. This drug may be useful for the treatment of bladder cancer due to its potent inhibitory activity against p2y receptors.

Formula: C₁₁H₁₁NO₃

Purity: Min. 95%

Molecular weight: 205.21 g/mol

Ref: 3D-CAA31480