329314-76-3 Usage
Description
(2Z)-2-(3-ethenyl-4-methyl-5-oxopyrrol-2-ylidene)acetamide is a chemical compound with the molecular formula C10H11NO2. It is an organic compound that contains a pyrrolidin-2-one backbone with an acetamide functional group attached to it. (2Z)-2-(3-ethenyl-4-methyl-5-oxopyrrol-2-ylidene)acetamide is classified as a ketamine derivative and has potential pharmacological activity. Its unique structure and properties make it a promising candidate for various applications in medicinal and pharmaceutical research.
Uses
Used in Pharmaceutical Research:
(2Z)-2-(3-ethenyl-4-methyl-5-oxopyrrol-2-ylidene)acetamide is used as a research compound for exploring its potential therapeutic applications. Its pharmacological activity and unique structure make it a valuable tool for studying various biological processes and developing new drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2Z)-2-(3-ethenyl-4-methyl-5-oxopyrrol-2-ylidene)acetamide is used as a starting material or intermediate for the synthesis of other bioactive compounds. Its versatile structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Drug Design:
(2Z)-2-(3-ethenyl-4-methyl-5-oxopyrrol-2-ylidene)acetamide is used as a template for drug design, providing a foundation for the creation of new molecules with specific therapeutic properties. Its unique features can be exploited to design drugs that target particular biological pathways or receptors.
Used in Drug Development:
In the process of drug development, (2Z)-2-(3-ethenyl-4-methyl-5-oxopyrrol-2-ylidene)acetamide can be used as a lead compound for further optimization and refinement. Its potential pharmacological activity and structural characteristics make it a valuable asset in the development of new therapeutic agents.
Overall, (2Z)-2-(3-ethenyl-4-methyl-5-oxopyrrol-2-ylidene)acetamide is a versatile and promising chemical compound with a wide range of applications in the fields of pharmaceutical research, medicinal chemistry, drug design, and drug development. Its unique structure and potential pharmacological activity make it an important tool for the discovery and development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 329314-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,3,1 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 329314-76:
(8*3)+(7*2)+(6*9)+(5*3)+(4*1)+(3*4)+(2*7)+(1*6)=143
143 % 10 = 3
So 329314-76-3 is a valid CAS Registry Number.
329314-76-3Relevant articles and documents
BOX A-type monopyrrolic heterocycles modified via the Suzuki-Miyaura cross-coupling reaction
Schulze, Daniel,Klopfleisch, Maurice,G?rls, Helmar,Westerhausen, Matthias
, p. 51 - 62 (2019/12/03)
The in vivo oxidation of heme yields bilirubin which is further degraded to the bilirubin oxidation end products (BOXes) that are biologically highly active. To study the mode of action and fate of (Z)-2-(4-methyl-5-oxo-3-vinyl-1,5-dihydro-2H-pyrrol-2-yli
Isolation and Identification of Intermediates of the Oxidative Bilirubin Degradation
Ritter, Marcel,Seidel, Raphael A.,Bellstedt, Peter,Schneider, Bernd,Bauer, Michael,G?rls, Helmar,Pohnert, Georg
supporting information, p. 4432 - 4435 (2016/09/09)
Four endogenous products of oxidative bilirubin degradation were isolated and fully characterized. The constitutional isomers belong to the propentdyopents (PDPs). Their structures and further oxidative transformations to biologically active bilirubin oxi
