2H-Imidazol-2-one, 1,3-dihydro-4-methyl-5-[4-(methylthio)benzoyl]-


Chemical Name: 2H-Imidazol-2-one, 1,3-dihydro-4-methyl-5-[4-(methylthio)benzoyl]-
CAS Number: 77671-31-9
Product Number: AG005GLA(AGN-PC-0JKZOX)
Synonyms:
MDL No: MFCD00867130
Molecular Formula: C12H12N2O2S
Molecular Weight: 248.3009

Identification/Properties


Properties
Storage:
2-8℃;Keep in dry area;
Computed Properties
Molecular Weight:
248.3g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
248.062g/mol
Monoisotopic Mass:
248.062g/mol
Topological Polar Surface Area:
83.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
371
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



Enoximone, also known as Phosphodiesterase III Inhibitor, is a valuable chemical compound widely utilized in the field of chemical synthesis. Its primary application lies in its ability to inhibit the enzyme phosphodiesterase III, which plays a crucial role in regulating cellular levels of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP). By inhibiting this enzyme, Enoximone modulates the intracellular levels of cAMP and cGMP, leading to various downstream effects that are beneficial in chemical reactions.In chemical synthesis, Enoximone is often used as a catalyst or additive to enhance specific reactions by altering the cellular signaling pathways involving cAMP and cGMP. Its ability to increase the levels of these cyclic nucleotides can influence key processes such as protein phosphorylation, gene expression, and ion channel activity. These effects can ultimately impact the outcome of chemical reactions, promoting desired product formation or yield.Additionally, Enoximone's pharmacological properties make it a versatile tool in designing and optimizing synthetic pathways for various compounds. Its unique mechanism of action and ability to modulate cellular signaling pathways offer researchers the flexibility to fine-tune reaction conditions and control specific reaction parameters to achieve the desired synthetic goals.Overall, the application of Enoximone in chemical synthesis showcases its importance as a catalyst and modulator of cellular signaling pathways, allowing for more precise and efficient control over synthetic reactions and processes.