The chemical substance known as "3-({2-[(E)-(1-{2-[(4-methylphenyl)amino]-2-oxoethyl}-2,5-dioxoimidazolidin-4-ylidene)methyl]phenoxy}methyl)benzoic acid" with CAS number 444780-45-4 is characterized by its complex molecular structure, which includes multiple functional groups such as carboxylic acids, imidazolidinones, and aromatic rings. This compound is likely to exhibit properties typical of both organic acids and amines, including potential solubility in polar solvents and the ability to form hydrogen bonds. The presence of the imidazolidinone moiety suggests possible biological activity, as many compounds with similar structures are known for their pharmacological properties. Additionally, the presence of a methylphenyl group may influence its lipophilicity and interaction with biological membranes. Overall, this compound's intricate structure may contribute to its reactivity and potential applications in medicinal chemistry or as a biochemical probe, although specific biological activities would require empirical investigation.

3-({2-[(E)-(1-{2-[(4-methylphenyl)amino]-2-oxoethyl}-2,5-dioxoimidazolidin-4-ylidene)methyl]phenoxy}methyl)benzoic acid

444780-45-4: The chemical substance known as "3-({2-[(E)-(1-{2-[(4-methylphenyl)amino]-2-oxoethyl}-2,5-dioxoimidazolidin-4-ylidene)methyl]phenoxy}methyl)benzoic acid" with CAS number 444780-45-4 is characterized by its complex molecular structure, which includes multiple functional groups such as carboxylic acids, imidazolidinones, and aromatic rings. This compound is likely to exhibit properties typical of both organic acids and amines, including potential solubility in polar solvents and the ability to form hydrogen bonds. The presence of the imidazolidinone moiety suggests possible biological activity, as many compounds with similar structures are known for their pharmacological properties. Additionally, the presence of a methylphenyl group may influence its lipophilicity and interaction with biological membranes. Overall, this compound's intricate structure may contribute to its reactivity and potential applications in medicinal chemistry or as a biochemical probe, although specific biological activities would require empirical investigation.

<p>WRN inhibitor 7 (Compound h6), a potent inhibitor of Werner syndrome helicase, demonstrates effective suppression of WRN's helicase and ATPase activities with IC50 values of 9.8 μM and 15.8 μM, respectively. This compound is utilized in the study of microsatellite instable (MSI) cancers [1].</p>

CAS 444780-45-4

3-({2-[(E)-(1-{2-[(4-methylphenyl)amino]-2-oxoethyl}-2,5-dioxoimidazolidin-4-ylidene)methyl]phenoxy}methyl)benzoic acid

WRN inhibitor 7

Ref: TM-T87635