Disodium 2,2'-[benzene-1,4-diylbis(nitrosoimino)]diacetate, identified by its CAS number 214211-69-5, is a chemical compound characterized by its unique structure, which includes a benzene ring substituted with nitrosoimino groups and acetate moieties. This compound typically exhibits properties associated with its functional groups, such as potential reactivity due to the presence of nitrosoimino functionalities, which can participate in various chemical reactions, including redox processes. The disodium salt form indicates that it is soluble in water, making it suitable for applications in aqueous environments. Its structural features suggest potential uses in fields such as organic synthesis, materials science, or as a reagent in analytical chemistry. Additionally, the presence of both acetate and nitrosoimino groups may impart specific biological activities, warranting further investigation into its pharmacological properties. Overall, this compound represents a complex interplay of organic chemistry principles, with implications for both practical applications and theoretical studies.

disodium 2,2'-[benzene-1,4-diylbis(nitrosoimino)]diacetate

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N,N-Dinitroso-p-phenylenediamine-N,N-diacetic acid (DNPD) is a water soluble molecule with a pyrimidine nucleus. It has been shown to have anti-inflammatory properties and is used for the treatment of skin conditions such as psoriasis. DNPD also modulates the apoptotic process by inhibiting the proliferation of endothelial cells. DNPD induces apoptosis in human keratinocytes by activating soluble guanylate cyclase, which leads to an increase in intracellular levels of guanosine 3',5'-cyclic monophosphate (cGMP). The activation of cGMP leads to an increase in the production of reactive oxygen species and mitochondrial dysfunction. This ultimately results in cell death.

CAS 214211-69-5: disodium 2,2'-[benzene-1,4-diylbis(nitrosoimino)]diacetate

N,N-Dinitroso-p-phenylenediamine-N,N-diacetic acid

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