7626-02-0Relevant articles and documents
Synthesis of N-aryl and N-arylcarbamoylamino derivatives of 1,3-diazinane-5-carboxamide and their activity against glioblastoma LN-229 cell line
Hron, Rebecca J.,Jursic, Branko S.,Neumann, Donna M.
, p. 6183 - 6193 (2016/12/06)
Six structural motifs based on the initial (lead) structure of merbarone were designed, prepared, and tested against the glioblastoma LN-229 cell line. Three different structural moieties were modified in the search for optimal glioblastoma activity: the 1,3-diazinane moiety, the aryl moiety, and the heteroatom linker. Calculated molecular descriptors such as lipophilicity (C log P), acidic strength (calculated pKa), and polar surface area (PSA) were used to design a diverse structural library of these compounds. From six different structural motifs and 136 compounds, a handful of examples with moderate (100 μg/ml), good (10 μg/ml) and excellent (1 μg/ml) glioblastoma activity were elucidated.
Cyano-, Nitro-, and Alkoxycarbonyl-Activated Observable Stable Enols of Carboxylic Acid Amides
Mukhopadhyaya, Jayanta Kumar,Sklenak, Stepan,Rappoport, Zvi
, p. 6856 - 6867 (2007/10/03)
A search for the enol structures of several amides YY′CHCONHPh with Y,Y′ = electron-withdrawing groups (EWGs) was conducted. When Y = CN, Y′ = CO2Me the solid structure is that of the enol (8b) MeO2CC(CN)=C(OH)NHPh, whereas in soluti
