“…For instance, a typical design for targeting the mitochondria and investigating their dynamics involves the incorporation of a cationic group, such as triphenylphosphonium (TPP + ), 11,12 a pyridinium group, and other substrates. [13][14][15][16][17][18][19][20][21][22] Similarly, for targeting the ER, the structural modifications include sulfonylurea, methyl sulfonamide motifs, or thiol-reactive functional groups such as halides. 18,19 The literature reveals many examples, majorly based on a naphthalimide scaffold bearing a sulfonamide functional moiety.…”