“…Indeed, a wealth of derivatives, mainly containing a primary sulfonamide (RSO 2 NH 2 ) [1, 2, 4–6] and its bioisosteres, such as the sulfamate (ROSO 2 NH 2 ) [1, 7, 8] and sulfamide (RNHSO 2 NH 2 ) [1, 2, 9–18] as zinc anchoring groups, have been investigated as CA inhibitors (CAIs) with some of them (principally sulfonamides and sulfamates) being explored for the treatment of a variety of disorders such as glaucoma [19–22], acid-base disequilibria [23], epilepsy [24, 25] neuromuscular diseases [26], edema [27], and obesity [28, 29] and for the management of hypoxic tumors [30]. Acetazolamide (AAZ) 1 [31], methazolamide (MZA) 2 [31], topiramate (TPM) 3 [32], ethoxzolamide (EZA) 4 [33], and dichlorphenamide (DCP) 5 [31] represent some examples of such pharmacologically relevant CAIs (Figure 1).…”