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Prior to the mid-1950s, the majority of commensals and pathogens were susceptible to tetracycline.
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That said, many infection-causing bacteria are already resistant to tetracyclines.
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One great advantage of this approach is the ease with which varying functionality can be added throughout the structure, particularly substituents at c5 x , c6 r , c7 y , c9 z , and even an extra e ring; a great many analogues have been made, and some of these combine strong antibacterial activity with activity against strains resistant to first- and second-generation tetracycline antibiotics myers et al.
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