From antibiotics to analgesics, explosives to pesticides, electrochemically activated (ECA) molecules is a very large class of application-based molecules, so large that they can be any type of molecule so long as they're electrochemically activated.

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The real power comes from antibiotics, like Penicillin: the scale and volume of antibiotic use for eight (8) billion people is driving global antibiotic resistances and deaths. The current World Health Organization estimates that nearly 4.95 million people die per year due to associated antimicrobial resistant infections [1]. However, if you were to protect existing antimicrobials from developing resistant strains of microorganisms with a CGP-specific charperone, one that microbes cannot metabolize, you can retain the effectiveness of your limited selection of antimicrobials longer. By only having antibacterial effects achieved via CGP use resistance development can be slowed, the reserved antimicrobials can be better protected, and new forms of antimicrobials can be developed.

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This self-same ECA-principle holds true for several other molecule classes like pain-killers; disinfectants; epoxies; glues and adhesives; additional oncologics; pesticides; demolition and explosive agents; colorful dyes and printer inks; and, even food flavors and ingredients.

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There almost is no limit with EAC or ECA molecular strategies, only increased control.

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1. World Health Organization. Antimicrobial Resistance. 2025. <https://www.who.int/news-room/fact-sheets/detail/antimicrobial-resistance>.

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