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We used a unique chemistry approach to tune the reactivity of our molecule, so that were targeting what would typically be considered a bad biomarker. The researchers tuned the dynamic range of the molecule so that it would not react to glutathione under healthy conditions but would react with the excess glutathione made by cancer cells

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doi: 10.1002/1873-3468.13216 39 RichterA

PRIMA-1 reactivates mutant p53 by covalent binding to the core domain

NONOates can be hydrolyzed under physiological conditions, releasing two moles of NO per donor

Glutathione is an endogenous antioxidant compound present in human tissues and organs