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They are both substrates and inhibitors/inducers of drug-metabolizing enzymes and drug transporters, making them victims and perpetrators of drugdrug interactions (DDIs) [1,2,3]

S., Hamill, R

in this study, we utilized BAR to compare the syn interactomes of both diseases to define better core molecular features, distinguishing MSA and PD/DLB

Heres the visual shorthand many readers find useful first: Common formulation GHK-Cu: 50 mg KPV: 10 mg BPC-157: 10 mg TB-500: 10 mg The term itself also has some history behind it