NAD+ scientific corpus · Two permanent publications
NAD+ is not a generic energy ingredient. It is a compartmented redox cofactor, a substrate for signalling and repair enzymes, and a metabolite governed by synthesis, transport, consumption and cellular demand. This collection separates those causal layers before examining human translation.
Scientific construction
The first publication establishes the complete NAD+ system. The second interrogates what may constrain persistence and utilisation after delivery. Neither document converts biochemical plausibility into a universal protocol.
IMolecular identity and reaction chemistry
IICellular mechanism and compartment
IIIAttainable exposure and in-vivo pharmacology
IVIntegrated physiology and individual terrain
VTerminal human translation
⊣Counterevidence and falsification
Identity, redox chemistry, salvage pathways, compartmentation, route-dependent exposure, active consumption, metrology, counterevidence and longitudinal response.
Delivery versus utilisation, CD38, precursor continuity, NNMT and methyl-donor economy, magnesium, MgATP, NAD kinase, NADP(H), mitochondrial transport and falsifiable response.
01Identity sources for identity claims
02Enzyme and structural records for causal claims
03Pharmacology for the exposure bridge
04Human studies as terminal translation tests