Cross-referencing clinical data
A pairing appears on this page only when a trial gave both ingredients together and measured the result. Rhus coriaria has none that clears that bar.
Stitching two separate single-ingredient studies into a pairing is the one thing this engine will not do. When a study of the combination itself holds up at source, it lands here with its citation.
No invented synergy. Where actives were studied on their own rather than together, the record shows each on its own evidence, never a combined effect no trial measured.
Research strength. Research strength says how much work stands behind the combination. It is never a product score.
Independent record. Every finding is cited to a named trial, dated, and never written by the brand.
20 pairings are live across the library today. Checked 20 July 2026.
No study gave these as a pair, so they are not in the card above. But the reason they belong together is settled biochemistry, not a guess, so it is worth knowing.
Ascorbate regenerates oxidised polyphenol radicals, extending the effective life of the tannin fraction in an aqueous formulation. The chemistry is settled and applies across polyphenol classes. It is a solution-phase effect, so it says nothing on its own about what happens after absorption.
Gallotannins bind iron in the gut lumen and form complexes the small intestine cannot take up. Sumac's tannin content is high enough that this is a practical consideration rather than a theoretical one, particularly for anyone working on low iron status. Spacing the two by a couple of hours resolves most of it.
Sumac has been examined in meta-analysed trials for its effect on glucose and insulin markers, and cinnamon occupies the same research space. Stacking two ingredients that both nudge glycaemic markers is worth noting for anyone already on glucose-lowering medication, because the effects can add. No trial has tested the combination as a unit.
Berberine is the more potent of the two on glucose handling by some margin. Adding sumac on top raises the chance of a larger combined shift, which matters most for people on prescribed glucose-lowering therapy. This is flagged as an interaction to supervise, not as a stack to assemble casually.
Tannin-protein complexation is what produces sumac's astringent mouthfeel, and it happens with supplemental protein too. Protein taken alongside sequesters part of the polyphenol dose while making the preparation more palatable. Both consequences follow from the same binding event.
Gallotannins are too large to absorb intact, so colonic bacteria carrying tannase hydrolyse them into gallic acid and pyrogallol derivatives. Those smaller metabolites are much of what circulates. Because tannase capacity differs between people, so does the metabolite profile from an identical dose.
Flavonols passing through the enterocyte compete for the same UGT and SULT capacity. A large added quercetin dose can shift the conjugated fraction of the native sumac flavonols and the other way round. The net direction depends on dose, so this is a flag rather than a dosing instruction.
Sumac's flavonols are extensively conjugated on first pass, which is the main reason plasma levels stay low. Piperine slows that step and raises measured exposure for compounds in this class. It raises exposure to everything else in the formula at the same time, which is the part that gets forgotten.
Nothing specific on file for Rhus coriaria. Match the label to the daily amount above, and tell your doctor what you take.
Not medical advice. Show the label to your pharmacist.These are the studies our verdict leans on, chosen from the 9 we read for Rhus coriaria. The full linked list is below.
3 sources behind our Rhus coriaria verdict: peer-reviewed studies and registered clinical trials. Every one links straight to PubMed, the journal, or ClinicalTrials.gov. Read them yourself.
Evidence surfaced via Semantic Scholar (Allen Institute for AI) and ClinicalTrials.gov. Ranked by study type and citation weight, not cherry-picked.
FDA Disclaimer: These statements have not been evaluated by the Food and Drug Administration. This information is for educational purposes only and is not intended to diagnose, treat, cure, or prevent any disease. Consult your healthcare provider before starting any supplement regimen.