LDH / Lactate Modulating Substances — Reference Table

LDH / Lactate Modulating Substances — Reference Table

Practical summary of reported LDH inhibitors and lactate-modulating agents. Columns: category, substance, mechanism/notes, best taken with, timing considerations, and evidence rank.

Category Substance Notes on LDH / Lactate Effect Best Taken With Timing Consideration Evidence Rank
Research-Grade Oxamate Classic LDH inhibitor (pyruvate analog). Primarily used in vitro/in vivo research. Not applicable Research use only
Research-Grade Galloflavin Flavonoid reported to selectively inhibit LDH-A in preclinical studies. With fats or bioenhancers (piperine, quercetin) Likely better in fasting or with a light fat-containing meal +
Research-Grade FX11 Small-molecule LDH-A inhibitor used in preclinical cancer models. Not available clinically Experimental / research only +
Research-Grade 3-Bromopyruvate (3-BP) Potent glycolysis and LDH inhibitor but highly toxic; not safe for general use. Unsafe for general use Research/clinical trial setting only
Natural EGCG (green tea) Direct LDH inhibition reported; reduces lactate production in multiple studies. Water or empty stomach (avoid iron-rich meals) Morning or fasting state for better absorption ++
Natural Resveratrol Downregulates LDH-A expression and lowers lactate output in preclinical work. With fat (olive oil, nuts) to improve bioavailability Morning / fasting favors NAD⁺ modulation ++
Natural Curcumin Suppresses LDH-A and other glycolytic enzymes; often combined with piperine. With fat + piperine (black pepper) With a meal (midday) for absorption ++
Natural Quercetin Inhibits LDH-A activity and reduces glycolytic flux in preclinical studies. With fat or phospholipids (lecithin) Midday; often synergistic with resveratrol ++
Natural Apigenin Reported to reduce LDH-A and suppress glycolysis; also has calming properties. With fat Evening (calming / possible GABAergic effects) +
Natural Silibinin (milk thistle) LDH suppression reported alongside hepatoprotective actions. With meal or fat Morning or evening (supports liver cycles) ++
Natural Baicalein Flavone from Scutellaria: reported LDH-A inhibition and glycolytic blockade. With fat; often as part of an herbal decoction Evening (may be sedating) +
Repurposed / Metabolic Metformin Indirectly reduces glycolysis / NADH load via AMPK and mitochondrial effects. With food (reduces GI upset) Typically morning ± evening dosing to maintain steady levels +++
Repurposed / Metabolic Dichloroacetate (DCA) Activates PDH (via PDK inhibition) pushing pyruvate into mitochondria — lowers lactate. Water; some protocols include thiamine support Morning or early afternoon (mitochondrial activation) ++
Repurposed / Metabolic Lonidamine Glycolysis / LDH targeting agent used investigationally in oncology settings. With food (per trials) Clinical trial / supervised use +
Repurposed / Metabolic Nicotinamide (B3, high dose) Alters NAD⁺/NADH balance, potentially reducing LDH activity in some contexts. With water Morning (can affect sleep if taken late) ++
Other / Experimental Gossypol Natural LDH-A inhibitor described in literature but toxic at active doses. Not recommended Research / clinical supervision only
Other / Experimental FX-11 derivatives Next-generation research LDH inhibitors derived from FX11 — preclinical pipeline. Not applicable Research setting +

Legend — Evidence Rank: +++ = clinical / human data; ++ = strong preclinical or animal evidence; + = cell culture / in vitro or early reports; = mostly experimental, unsafe, or not practical for general use.

This way you can see at a glance:

  • Strongest practical evidenceMetformin, Curcumin, Resveratrol, Quercetin, EGCG, DCA, Silibinin.
  • Moderate evidence → Apigenin, Baicalein, Nicotinamide.
  • Experimental / unsafe → Oxamate, FX11, 3-BP, Gossypol.