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PreclinicalResearch compoundLimited evidence

7,8‑DHF

Natural flavone and putative small-molecule BDNF mimetic (TrkB agonist), preclinical data only.

NootropicNeuroprotectiveBDNFNeuroprotectionBDNFnoo.affects.neuroprotectionnoo.affects.mood
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Pharmacology

ClassBDNF · Neuroprotection
Primary targetTrkB receptor selective agonism (dimerization and autophosphorylation)
Targets3 receptor targets
Half-lifeShort in rodents (roughly a couple of hours) with low oral bioavailability; no human pharmacokinetic data
OnsetNo established human protocol (community users typically dose once or twice daily, often in the morning)
EvidenceLimited evidence
Affected systemsBDNFnoo.affects.neuroprotectionnoo.affects.mood

Contents

WHAT IS 7,8-DHF?

Detailed overview

7,8-DHF (7,8-dihydroxyflavone, tropoflavin) is a naturally occurring flavone described as a small-molecule BDNF mimetic: it is proposed to bind the TrkB receptor, trigger its dimerization and autophosphorylation, and engage the downstream PI3K/Akt and MAPK/ERK neurotrophic pathways, while also acting as an independent antioxidant. It has been studied extensively in rodent models of depression, fear extinction (PTSD), Alzheimer's disease and neuroprotection, often with favorable results. Importantly, several independent laboratories could not reproduce the claim of direct TrkB activation, so the exact mechanism is disputed. There are no human clinical trials, oral bioavailability is low and clearance is rapid, so efficacy and safety in humans are essentially unstudied; it is currently available only as research-grade or supplement-grade material.

Mechanism

Putative TrkB agonist (BDNF mimetic)

Evidence

Preclinical only (no human data)

Legal status

Research-grade / supplement-grade powder

Receptor profile

  • TrkB receptor (BDNF receptor)Strong
  • PI3K/Akt and MAPK/ERK signaling (downstream)Moderate
  • Antioxidant / oxidative stress reductionWeak

Safety

Side effects, stop signs, contraindications

Side effects · 6

  • No formal human safety or toxicology data: the evidence comes almost entirely from rodent studies
  • Low oral bioavailability and rapid clearance in rodents, so human exposure is uncertain
  • Whether it truly activates TrkB directly in humans is scientifically disputed (several independent groups could not reproduce it)
  • Purity of research-grade or supplement-grade powder can be variable
  • Theoretical pro-oxidant/quinone effect at very high concentrations (catechol structure)
  • Use in pregnancy and drug interactions are unstudied

Contraindications · 4

  • Pregnancy and breastfeeding: safety not established, avoid
  • Not an approved medicine; exists only as research-grade or supplement-grade material, not recommended without clinical supervision
  • Unknown interaction profile: caution with other neuroactive agents and antidepressants
  • Uncertain sourcing and purity risk due to unregulated supply

Related Nootropics

Same therapeutic category

Studies

Related research and clinical findings

FAQ

FAQ

Natural flavone and putative small-molecule BDNF mimetic (TrkB agonist), preclinical data only.

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Structure & chemistry

TypeNootropic
FormulaC15H10O4
UpdatedJuly 10, 2026
MolekulaX Editorial Team·Source-verified · PubMed · FDA · EMA
Updated: July 10, 2026

The information here is strictly for educational and scientific purposes. It does not replace medical advice or clinical consultation, and it does not encourage illegal substance or pharmaceutical use. Data is sourced. When in doubt, consult your doctor.