L-Tryptophan — Hermetica Encyclopedia
Amino Acid & Peptide · Compound

L-Tryptophan

Provisional Moderate Scoreamino_acid1 Screened PMID Record

Hermetica Superfood Encyclopedia

Evidence review status: needs_human_review

Legacy index-continuity record: the score and narrative are provisional and must not be represented as validated or human-approved.

Review flags: CLAIM_LEVEL_HUMAN_REVIEW_REQUIRED

Provisional Summary

A meta-analysis found the clearest L-tryptophan sleep signal for wake after sleep onset at intakes of at least 1 gram per day. It did not establish broad improvement across every sleep outcome or validate unspecified tryptophan forms.

1
Screened PMID Records
Reported Benefits
Pending
Synergy Review
At a Glance
CategoryAmino Acid & Peptide
GroupCompound
Public Score StatusProvisional Moderate
Primary KeywordL-tryptophan sleep evidence
Tryptophan close-up macro showing natural texture and detail — rich in anticoagulant, serotonergic, thyroid-active
L-Tryptophan — botanical close-up

Origin & History

Tryptophan growing in natural environment — natural habitat
Natural habitat

Tryptophan is an essential amino acid renowned for its role in the synthesis of serotonin and melatonin, key molecules that regulate mood, sleep, and emotional balance. Found in protein-rich foods such as turkey, dairy, eggs, seeds, and legumes, tryptophan is critical for neurological function, appetite regulation, and circadian rhythm support. It also plays a secondary role in pain modulation and cognitive clarity.

Modern biochemical compound without traditional medicinal history.Traditional Medicine

Research Narrative (Provisional)

A systematic review, meta-analysis and meta-regression evaluated tryptophan supplementation and sleep quality (PMID 33942088). The clearest finding concerned wake after sleep onset at at least 1 gram/day; other outcomes were less consistent.

Preparation & Dosage

Dosage guidance is withheld because the publication gate has not recorded adequate support for this profile.

Nutritional Profile

- Essential amino acid - Precursor to serotonin - Precursor to melatonin - Involved in neurotransmitter modulation

Reported Mechanism (Provisional)

Mechanism of Action

Tryptophan is primarily metabolized via the kynurenine pathway (95-99%), producing NAD+, kynurenic acid (a neuroprotective NMDA antagonist), and quinolinic acid. A smaller but crucial portion enters the serotonin pathway (~1-5%), where tryptophan hydroxylase converts it to 5-hydroxytryptophan, leading to serotonin (5-HT) and subsequently melatonin synthesis. Additionally, gut microbiota can metabolize tryptophan into indole derivatives through the indole pathway.

Clinical Narrative (Provisional)

Identity is pinned to L-tryptophan. Evidence should not be transferred to unspecified isomers or trace-dose combinations.

Also Known As

L-TryptophanTRP2-Amino-3-(1H-indol-3-yl)propanoic acid

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These statements have not been evaluated by the Food and Drug Administration. This content is for informational purposes only and is not intended to diagnose, treat, cure, or prevent any disease.
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