Skip to content
    Back to Database
    Amino AcidsNatural

    L-Serine

    Also known as: Serine, L-Ser

    Randomised trials report that high‑dose oral L‑serine (400 mg/kg/day) reduced disease progression measures and pathogenic deoxysphingolipids in HSAN1. Small n‑of‑1 trials in rare GRIN2B loss‑of‑function disorders showed individual improvements in some children but mixed overall results. Several randomised, placebo‑controlled trials used L‑serine as a major component of combined metabolic activator formulations that reported faster recovery from mild‑to‑moderate COVID‑19 and improved cognitive scores in Alzheimer’s disease, but effects cannot be attributed solely to L‑serine within those mixtures.

    Last reviewed: 2026-10-14 · 4 indexed studies

    Evidence Score
    64/100
    Neurological supportSupport for inherited sphingolipid disordersAdjunct in multi‑nutrient metabolic therapies
    Data Completeness4/4 · 100%
    Evidence ScoreDosageSafetyLinked Studies

    Set your location for accurate regulatory status

    Saved on this device — no sign-in needed.

    Overview

    L‑serine is a non‑essential amino acid available as an oral supplement. Human trials have tested L‑serine alone for hereditary sensory and autonomic neuropathy type 1 (HSAN1) and in multi‑component metabolic formulations for conditions such as COVID‑19 and Alzheimer’s disease; evidence for benefit is condition specific and often from combined formulations.

    Mechanism & Function

    Mechanism of Action

    In the included abstracts L‑serine is characterised as a metabolic precursor relevant to sphingolipid metabolism (lowering toxic deoxysphingolipids in HSAN1) and as a precursor to d‑serine which modulates N‑methyl D‑aspartate receptor function in GRIN2B disorders. In the combined metabolic activator trials it is a major component intended to support mitochondrial and antioxidant metabolic pathways, though individual contribution is not isolated in those studies.

    Physiological Role

    Precursor for sphingolipids and for d‑serine (a modulator of NMDA receptors); implicated in cellular metabolic and antioxidant pathways in the context of combined metabolic supplementation.

    Primary Pathways

    Sphingolipid metabolism / deoxysphingolipid reductionNMDA receptor modulation via d‑serineCellular metabolic/mitochondrial and antioxidant pathways (as part of combined metabolic activators)

    Performance / Health Relevance

    Direct performance or ergogenic effects are not demonstrated in the supplied human trials; evidence pertains to specific clinical neurological and recovery outcomes rather than athletic performance.

    Evidence Review

    Overall64/100
    Human Clinical65/100
    Meta-AnalysisN/A

    No meta-analyses or systematic reviews indexed for this ingredient yet.

    Mechanistic70/100
    Real-World50/100
    Safety70/100

    Dimensions marked N/A have no indexed evidence of that class. They are shown as unavailable rather than scored.

    Practical Use & Dosage

    Minimum Effective Dose
    Not established from isolated‑ingredient trials for most indications; clinical benefit in HSAN1 was observed at 400 mg/kg/day.
    Optimal Range
    Not established. Trials used doses such as 400 mg/kg/day (HSAN1) and 12.35 g per dose within a combined formula (AD trial; given once daily then twice daily).
    Upper / Caution Level
    Not established. High oral doses up to ~400 mg/kg/day (~28 g/day for a 70 kg adult) were used and reported without serious adverse effects in the HSAN1 trial.
    Timing
    Varied by trial; HSAN1 dosed daily, Alzheimer’s combined formula given once daily then twice daily in later weeks.
    Best Format
    Oral powder/capsule as used in trials; often administered as part of a combined metabolic formula in some studies.
    Bioavailability
    No specific human bioavailability data reported in the provided abstracts.
    Absorption Considerations
    Not specified in the provided abstracts.

    Safety & Interactions

    Side Effects

    • •No serious adverse effects reported in the HSAN1 trial (per abstract)
    • •Adverse events not detailed in the provided abstracts for other trials

    Contraindications

    • Not specified in the provided abstracts

    Drug Interactions

    • •Not specified in the provided abstracts

    Who Should Avoid

    • •Not specified in the provided abstracts

    Monitoring

    For clinical use in HSAN1, plasma sphingolipid levels were an outcome measure in the trial; trials report monitoring but specific monitoring guidance is not provided in the abstracts.

    Frequently Asked Questions

    Auto-generated from indexed evidence — dosage, safety, interactions, and more.

    When is L-Serine typically used or indicated?

    L-Serine is most commonly used for: Neurological support, Support for inherited sphingolipid disorders, Adjunct in multi‑nutrient metabolic therapies. Precursor for sphingolipids and for d‑serine (a modulator of NMDA receptors); implicated in cellular metabolic and antioxidant pathways in the context of combined metabolic supplementation.

    How does L-Serine work?

    In the included abstracts L‑serine is characterised as a metabolic precursor relevant to sphingolipid metabolism (lowering toxic deoxysphingolipids in HSAN1) and as a precursor to d‑serine which modulates N‑methyl D‑aspartate receptor function in GRIN2B disorders. In the combined metabolic activator trials it is a major component intended to support mitochondrial and antioxidant metabolic pathways, though individual contribution is not isolated in those studies.

    What is the recommended dose of L-Serine?

    The optimal range is Not established. Trials used doses such as 400 mg/kg/day (HSAN1) and 12.35 g per dose within a combined formula (AD trial; given once daily then twice daily).. with a minimum effective dose of Not established from isolated‑ingredient trials for most indications; clinical benefit in HSAN1 was observed at 400 mg/kg/day.. Best taken: Varied by trial; HSAN1 dosed daily, Alzheimer’s combined formula given once daily then twice daily in later weeks.. Upper / caution level: Not established. High oral doses up to ~400 mg/kg/day (~28 g/day for a 70 kg adult) were used and reported without serious adverse effects in the HSAN1 trial..

    What are the side effects of L-Serine?

    Reported side effects include: No serious adverse effects reported in the HSAN1 trial (per abstract); and Adverse events not detailed in the provided abstracts for other trials. Monitoring: For clinical use in HSAN1, plasma sphingolipid levels were an outcome measure in the trial; trials report monitoring but specific monitoring guidance is not provided in the abstracts.

    Does L-Serine interact with medications?

    Known or theoretical interactions: Not specified in the provided abstracts. Always check with a clinician before combining with prescription medication.

    Who should avoid L-Serine?

    L-Serine is generally not recommended for: Not specified in the provided abstracts; and Not specified in the provided abstracts.

    How strong is the evidence for L-Serine?

    Evidence level: Moderate (overall score 64/100), based on 4 indexed studies on SuppIndex.

    Research & References (4)

    Combined Metabolic Activators Accelerates Recovery in Mild-to-Moderate COVID-19.

    RCT2021
    PubMed

    Randomised phase 2 and phase 3 trials of a combined metabolic activator (containing L‑serine plus N‑acetyl‑L‑cysteine, nicotinamide riboside and L‑carnitine tartrate) in ambulatory patients with mild‑to‑moderate COVID‑19 compared to placebo.

    Combined metabolic activators improve cognitive functions in Alzheimer's disease patients: a randomised, double-blinded, placebo-controlled phase-II trial.

    RCT2023
    PubMed

    Randomised, double‑blind, placebo‑controlled phase II trial administering a combined metabolic activator with L‑serine as the major component (one dose contained 12.35 g L‑serine) to patients with Alzheimer’s disease, assessing cognitive outcomes and safety.

    Potential benefits of l-serine in children with GRIN2B loss-of-function variants: Randomized n-of-1 trials.

    RCT2025
    PubMed

    Randomised, double‑blind, placebo‑controlled n‑of‑1 trials of oral L‑serine in four children with GRIN2B loss‑of‑function variants, assessing individual patient outcomes over two 6‑month cycles.

    Randomized trial of l-serine in patients with hereditary sensory and autonomic neuropathy type 1.

    RCT2019
    PubMed

    Randomised, placebo‑controlled trial in patients with hereditary sensory and autonomic neuropathy type 1 (HSAN1) comparing oral L‑serine 400 mg/kg/day to placebo for 1 year, with an open‑label extension.

    Related Ingredients

    Other top-rated ingredients in Amino Acids.

    Research Overview

    Moderate Evidence
    4Total Studies
    4Human Trials
    0Meta-Analyses
    2025Latest Study
    0Animal / In Vitro
    0Athlete Studies
    Primary data sourceClinical Patients
    Pooled evidence (meta-analysis / systematic review)No

    Cite this ingredient

    One-click citation export in APA, MLA, Chicago, BibTeX, or HTML. The URL below is stable and safe to link.

    Stable URL

    https://thesuppindex.com/ingredients/l-serine

    SuppIndex. (2026). L-Serine: Evidence summary, dosage and clinical studies. Retrieved October 16, 2026, from https://thesuppindex.com/ingredients/l-serine

    Based on 4 indexed studies · Evidence level: Moderate.

    Goal Ratings

    Cognition
    Recovery
    General Health

    Stack Compatibility

    L‑serine has been administered as part of multi‑component metabolic activator formulations in clinical trials; effects observed in such trials cannot be attributed to L‑serine alone.

    Often studied as part of combined metabolic activators (with N‑acetylcysteine, nicotinamide riboside, L‑carnitine tartrate)