A reference work, not a recommendation to use: this profile describes mechanism and evidence and does not replace medical advice. The claims come from marketing and forums and are tested here, not endorsed.
Claims checked
Protects the liver
Not studiedNo study of liver protection or liver values in healthy people found. NAC is established as an antidote in paracetamol poisoning, on a weak RCT and mainly observational basis [3]; this is a drug use in poisoned patients and not evidence for healthy people. The advertising claim “Raises glutathione and protects the liver” is split according to K4; the glutathione part appears as a marker in the next claim.
Raises glutathione levels (marker only)
Mixed resultsMarker only. In a double-blind crossover study, glutathione rose only in people with a low baseline value, not at medium or high values [7]; a systematic review in men reports mostly an improved glutathione balance [8]. Area as for the split main claim.
More endurance and athletic performance
Mixed resultsPerformance gains (VO2max +13.6%, time trial +15.4%, Wingate +11.4%) only in the group with low glutathione, not at medium or high baseline values [7]. A systematic review of 16 controlled studies in men reports mostly benefits, without meta-analysis [8].
Helps against depression
Small benefitMeta-analysis of twelve RCTs with 904 patients: SMD −0.24 (95% CI −0.44 to −0.05) in favor of NAC as an add-on, most clearly in bipolar disorder; because of the wide confidence interval, the authors consider larger studies necessary [9].
Mechanism of action
Evidence map: N-Acetylcysteine (NAC)
Glutathione is formed in the cell from glutamate, cysteine, and glycine; the supply of cysteine and the activity of the rate-limiting enzyme glutamate-cysteine ligase are decisive for the synthesis rate [1]. NAC is used as a cysteine donor for this pathway. After oral intake, however, only 6 to 10% reaches the circulation unchanged; the elimination half-life after infusion was about 2.3 hours, and the volume of distribution corresponded essentially to the extracellular space [2].
Intravenously, acetylcysteine serves as an antidote in paracetamol poisoning. A Cochrane review found only a few small RCTs with a high risk of bias: acetylcysteine appeared superior to placebo and had fewer adverse effects than dimercaprol or cysteamine; one small study pointed to lower mortality in fulminant liver failure. Current treatment rests mainly on observational studies [3]. With intravenous administration, non-allergic anaphylactoid reactions occur; simplified infusion regimens reduced them markedly in a meta-analysis, without more liver injury [4]. Errors in infusions with accidental overdose led in case reports to brain edema, hemolytic uremic syndrome, and deaths [5]. These drug findings concern poisoned patients and say nothing about liver protection in healthy people. Orally, acetylcysteine is approved as a mucolytic; the package leaflet of such a product names the liquefaction of mucus in cold-related bronchitis as an indication and describes, among other things, rare bronchospasms, very rare severe skin and hypersensitivity reactions, and interactions with glyceryl trinitrate and carbamazepine [6].
On the supplement claims: in a double-blind crossover study with 36 of 100 screened people, NAC over 30 days raised the glutathione level only in people with low glutathione, lowered oxidation markers, and increased performance (VO2max, time trial, Wingate); at medium and high baseline values, performance and redox status remained unchanged [7]. A systematic review of 16 controlled studies in men reports mostly benefits for performance, antioxidant capacity, and glutathione balance, but no clear effects on blood count, inflammatory response, and muscle parameters [8]. As adjunctive treatment in depression (mainly in bipolar disorder), a meta-analysis of twelve RCTs with 904 patients found a small effect (standardized mean difference −0.24; 95% CI −0.44 to −0.05) [9]. Studies with the combination GlyNAC (glycine and NAC) do not count for NAC alone; they are covered in the glynac profile.
Formulations and origin: NAC is available as effervescent tablets, granules, and capsules, as an extended-release tablet, and as an infusion solution (medicinal products). An extended-release tablet gave a flatter concentration curve and the lowest oral availability, a fast-dissolving tablet the highest (6 to 10% overall) [2]. Comparative data with a clinical endpoint were not found.
Synaptik serves solely to explain biochemistry and pharmacology and is not medical advice or a recommendation to take anything.
superoxide, H₂O₂, radicals glutathione (GSH) selected drug gold = the drug's site of action
Baseline
N-acetylcysteine (NAC)
The baseline panel shows the cell without a drug, the other the same cell with the selected drug. Both panels run the same model; particles and speeds only show where the drug acts and in which direction, not the size of the effect in humans.
N-acetylcysteine serves as a cysteine source for glutathione synthesis; cysteine is the limiting building block, glutamate-cysteine ligase (GCL) sets the rate, and GSH inhibits GCL by feedback [1]. This fits the human data: in a double-blind crossover study of 36 people, glutathione rose only in those with low baseline levels; with medium or high baseline, redox status and performance did not change [15]. Liver protection in healthy people has not been studied.
Tap or focus a labelled part for a one-line explanation.
Also acting here, not drawn
- Alpha-lipoic acid (racemate): not selected (evidence level below 3)
- Centrophenoxine: only one animal finding (rat brain)
- Coenzyme Q10: same finding as ubiquinol, which is drawn
- Emoxypine: only one Russian review
- Hericium erinaceus (erinacine A-enriched mycelium): not selected (evidence level below 3)
- Chaga (Inonotus obliquus): not selected (evidence level below 3)
- L-ergothioneine: its transporter ETT (OCTN1) is not part of the scene
- MOTS-c: not selected (evidence level below 3)
- N-acetyl-L-tyrosine: only one finding in fruit flies
- Pinealon: not selected (evidence level below 3)
- Tocotrienol–tocopherol mixture: not selected (evidence level below 3)
Targets
| Target | Type | Action | Key data | Evidence |
|---|---|---|---|---|
| Glutathione synthesis (glutamate-cysteine ligase, cysteine supply) | Signaling pathway | Activator | cysteine is the scarce building block; GCL rate-limiting | Laboratory[1] |
| Erythrocyte glutathione | Other | Expression ↑ | rise only at low baseline (crossover study, 36 people) | Human, randomised[7] |
Effect profile
- Dopamine
- Noradrenaline
- Serotonin
- Acetylcholine
- Glutamate · AMPA
- Glutamate · NMDA
- GABA
- Histamine
- Orexin
- Adenosine
- Opioids
- Melatonin
- Neurotrophins
- Blood flow
- Nitric oxide
- Energy metabolism
- Insulin · glucose
- Inflammation · oxidativeGlutathione ↑ and oxidation markers ↓ only at low baseline glutathione; otherwise unchanged[7][8]
- Stress axis
- Testosterone axis
- Endocannabinoids
- Autophagy · senescence
- Immune system
- Lipid metabolism
- Coagulation · fibrinolysis
- Methylation
Routes of administration and bioavailability
Oral (swallowed) · Tablets, effervescent tablets, extended-release tablet
6–10% (human)Rapid absorption with fast-dissolving forms; extended-release tablet with a flatter curve and lowest availability [2].
Human, non-randomised
Intravenous · Infusion (antidote)
100%Standard route in paracetamol poisoning; anaphylactoid reactions possible, less frequent with simplified regimens [3][4].[3][4]
Human, non-randomised
Human studies
Pharmacokinetics oral and intravenous
Measured: plasma levels, excretion
Result: Oral availability 6–10%, t½ 2.27 h, volume of distribution 0.33 l/kg.[2]
Human, non-randomised
Paracetamol poisoning
Measured: liver injury, mortality, adverse effects
Result: Acetylcysteine superior to placebo; quality of evidence low to very low.[3]
Human, randomised
Performance by glutathione status
Measured: VO2max, time trial, Wingate, redox markers
Result: Better only at low glutathione; no effect at medium and high.[7]
Human, randomised
Performance and biomarkers in men
Measured: performance, laboratory values, adverse effects
Result: Mostly benefits for performance and glutathione; no severe adverse effects.[8]
Human, randomised
Depression
Measured: depression score
Result: SMD −0.24 (CI −0.44 to −0.05).[9]
Human, randomised
Risks and warnings
Anaphylactoid reactions during infusion
With intravenous administration as an antidote, non-allergic anaphylactoid, skin, and gastrointestinal reactions occur; simplified infusion regimens reduced them markedly (OR 0.24) [4].
Human, non-randomised
Severe consequences of infusion errors
After accidental intravenous overdose, brain edema, seizures, hemolytic uremic syndrome, and deaths were described (review of 16 case reports) [5].
Human, non-randomised
Adverse effects with oral intake (product information)
The package leaflet of an oral product lists occasional allergic reactions (rash, swelling, itching, hives, shortness of breath, rapid heartbeat, drop in blood pressure), headache, fever, inflammation of the oral mucosa, abdominal pain, nausea, vomiting, diarrhea, and tinnitus; rarely shortness of breath and bronchospasm, especially in asthma; very rarely bleeding, anaphylactic shock, and severe skin reactions (Stevens-Johnson and Lyell syndromes, usually with concurrent intake of other medicines). Platelet aggregation was impaired in several studies, with unclear clinical significance. As warnings it names bronchial asthma, previous or existing gastrointestinal ulcers, and histamine intolerance (with longer use) [6].
Human, non-randomised
Oral intake in sports studies
No severe adverse effects were reported in the controlled sports studies [8].
Human, randomised
Interactions
- Glyceryl trinitrate (nitroglycerin): According to the product information, possibly increased vasodilation with a drop in blood pressure that can be severe and manifest as headache [6].
- Carbamazepine: Decrease in the plasma carbamazepine level with possibly reduced efficacy [6].
- Cough suppressants: With concurrent use, a dangerous accumulation of secretions can occur because of the suppressed cough reflex [6].
- Antibiotics (tetracyclines, aminoglycosides, penicillins): Indications from experimental studies of reduced effect; cefixime and loracarbef are not affected according to the product information [6].
- Activated charcoal: Activated charcoal can reduce the effect of acetylcysteine [6].
- Laboratory tests: Acetylcysteine can affect the determination of salicylates and of ketone bodies in urine [6].
Fact check: common claims
- refuted
“NAC replenishes glutathione stores in everyone”
In a double-blind crossover study, glutathione rose only at a low baseline value, not at medium or high [7].
- not supported
“NAC protects the liver because it helps in paracetamol poisoning”
The antidote effect concerns poisoned patients [3]; for healthy people without poisoning there is no study of liver protection.
- partly supported
“NAC is a natural antidepressant”
As an add-on to a treatment, a small effect with a wide confidence interval, mainly in bipolar disorder [9]; not tested as sole treatment.
Pharmacokinetics
- Absorption
- Oral availability 6–10% [2].
- Half-life
- About 2.3 hours (late elimination phase after infusion) [2].
- Metabolism
- About 30% of total clearance via the kidney [2].
Legal status
- Germany
- Acetylcysteine is prescription-only, except for oral use in acute common cold illnesses in humans (AMVV Annex 1) [10]. The entry concerns medicinal products; whether NAC may be marketed as a dietary supplement was not checked (not verified). According to the package leaflet of an effervescent tablet product approved by the Belgian medicines agency, the same medicinal product is authorized in the European Economic Area, in Germany as an acetylcysteine product from Hexal; indication there: liquefaction of mucus and easier expectoration in cold-related bronchitis [6]. The German marketing authorization itself (AMIce) and the summary of product characteristics were not queried.
- EU
- No entry “acetylcysteine” or “cysteine” in the consolidated Union list of novel foods, as of August 10, 2026 [11]; in the EMA data export (October 24, 2026) no centrally authorized medicinal product with acetylcysteine.
- USA
- Not verified.
Related compounds
Open questions
- Do only people with low glutathione benefit, and how common is that in healthy people?
- How well tolerated is NAC as a long-term supplement, also with regard to training adaptations?
- Is the small effect in depression confirmed in large RCTs?
References
- Lu SC. Glutathione synthesis. Biochim Biophys Acta. 2013;1830(5):3143–53. doi:10.1016/j.bbagen.2012.09.008 · PubMed
- Borgström L, Kågedal B, Paulsen O. Pharmacokinetics of N-acetylcysteine in man. Eur J Clin Pharmacol. 1986;31(2):217–22. doi:10.1007/BF00606662 · PubMed
- Chiew AL, Gluud C, Brok J, Buckley NA. Interventions for paracetamol (acetaminophen) overdose. Cochrane Database Syst Rev. 2018;2(2):CD003328. doi:10.1002/14651858.CD003328.pub3 · PubMed
- Nakatsu L, Lopez JR, Garcia CM, Cherian M, Nash J, Tofighi D, et al. Comparison of two-bag and three-bag acetylcysteine regimens in the treatment of paracetamol poisoning: a systematic review and meta-analysis. Clin Toxicol (Phila). 2025;63(3):155–65. doi:10.1080/15563650.2025.2456116 · PubMed
- Baker MB, Young J, Binda DD, Dienes E, Kennedy JM. Safety of acetylcysteine: a scoping review of iatrogenic overdose cases and their associated complications. Clin Toxicol (Phila). 2026;64(8):636–47. doi:10.1080/15563650.2026.2673132 · PubMed
- Föderalagentur für Arzneimittel und Gesundheitsprodukte (FAGG, Belgien). Gebrauchsinformation: Information für Anwender. Acetylcysteïn Sandoz 600 mg Brausetabletten. Sandoz nv/sa, Zulassungsnummern BE459546 und BE459511; zuletzt genehmigt 02/2020 [Internet]. Abgerufen am 24.10.2026. Verfügbar unter: https://app.fagg-afmps.be/pharma-status/api/files/62bc58c11e5c015ab3bf2ff3
- Paschalis V, Theodorou AA, Margaritelis NV, Kyparos A, Nikolaidis MG. N-acetylcysteine supplementation increases exercise performance and reduces oxidative stress only in individuals with low levels of glutathione. Free Radic Biol Med. 2018;115:288–97. doi:10.1016/j.freeradbiomed.2017.12.007 · PubMed
- Fernández-Lázaro D, Domínguez-Ortega C, Busto N, Santamaría-Peláez M, Roche E, Gutiérez-Abejón E, et al. Influence of N-acetylcysteine supplementation on physical performance and laboratory biomarkers in adult males: a systematic review of controlled trials. Nutrients. 2023;15(11):2463. doi:10.3390/nu15112463 · PubMed
- Peng TR, Lin HH, Tseng TL, Huang YH, Tsai PY, Lin CY, et al. Efficacy of N-acetylcysteine for patients with depression: an updated systematic review and meta-analysis. Gen Hosp Psychiatry. 2024;91:151–9. doi:10.1016/j.genhosppsych.2024.10.018 · PubMed
- Verordnung über die Verschreibungspflicht von Arzneimitteln (Arzneimittelverschreibungsverordnung – AMVV), Anlage 1 (zu § 1 Nr. 1 und § 5): Stoffe und Zubereitungen nach § 1 Nr. 1, Eintrag „Acetylcystein“. Bundesministerium der Justiz [Internet]. Abgerufen am 24.10.2026. Verfügbar unter: https://www.gesetze-im-internet.de/amvv/anlage_1.html
- Durchführungsverordnung (EU) 2017/2470 der Kommission vom 20. Dezember 2017 zur Erstellung der Unionsliste der neuartigen Lebensmittel gemäß der Verordnung (EU) 2015/2283 des Europäischen Parlaments und des Rates über neuartige Lebensmittel. ABl. L 351 vom 30.12.2017, S. 72. Konsolidierte Fassung vom 10.08.2026 (CELEX 02017R2470-20260810).
How this profile was checked
Last reviewed: 2026-10-25. All sources with a DOI or PMID were resolved automatically via Crossref or doi.org and PubMed.
Translated from the German profile (version of 2026-10-25); translation checked on 2026-10-26.
Checked
- All PMIDs resolved via PubMed efetch; DOIs taken from the PubMed record and checked via Crossref with tools/pruefe_profile.py.
- Abstracts: [2] n = 10, oral availability 6–10%, t½ 2.27 h, Vd 0.33 l/kg, renal clearance ≈ 30%; [3] 11 RCTs, 700 participants, quality low to very low, acetylcysteine superior to placebo; [4] OR 0.24 for anaphylactoid reactions; [5] 16 case reports, brain edema, HUS, deaths; [7] 100 screened, 36 included, performance gains only in the low group; [8] 16 studies, no severe adverse effects; [9] 12 RCTs, 904 patients, SMD −0.24.
- Full text [1] (PMC3549305): cysteine and GCL as main determinants, GGT cleaves glutathione extracellularly.
- AMVV Annex 1 (“gesetze-im-internet.de”, October 24, 2026), wording (translated): “Acetylcysteine – except for oral use in acute common cold illnesses in humans –”.
- Union list (CELEX 02017R2470-20260810): no hits for acetylcysteine and cysteine. EMA data export (timestamp October 24, 2026): no product with acetylcysteine.
- Fix round October 24, 2026: package leaflet Acetylcysteïn Sandoz 600 mg effervescent tablets (FAGG database, last approved 02.2020) read in full: indication, contraindications, warnings, interactions, adverse effects with frequencies; list of EEA authorizations with “Germany: Acetylcystein HEXAL … effervescent tablets”. Read for comparison: package leaflet Acetylcysteine EG (FAGG, 10.2025), same interactions (nitroglycerin, carbamazepine, antitussives, antibiotics, activated charcoal).
- October 25, 2026: decision q043 (Tilman) confirms kategorie “Arzneimittel” (level unchanged). q018 trade names: a trade name in common use in DE/EU is documented neither via an EPAR (no centrally authorized product, see EMA data export) nor via a German summary of product characteristics or Drugs@FDA; the available package leaflet [6] names for Germany only a generic with a company name. synonyme therefore unchanged. German summary of product characteristics: research assignment docs/AUFTRAG-RECHTSSTATUS.md (q113).
- October 25, 2026, q012: full text read [1], package leaflet [6] read in full; all other study findings abstract only checked. q068 (K4 split approved: “Protects the liver” 0 · not studied and “Raises glutathione levels (marker only)”, both under “Liver & bile”) and q098: level as set, back-reference n-acetylcystein → glynac “component” present.
- October 25, 2026, trade names harmonized (q018; guideline “Handelsnamen”, decision of October 25, 2026: Article 57 database as a source on a par with EPAR, summary of product characteristics, and Drugs@FDA; US names only where there are no DE/EU names; no combination products): “Fluimucil” added to synonyme; the note above that a DE/EU trade name was not documented is thereby superseded. Source: EMA Article 57 database (Article 57 product data, EMA/518502/2018 Rev. 90, data as of October 9, 2026, retrieved October 25, 2026): “Fluimucil” (acetylcysteine; oral, inhaled, intravenous) in eleven countries (including Austria, Italy, the Netherlands, Spain), in Germany in variants with an addition in the name. “ACC” is listed for Germany and nine other countries but is not included because the abbreviation stands for acetyl-CoA carboxylase in the library (synonym collision, guideline). Products made up of active substance and company name not included.
Not verified
- German marketing authorization (AMIce/PharmNet.Bund) and summary of product characteristics (SmPC) of NAC medicinal products; risks and interactions come from the package leaflet approved by the Belgian agency [6], whose indication and wording may differ from German products. The package leaflet has no recognized identifier (check script warning expected).
- Classification of NAC under food law in dietary supplements (DE and EU) and FDA status.
No dosages, no sources of supply. This information does not replace medical advice.
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