
Chaga
Inonotus obliquus
Capsules · PRIME189 zł
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Inonotus obliquus
Capsules · PRIME189 zł

Inonotus obliquus
Powders · LONGEVITY119 zł

Inonotus obliquus
Powders · PRIME189 zł

Inonotus obliquus
Capsules · LONGEVITY129 zł

Inonotus obliquus
Drops · PRIME169 zł
Version 1.0 · Updated: 21 June 2026 · Subject-matter reviewer: Mateusz Rosa, founder of Aloha Fungi, international TCM therapist, Doctor of Acupuncture (WFAS), author.
Chaga in 60 seconds
Chaga is the common name for the mushroom Inonotus obliquus of the Hymenochaetaceae family. In Polish czerniak brzozy, regionally błyskoporek podkorowy, czyreń, czarcie oko, in Siberian czanga. It is a parasitic mushroom that attacks living trees, mainly birches, and develops inside for 10-20 years, forming on the outside a black, irregular growth that looks like a burnt crust.
Inside, beneath that crust, is an orange-rust coloured core. It is the core, not the crust, that holds the highest concentration of bioactive compounds. The black outer shell of Chaga is not burnt wood but concentrated melanin, which the mushroom produces to protect itself from UV radiation and microbes.
In Poland Chaga is a partially protected species and wild harvest is restricted. Aloha Fungi sources its raw material only from certified controlled-harvest regions (mainly Siberia and Eastern Europe), never from Polish forests.
The earliest documented use goes back to the Khanty people (Western Siberia), who used Chaga for stomach and liver complaints. From Siberia, through Russia, the tradition spread to Poland and the Baltic countries by the 16th century. In Polish villages Chaga was used as a strengthening tea, a digestive aid and a coffee substitute in times of shortage.
Marta Kinga Lemieszek, in her 2011 work, describes Chaga as a traditional folk-medicine remedy in Russia, Poland and the Baltic countries, used for digestive and liver conditions. Modern research on Inonotus obliquus has partly Polish roots, including the team from UMCS in Lublin and the Institute of Rural Medicine.
More than 200 bioactive compounds have been identified in Chaga. The main groups are polysaccharides, melanin, polyphenols and triterpenoids. Standardised in our extract to above 30% β-glucans.
β-glucans (1→3, 1→6 and 1→4), the main immunomodulatory agent, including heteropolysaccharides built from β-Glc, β-Xyl, α-Man and α-Rha (Wold et al. 2018).
Melanin, the pigment giving Chaga its black exterior. It is the same type of compound found in human skin and one of the strongest antioxidants in the mushroom.
Polyphenols, betulinic acid, styrylpyrone derivatives and phenolic acids account for part of the antioxidant action.
Triterpenoids: inotodiol, lanosterol, ergosterol and trametenolic acid. In addition, betulin and betulinic acid, which the mushroom accumulates from the host birch.
Chaga β-glucans bind to Dectin-1 and TLR4 receptors on macrophages and dendritic cells, triggering NF-κB and MAPK signalling cascades that modulate cytokine production (Sang et al. 2022, Shen et al. 2022).
A key observation from Shen et al. (2022) on RAW264.7 macrophage lines: Chaga extracts had a bidirectional effect. In the resting state (M0) they raised macrophage activity, while in the overactive state (M1, LPS-induced) they lowered production of IL-1β and TNF-α. This is regulatory rather than purely stimulatory action. Wold et al. (2018) identified specific polysaccharide fractions (IOE-WN) inducing NO production in macrophages and dendritic cells in vitro.
Melanin shows strong free-radical scavenging in DPPH assays. Polyphenols, including betulinic acid and styrylpyrones, act synergistically. Chaga activates the Nrf2 transcription factor, which upregulates phase II detoxification enzymes: superoxide dismutase (SOD), catalase and glutathione-S-transferase (Glamočlija et al. 2015).
Bidirectional modulation of TNF-α, IL-1β and IL-6 (Shen et al. 2022) points to regulatory rather than classically anti-inflammatory action. In addition, inhibition of the NF-κB pathway in inflamed cells (Sang et al. 2022), modulation of prostaglandin and leukotriene production (2024 review) and a protective effect on the liver against oxidative stress (Fang et al. 2020) have been described.
Chaga does not cure cancers in humans. All available studies are in vitro and animal models, and a therapeutic claim is prohibited by regulation. Chaga does not „flush toxins"; only modulation of phase II detoxification enzymes through Nrf2 can be described. It does not replace immunosuppressive, hormonal, anticoagulant or oncological medicines. It also has no fast, noticeable effect like coffee or adrenaline. It is a tonifying mushroom; the first changes appear after 4-12 weeks of regular use.
Chaga works in the morning and before noon, up to about 2 pm. It is tonifying and strengthens Yang, so in the evening it may make it harder to fall asleep for sensitive people. Exception: sublingual drops (15-20 drops) can be taken with lunch.
For prevention, preferably in the morning: 1 g of extract a day as powder (1 teaspoon) or drops (30 drops), and in capsules the standard serving is 3. Intensively: 2-3 g of extract a day in two servings, morning and before noon. Do not exceed 4 g a day without individual recommendation.
Chaga extract absorbs best 20-30 minutes before a meal, on a slightly empty stomach, with warm water, coffee or cacao. Hold sublingual drops under the tongue for 30-60 seconds, then swallow. If discomfort appears on an empty stomach, take it with a light meal. You can also add 1 teaspoon of powder to your morning coffee.
The classic rhythm is 5 days on, 2 days off (usually the weekend). The break maintains receptor responsiveness to β-glucans and triterpenes and limits adaptation. Prevention and everyday support: 8-12 weeks, then a 2-4 week break and a repeat cycle. Targeted protocol under a therapist: 12-16 weeks. Seasonal variant (autumn-winter): 4-8 weeks.
Week 1-2: subtle effects, sometimes mild fatigue (in TCM a „cleansing reaction"). If it is strong, reduce the serving by half.
Week 3-6: steadier daytime energy, better stress tolerance, some people report changes in skin and digestion.
Week 8-12: a cumulative effect, greater resistance to infection, a steadier overall state. Individual variation is large.
Chaga in the morning (tonifying, strengthens Yang and Wei Qi), Reishi in the evening (calming, supports Yin). This gives 24-hour immune support without night-time stimulation. Duration: 8-12 weeks.
For people doing intensive mental work and exposed to oxidative stress. Lion’s Mane supports the NGF/BDNF neuronal growth factors. Chaga 1 g in the morning, Lion’s Mane 0.5-1 g in the morning or split between morning and afternoon. Duration: 12 weeks.
Coriolus contains the unique polysaccharide-peptides PSK and PSP. Chaga 1 g in the morning, Coriolus 1 g before noon. Broad support of immune function, an autumn-winter classic. Duration: 8 weeks, seasonally.
Immune support combined with daytime energy. Cordyceps 0.5-1 g in the morning on an empty stomach, Chaga 1 g in the morning or before noon. Both mushrooms are tonifying, so avoid them after 2 pm. Duration: 8-12 weeks.
Chaga 1 g in the morning (antioxidant protection), Tremella 1 g in the evening with dinner (water-binding, support for the skin barrier). For people with atopic tendencies or an aggressive skincare regimen. Duration: 12 weeks.
In TCM Chaga tonifies Wei Qi (defensive energy), supports Kidney Yang, clears Heat from the Liver and moves Blood. In the OOTI model it is most often used in the Cleansing phase, where it supports the Liver and phase II detoxification through regulation of Nrf2 and glutathione-S-transferase, and in the Nourishment phase, where it strengthens Wei Qi and the recovery of cellular immunity, often combined with Reishi or Tremella.
Caution according to TCM with Spleen Yang deficiency (chronic diarrhoea, weak digestion, cold extremities), because Chaga’s cool nature burdens the Spleen in deep Yang deficiency, and also with Blood deficiency and in acute viral infections. This is a frame of cultural observation, not a medical diagnosis. Concepts such as Qi, Yang or meridian do not correspond one to one with Western anatomy or physiology.
| Taste | bitter (苦 kǔ), slightly sweet (甘 gān) |
| Nature | cool to neutral (微寒 wēi hán) |
| Meridians | Liver (肝), Kidney (腎), Spleen (脾) |
| Category | tonic of Wei Qi and Kidney Yang, clears Heat from the Liver |
Pregnancy and breastfeeding (insufficient clinical safety data).
Active kidney stones or a history of oxalate calculi. This is a real, documented risk: Chaga contains relatively high oxalate levels, and long, intense use has been associated with acute kidney failure in predisposed individuals (Kikuchi et al. 2014, Clin Nephrol).
Active immunosuppressive treatment (after organ transplant, active autoimmune disease in flare), because Chaga modifies immune signalling through macrophage activation.
Anticoagulants (warfarin, acenocoumarol, NOAC): Chaga has anticoagulant activity, may potentiate the drug effect and increase bleeding risk.
Antidiabetic medicines: Chaga lowers blood glucose (animal studies), and combined with metformin or insulin it risks hypoglycaemia.
Antihypertensive medicines: possible potentiation of the blood-pressure-lowering effect.
Active autoimmune diseases (RA, lupus, Hashimoto’s in flare).
Planned surgery: stop at least 14 days before the procedure (anticoagulant activity).
Reported: mild gastrointestinal discomfort on an empty stomach (take with a light meal), a „cleansing reaction" in the first 5-7 days (fatigue, mild migraine, reduce the serving by half), rare allergic reactions (itching, rash, stop immediately). With long-term use, increased urinary oxalate excretion, so drink at least 2 L of water a day.
Up to 3 g of extract a day is well tolerated by healthy people. Above that requires therapist oversight. Do not exceed 4 g a day without a specific recommendation.
Evidence verdict
We also show what is not proven. This is a dietary supplement, not a medicine.
3
Strong evidence
confirmed composition
3
Preliminary
in vitro and animal studies
2
Not proven
no human studies
Reviewed by
Mateusz Rosa · Doctor of Acupuncture (WFAS)
Version 1.0 · Updated: 21 June 2026 · Subject-matter reviewer: Mateusz Rosa, founder of Aloha Fungi, international TCM therapist, Doctor of Acupuncture (WFAS), author.
Based on 10 verified sources
See sources ↓| Claim | Type of evidence | Strength |
|---|---|---|
| β-glucans activate Dectin-1 and TLR4 (immunomodulation) | in vitro (Wold 2018, Shen 2022), multiple independent studies | MOCNY |
| Bidirectional regulation of TNF-α and IL-1β on M0/M1 macrophages (regulatory, not stimulant) | in vitro (Shen 2022, RAW264.7 lines) | MOCNY |
| Antioxidant activity (DPPH, FRAP), melanin and polyphenols | in vitro (Glamočlija 2015), multiple independent studies | MOCNY |
| Hepatoprotective action | animal models (Fang 2020), no human RCT | WSTĘPNY |
| Support in atopic dermatitis (IgE and cytokine modulation) | mouse DNCB-AD model (Liu 2026), needs human replication | WSTĘPNY |
| Anti-fatigue action (liver glycogen, lactic acid) | exhaustion swim test in mice (Xiuhong 2015) | WSTĘPNY |
| „Cures" cancers in humans | none, only in vitro and animal models, claim prohibited by regulation | BRAK |
| „Flushes toxins" from the whole body | none, only modulation of phase II enzymes (Nrf2) can be discussed | BRAK |
MOCNY = solid evidence · WSTĘPNY = moderate or preliminary · BRAK = unsupported or prohibited by regulation.
The educational content on this page does not replace medical advice. A dietary supplement is not a medicine and should not replace a varied diet or medical consultation. Before starting supplementation, especially with chronic conditions, pregnancy, breastfeeding or when taking medication, consult your doctor. All cited studies come from peer-reviewed scientific journals (DOI and PMID in the bibliography). Aloha Fungi does not claim therapeutic efficacy for any product; the mechanisms described are based on the current state of the literature. All products are dietary supplements notified to the Polish Chief Sanitary Inspectorate (GIS).