⚠️ FDA Banned Compound

"Vitamin B17" (Amygdalin / Laetrile)
What the Research Shows

Not a vitamin. Not proven against cancer. Metabolizes to cyanide. Here's the full picture — from mechanism theory to why the FDA banned it.

0
Validated Clinical Trials Showing Benefit
0
Patients in NEJM Phase II Trial
BANNED
FDA Status Since 1980
HCN
Primary Metabolite (Hydrogen Cyanide)

What Is "Vitamin B17"?

The name is a marketing construct. Here's what the compound actually is and where the name came from.

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Amygdalin — The Natural Form

A cyanogenic glycoside found naturally in the seeds (kernels) of apricots, bitter almonds, apples, peaches, and cherries. First isolated in 1830 by chemists Robiquet and Boutron-Charlard. Plants use it as a defense mechanism; when the seed is crushed or digested, enzymes release hydrogen cyanide — which deters pests.

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Laetrile — The Semi-Synthetic Form

A patented semi-synthetic derivative of amygdalin developed by Ernst T. Krebs Jr. in the 1950s. Chemically distinct from pure amygdalin but similarly releases cyanide upon hydrolysis. Marketed as a cancer treatment under various brand names. The terms "laetrile" and "amygdalin" are often used interchangeably by the media but refer to different molecular structures.

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"Vitamin B17" — A Marketing Term

The "vitamin" label was coined by Krebs Jr. as a commercial strategy, not a scientific classification. Amygdalin is not a vitamin by any accepted definition: no human deficiency state exists, the body does not require it, and no nutritional authority — including WHO, FDA, or EFSA — recognizes it as a vitamin. The B17 designation was designed to imply essentiality and safety that the evidence does not support.

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Chemical Classification

Amygdalin is formally classified as a cyanogenic glycoside with the molecular formula C₂₀H₂₇NO₁₁. On hydrolysis (by beta-glucosidase, stomach acid, or gut microbiota), it breaks down into: glucose, benzaldehyde, and hydrogen cyanide (HCN). The cyanide is the biologically active — and toxic — component. There is no form of amygdalin that circumvents this chemistry.

The Claimed Mechanism vs. What Science Found

Proponents proposed a "selective" anti-cancer mechanism. Here's the theory — and why the evidence doesn't support it.

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The Proposed Theory

Krebs Jr. theorized that cancer cells express elevated levels of beta-glucosidase — the enzyme that cleaves amygdalin into HCN. The idea: cancer cells would selectively absorb amygdalin, cleave it into cyanide, and self-destruct. Normal cells were proposed to be protected by rhodanese (an enzyme that detoxifies HCN). This is the "selective toxicity" hypothesis.

Why the Theory Failed

The selective toxicity model was never validated in rigorous human trials. Beta-glucosidase is found throughout the gut microbiome, not uniquely in cancer cells. Rhodanese is present in both healthy and cancerous tissues in similar concentrations. HCN released systemically does not discriminate between cell types — it inhibits cytochrome c oxidase in all cells, disrupting cellular respiration universally. The selectivity claimed was not observed.

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What In Vitro Data Shows

Chang et al. (2006) and similar studies do show cytotoxic effects in cancer cell lines in controlled lab settings. However, cytotoxicity in a petri dish does not equal selective anti-cancer activity in a living organism. Bleach is also cytotoxic in vitro. The question is whether the concentration that kills cancer cells in isolation can be safely delivered to a human — and the clinical data says it cannot.

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The Evidence Gap

The critical gap between in vitro cytotoxicity and in vivo clinical benefit is where laetrile research collapsed entirely. No dose that produced anti-tumor effects in animal or cell studies could be administered to humans without causing systemic cyanide poisoning. This "therapeutic window" — the gap between effective and toxic doses — essentially does not exist in a usable form for amygdalin.

In Vitro EvidenceModerate
Animal Model EvidenceWeak
Human Clinical EvidenceNone

What the Studies Actually Found

A chronological review of the key human evidence — from the pivotal NEJM trial to the definitive Cochrane Review.

Phase II RCT NEJM · 1982 N=178

Moertel et al. (1982) — The Definitive Clinical Trial

The most rigorous human trial of laetrile ever conducted, published in the New England Journal of Medicine. 178 cancer patients with a variety of advanced cancers were treated with laetrile plus a metabolic therapy program (vitamins, pancreatic enzymes, diet). The researchers were led by Charles Moertel of the Mayo Clinic — one of the era's most respected oncologists.

Verdict: "No substantive benefit was observed in terms of cure, improvement, or stabilization of cancer, or improvement of symptoms." Measurable cyanide toxicity was documented in patients. The study effectively ended mainstream scientific interest in laetrile as a cancer treatment.
Cochrane Systematic Review Cochrane Database · 2015 All Available Evidence

Milazzo et al. (2015) — Cochrane Collaboration Review

The gold standard of evidence synthesis. Milazzo and colleagues systematically searched all available databases for randomized controlled trials and controlled clinical trials investigating laetrile or amygdalin for cancer. The review methodology was pre-registered and independent.

Verdict: "The claims that laetrile or amygdalin have beneficial effects for cancer patients are not currently supported by sound clinical data. There is a considerable risk of serious adverse effects from cyanide poisoning after laetrile or amygdalin, especially after oral ingestion." The Cochrane Review found no reliable evidence of benefit from any identified study.
In Vitro Biochem Pharmacol · 2006 Cell Line Study

Chang et al. (2006) — In Vitro Cytotoxicity

Investigated the effects of amygdalin on bladder cancer cell lines in controlled laboratory conditions. Found cytotoxic effects at certain concentrations. This study is frequently cited by proponents as evidence of anti-cancer activity.

Context: Cell-line cytotoxicity is not clinical evidence. The concentrations required to produce in vitro toxicity would result in lethal or near-lethal cyanide poisoning if achieved in a human body. The researchers themselves noted the limitations. In vitro studies like this are hypothesis-generators, not treatment validations.
Safety Review EFSA · 2016 Consumer Advisory

EFSA (2016) — Apricot Kernel Consumer Safety Opinion

The European Food Safety Authority conducted a formal risk assessment on bitter apricot kernels sold as food products, in response to growing popularity. The assessment modeled HCN release from realistic consumption scenarios.

Verdict: A single bitter apricot kernel serving (3 kernels, ~19g) is enough to exceed safe HCN exposure thresholds for adults. For children, even one kernel may be sufficient. EFSA recommended member states take action to restrict sale and add mandatory warnings.

The FDA Ban: A Timeline

The regulatory history of laetrile is long, contested, and ultimately resolved in favor of the ban. Here's how it unfolded.

1920s–1950s

Early Promotion

Amygdalin was used sporadically as a cancer remedy in Europe and the US. Ernst T. Krebs Jr. develops and patents "laetrile" in the 1950s, marketing it as Vitamin B17 and claiming it is non-toxic and selectively anti-cancerous. No supporting clinical data existed.

1962

First FDA Action

The FDA declares laetrile a "new drug" requiring proof of safety and efficacy before sale. Manufacturers had no data to submit. Interstate shipment is blocked, though individual states began passing laws to permit its use within state lines.

1970s

Peak Popularity & Legal Battles

Laetrile reaches peak popularity — an estimated 70,000 Americans per year are using it. 27 states legalize it for in-state use. Proponents argue it is a "natural" substance and a matter of personal freedom. Court battles proliferate as patients seek access through emergency injunctions.

1979

U.S. Supreme Court Rules

United States v. Rutherford: The Supreme Court unanimously rules that terminally ill patients do not have a constitutional right to unapproved cancer treatments. The FDA's authority to regulate laetrile is upheld. This eliminates the primary legal avenue used to circumvent the ban.

1980

Federal Ban Formalized

Following the Rutherford ruling and in the absence of any clinical evidence of efficacy, the FDA formally bans the interstate sale of laetrile. State laws permitting intrastate use become largely moot as supply chains are cut. The ban remains in effect today.

1982

NEJM Trial Closes the Chapter

Moertel et al. publish the definitive Phase II trial results. No benefit. Documented toxicity. The scientific case for laetrile is effectively closed. Remaining proponents retreat to anecdotes and alternative media.

Present

Ongoing Enforcement & "Medical Tourism"

Laetrile clinics continue to operate in Mexico and other countries, marketing to US patients. The FDA actively warns consumers and intercepts illegal imports. The compound is banned in Australia, UK, and throughout the EU as well. Deaths continue to be reported in medical literature.

Toxicity & Risk Profile

This is the most important section on this page. The safety data is unambiguous.

⚠️ Clinical Symptoms of Amygdalin/Cyanide Toxicity

Symptoms typically appear within 30–60 minutes of oral ingestion. Severity depends on dose, individual body weight, gut microbiome composition, and whether Vitamin C or vitamin B12 co-ingestion reduces/potentiates effects.

Nausea and vomiting
Headache
Dizziness and weakness
Hypotension (low blood pressure)
Cyanosis (blue discoloration)
Tachycardia then bradycardia
Confusion and disorientation
Liver enzyme elevation
Peripheral neuropathy
Seizures
Loss of consciousness / coma
Death (documented)

📊 Oral vs. Intravenous Risk Comparison

Factor Oral Route Intravenous Route
HCN Release Amplified by gut bacteria (beta-glucosidase) Less enhancement from gut microbiome
Onset of Toxicity 30–60 min (unpredictable) More immediate, more predictable
Documented Fatal Cases Multiple in literature Fewer, but documented
Vitamin C Interaction Increases HCN release Also increases HCN release
Legal Status (US) Illegal / FDA banned Illegal / FDA banned

🚨 Emergency Information

If you or someone you know has ingested bitter apricot kernels, amygdalin, or laetrile and is showing symptoms of poisoning, call emergency services immediately (911 in the US, 999 in UK, 112 in EU). Inform them of amygdalin/cyanide exposure. Time-critical antidotes (hydroxocobalamin, sodium nitrite/thiosulfate) are available in emergency settings. Do not attempt to induce vomiting without medical guidance.

Supporting Liver Function

Amygdalin toxicity causes documented liver enzyme elevation and hepatotoxicity. If you are researching alternative health approaches, these liver-support supplements have an actual evidence base.

Evidence-Based Liver Support Options

Unlike amygdalin, the following compounds have meaningful clinical or mechanistic evidence supporting liver health. These are not replacements for medical care.

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TUDCA
Tauroursodeoxycholic acid — bile acid with documented hepatoprotective effects in clinical studies
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Milk Thistle (Silymarin)
Most studied liver-protective botanical. Antioxidant, anti-inflammatory, hepatocyte regeneration support
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NAC (N-Acetyl Cysteine)
Glutathione precursor. Standard medical treatment for acetaminophen overdose. Supports detox pathways
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Alpha Lipoic Acid
Potent antioxidant with hepatoprotective properties. Regenerates other antioxidants including Vitamin E and glutathione
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Common Questions Answered

Straightforward answers to the questions we see most often.

Is "Vitamin B17" a real vitamin? +
No. "Vitamin B17" is a marketing term with no scientific basis. Amygdalin is not a vitamin — it is not essential for human life, the body produces no deficiency state without it, and no recognized nutrition body classifies it as a vitamin. The name was coined in the 1950s by Ernst T. Krebs Jr. as a commercial strategy.
What is the difference between amygdalin and laetrile? +
Amygdalin is the naturally occurring compound found in the seeds of apricots, bitter almonds, apples, and other stone fruits. Laetrile is a semi-synthetic, patented derivative developed and promoted as a cancer treatment. Both metabolize to release hydrogen cyanide (HCN) in the body. The terms are often used interchangeably in the media, though they are chemically distinct.
Did any clinical trials show laetrile works against cancer? +
No. The most rigorous clinical evaluation — a 1982 Phase II trial by Moertel et al. published in the New England Journal of Medicine — enrolled 178 cancer patients and found no anticancer activity. Patients experienced measurable cyanide toxicity. A 2015 Cochrane Systematic Review by Milazzo et al. surveyed all available evidence and concluded there is "no reliable evidence" that laetrile or amygdalin is effective against cancer in humans.
Why is laetrile banned by the FDA? +
The FDA banned interstate commerce of laetrile in 1980 after clinical evidence showed no anticancer benefit and significant cyanide poisoning risk. The ban was upheld by the U.S. Supreme Court in 1979 (United States v. Rutherford). It is classified as an unapproved new drug and cannot legally be sold as a cancer treatment in the United States. Several other countries have similar restrictions.
How dangerous is amygdalin / laetrile? +
It can be lethal. Amygdalin is metabolized to hydrogen cyanide (HCN), which inhibits cellular respiration. Oral ingestion is significantly more toxic than intravenous administration because gut bacteria enhance cyanide release. Documented symptoms range from nausea, vomiting, headache, and dizziness to cyanosis, liver damage, seizures, coma, and death. Multiple fatalities have been reported in medical literature. Children are at especially high risk from apricot kernel consumption.
Are apricot kernels safe to eat? +
Bitter apricot kernels contain high concentrations of amygdalin and pose a real cyanide poisoning risk, particularly for children. The European Food Safety Authority (EFSA) issued a 2016 opinion warning that even 3 small bitter apricot kernels can exceed the safe HCN threshold for adults, and a single kernel may be enough for a child. Sweet apricot kernels have much lower amygdalin content. Regulatory agencies in multiple countries have issued formal consumer warnings.
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Medical Disclaimer: This page is for informational and educational purposes only. It does not constitute medical advice, diagnosis, or treatment recommendation. The content on this page explicitly does not recommend or endorse the use of amygdalin, laetrile, or "Vitamin B17" — including for cancer treatment. If you or someone you know is dealing with cancer, consult a licensed oncologist. If you are considering alternative or complementary approaches, discuss them with your physician. MeetPeptide is not responsible for any decisions made based on the information provided here. Emergency: If you suspect cyanide poisoning, call 911 immediately.