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Isolated phytochemicals & plant compounds

Indole-3-carbinol

Indole-3-carbinol / I3C cruciferous-vegetable indole

Indole-3-carbinol (I3C) is a cruciferous-vegetable indole studied mainly for estrogen-metabolite markers and small gynecologic research settings, not cognition. Those studies do not establish a healthy-user focus, memory, mood, or productivity benefit, or a consumer dose, product, combination, or long-term safety framework. The only indexed I3C listing is currently unavailable.

Hormone SupportHormonal Axis RelatedIsolated CompoundFood DerivedClinical ResearchLimited Human EvidenceMixed Evidence
Updated August 2026/5 min read/8 citations
Reviewed by the NootropicsIndex editorial team.Method: prioritize cited human research and official safety or regulatory sources; compare retailer-listed prices without endorsing products.Affiliate disclosure
01

What is it?

What Indole-3-carbinol is

2

Indole-3-carbinol, or I3C, forms when glucobrassicin from cruciferous vegetables breaks down. A capsule of isolated I3C is not the same exposure as eating broccoli, cabbage, kale, or Brussels sprouts.

Main evidence is hormonal, not cognitive3
Human I3C studies mainly involve urinary estrogen metabolites and small gynecologic dysplasia trials. Reliable human evidence for focus, memory, mood, or productivity was not found.
How the evidence is used2
This profile keeps cruciferous vegetable intake, isolated I3C, DIM, population-specific clinical research, and nootropic claims separate. The listing is used only for product-form context.
02

Names, aliases and forms

Common NameIndole-3-carbinol
AbbreviationI3C
Chemical NamesIndole-3-methanol; 3-hydroxymethylindole; 3-indolylcarbinol
Iupac Name1H-indol-3-ylmethanol
Active ConstituentGlucobrassicin breakdown product
Cas Number700-06-1
Pubchem Cid3712
Molecular FormulaC9H9NO
03

Mechanisms of action

Estrogen-metabolism shift

3

Human studies report shifts in estrogen-metabolite ratios after I3C. That is why I3C is marketed for hormone support, but the marker shift is not the same as a proven disease-prevention, fertility, testosterone, or mood effect.

I3C versus DIM

2

I3C can form acid-condensation products such as DIM in the stomach, but I3C, DIM, cruciferous vegetables, and blended hormone-support formulas are distinct exposures and products.

04

Potential effects and evidence map

Reviewed I3C evidence includes a small human estrogen-metabolism study, small gynecologic research studies, and a phase I study in high-risk women. These findings are population- and context-specific, not cognitive outcomes or a consumer-use framework. Animal toxicology does not establish the safety of concentrated, long-term self-use.

Effect domainMagnitudeGrade
Cellular / long-term brain support4
CumulativeConfidence: Low

Human evidence is mainly estrogen-metabolism and gynecologic dysplasia context, not brain-specific support or cognitive enhancement.

Note Used as a broad cellular-research placeholder because the taxonomy lacks an endocrine effect domain.

1/5
C
Mood / wellbeing2
UnknownConfidence: Low

No reliable human mood or wellbeing benefit was found for I3C supplementation.

Note Hormone-support marketing should not be converted into mood claims.

0/5
E
Memory / learning2
UnknownConfidence: Low

No reliable human memory, learning, focus, or productivity evidence was found.

Note Not a cognitive nootropic based on current evidence.

0/5
E
05

Typical dosages and timing

Research context4Study-specific

Separate small studies included 200 mg and 400 mg daily arms. A phase I study in high-risk women used 400 mg daily before 800 mg daily. These research protocols do not establish a consumer amount, route, timing, or repeat-use plan.

06

Timing & effect horizon

Effect horizonUnknown
Unknown
No nootropic timing data5

Reliable onset, duration, half life, tolerance, and cycling data for cognitive or mood use were not found. Estrogen-metabolite studies measured changes over weeks to months.

07

Safety, side effects and risk profile

Hormonal caution3
Confidence: Medium

I3C changes estrogen-metabolism markers, so caution is appropriate with hormone-sensitive conditions or hormone therapy.

Note Separate food-level cruciferous intake from concentrated I3C capsules.

3/5
C
Interaction risk5
Confidence: Medium

I3C can induce CYP1A2 in human studies and MSKCC warns that CYP1A2 substrate drug effectiveness may be reduced.

Note Medication review matters for clozapine, olanzapine, theophylline, caffeine-sensitive users, and other CYP1A2 substrates.

3/5
C
Pregnancy / lactation caution2
Confidence: Low

Avoid concentrated I3C during pregnancy or lactation unless a clinician specifically directs use.

Note Hormonal and reproductive safety are not established for supplement-dose self-use.

3/5
E
GI discomfort2
Confidence: Low

GI effects and rash are plausible; NTP and animal work point to intestine as a toxicity target in some models.

Note Stop and review if persistent GI symptoms, rash, or allergy-like reactions occur.

2/5
D
Liver / kidney caution2
Confidence: Low

MSKCC notes rare small ALT increases, and I3C strongly affects xenobiotic-metabolism pathways.

Note Use caution with liver disease, abnormal liver enzymes, heavy alcohol use, or hepatotoxic medication plans.

2/5
D
Evidence uncertainty7
Confidence: Medium

NTP rodent findings and mixed preclinical cancer models make high-dose, long-term self-use a poor extrapolation from vegetable intake.

Note Human trials are small and not nootropic-focused.

3/5
C
CYP1A2 interaction caution5

In the phase I study, CYP1A2 activity rose after I3C. MSKCC warns that lab and human evidence suggest I3C may affect CYP1A2 substrate drugs, with clinical relevance still uncertain.

Hormone-sensitive context2

Because I3C changes estrogen-metabolism markers, people with hormone-sensitive cancers, endometriosis, fibroids, fertility care, hormone therapy, oral contraceptives, or anti-estrogen drugs should seek individual clinical guidance rather than self-experimenting.

Animal toxicology is mixed7

NTP rodent gavage studies found different carcinogenicity conclusions by species and sex, including clear evidence in male mice for liver neoplasms and some evidence in female rats for uterine neoplasms. This argues against assuming high-dose long-term supplement use is benign.

08

Interactions and cautions

Medication review2

Review I3C with CYP1A2 substrate drugs, hormone therapy, oral contraceptives, anti-estrogen drugs, chemotherapy or cancer-care plans, immunosuppressive conditions, caffeine sensitivity, smoking changes, and liver-risk medication combinations.

10

Practical buying and quality notes

  • The only indexed product row is I3C Indole-3-Carbinol 200 mg capsules, but it is marked unavailable in current variant data. Use it as historical listing context only.8
  • For I3C products, compare whether the product is I3C or DIM, the mg per capsule, serving count, lot testing, excipients, storage, expiry, and whether it is a single-ingredient product or a hormone-support blend.8
  • Cruciferous vegetables provide glucosinolate precursors in a food matrix. A 200 mg isolated I3C capsule is a concentrated and chemically different exposure from normal dietary servings.2
11

FAQ

What is Indole-3-carbinol?

1

Indole-3-carbinol is a plant indole formed from glucobrassicin in cruciferous vegetables. It is commonly abbreviated I3C.

What amounts appeared in I3C studies?

5

The cited small trials and phase I study used differing protocol amounts. They do not establish a consumer amount, route, timing, or long-term self-use plan.

Does I3C help focus or memory?

3

No reliable human focus, memory, mood, or productivity evidence was found. The better-supported human context is estrogen-metabolism markers and small gynecologic dysplasia studies.

Is I3C the same as DIM?

2

No. DIM can form from I3C under acidic conditions, and both appear in related supplement markets, but they are distinct compounds with different product labels and evidence boundaries.

Who should avoid I3C?

2

Seek individual clinical guidance with pregnancy, lactation, hormone-sensitive conditions, cancer-care plans, hormone therapy, anti-estrogen drugs, oral contraceptives, liver disease, abnormal liver enzymes, CYP1A2 substrate drugs, or complex medication plans.

12

References

  1. PubChem. Indole-3-carbinol (CID 3712). Accessed 2026-07-01.
  2. Memorial Sloan Kettering Cancer Center. Indole-3-Carbinol. Accessed 2026-07-01.
  3. Michnovicz JJ, et al. Changes in levels of urinary estrogen metabolites after oral indole-3-carbinol treatment in humans. J Natl Cancer Inst. 1997;89(10):718-723.
  4. Bell MC, et al. Placebo-controlled trial of indole-3-carbinol in the treatment of CIN. Gynecol Oncol. 2000;78(2):123-129.
  5. Reed GA, et al. A phase I study of indole-3-carbinol in women: tolerability and effects. Cancer Epidemiol Biomarkers Prev. 2005;14(8):1953-1960.
  6. Naik R, et al. A randomized phase II trial of indole-3-carbinol in the treatment of vulvar intraepithelial neoplasia. Int J Gynecol Cancer. 2006;16(2):786-790.
  7. National Toxicology Program. Toxicology and carcinogenesis studies of indole-3-carbinol. Technical Report 584. July 2017.
  8. NootropicsIndex indexed listing. I3C Indole-3-Carbinol 200 mg capsules. Accessed 2026-07-01.
Note

This page is informational and summarizes available evidence. It is not medical advice, a recommendation, or a substitute for guidance from a qualified clinician.