Silbinol® (Indian Kino Pterostilbene Extract — Sabinsa)

Pterocarpus marsupium
Evidence Level
Limited
3 Clinical Trials
9 Documented Benefits
2/5 Evidence Score

Silbinol is Sabinsa's standardized extract from the heartwood of Pterocarpus marsupium (Indian Kino tree, known as 'Vijayasar' in Hindi/Sanskrit), studied for blood sugar support, though the only human trial of this branded extract measured safety and found no change in glucose or blood lipids. Pterostilbene is the key bioactive, a dimethylated version of resveratrol but more bioavailable, potent, and metabolically stable. Available in three standardizations: 5%, 30%, or 90% pterostilbene. Also contains (-)-epicatechin (>=0.01%) with documented insulin-like activity. Backed by an ICMR trial of P. marsupium decoction in newly-diagnosed Type 2 diabetics plus a published safety trial of the 90% pterostilbene extract.

Studied Dose 200 mg/day (100 mg twice daily) of 90% pterostilbene; consumer form 450 mg Indian Kino providing 22.5 mg pterostilbene.
Active Compound Pterostilbene (dimethylated stilbene) from Pterocarpus marsupium (Indian Kino) heartwood/bark, standardized to 5%, 30%, or 90%; plus min 0.01% (-)-epicatechin.

Benefits

Blood sugar support (open-label decoction trial)

A trial conducted by the Indian Council of Medical Research (ICMR) tested P. marsupium decoction in newly-diagnosed non-insulin-dependent diabetes mellitus (NIDDM) patients, measuring blood glucose and HbA1c. This was an open-label trial (no placebo) of a decoction of the plant, a different preparation than this branded pterostilbene extract, which has not itself been tested for blood-sugar efficacy.

Pterostilbene — more bioavailable than resveratrol

Pterostilbene is structurally a di-methylated version of resveratrol but with better bioavailability, potency, and metabolic stability. The methylation increases lipid solubility and resistance to first-pass metabolism. Practical advantage over resveratrol which has poor oral bioavailability (<1% in some studies). Same molecular target class but better drug-like properties.

Antioxidant activity (laboratory studies)

In test-tube assays, pterostilbene resisted lipid peroxidation more than resveratrol. This is laboratory chemistry, not a measured human antioxidant outcome. In the one human trial of Silbinol, the serum antioxidant profile did not differ significantly from placebo, although glutathione trended higher.

PPARα induction (preclinical mechanism)

Pterostilbene shows the highest induction of PPAR-alpha among stilbenes. PPAR-alpha regulates fatty acid metabolism and lipid handling. This is a laboratory mechanism, not a measured human outcome, and the human safety trial of Silbinol found no change in blood lipids. The drug comparison to fenofibrate comes from preclinical work.

Insulin sensitivity improvement

In animal and cell studies, pterostilbene and the (-)-epicatechin component affected insulin signaling. This is preclinical work; no human trial of Silbinol has measured insulin sensitivity, and the comparison to metformin comes from animal data. Combined mechanisms address both insulin sensitivity (cells responding to insulin) and insulin secretion.

Antimicrobial activity (laboratory studies only)

Pterostilbene has shown antimicrobial activity in laboratory tests. These are cell and culture studies, not trials in people, and this has not been tested as a benefit of the supplement in humans.

Anti-inflammatory (COX-2 inhibition)

Pterostilbene has documented anti-inflammatory effects via COX-2 inhibition, the same target class as NSAIDs. The mechanism supports applications in inflammatory metabolic disease (chronic low-grade inflammation drives metabolic syndrome). It also has analgesic effects.

TMAO effects (preclinical)

Pterostilbene has been examined for effects on trimethylamine N-oxide (TMAO) in preclinical work. No human trial of Silbinol has measured TMAO or any cardiovascular outcome.

Safety established — 200 mg/day clinical trial

A safety trial gave healthy adults Silbinol 90% pterostilbene 100 mg twice daily (200 mg/day) or placebo for 2 months. Hematological, lipid, glycemic, thyroid, liver, and renal function parameters remained within normal range, with no serious adverse events. Trial registration CTRI/2019/08/020736.

Mechanism of action

1

PPARα activation

Pterostilbene induces PPARα in laboratory studies. PPARα regulates fatty acid oxidation and lipid metabolism, and the comparison to fibrate drugs (fenofibrate) comes from preclinical work. This is a mechanism, not a human outcome: the one human trial of Silbinol found no change in blood lipids.

2

Insulin signaling enhancement

(-)-Epicatechin in Silbinol has documented insulin-like activity — directly supporting insulin signaling. Combined with pterostilbene's effects on insulin sensitivity, Silbinol addresses multiple aspects of glucose homeostasis. Comparative studies confirm similarity between (-)-epicatechin and insulin mechanisms.

3

COX-2 anti-inflammatory inhibition

Pterostilbene inhibits cyclooxygenase-2 (COX-2) — the inflammatory isoform of the enzyme producing prostaglandins. Same target as NSAIDs (with milder magnitude). Mechanism reduces inflammatory contribution to metabolic and cardiovascular disease.

4

Lipid peroxidation prevention

Pterostilbene's antioxidant activity exceeds resveratrol against lipid peroxidation. Lipid peroxidation drives atherosclerosis via oxidized LDL formation. Preventing lipid peroxidation supports cardiovascular health alongside the direct lipid-lowering effects.

5

Methylation-enhanced bioavailability

Pterostilbene's two methyl groups (vs resveratrol's hydroxyl groups) increase lipid solubility and resistance to phase II metabolism (glucuronidation, sulfation). Animal pharmacokinetic work reported markedly higher oral bioavailability for pterostilbene (around 80 percent in rats) than for resveratrol (commonly under 1 percent). The bioavailability advantage explains why pterostilbene produces effects at lower doses than resveratrol.

Clinical trials

1
Silbinol Safety RCT — 90% Pterostilbene
PubMed

Randomized double-blind placebo-controlled study evaluating Silbinol® at 100 mg twice daily (200 mg/day) for 2 months in healthy adults. Primary outcomes: changes in laboratory parameters, vital signs, adverse events. Secondary: serum antioxidant enzyme levels. Published in peer-reviewed journal. CTRI/2019/08/020736.

60 healthy adult participants (27 males, 33 females). 2-month intervention with 100 mg Silbinol bid or placebo.

Hematological, lipid, glycemic, thyroid profiles, liver and renal functions remained within normal range — no differences between groups. No serious adverse events. The serum antioxidant profile did not differ significantly between groups, although glutathione levels trended higher in the pterostilbene group. Established safety of >90% pterostilbene at 200 mg/day for human use. Foundation for therapeutic applications.

2
P. marsupium Plant Extract: Open-Label ICMR Antidiabetic Trial (not the branded 90% pterostilbene extract)
PubMed

Phase 2 open trial conducted by the Indian Council of Medical Research (ICMR) at 4 centers in India testing P. marsupium decoction for 12 weeks in newly-diagnosed non-insulin-dependent diabetes mellitus (NIDDM) patients. Foundational efficacy evidence. Published in Indian Journal of Medical Research.

93 newly-diagnosed NIDDM patients. 12-week intervention with P. marsupium decoction.

Documented improvements in blood glucose levels and glycosylated hemoglobin (HbA1c) with P. marsupium intervention. Foundational evidence supporting Silbinol's metabolic positioning. Traditional decoctions and modern standardized extracts provide consistent antidiabetic effects in NIDDM patients.

3
PRECLINICAL ONLY (not a human trial): Pterostilbene Pharmacology in Animal and Cell Studies

Class evidence for pterostilbene pharmacology across preclinical and clinical research. Studies include Rimando et al. (PPARα induction), Manickam et al. (insulin sensitivity), Remsberg et al. (analgesic), Satheesh and Pari (antidiabetic mechanism), and others.

Various — animal models and in vitro studies of pterostilbene pharmacology.

Pterostilbene consistently demonstrates: PPARα activation (highest among stilbenes), insulin sensitivity effects, anti-inflammatory activity via COX-2 inhibition, antioxidant activity in vitro, and antimicrobial activity in culture, all observed in animal or cell models rather than human trials. Multi-mechanism profile supports broad applications across metabolic, cardiovascular, and inflammatory health.

Side effects and drug interactions

Common Potential side effects

Excellent safety profile — no significant adverse events in published RCT at 200 mg/day for 2 months.
Mild GI effects rare.
Pterostilbene is more bioavailable than resveratrol — lower doses produce equivalent or greater effects.
Long-term safety supported by traditional Ayurvedic use of Pterocarpus marsupium.
Possible mild blood-thinning effect at high doses — relevant before surgery.
Pregnancy and lactation: insufficient data; consult clinician.
Available in three standardizations (5%, 30%, 90%) for different application potency requirements.

Important Drug interactions

Diabetes medications (metformin, sulfonylureas, insulin) — additive glucose-lowering effects; monitor blood glucose.
Statins and fibrate drugs — pterostilbene activates PPARα (same as fibrates); theoretical additive effect.
Anticoagulants (warfarin) — stilbenes may have mild antiplatelet effects; monitor INR.
NSAIDs — pterostilbene has COX-2 inhibition activity; minimal clinical interaction concern.
Antihypertensive medications — possible mild additive effects.
Other resveratrol/stilbene supplements — complementary; similar mechanism class.
Pregnancy and lactation: consult clinician.

Frequently asked questions about Silbinol® (Indian Kino Pterostilbene Extract — Sabinsa)

What is Silbinol?

Silbinol is Sabinsa's standardized extract from the heartwood of Pterocarpus marsupium (Indian Kino tree, known as 'Vijayasar' in Hindi/Sanskrit), studied for blood sugar support, though the only human trial of this branded extract measured safety and found no change in glucose or blood lipids.

What is Silbinol used for?

Silbinol is researched primarily for Metabolic Health. A trial conducted by the Indian Council of Medical Research (ICMR) tested P. marsupium decoction in newly-diagnosed non-insulin-dependent diabetes mellitus (NIDDM) patients, measuring blood glucose and HbA1c.

What is the recommended dosage of Silbinol?

The clinically studied dose is 200 mg/day (100 mg twice daily) of 90% pterostilbene; consumer form 450 mg Indian Kino providing 22.5 mg pterostilbene. Always follow the product label and check with a healthcare provider for personal advice.

Is Silbinol safe, and does it have side effects?

For most healthy adults, Silbinol is well tolerated at studied doses. Reported effects can include: Excellent safety profile — no significant adverse events in published RCT at 200 mg/day for 2 months. Mild GI effects rare. It may also interact with some medications. Silbinol is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does Silbinol interact with any medications?

Possible interactions include: Diabetes medications (metformin, sulfonylureas, insulin) — additive glucose-lowering effects; monitor blood glucose. Statins and fibrate drugs — pterostilbene activates PPARα (same as fibrates); theoretical additive effect. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Silbinol?

NutraSmarts rates the evidence for Silbinol as Limited (2 out of 5). It is backed by 3 clinical trials and 3 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(3 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Majeed M, Nagabhushanam K, Paulose S, Mundkur L A Short-Term Safety Evaluation of Silbinol® — an Extract from Pterocarpus marsupium in Healthy Adults — a Randomized, Double-Blind, Placebo-Controlled Study Journal of Evidence-Based Integrative Medicine. 2023;28:2515690X231198312. doi: 10.1177/2515690X231198312.PubMedUsed to support: Manufacturer-run double-blind RCT (n=60 healthy adults, 8 weeks) by Sami-Sabinsa evaluating the safety of Silbinol at 200 mg/day (90 percent pterostilbene). No serious adverse events; hematology, lipid, glycemic, thyroid, liver and renal parameters stayed within the normal range with no difference from placebo. The serum antioxidant profile did not differ significantly from placebo. The trial was not powered for glycaemic or any other efficacy endpoint.
  2. Indian Council of Medical Research (ICMR) Collaborating Centres, New Delhi Flexible dose open trial of Vijayasar in cases of newly-diagnosed non-insulin-dependent diabetes mellitus Indian Journal of Medical Research. 1998;108:24-29.PubMedUsed to support: Open-label, non-randomised multicentre trial (n=97) in which an aqueous extract of Pterocarpus marsupium (2 to 4 g/day), not the branded 90 percent pterostilbene extract, brought blood glucose under control in 69 percent of newly-diagnosed NIDDM patients, with fasting glucose down 32 mg/dL and postprandial down 45 mg/dL (both p<0.001) and HbA1c down from 9.8 to 9.4 percent at 12 weeks; blood lipids did not change and no adverse events occurred. This is a different preparation than Silbinol and had no placebo control.
  3. Dellinger RW, Santos SR, Morris M, Evans M, Alminana D, Guarente L, Marcotulli E Repeat dose NRPT (nicotinamide riboside and pterostilbene) increases NAD+ levels in humans safely and sustainably: a randomized, double-blind, placebo-controlled study NPJ Aging and Mechanisms of Disease. 2017;3:17. doi: 10.1038/s41514-017-0016-9.PubMedUsed to support: Double-blind RCT (n=120 healthy adults aged 60 to 80, 8 weeks) of a combination product containing nicotinamide riboside plus pterostilbene, not pterostilbene alone. It measured blood NAD+ (a biochemical marker, raised 40 to 90 percent) and safety, not blood glucose, blood lipids or any clinical outcome. Industry-funded (Elysium Health). Relevant only to the pterostilbene safety profile and the NAD+ surrogate, not to any metabolic or antioxidant benefit of Silbinol.