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Coptisine

Coptisine

Research reviewed: Up until 03/2026

Coptisine is a dietary supplement with 8 published peer-reviewed studies involving 260 participants, researched for Blood Sugar Control, Antimicrobial Activity, Anti-inflammatory Activity and 1 more areas.

8
Studies
260
Participants
2013–2021
Research Span

Evidence at a Glance

Strength is scored by study design, sample size, study type, and outcomes

Overall: Weak Evidence

Blood Sugar Control

Weak
2 studies 1 of 2 positive 33 participants 0 human

Antimicrobial Activity

Weak
2 studies 0 of 2 positive 0 participants 0 human

Anti-inflammatory Activity

Weak
1 study 1 of 1 positive 20 participants 0 human

Anti-cancer Activity

Weak
3 studies 1 of 3 positive 7,956 participants 0 human

Research Visualised

Visual breakdown of the clinical data.

Study Quality Breakdown

What types of studies were conducted

0/8
Randomised
0/8
Double-Blind
0/8
Placebo-Controlled

Participants Per Study

Larger samples = more reliable results

Study 1 (2013)
30
Study 2 (2017)
3
Study 1 (2019)
0
Study 2 (2021)
0
Study 1 (2016)
20
Study 1 (2014)
7,901
Study 2 (2020)
20
Study 3 (2021)
35

Research Timeline

When the studies were published

1
2013
1
2014
1
2016
1
2017
1
2019
1
2020
2
2021

All Studies

Detailed breakdown of each trial. Click to expand.

Blood Sugar Control

1

To evaluate hypoglycemic effects of Coptisine in STZ-induced diabetic mice

2013 30 participants 4 weeks 25-100 mg/kg Coptisine
Review/Other Positive

Study Type

Animal study

Purpose

To evaluate hypoglycemic effects of Coptisine in STZ-induced diabetic mice

Dose

25-100 mg/kg Coptisine

Participants

30 STZ-induced diabetic mice

Duration

4 weeks

Results

Coptisine significantly reduced fasting blood glucose, improved insulin sensitivity, activated AMPK pathway, and partially preserved pancreatic β-cell function. Effects were dose-dependent and comparable to Berberine.

How They Measured It

Fasting blood glucose, insulin, HOMA-IR, pancreatic β-cell markers, AMPK activation

Read full study
2

To investigate mechanisms of Coptisine-induced glucose uptake in adipocytes

2017 3 participants 2 hours 1-100 μM Coptisine
Review/Other Mixed

Study Type

In vitro study

Purpose

To investigate mechanisms of Coptisine-induced glucose uptake in adipocytes

Dose

1-100 μM Coptisine

Participants

3T3-L1 adipocytes

Duration

2 hours

Results

Coptisine stimulated glucose uptake in adipocytes through GLUT4 translocation via insulin-dependent (IR/Akt) and AMPK-dependent pathways, with an additive effect when combined with insulin.

How They Measured It

Glucose uptake assay (2-NBDG), GLUT4 translocation, Akt/mTOR signaling, IR activation

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Antimicrobial Activity

1

To evaluate antibacterial activity of Coptisine against drug-resistant bacterial pathogens

2019 ? participants 24-72 hours Coptisine 0.5-128 μg/mL
Review/Other Positive

Study Type

In vitro study

Purpose

To evaluate antibacterial activity of Coptisine against drug-resistant bacterial pathogens

Dose

Coptisine 0.5-128 μg/mL

Participants

MRSA, VRSA, MDR E. coli, Klebsiella pneumoniae

Duration

24-72 hours

Results

Coptisine exhibited significant bactericidal activity against MRSA (MIC 4 μg/mL) and MDR Gram-negative pathogens. Mechanism involves membrane disruption and DNA gyrase inhibition. Strong antibiofilm activity also demonstrated.

How They Measured It

MIC determination, time-kill kinetics, membrane permeability assay, biofilm inhibition

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2

To assess antifungal activity of Coptisine against Candida species

2021 ? participants 48 hours Coptisine 1-64 μg/mL
Review/Other Mixed

Study Type

In vitro study

Purpose

To assess antifungal activity of Coptisine against Candida species

Dose

Coptisine 1-64 μg/mL

Participants

Candida albicans, C. glabrata, C. tropicalis

Duration

48 hours

Results

Coptisine demonstrated antifungal activity against all Candida species tested (MIC 4-32 μg/mL), disrupted biofilm formation, and synergized with fluconazole against fluconazole-resistant strains.

How They Measured It

MIC/MFC determination, anti-biofilm assays, ERG11 expression, cell wall integrity analysis

Read full study

Anti-inflammatory Activity

1

To characterize anti-inflammatory mechanisms of Coptisine in models of acute inflammation

2016 20 participants 24 hours (in vitro), 6 hours (animal) 5-50 μM (in vitro), 20-80 mg/kg (animal)
Review/Other Positive

Study Type

In vitro and animal study

Purpose

To characterize anti-inflammatory mechanisms of Coptisine in models of acute inflammation

Dose

5-50 μM (in vitro), 20-80 mg/kg (animal)

Participants

Macrophage cells and 20 mice with carrageenan edema

Duration

24 hours (in vitro), 6 hours (animal)

Results

Coptisine inhibited NLRP3 inflammasome activation, reduced IL-1β maturation, suppressed NF-κB signaling, and significantly attenuated carrageenan-induced paw edema in rodent inflammation models.

How They Measured It

Cytokine profiling (IL-1β, IL-6, TNF-α), NLRP3 inflammasome, NF-κB, carrageenan edema model

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Anti-cancer Activity

1

To evaluate the anticancer mechanism of Coptisine in gastric cancer cells

2014 7901 participants 48 hours 5-50 μM Coptisine
Review/Other Mixed

Study Type

In vitro study

Purpose

To evaluate the anticancer mechanism of Coptisine in gastric cancer cells

Dose

5-50 μM Coptisine

Participants

SGC-7901 and AGS gastric cancer cell lines

Duration

48 hours

Results

Coptisine potently inhibited gastric cancer cell proliferation (IC50 12-18 μM), induced G2/M cell cycle arrest, caused DNA double-strand breaks, and inhibited topoisomerase I and II activity.

How They Measured It

Cell viability, apoptosis, cell cycle analysis, DNA damage markers (γH2AX), topoisomerase inhibition

Read full study
2

To evaluate Coptisine antitumor activity in a colon cancer xenograft model

2020 20 participants 21 days 20-40 mg/kg Coptisine
Review/Other Positive

Study Type

Animal study

Purpose

To evaluate Coptisine antitumor activity in a colon cancer xenograft model

Dose

20-40 mg/kg Coptisine

Participants

20 nude mice with HCT116 xenografts

Duration

21 days

Results

Coptisine significantly reduced tumor growth, increased tumor apoptosis, reduced Ki67 proliferation index, and suppressed Wnt/β-catenin signaling without significant organ toxicity.

How They Measured It

Tumor volume, body weight, apoptosis (TUNEL), Ki67, Wnt/β-catenin signaling

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3

To review the pharmacological properties and anticancer mechanisms of Coptisine

2021 35 participants Various Various formulations
Review/Other Mixed

Study Type

Systematic review

Purpose

To review the pharmacological properties and anticancer mechanisms of Coptisine

Dose

Various formulations

Participants

Review of 35 pre-clinical studies

Duration

Various

Results

Coptisine demonstrates anticancer activity against gastric, colon, hepatic, and lung cancers via multiple mechanisms including topoisomerase inhibition, apoptosis induction, cell cycle arrest, and Wnt signaling suppression.

How They Measured It

Systematic review of pre-clinical studies

Read full study

Frequently Asked Questions

Common questions about Coptisine research

What does the research say about Coptisine?

There are currently 8 peer-reviewed studies on Coptisine (Coptisine), involving 260 total participants. Research covers Blood sugar control, Antimicrobial activity, Anti-inflammatory activity and 1 more areas. The overall evidence strength is rated as Weak.

How strong is the evidence for Coptisine?

The evidence is currently rated as "Weak Evidence". This rating is based on study design quality (randomisation, blinding, placebo controls), sample sizes, study types (0 human studies), and reported outcomes.

What health goals has Coptisine been studied for?

Coptisine has been researched for: Blood sugar control, Antimicrobial activity, Anti-inflammatory activity, Anti-cancer activity. Each area has its own body of evidence which you can explore in the study breakdowns above.

Are the studies on Coptisine based on human trials?

Currently all 8 studies on Coptisine are animal or in-vitro studies. Human clinical trials are needed before the evidence can be rated above "Weak".