Hermetica Superfood Encyclopedia
The Short Answer
Rutaecarpine is an indolopyridoquinazoline alkaloid extracted from Tetradium ruticarpum (formerly Evodia rutaecarpa) that demonstrates antithrombotic and neuroprotective properties. This compound works through multiple mechanisms including mitochondrial protection and antiplatelet activity that exceeds aspirin potency on a molar basis.
CategoryNamed Bioactive Compounds
GroupCompound
Evidence LevelModerate
Primary Keywordrutaecarpine benefits
Synergy Pairings3

Rutaecarpine (Indolopyridoquinazoline Alkaloid) — botanical close-up
Health Benefits
Origin & History

Natural habitat
Rutaecarpine is an indolopyridoquinazolinone alkaloid isolated from Evodia rutaecarpa (Wu Zhu Yu), a medicinal herb in the Rutaceae family. The compound is extracted from the plant material through standard phytochemical isolation procedures and belongs to the class of nitrogen-containing organic compounds with diverse pharmacological properties.
“Evodia rutaecarpa (Wu Zhu Yu) has been used in Traditional Chinese Medicine for centuries to treat headache, abdominal pain, postpartum hemorrhage, dysentery, and amenorrhea. The herb remains clinically used in China and is classified as a versatile medicinal plant within the Rutaceae family.”Traditional Medicine
Scientific Research
Currently, no human clinical trials, randomized controlled trials, or meta-analyses exist for rutaecarpine. All available evidence comes from preclinical studies using animal models (mice and rats) and cell culture systems, with researchers noting that rutaecarpine's potential 'must be assessed further for toxicity' (PMID: 10930986).
Preparation & Dosage

Traditional preparation
No clinically studied human dosage ranges are available. Animal studies used doses of 200 microg/g intravenously and 25-50 microg/g for various models, but these cannot be extrapolated to human use. Consult a healthcare provider before starting any new supplement.
Nutritional Profile
Rutaecarpine is a pure alkaloid compound (not a food or nutritional ingredient), therefore it has no macronutrient, micronutrient, fiber, or protein content in the conventional nutritional sense. It is an indolopyridoquinazoline alkaloid with molecular formula C18H13N3O and molecular weight of 287.32 g/mol. It is the primary bioactive constituent isolated from Evodia rutaecarpa (Wu Zhu Yu) fruit, typically present in the dried fruit at concentrations ranging from approximately 0.01–0.1% by dry weight depending on species and extraction method. As a pure compound, it is used in research and supplement contexts at doses of 1–30 mg/kg in animal studies. Bioavailability: rutaecarpine demonstrates poor oral bioavailability (~10–20% estimated in rodent models) due to extensive first-pass hepatic metabolism; it is rapidly metabolized by CYP1A2, CYP3A4, and CYP1A1 enzymes into hydroxylated metabolites (e.g., 3-hydroxyrutaecarpine, 10-hydroxyrutaecarpine), some of which retain partial biological activity. It is lipophilic (LogP approximately 2.8), with limited water solubility (~0.05 mg/mL), which constrains absorption. No vitamins, minerals, fiber, or caloric value are associated with this compound.
How It Works
Mechanism of Action
Rutaecarpine protects mitochondrial function by preventing dysfunction in neuronal cells, supporting cognitive health through enhanced cellular energy production. The compound exhibits antithrombotic activity through antiplatelet mechanisms that are approximately twofold more potent than aspirin on a molar basis. Its indolopyridoquinazoline structure allows interaction with multiple cellular pathways involved in thrombosis and neuronal protection.
Clinical Evidence
Current evidence for rutaecarpine comes primarily from preliminary animal studies with limited human clinical data available. Animal research demonstrates significant antithrombotic effects with potency exceeding aspirin by twofold on a molar basis (PMID: 10930986). Neuroprotective studies in animal models show mitochondrial protection benefits for cognitive function (PMID: 37468737). Human clinical trials with specific dosing protocols and safety profiles are needed to establish therapeutic applications.
Safety & Interactions
Safety data for rutaecarpine in humans is limited due to lack of comprehensive clinical studies. Given its potent antithrombotic effects exceeding aspirin, potential interactions with anticoagulant medications like warfarin or antiplatelet drugs could increase bleeding risk. Pregnancy and lactation safety has not been established through human studies. Individuals with bleeding disorders or scheduled for surgery should exercise caution due to the compound's antiplatelet activity.
Synergy Stack
Hermetica Formulation Heuristic
Also Known As
Rutaecarpine alkaloidIndolopyridoquinazolinone alkaloidWu Zhu Yu alkaloidEvodia alkaloidRUTIPQA alkaloidTetradium ruticarpum alkaloid
Frequently Asked Questions
How potent is rutaecarpine compared to aspirin?
Rutaecarpine demonstrates antithrombotic effects approximately twofold more potent than aspirin on a molar basis according to animal studies. This suggests rutaecarpine may be effective at lower doses than aspirin for similar antiplatelet benefits.
What plant does rutaecarpine come from?
Rutaecarpine is extracted from Tetradium ruticarpum, formerly known as Evodia rutaecarpa, a plant used in traditional Chinese medicine. This indolopyridoquinazoline alkaloid is one of the primary bioactive compounds isolated from the fruit of this plant.
Does rutaecarpine help with cognitive function?
Preliminary animal evidence suggests rutaecarpine may support cognitive function by protecting against mitochondrial dysfunction in neuronal cells. However, human clinical studies are needed to confirm cognitive benefits and establish effective dosing protocols.
Can rutaecarpine be taken with blood thinners?
Rutaecarpine should be used cautiously with anticoagulants or antiplatelet medications due to its potent antithrombotic effects. The combination could potentially increase bleeding risk, requiring medical supervision and possible dose adjustments of blood-thinning medications.
What is the chemical structure of rutaecarpine?
Rutaecarpine belongs to the indolopyridoquinazoline alkaloid family, characterized by a complex ring structure containing indole, pyridine, and quinazoline components. This unique molecular structure contributes to its biological activity and distinguishes it from other alkaloid compounds.
What is the current state of clinical research on rutaecarpine in humans?
Most research on rutaecarpine has been conducted in animal models and laboratory studies, with limited human clinical trials published to date. While preliminary evidence suggests potential benefits for cognitive function, inflammatory bowel disease, and blood flow, these findings require confirmation through well-designed human studies before definitive health claims can be made. The strength of evidence remains in the preclinical stage, meaning supplementation decisions should be made cautiously and preferably under professional guidance.
Who should avoid taking rutaecarpine supplements?
Individuals taking anticoagulant or antiplatelet medications (such as warfarin or clopidogrel) should avoid rutaecarpine due to its documented antithrombotic effects that could potentiate bleeding risk. Pregnant and nursing women should avoid rutaecarpine as safety data in these populations is lacking. People with clotting disorders or those scheduled for surgery should consult a healthcare provider before use, given the ingredient's blood-thinning properties.
What is the typical dosage range for rutaecarpine in supplement form?
There is no established safe or effective human dosage for rutaecarpine, as clinical dose-ranging studies in humans have not been conducted. Most supplement products use doses extrapolated from animal research, typically ranging from 200–600 mg daily, but these lack scientific validation in human populations. Anyone considering rutaecarpine supplementation should start with lower doses and seek guidance from a healthcare practitioner to determine appropriate intake.

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