L-THP

L-THP is the left-handed form of tetrahydropalmatine, an alkaloid from Corydalis and Stephania plants whose preparations have long been used for sedation and pain relief.

Human trialsNon-peptide compound reference

Also known as: Levo-Tetrahydropalmatine, levo-Tetrahydropalmatine, (-)-Tetrahydropalmatine, Rotundine, (-)-rotundine, Gindarine, Hyndarine, (-)-Corydalis B

(how we review)

Dosing & scaling, explained

Amounts reported for L-THP are listed under Reported protocols, each with its source and study kind. No amount ladder is inferred from them. This is educational source context, not a protocol or recommendation.

No source-supported amount ladder is shown

Enter a target amount only from your own reviewed source. The calculator can convert it into concentration, volume and device markings, but it will not infer an amount from product availability or another compound.

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No independently verified schedule

Clinical context

Human study rows are described per source under Reported protocols; they belong to their trial populations and are not a general amount.

Storage, handling and interpretation

Product identity

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Storage & handling

Follow the product label, certificate and validated laboratory SOP; no universal storage assumption is applied here.

Prepared solutions

Label concentration and preparation date, use sterile technique where applicable, and follow a validated stability protocol.

Reported protocols for L-THP

What published studies and recent community write-ups report about amounts, timing and course length. 5 clinical, 1 preclinical and 1 community-reported rows, each linked to its source. These are descriptions of what others report, not instructions, and nothing here is medical advice.

ContextDoseFrequencyRouteCourseSource
Clinical5 rows
Safety and pharmacokinetics with a cocaine challenge24 adult men who use cocaine, randomised double-blind; 20 completed and 19 gave full pharmacokinetic data30 mg twice daily (60 mg per day)Twice dailyOral capsulesA 3.5 day course, with an intranasal cocaine challenge of 40 mg on day 4Not applicableJournal of Clinical Pharmacology (PubMed Central)2017
The short course was safe and well tolerated, did not change cocaine's pharmacokinetics and did not change its acute cardiovascular effects, with no difference in side-effect counts against placebo. The authors chose 30 mg twice daily specifically to stay below the amounts where sedation appears, and the study was designed to test safety rather than whether the drug reduces cocaine use.
Randomised trial in heroin dependence120 heroin-dependent inpatients, randomised double-blind against placeboTwo 30 mg tablets twice daily (120 mg per day)Twice dailyOral tablets4 weeks of treatment, 4 weeks of observation, then 3 months of follow-up after dischargeNone describedActa Pharmacologica Sinica (PubMed Central)2008
Four weeks of treatment reduced the severity of protracted withdrawal, including physical symptoms, mood, insomnia and craving, and among those who stayed in the programme past the first two weeks the abstinence rate at three months was 47.8 percent against 15.2 percent on placebo. The paper calls itself a pilot study, the dose was deliberately kept low to limit liver risk and the figures come from one site.
Long-standing approved use in China, reviewedPatients treated under the Chinese drug name RotundineSedation is described as appearing above roughly 100 mg per 70 kg of body weight, which is why trial doses sit below thatNot statedOralIn use as an approved medicine for more than 40 yearsNot describedFuture Medicinal Chemistry (PubMed Central)2012
This review sets out the case for developing L-THP as an addiction medicine and notes it is already approved and marketed in China as Rotundine or Rotundin for analgesia and sedation. It is candid about the problem that the sedative and reward-blunting effects of a dopamine antagonist can interfere with the very behaviours being measured, and about the regulatory work a United States approval would need.
Trial in schizophrenia63 participants randomised to L-THP or placebo30 mg twice dailyTwice dailyOralThe registered study ran from September 2014Not describedClinicalTrials.gov2014
Registered at the Maryland Psychiatric Research Center on the reasoning that L-THP is a dopamine antagonist with anti-inflammatory and antiprotozoal activity, with positive and negative symptom improvement as the primary outcome. The record is marked completed with no results posted, so the dose and design are public but the findings are not.
Multi-ingredient pain formula trial27 healthy adults aged 22 to 63 with unresolved non-pathological aches, in a crossover design2 capsules daily of a 10-ingredient formula containing L-THP; the paper does not state the L-THP amountDailyOral capsulesThree 7-day periods separated by 7-day washouts7-day washout between periodsNutrients (PubMed Central)2020
The formula scored better than 325 mg of acetaminophen on worst-pain scores and reduced musculoskeletal discomfort totals after a week. L-THP is only one of ten ingredients alongside B vitamins, white willow bark, Angelica root, acetyl L-carnitine, caffeine, L-theanine and benfotiamine, so nothing in this result can be attributed to L-THP on its own, and an employee of the product's maker was an author.
Preclinical1 row
Reinstatement of cocaine seeking in ratsMale Sprague-Dawley rats trained to self-administer cocaine, then extinguished3.0 or 10.0 mg/kgSingle dose, one hour before each testOral gavageSingle-dose test sessionsNot applicableDrug and Alcohol Dependence (PubMed Central)2011
Both doses blocked the return of drug-seeking triggered by a cocaine challenge, by footshock stress and by drug-associated cues. At 10 mg/kg the animals also responded less for food, which suggests general sedation, while at 3 mg/kg they did not, so the lower dose is the cleaner result. These are rat amounts given by gavage and they do not convert to a human dose.
Sources for this section (8)
  1. Pharmacokinetics and Safety Assessment of l-Tetrahydropalmatine in Cocaine Users: A Randomized, Double-Blind, Placebo-Controlled StudyJournal of Clinical Pharmacology (PubMed Central)2017Clinical
  2. Medication of l-tetrahydropalmatine significantly ameliorates opiate craving and increases the abstinence rate in heroin users: a pilot studyActa Pharmacologica Sinica (PubMed Central)2008Clinical
  3. l-tetrahydropalmatine: a potential new medication for the treatment of cocaine addictionFuture Medicinal Chemistry (PubMed Central)2012Clinical
  4. Treatment of Schizophrenia With L-tetrahydropalmatine (NCT02118610)ClinicalTrials.gov2014Clinical
  5. Pain Bloc-R Alleviates Unresolved, Non-Pathological Aches and Discomfort in Healthy AdultsNutrients (PubMed Central)2020Clinical
  6. Oral administration of levo-tetrahydropalmatine attenuates reinstatement of extinguished cocaine seeking by cocaine, stress or drug-associated cues in ratsDrug and Alcohol Dependence (PubMed Central)2011Preclinical

Plus 2 community resources (dosing guides, forum threads and vendor write-ups), reported above but not linked.

Overview

L-THP is the left-handed form of tetrahydropalmatine, an alkaloid from Corydalis and Stephania plants whose preparations have long been used for sedation and pain relief. Purified or synthetic L-THP has been sold in China as Rotundine for more than forty years as an analgesic and sedative, and its pharmacology is unusual for a plant compound: it blocks dopamine D1 and D2 receptors and also acts at D3, alpha-adrenergic and serotonin receptors. That profile drew interest in addiction medicine, and human studies have given 30 mg twice daily to cocaine users and four weeks of treatment to heroin users, alongside rat work showing it blocks cocaine-seeking triggered by drug, stress or cues.

What researchers are exploring

These themes describe recurring questions in published research. They are not claims of effectiveness or recommendations for use.

  • 1

    Cognitive & neural

    Neuroplasticity, cognition, stress and sleep models.

  • 2

    Safety and pharmacokinetics with a cocaine challenge

    The short course was safe and well tolerated, did not change cocaine's pharmacokinetics and did not change its acute cardiovascular effects, with no difference in side-effect counts against placebo. The authors chose.

  • 3

    Randomised trial in heroin dependence

    Four weeks of treatment reduced the severity of protracted withdrawal, including physical symptoms, mood, insomnia and craving, and among those who stayed in the programme past the first two weeks the abstinence rate.

  • 4

    Long-standing approved use in China, reviewed

    This review sets out the case for developing L-THP as an addiction medicine and notes it is already approved and marketed in China as Rotundine or Rotundin for analgesia and sedation. It is candid about the problem.

  • 5

    Trial in schizophrenia

    Registered at the Maryland Psychiatric Research Center on the reasoning that L-THP is a dopamine antagonist with anti-inflammatory and antiprotozoal activity, with positive and negative symptom improvement as the.

  • 6

    Multi-ingredient pain formula trial

    The formula scored better than 325 mg of acetaminophen on worst-pain scores and reduced musculoskeletal discomfort totals after a week. L-THP is only one of ten ingredients alongside B vitamins, white willow bark.

What the current evidence can support

Study models remain visible so laboratory and animal findings are not mistaken for established human outcomes.

  • Human

    Human studies and registrations

    5 protocol rows on this page come from human trials, trial registrations, regulator labels or reviews of human data. Approval status and populations are stated per row.

  • Animal

    Preclinical models

    1 protocol row describe animal, cell or toxicology work. Amounts from these rows do not translate to people.

  • Not graded

    Community-reported use

    1 row record what blogs, vendor write-ups or forums describe for L-THP. None has been verified against primary literature.

Chemistry identifiers

Sequence, synonyms and registry identifiers as recorded in PubChem, the National Library of Medicine's open chemistry database. Formula, mass and CAS number are summarized at the top of the page.

Also listed as

levo-Tetrahydropalmatine, (-)-Tetrahydropalmatine, Rotundine, (-)-rotundine, Gindarine, Hyndarine, (-)-Corydalis B, UNII 3X69CO5I79

InChIKey

AEQDJSLRWYMAQI-KRWDZBQOSA-N

IUPAC name

(13aS)-2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline

Limitations and unknowns

Important limitations

  • Every amount on this page is a report of what a source describes, not a protocol to follow.
  • Preclinical and community rows do not establish a human amount, schedule or route.
  • Formulation, purity and presentation vary by supplier and are not covered by the dossier.

Sources

7 curated references, each with its journal, year and study model, plus 2 community resources reported but not linked.

  1. (-)-Tetrahydropalmatine (PubChem CID 72301)PubChem, National Library of Medicine2026Not graded
  2. Pharmacokinetics and Safety Assessment of l-Tetrahydropalmatine in Cocaine Users: A Randomized, Double-Blind, Placebo-Controlled StudyJournal of Clinical Pharmacology (PubMed Central)2017Human
  3. Medication of l-tetrahydropalmatine significantly ameliorates opiate craving and increases the abstinence rate in heroin users: a pilot studyActa Pharmacologica Sinica (PubMed Central)2008Human
  4. l-tetrahydropalmatine: a potential new medication for the treatment of cocaine addictionFuture Medicinal Chemistry (PubMed Central)2012Human
  5. Treatment of Schizophrenia With L-tetrahydropalmatine (NCT02118610)ClinicalTrials.gov2014Human
  6. Pain Bloc-R Alleviates Unresolved, Non-Pathological Aches and Discomfort in Healthy AdultsNutrients (PubMed Central)2020Human
  7. Oral administration of levo-tetrahydropalmatine attenuates reinstatement of extinguished cocaine seeking by cocaine, stress or drug-associated cues in ratsDrug and Alcohol Dependence (PubMed Central)2011Animal