L-Tetrahydropalmatine (L-THP)
L-Tetrahydropalmatine (L-THP) is the levorotatory enantiomer of tetrahydropalmatine, a tetracyclic protoberberine-type isoquinoline alkaloid isolated from plants of the Corydalis and Stephania genera. As an isolated stereoisomer, L-THP is utilized in receptor-based research due to the distinct pharmacological activity of the (−)-enantiomer compared to its racemate or the (+)-enantiomer. It is primarily used as a multi-receptor probe in monoamine receptor research.
Technical Specifications
| Property | Specification |
| Product Name | L-Tetrahydropalmatine (L-THP) |
| IUPAC Name | (−)-Tetrahydropalmatine |
| CAS Number | 2934-97-6 |
| Molecular Formula | C21H25NO4 |
| Molecular Weight | 355.43 g/mol |
| Chemical Class | Protoberberine isoquinoline alkaloid |
| Appearance | White to off-white crystalline powder |
| Solubility | Poor in water; soluble in DMSO and organic solvents |
| Assay Purity | Established by HPLC-UV with MS confirmation |
Pharmacology & Research Context
L-THP is characterized by broad, moderate-affinity engagement across multiple monoamine receptor families, acting as an antagonist at dopamine D1, D2, and D3 receptors, with additional affinity at α-adrenergic and serotonergic sites. Consequently, it functions effectively as a multi-receptor probe in in vitro assays rather than a highly selective tool compound.
Safety Warning: Hepatotoxicity
L-THP is a documented cause of drug-induced liver injury. It has been associated with cases of acute hepatitis and, in historical contexts involving traditional preparations, serious toxicological events. L-THP is not FDA-approved for any indication. Investigators should treat this compound as a known hepatotoxin and utilize appropriate laboratory safety protocols when handling.
Research Applications
L-THP is utilized for its role in investigating dopaminergic signaling and monoamine receptor dynamics.
Primary fields of in vitro laboratory investigation include:
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Receptor Binding Studies: Mapping affinity profiles across dopamine, adrenergic, and serotonergic receptor families.
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Monoamine System Probing: Utilizing the compound as a multi-receptor agent in neurobiological cell models.
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Structural/Enantiomeric Analysis: Comparative research between L-THP, the racemate, and the (+)-enantiomer.
Storage & Handling Guidelines
To maintain the structural integrity and enantiomeric purity of the compound:
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Storage Environment: Store in a dry, cool environment protected from light.
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Solvent Preparation: Due to poor aqueous solubility, prepare stock solutions in DMSO or other suitable organic solvents.
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Analytical Documentation: Refer to the lot-specific Certificate of Analysis (COA) for purity and enantiomeric composition data.
Research Use Disclaimer
Research Use Only Disclaimer: This product is developed and distributed strictly as a Research Use Only (RUO) laboratory reference chemical intended exclusively for non-clinical analytical and scientific investigation. It is not an FDA-approved drug, food, cosmetic, or dietary supplement, and is strictly prohibited for human or animal consumption. Kimera Chems supplies these high-purity research materials solely to accredited institutional laboratories and qualified scientific investigators.
| CAS Number | 483-14-7 |
| Other Names | L-THP, Rotundine, 5,8,13,13aS-tetrahydro-2,3,9,10-tetramethoxy-6H-dibenzo[a,g]quinolizine |
| IUPAC Name | (13aS)-2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline |
| Molecular Formula | C21H25NO4 |
| Molecular Weight | 355.434 g/mol |




