Structure via PubChem · Public domain (PubChem)
میراگینین
Sign in to saveMitragynine is an indole-based alkaloid and is one of the main psychoactive constituents in the Southeast Asian plant Mitragyna speciosa, commonly known as kratom. It has also been researched for its use to potentially manage symptoms of opioid withdrawal. It is a partial agonist of the mu-opioid receptors; and as such can produce effects similar to those of classical opioids such as morphine.
Key facts
- Drug.bioavailability
- 21%
- Drug.drug_name
- Mitragynine
- Drug.image
- Mitragynine v2.svg
- Drug.image_class
- skin-invert-image
- Drug.image2
- Mitragynine molecule ball.png
- Drug.image_class2
- bg-transparent
- Drug.legal_AU
- S8
- Drug.legal_BR
- B1
- Drug.legal_CA
- Unscheduled
- Drug.legal_DE
- NPSG
- Drug.legal_NZ
- Unscheduled
- Drug.legal_UK
- PSA
- Drug.legal_US
- unscheduled
- Drug.legal_UN
- unscheduled
- Drug.legal_status
- In general legal for medical and research uses as a research chemical.
- Drug.routes_of_administration
- By mouth
- Drug.IUPAC_name
- methyl (16E)-9,17-dimethoxy-16,17-didehydro-20β-corynan-16-carboxylate
- Drug.metabolites
- 7-Hydroxymitragynine
via Wikipedia infobox
Chemical data
- Formula
- C23H30N2O4
- Molecular weight
- 398.5 g/mol
- IUPAC name
- methyl (E)-2-[(2S,3S,12bS)-3-ethyl-8-methoxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate
- SMILES
- CC[C@@H]1CN2CCC3=C([C@@H]2C[C@@H]1/C(=C\OC)/C(=O)OC)NC4=C3C(=CC=C4)OC
- InChIKey
- LELBFTMXCIIKKX-QVRQZEMUSA-N
- XLogP
- 3.4
- Polar surface area
- 63.8 Ų
- H-bond donors
- 1
- H-bond acceptors
- 5
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Has part
- oxygen
- Mass
- 398.221
Show 5 more facts
- chemical formula
- C₂₃H₃₀N₂O₄
- canonical SMILES
- CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=CC=C4)OC
- isomeric SMILES
- CC[C@@H]1CN2CCC3=C([C@@H]2C[C@@H]1/C(=C\OC)/C(=O)OC)NC4=C3C(=CC=C4)OC
- Commons category
- Mitragynine
- found in taxon
- Mitragyna speciosa
Sources (2)
via Wikidata · CC0