Structure via PubChem · Public domain (PubChem)
lobelanine
Sign in to saveLobelanine is a chemical precursor in the biosynthesis of lobeline.
In the Vinony graph
Within Vinony's link graph, lobelanine is referenced by 4 other articles, and connects out to digital object identifier, chemical formula and alkaloid.
It is catalogued under topics including Biosynthesis, Chembox image size set and Piperidine alkaloids.
Its subject is documented across 5 Wikipedia language editions.
Chemical data
- Formula
- C22H25NO2
- Molecular weight
- 335.4 g/mol
- IUPAC name
- 2-[(2R,6S)-1-methyl-6-phenacylpiperidin-2-yl]-1-phenylethanone
- SMILES
- CN1[C@H](CCC[C@H]1CC(=O)C2=CC=CC=C2)CC(=O)C3=CC=CC=C3
- InChIKey
- IDEMKXUAULKYJV-BGYRXZFFSA-N
- XLogP
- 3.9
- Polar surface area
- 37.4 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Mass
- 335.188529
Show 4 more facts
- found in taxon
- Lobelia siphilitica
- chemical formula
- C₂₂H₂₅NO₂
- canonical SMILES
- CN1C(CCCC1CC(=O)C2=CC=CC=C2)CC(=O)C3=CC=CC=C3
- isomeric SMILES
- CN1[C@H](CCC[C@H]1CC(=O)C2=CC=CC=C2)CC(=O)C3=CC=CC=C3
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Lobelanine is a chemical precursor in the biosynthesis of lobeline.
==References==
Excerpted from Wikipedia’s “lobelanine” article, available under the CC BY-SA 4.0 licence.