Structure via PubChem · Public domain (PubChem)
vindoline
Sign in to saveVindoline is a chemical precursor to vinblastine. Vindoline is formed through biosynthesis from Tabersonine.
Chemical data
- Formula
- C25H32N2O6
- Molecular weight
- 456.5 g/mol
- IUPAC name
- methyl (1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-10-hydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,13-tetraene-10-carboxylate
- SMILES
- CC[C@@]12C=CCN3[C@@H]1[C@]4(CC3)[C@H]([C@]([C@@H]2OC(=O)C)(C(=O)OC)O)N(C5=C4C=CC(=C5)OC)C
- InChIKey
- CXBGOBGJHGGWIE-ACSXSLCXSA-N
- XLogP
- 1.3
- Polar surface area
- 88.5 Ų
- H-bond donors
- 1
- H-bond acceptors
- 8
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Mass
- 456.226
Show 5 more facts
- found in taxon
- Lonicera morrowii
- chemical formula
- C₂₅H₃₂N₂O₆
- isomeric SMILES
- CC[C@@]12C=CCN3[C@@H]1[C@]4(CC3)[C@H]([C@]([C@@H]2OC(=O)C)(C(=O)OC)O)N(C5=C4C=CC(=C5)OC)C
- canonical SMILES
- CCC12C=CCN3C1C4(CC3)C(C(C2OC(=O)C)(C(=O)OC)O)N(C5=C4C=CC(=C5)OC)C
- Commons category
- Vindoline
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- See also
- References
Vindoline is a chemical precursor to vinblastine. Vindoline is formed through biosynthesis from Tabersonine.
==See also== Lochnericine Dimerization of catharanthine and vindoline
Excerpted from Wikipedia’s “vindoline” article, available under the CC BY-SA 4.0 licence.