Structure via PubChem · Public domain (PubChem)
veracevine
Sign in to saveAlso known as Cevane-3-beta,4-beta,12,14,16-beta,17,20-heptol, 4,9-epoxy-, Veracevin, Protocevin, Protocevine, 4,9-epoxycevane-3beta,4beta,12,14,16beta,17,20-heptol
Veracevine is an alkaloid that occurs in the seeds of Schoenocaulon officinale. It is used as an insecticide in veterinary medicine.
In the Vinony graph
Within Vinony's link graph, veracevine is referenced by 206 other articles, and connects out to International Standard Book Number, chemical formula and veterinary medicine.
Vinony files it under Chembox image size set, Insecticides and Isoquinoline alkaloids.
Its subject is documented across 8 Wikipedia language editions.
Chemical data
- Formula
- C27H43NO8
- Molecular weight
- 509.6 g/mol
- IUPAC name
- (1R,2S,6S,9S,10R,11S,12S,14R,15S,18S,19S,22S,23S,25R)-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosane-1,10,11,12,14,22,23-heptol
- SMILES
- C[C@H]1CC[C@H]2[C@@]([C@]3([C@H](C[C@]4([C@@H]5CC[C@H]6[C@]7([C@]5(C[C@]4([C@@H]3CN2C1)O)O[C@@]6([C@H](CC7)O)O)C)O)O)O)(C)O
- InChIKey
- MZHXYVMEVBEFAL-XXFAKQOHSA-N
- XLogP
- -1.2
- Polar surface area
- 154 Ų
- H-bond donors
- 7
- H-bond acceptors
- 9
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 509.298867
Show 3 more facts
- canonical SMILES
- CC1CCC2C(C3(C(CC4(C5CCC6C7(C5(CC4(C3CN2C1)O)OC6(C(CC7)O)O)C)O)O)O)(C)O
- chemical formula
- C₂₇H₄₃NO₈
- isomeric SMILES
- C[C@H]1CC[C@H]2[C@@]([C@]3([C@H](C[C@]4([C@@H]5CC[C@H]6[C@]7([C@]5(C[C@]4([C@@H]3CN2C1)O)O[C@@]6([C@H](CC7)O)O)C)O)O)O)(C)O
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- See also
- References
Veracevine is an alkaloid that occurs in the seeds of Schoenocaulon officinale. It is used as an insecticide in veterinary medicine.
== See also == Veratridine, a related alkaloid
Excerpted from Wikipedia’s “veracevine” article, available under the CC BY-SA 4.0 licence.