CHEBI:156445 - loline alkaloid

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ChEBI Name loline alkaloid
ChEBI ID CHEBI:156445
Definition A pyrrolizidine alkaloid that is hexahydro-1H-pyrrolizine carrying an exo-1-amino group at position 1 and an ether bridge between C-2 and C-7. It is a class of natural insecticides produced by fungal symbionts of Poaceae.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Martin Larralde
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Formula C7H10N2O
Net Charge 0
Average Mass (excl. R groups) 138.167
Monoisotopic Mass (excl. R groups) 138.07931
SMILES [H][C@]12[C@@H]3CCN1C[C@@H](O3)[C@@H]2N([*])[*]
Roles Classification
Biological Role(s): fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
mycotoxin
Poisonous substance produced by fungi.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
Application(s): insecticide
Strictly, a substance intended to kill members of the class Insecta. In common usage, any substance used for preventing, destroying, repelling or controlling insects.
antifeedant
A substance that prevents pests from feeding.
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ChEBI Ontology
Outgoing loline alkaloid (CHEBI:156445) has role antifeedant (CHEBI:22583)
loline alkaloid (CHEBI:156445) has role fungal metabolite (CHEBI:76946)
loline alkaloid (CHEBI:156445) has role insecticide (CHEBI:24852)
loline alkaloid (CHEBI:156445) has role mycotoxin (CHEBI:25442)
loline alkaloid (CHEBI:156445) is a cyclic ether (CHEBI:37407)
loline alkaloid (CHEBI:156445) is a organic heterotricyclic compound (CHEBI:26979)
loline alkaloid (CHEBI:156445) is a pyrrolizidine alkaloid (CHEBI:64948)
Incoming loline (CHEBI:156448) is a loline alkaloid (CHEBI:156445)
norloline (CHEBI:156447) is a loline alkaloid (CHEBI:156445)
Synonyms Sources
loline alkaloids ChEBI
lolines SUBMITTER
Manual Xref Database
Loline_alkaloid Wikipedia
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IND44135949 Agricola citation Europe PMC
Last Modified
15 April 2021