quinolizidine alkaloid
Let an agent describe quinolizidine alkaloids, their sources, structures and toxicity in general terms, and point to food safety guidance, without giving medical advice.
Bundle → Layer → Finding → Questions Filled
4 bundles · 8 layers · 8 findings · 16 questions
Compound Which alkaloid.
Identity
Name and identifiers.
Compound
Name and IDs.
- Which compound? provenance
- What are its identifiers? provenance
Structure
Skeleton type.
Structure
Type.
- Which structural type? provenance
- How many rings? measurement
Occurrence Sources.
Plants
Species.
Plant source
Species and part.
- Which plants contain it? provenance
- At what levels? measurement
Foods
Lupin products.
Food content
Measured alkaloids, method, units, fresh weight or dry matter, and the survey or source.
- What levels occur in foods? measurement
- From which survey? provenance
Toxicology Effects.
Effects
Mechanism.
Toxic effect
Effect and source.
- What effects are reported? provenance
- At what exposure? measurement
Guidance
Limits.
Guidance value
Value and body.
- Which guidance values exist? provenance
- From which assessment? provenance
Uses Pharmacology.
Medicines
Approved uses.
Medicine
Compound and approval.
- Which compounds are medicines? provenance
- Where approved? provenance
Agriculture
Breeding.
Breeding
Varieties.
- How are low-alkaloid varieties bred? provenance
- Which varieties? provenance
Classifiers Filled
- Family
- Thing Registry
- Category
- Physical world and living systems
- Entry kind
- thing
- Plane
- PHY
- Domain
- PHY.MAT
- Other names and narrower kinds
- 11-[(16-Hydroxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-17-yl)methyl]-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one, 11-[(16-Hydroxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-15-yl)methyl]-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one, Feruloyllupinine, octahydro-1H-quinolizin-1-ylmethyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate, 2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethyl 3-[3-methoxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]prop-2-enoate, 2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethyl 3-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate, Nupharolutine, [(3R,6S,9R,9aS)-6-(furan-3-yl)-9-methyl-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-3-yl]methanol, (3R,9S,9aR)-6-(furan-3-yl)-3,9-dimethyl-2,3,4,8,9,9a-hexahydro-1H-quinolizine, (16-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl) 1H-pyrrole-2-carboxylate, [(1S,2S,9aR)-2-hydroxy-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl 1H-pyrrole-2-carboxylate, [(1S,2S,4S,9S,10R,12R,13S)-12,13-dihydroxy-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] 1H-pyrrole-2-carboxylate
What it is Filled
A class of alkaloids containing a quinolizidine ring system, found mainly in legumes of the family Fabaceae, especially lupins (Lupinus) and related genera; examples include lupinine, sparteine, lupanine and cytisine.
Why it exists Filled
Let an agent describe quinolizidine alkaloids, their sources, structures and toxicity in general terms, and point to food safety guidance, without giving medical advice.
Distinguishing features Filled
- Bitter lupins contain high levels; sweet lupin varieties have low levels.
- Cytisine is used as a smoking cessation medicine in some countries.
- Debittering is needed before eating bitter lupin seeds.
What robots and AI may and may not do Filled
Must not
- give dosing advice
- advise eating raw bitter lupins
Only with a human decision
- suspected poisoning, which goes to poison centres
May
- describe chemistry and point to food safety guidance
Moral aspects Filled
- food safety
Who is affected
- consumers
- farmers
Owners Filled
Steward
nobody; a compound class
Master systems
- ChEBI
- PubChem
Links to other meta-models Filled
parent
- Q70702 - registry parent class
- Q76516005 - registry parent class
related
- alkaloid - chemistry
- lupin - plant source
- lupin poisoning - toxicity
contains
- quinolizidine ring - structure
What else AI and robots need to interact with it Filled
Identity and identifiers required Filled
- Vercy registry: vr.tr.quinolizidine-alkaloid
- Wikidata: Q76515995 (https://www.wikidata.org/wiki/Q76515995)
- ChEBI: CHEBI:26515 quinolizidine alkaloid class
- ChEBI or PubChem: per compound individual alkaloids
Direct properties not applicable Not applicable
Not applicable
A compound class: properties belong to each compound.
Recognition required Filled
- Appearance cannot establish identity or concentration; chromatography and mass spectrometry are used
- Pure compounds are typically crystalline solids or oils.
Capabilities and actions required Filled
- describe structures and examples
- describe occurrence in lupins
- explain food safety limits in general terms
- point to toxicology sources
Hazards and failure modes required Filled
- Anticholinergic poisoning from improperly debittered lupins
- Livestock poisoning
Standards and interfaces required Filled
- Food safety assessments of lupin alkaloids, such as the EFSA opinion (2019)
- National limits for alkaloids in lupin foods where set
Context of use required Filled
- Plant defence compounds; relevant to food safety of lupin products and to pharmacology.
- lupinine type
- sparteine and lupanine types
- cytisine type
- matrine type
Sources Filled
- Q76515995 - identity of the registry item, labels and sitelinks
- Quinolizidine alkaloids - class description
- Quinolizidine alkaloid - CHEBI:26515 - Chemical class identity and class-level identifier.
- Scientific opinion on quinolizidine alkaloids in feed and food, particularly lupins and lupin-derived products - 2019 assessment, structures, occurrence, analytical methods, bitter and sweet lupins, human and animal toxicity.
- Alkaloids and allergies: current data on health risks from lupin seeds in food - Variable alkaloid profiles and concentrations, analytical limitations and food-safety context.
- Cytisinicline (cytisine) - Cytisine's medicinal use for smoking cessation and its alternative name cytisinicline.
Open questions
- The registry merges individual compounds named by systematic names; they should be separate entries.
Machine files
Provenance
thing registry research (pass 2) · unreviewed
Built from: models/things/publications/thing-q76515995/spec.json