CHEBI:141968 - caracurine VII

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ChEBI Name caracurine VII
ChEBI ID CHEBI:141968
Definition A monoterpenoid indole alkaloid with formula C19H22N2O2, isolated from several species of Strychnos.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Mark Williams
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Formula C19H22N2O2
Net Charge 0
Average Mass 310.391
Monoisotopic Mass 310.16813
InChI InChI=1S/C19H22N2O2/c22-18-16-12-9-15-19(6-7-21(15)10-11(12)5-8-23-18)13-3-1-2-4-14(13)20-17(16)19/h1-5,12,15-18,20,22H,6-10H2/t12-,15-,16+,17-,18+,19+/m0/s1
InChIKey UFUDXCDPABDFHK-SRCYXDNASA-N
SMILES C1=CC=C2C(=C1)[C@]34CCN5CC6=CCO[C@H]([C@]([C@]6(C[C@@]35[H])[H])([C@@]4(N2)[H])[H])O
Metabolite of Species Details
Strychnos dolichothyrsa (IPNI:547167-1) Found in bark (BTO:0001301). See: PubMed
Strychnos matopensis (NCBI:txid1040897) Found in root (BTO:0001188). See: Massiot, G et al. Alkaloids from roots of Strychnos matopensis (1988). Phytochemistry, Vol 27(10), p 3293-3304.
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
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ChEBI Ontology
Outgoing caracurine VII (CHEBI:141968) has role plant metabolite (CHEBI:76924)
caracurine VII (CHEBI:141968) is a monoterpenoid indole alkaloid (CHEBI:65323)
caracurine VII (CHEBI:141968) is a organic heterohexacyclic compound (CHEBI:51914)
caracurine VII (CHEBI:141968) is a primary alcohol (CHEBI:15734)
caracurine VII (CHEBI:141968) is a tertiary amino compound (CHEBI:50996)
IUPAC Name
(17R)-19,20-didehydro-17,18-epoxycuran-17-ol
Synonyms Sources
1-deacetyldiaboline ChemIDplus
caracurin VII ChEBI
caracurine ChemIDplus
caracurine VII ChemIDplus
deacetyldiaboline ChemIDplus
desacetyldiaboline ChEBI
Wieland-Gumlich aldehyde ChemIDplus
Manual Xref Database
Wieland-Gumlich_aldehyde Wikipedia
View more database links
Registry Numbers Types Sources
43170 Reaxys Registry Number Reaxys
466-85-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10807177 PubMed citation Europe PMC
15647330 PubMed citation Europe PMC
17402076 PubMed citation Europe PMC
29711638 PubMed citation Europe PMC
Last Modified
13 September 2018