CHEBI:142029 - rauvomitine

ChEBI IDCHEBI:142029
ChEBI Namerauvomitine
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DefinitionA monoterpenoid indole alkaloid with formula C30H34N2O5.
Last Modified2 October 2018
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FormulaC30H34N2O5
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Average Mass502.611
Monoisotopic Mass502.24677
SMILES[H][C@@]12[C@@H]3C[C@]4(c5ccccc5N(C)[C@@]4([H])[C@]4([H])C[C@H]1/C(=C\C)CN34)[C@@H]2OC(=O)c1cc(OC)c(OC)c(OC)c1
InChIInChI=1S/C30H34N2O5/c1-6-16-15-32-21-13-18(16)25-22(32)14-30(19-9-7-8-10-20(19)31(2)27(21)30)28(25)37-29(33)17-11-23(34-3)26(36-5)24(12-17)35-4/h6-12,18,21-22,25,27-28H,13-15H2,1-5H3/b16-6-/t18-,21-,22-,25-,27-,28+,30+/m0/s1
InChIKeyJHWXXJLDNKFDNH-OGWDYSPGSA-N
Species of MetaboliteComponentSourceComments
Rauvolfia obscura (IPNI:81602-1) root (BTO:0001188) PubMed (948531)
Rauvolfia vomitoria (ncbitaxon:403115)
fruit (BTO:0000486) Article (Iwu, M.M. (1980) Alkaloids of Rauwolfia vomitoria fruits. Planta. Med., 40, 13-16.)
root (BTO:0001188) PubMed (905421)
Roles Classification
Chemical Role:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Biological Roles:
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.
ChEBI Ontology
Outgoing Relation(s)
rauvomitine (CHEBI:142029) has functional parent 3,4,5-trimethoxybenzoic acid (CHEBI:454991)
rauvomitine (CHEBI:142029) has role plant metabolite (CHEBI:76924)
rauvomitine (CHEBI:142029) is a benzoate ester (CHEBI:36054)
rauvomitine (CHEBI:142029) is a monoterpenoid indole alkaloid (CHEBI:65323)
rauvomitine (CHEBI:142029) is a organic heterohexacyclic compound (CHEBI:51914)
rauvomitine (CHEBI:142029) is a tertiary amino compound (CHEBI:50996)
IUPAC Name 
(16ξ,17R,19E)-ajmal-19-en-17-yl 3,4,5-trimethoxybenzoate
Synonyms  Source
(−)-rauvomitineKNApSAcK
rauvomitinChemIDplus
Manual XrefsDatabases
C00024334KNApSAcK
Registry NumbersSources
CAS:466-57-9KNApSAcK
CAS:466-57-9ChemIDplus
Citations