CHEBI:70215 - Dichotomide VII

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ChEBI Name Dichotomide VII
ChEBI ID CHEBI:70215
Definition A natural product found in Stellaria dichotoma var. lanceolata.
Stars This entity has been manually annotated by a third party.
Supplier Information
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Formula C20H21N3O8
Net Charge 0
Average Mass 431.39600
Monoisotopic Mass 431.13286
InChI InChI=1S/C20H21N3O8/c1-7(25)13-15-9(5-10(22-13)19(21)29)8-3-2-4-11(14(8)23-15)30-20-18(28)17(27)16(26)12(6-24)31-20/h2-5,12,16-18,20,23-24,26-28H,6H2,1H3,(H2,21,29)/t12-,16-,17+,18-,20-/m1/s1
InChIKey OWGHIJSRWBEFSS-GUPBPSBKSA-N
SMILES CC(=O)c1nc(cc2c3cccc(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)c3[nH]c12)C(N)=O
Metabolite of Species Details
Stellaria dichotoma var. lanceolata (IPNI:50920984-1) Found in root (BTO:0001188). Methanolic extract of air-dried, powdered roots See: PubMed
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing Dichotomide VII (CHEBI:70215) has role metabolite (CHEBI:25212)
Dichotomide VII (CHEBI:70215) is a harmala alkaloid (CHEBI:61379)
Citation Waiting for Citations Type Source
21090796 PubMed citation Europe PMC
Last Modified
22 September 2014
General Comment
2014-10-17 Suggested Classification: ISA:beta-carbolines(CHEBI:60834); ISA:hexose(CHEBI:18133); ISA:glycoside(CHEBI:24400); ISA:pyridinemonocarboxylic acid(CHEBI:26420); ISA:aromatic carboxylic acid(CHEBI:33859); ISA:indoles(CHEBI:24828); ISA:aromatic ketone(CHEBI:76224); ISA:aralkylamine(CHEBI:18000); ISA:oxanes(CHEBI:46942); ISA:benzenoid aromatic compound(CHEBI:33836); ISA:enol ether(CHEBI:47985); ISA:enone(CHEBI:51689); ISA:pyrroles(CHEBI:26455); ISA:enamine(CHEBI:47989); ISA:polyol(CHEBI:26191); ISA:carboxamide(CHEBI:37622); ISA:secondary alcohol(CHEBI:35681); ISA:organonitrogen compound(CHEBI:35352); ISA:acetal(CHEBI:59769); ISA:carboxylic acid(CHEBI:33575); ISA:primary alcohol(CHEBI:15734);