CHEBI:49212 - (−)-syringaresinol

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ChEBI Name (−)-syringaresinol
ChEBI ASCII Name (-)-syringaresinol
Definition The (7β,7'β,8β,8'β)-stereoisomer of syringaresinol.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C22H26O8
Net Charge 0
Average Mass 418.43704
Monoisotopic Mass 418.16277
InChI InChI=1S/C22H26O8/c1-25-15-5-11(6-16(26-2)19(15)23)21-13-9-30-22(14(13)10-29-21)12-7-17(27-3)20(24)18(8-12)28-4/h5-8,13-14,21-24H,9-10H2,1-4H3/t13-,14-,21+,22+/m1/s1
SMILES [H][C@@]12CO[C@@H](c3cc(OC)c(O)c(OC)c3)[C@]1([H])CO[C@H]2c1cc(OC)c(O)c(OC)c1
Metabolite of Species Details
Garcia parviflora (IPNI:107401-2) Found in leaf (BTO:0000713). MeOH extract of air-dried, powdered branch and leaves See: PubMed
Garcia parviflora (IPNI:107401-2) Found in branch (BTO:0000148). MeOH extract of air-dried, powdered branch and leaves See: PubMed
Sinocalamus affinis (IPNI:421970-1) Found in stem (BTO:0001300). 95% Ethanolic extract of skin-removed, air-dried, powdered stems. See: PubMed
Machilus robusta (NCBI:txid460780) Found in bark (BTO:0001301). 95%aqueous EtOH extract of air-dried bark See: PubMed
Roles Classification
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.
(via syringaresinol )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (−)-syringaresinol (CHEBI:49212) is a syringaresinol (CHEBI:49211)
(−)-syringaresinol (CHEBI:49212) is enantiomer of (+)-syringaresinol (CHEBI:47)
Incoming (−)-syringaresinol O,O'-bis(β-D-glucoside) (CHEBI:2375) has functional parent (−)-syringaresinol (CHEBI:49212)
(+)-syringaresinol (CHEBI:47) is enantiomer of (−)-syringaresinol (CHEBI:49212)
Registry Numbers Types Sources
6577407 Reaxys Registry Number Reaxys
6577407 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
20958014 PubMed citation Europe PMC
21469695 PubMed citation Europe PMC
21627109 PubMed citation Europe PMC
Last Modified
29 January 2015