CHEBI:7638 - norswertianolin

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ChEBI Name norswertianolin
Definition A β-D-glucoside that is bellidin in which a β-D-glucopyranosyl residue is attached at position O-8. A natural product found particularly in Gentiana campestris and Gentiana germanica.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:65481
Supplier Information
Download Molfile XML SDF
Formula C19H18O11
Net Charge 0
Average Mass 422.33960
Monoisotopic Mass 422.08491
InChI InChI=1S/C19H18O11/c20-5-11-14(24)16(26)17(27)19(30-11)29-9-2-1-7(22)18-13(9)15(25)12-8(23)3-6(21)4-10(12)28-18/h1-4,11,14,16-17,19-24,26-27H,5H2/t11-,14-,16+,17-,19-/m1/s1
SMILES OC[C@H]1O[C@@H](Oc2ccc(O)c3oc4cc(O)cc(O)c4c(=O)c23)[C@H](O)[C@@H](O)[C@@H]1O
Metabolite of Species Details
Gentiana germanica (IPNI:368223-1) See: DOI
Gentiana ramosa (IPNI:368797-1) See: DOI
Swertia randaiensis (IPNI:371063-1) See: INDIAN J CHEM,1980,19B,10,929
Swertia japonica (NCBI:txid137129) See: DOI
Gentianella campestris (NCBI:txid49940) See: PubMed
Roles Classification
Biological Role(s): EC (acetylcholinesterase) inhibitor
An EC 3.1.1.* (carboxylic ester hydrolase) inhibitor that interferes with the action of enzyme acetylcholinesterase (EC, which helps breaking down of acetylcholine into choline and acetic acid.
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing norswertianolin (CHEBI:7638) has functional parent bellidin (CHEBI:65480)
norswertianolin (CHEBI:7638) has role EC (acetylcholinesterase) inhibitor (CHEBI:38462)
norswertianolin (CHEBI:7638) has role metabolite (CHEBI:25212)
norswertianolin (CHEBI:7638) is a β-D-glucoside (CHEBI:22798)
norswertianolin (CHEBI:7638) is a xanthones (CHEBI:51149)
4,6,8-trihydroxy-9-oxo-9H-xanthen-1-yl β-D-glucopyranoside
Synonyms Sources
8-(β-D-glucopyranosyloxy)-1,3,5-trihydroxy-9H-xanthen-9-one ChemIDplus
bellidin-8-O-β-D-glucopyranoside ChEBI
Manual Xrefs Databases
C00002971 KNApSAcK
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Registry Numbers Types Sources
1694897 Reaxys Registry Number Reaxys
54954-12-0 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
15490334 PubMed citation Europe PMC
18336006 PubMed citation Europe PMC
19771868 PubMed citation Europe PMC
21355239 PubMed citation Europe PMC
3482877 PubMed citation Europe PMC
3889613 PubMed citation Europe PMC
520863 Chinese Abstracts citation Europe PMC
Last Modified
28 July 2014
General Comment
2012-07-27 INDIAN J CHEM,1980,19B,10,929