CHEBI:74867 - β-peltatin

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ChEBI Name β-peltatin
ChEBI ID CHEBI:74867
ChEBI ASCII Name beta-peltatin
Definition An organic heterotetracyclic compound that is α-peltatin in which the phenolic hydroxy group of the 4-hydroxy-3,5-dimethoxyphenyl substitutent had been converted into the corresponding methyl ether.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C22H22O8
Net Charge 0
Average Mass 414.40530
Monoisotopic Mass 414.13147
InChI InChI=1S/C22H22O8/c1-25-14-5-10(6-15(26-2)20(14)27-3)17-12-7-16-21(30-9-29-16)19(23)13(12)4-11-8-28-22(24)18(11)17/h5-7,11,17-18,23H,4,8-9H2,1-3H3/t11-,17+,18-/m0/s1
InChIKey HLBPOYVRLSXWJJ-PDSMFRHLSA-N
SMILES [H][C@]12COC(=O)[C@]1([H])[C@H](c1cc(OC)c(OC)c(OC)c1)c1cc3OCOc3c(O)c1C2
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.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing β-peltatin (CHEBI:74867) has functional parent α-peltatin (CHEBI:10324)
β-peltatin (CHEBI:74867) has role antineoplastic agent (CHEBI:35610)
β-peltatin (CHEBI:74867) has role plant metabolite (CHEBI:76924)
β-peltatin (CHEBI:74867) is a γ-lactone (CHEBI:37581)
β-peltatin (CHEBI:74867) is a furonaphthodioxole (CHEBI:50307)
β-peltatin (CHEBI:74867) is a lignan (CHEBI:25036)
β-peltatin (CHEBI:74867) is a organic heterotetracyclic compound (CHEBI:38163)
β-peltatin (CHEBI:74867) is a phenols (CHEBI:33853)
IUPAC Name
(5R,5aR,8aR)-10-hydroxy-5-(3,4,5-trimethoxyphenyl)-5,8,8a,9-tetrahydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(5aH)-one
Synonyms Sources
(−)-β-peltatin ChEBI
AI3-50532 ChemIDplus
β-peltatin A ChemIDplus
BRN 0099483 ChemIDplus
NSC 24819 ChemIDplus
peltatin methyl ether ChemIDplus
Manual Xrefs Databases
CPD-8960 MetaCyc
LSM-19963 LINCS
View more database links
Registry Numbers Types Sources
518-29-6 CAS Registry Number ChemIDplus
99483 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
12943762 PubMed citation Europe PMC
12991048 PubMed citation Europe PMC
14380575 PubMed citation Europe PMC
14774701 PubMed citation Europe PMC
14774702 PubMed citation Europe PMC
18876991 PubMed citation Europe PMC
3430175 PubMed citation Europe PMC
Last Modified
28 April 2020