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CHEBI:27566 - 6-prenylnaringenin

ChEBI IDCHEBI:27566
ChEBI Name6-prenylnaringenin
Stars
DefinitionA trihydroxyflavanone having a structure of naringenin prenylated at C-6.
Secondary ChEBI IDsCHEBI:2234, CHEBI:20756
Last Modified6 February 2023
DownloadsMolfile
FormulaC20H20O5
Net Charge0
Average Mass340.375
Monoisotopic Mass340.13107
SMILESCC(C)=CCc1c(O)cc2c(c1O)C(=O)C[C@@H](c1ccc(O)cc1)O2
InChIInChI=1S/C20H20O5/c1-11(2)3-8-14-15(22)9-18-19(20(14)24)16(23)10-17(25-18)12-4-6-13(21)7-5-12/h3-7,9,17,21-22,24H,8,10H2,1-2H3/t17-/m0/s1
InChIKeyYHWNASRGLKJRJJ-KRWDZBQOSA-N
Roles Classification
Biological Role:
T-type calcium channel blocker  Any agent that interferes with the activity of T-type calcium channels.
ChEBI Ontology
Outgoing Relation(s)
6-prenylnaringenin (CHEBI:27566) has functional parent (S)-naringenin (CHEBI:17846)
6-prenylnaringenin (CHEBI:27566) has role T-type calcium channel blocker (CHEBI:194338)
6-prenylnaringenin (CHEBI:27566) is a (2S)-flavan-4-one (CHEBI:140377)
6-prenylnaringenin (CHEBI:27566) is a 4'-hydroxyflavanones (CHEBI:140331)
6-prenylnaringenin (CHEBI:27566) is a trihydroxyflavanone (CHEBI:38739)
Synonyms  Source
(2S)-2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-6-(3-methyl-2-butenyl)-4H-1-benzopyran-4-oneChemIDplus
sophoraflavanone BChEBI
Manual XrefsDatabases
C00000997KNApSAcK
Registry NumbersSources
Reaxys:6233280Reaxys
CAS:68236-13-5ChemIDplus
Citations