CHEBI:142229 - (2R)-2-hydroxynaringenin

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ChEBI Name (2R)-2-hydroxynaringenin
ChEBI ID CHEBI:142229
ChEBI ASCII Name (2R)-2-hydroxynaringenin
Definition A 2,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one that has (R) configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C15H12O6
Net Charge 0
Average Mass 288.253
Monoisotopic Mass 288.06339
InChI InChI=1S/C15H12O6/c16-9-3-1-8(2-4-9)15(20)7-12(19)14-11(18)5-10(17)6-13(14)21-15/h1-6,16-18,20H,7H2/t15-/m1/s1
InChIKey NFENYLPEYDNIMO-OAHLLOKOSA-N
SMILES O1C2=C(C(C[C@@]1(C3=CC=C(C=C3)O)O)=O)C(=CC(=C2)O)O
Metabolite of Species Details
Ziziphus jujuba var. sp.nosa (NCBI:txid714518) Found in root (BTO:0001188). See: Yue-Juan Meng, Yu-Wei Zhang, Hong-Yu Jiang, Yong-Li Bao, Yin Wu, Lu-Guo Sun, Chun-Lei Yu, Yan-Xin Huang and Yu-Xin Li. Chemical constituents from the roots of Zizyphus jujuba Mill. var. spinosa (2013). Biochemical Systematics and Ecology, vol 50, p 182-186.
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 2,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (2R)-2-hydroxynaringenin (CHEBI:142229) has functional parent (R)-naringenin (CHEBI:50201)
(2R)-2-hydroxynaringenin (CHEBI:142229) has role plant metabolite (CHEBI:76924)
(2R)-2-hydroxynaringenin (CHEBI:142229) is a 2,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one (CHEBI:142230)
(2R)-2-hydroxynaringenin (CHEBI:142229) is enantiomer of (2S)-2-hydroxynaringenin (CHEBI:141994)
Incoming (2S)-2-hydroxynaringenin (CHEBI:141994) is enantiomer of (2R)-2-hydroxynaringenin (CHEBI:142229)
IUPAC Name
(2R)-2,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one
Synonyms Sources
(2R)-2-hydroxynaringenin ChEBI
(R)-2-hydroxynaringenin ChEBI
Registry Number Type Source
33237761 Reaxys Registry Number Reaxys
Last Modified
20 September 2018