8-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]-7-hydroxy-2-(4-hydroxyphenyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

8-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]-7-hydroxy-2-(4-hydroxyphenyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

SPWIYFDXMWFJMA-UHFFFAOYSA-N CHEBI:182736 0 Reactome links 1 studies

Metabolite details

Identifier: SPWIYFDXMWFJMA-UHFFFAOYSA-N
InChI Key: SPWIYFDXMWFJMA-UHFFFAOYSA-N
IUPAC name: 8-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]-7-hydroxy-2-(4-hydroxyphenyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Preferred name: 8-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]-7-hydroxy-2-(4-hydroxyphenyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
INN name: —
Synonym: —
ChEBI: CHEBI:182736

Reactome pathways

No Reactome pathways listed for this metabolite.

Observed in studies

Distinct metabolic profiling is correlated with bisexual flowers formation resulting from exogenous ethephon induction in melon (<i>Cucumis melo</i> L.)

Observed in differential profiles

Control_vs_Ethephon_Treatment