(Q105374544)

English

7-hydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

chemical compound

In more languages

Statements

type of chemical entity

0 references

1 reference

based on heuristic

inferred from SMILES

7-hydroxy-2-(4-hydroxyphenyl)-5-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

1 reference

based on heuristic

inferred from SMILES

432.10564684 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

Apigenin 5-O-beta-D-glucopyranoside

1 reference

based on heuristic

inferred from InChI

Apigenin 5-O-glucoside

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₁H₂₀O₁₀

0 references

canonical SMILES

O=C1C=C(OC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O)=C12)C=4C=CC(O)=CC4

0 references

isomeric SMILES

O=c1cc(-c2ccc(O)cc2)oc2cc(O)cc(O[C@@H]3O[C@@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c12

0 references

Cephalotaxus harringtonii var. harringtonii

1 reference

Inhibitors of osteoclast differentiation from Cephalotaxus koreana

1 reference

Comprehensive profiling and natural variation of flavonoids in rice

Capsicum annuum

1 reference

Integrative analysis of metabolome and transcriptome reveals the mechanism of color formation in pepper fruit (Capsicum annuum L.).

Identifiers

InChI=1S/C21H20O10/c22-8-16-18(26)19(27)20(28)21(31-16)30-15-6-11(24)5-14-17(15)12(25)7-13(29-14)9-1-3-10(23)4-2-9/h1-7,16,18-24,26-28H,8H2/t16-,18+,19-,20+,21+/m0/s1

0 references

ZFPMFULXUJZHFG-JOZSIVFUSA-N

0 references

1 reference

17 September 2022

based on heuristic

inferred from InChIKey

Sitelinks

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