(Q105133322)

inferred from SMILES

mass

448.10056146 dalton

1 reference

2 references

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

2 references

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

2 references

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one

2 references

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

2 references

kaempferol 3-O-alpha-L-glucopyranoside

2 references

kaempferol 3-O-beta-D-allopyranoside

1 reference

1 reference

kaempferol 3-O-beta-L-glucopyranoside

1 reference

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

1 reference

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

1 reference

chemical formula

C₂₁H₂₀O₁₁

0 references

canonical SMILES

O=C1C(OC2OC(CO)C(O)C(O)C2O)=C(OC=3C=C(O)C=C(O)C13)C=4C=CC(O)=CC4

0 references

isomeric SMILES

O=c1c(O[C@@H]2O[C@H](CO)[C@H](O)[C@@H](O)[C@H]2O)c(-c2ccc(O)cc2)oc2cc(O)cc(O)c12

0 references

found in taxon

Sinoadina racemosa

1 reference

Six secoiridoid glucosides from Adina racemosa

Annona crassiflora

1 reference

Foliar flavonoids of Annonaceae from Brazil: taxonomic significance

Camellia sinensis

2 references

Medicinal flowers. XXII. Structures of chakasaponins V and VI, chakanoside I, and chakaflavonoside A from flower buds of Chinese tea plant (Camellia sinensis).

Bioactive saponins and glycosides. XXVIII. New triterpene saponins, foliatheasaponins I, II, III, IV, and V, from Tencha (the leaves of Camellia sinensis).

Campanula glomerata

1 reference

Natural acetylenes. Part XXIX. Polyacetylenes from the Campanulaceae plant family. Tetrahydropyranyl polyacetylenic alcohols from the clustered bellflower (Campanula glomerata L.)

Fagopyrum megacarpum

1 reference

Studies on nepalese crude drugs. XXVIII. Chemical constituents of Bhote Khair, the underground parts of Eskemukerjea megacarpum HARA.

Euphorbia

1 reference

Trifolin from Euphorbia condylocarpa

Hypericum erectum

1 reference

Chemical constituents of Hypericum erectum Thunb.

Lupinus albus

1 reference

Profiling changes in metabolism of isoflavonoids and their conjugates in Lupinus albus treated with biotic elicitor.

Monochaetum multiflorum

1 reference

A flavonol glycoside-lignan ester and accompanying acylated glucosides from Monochaetum multiflorum

Pelargonium reniforme

1 reference

O-Galloyl-C-glycosylflavones from Pelargonium reniforme

Silphium perfoliatum

1 reference

Kaempferol triosides from Silphium perfoliatum

Strychnos spinosa

1 reference

Secoiridoid glucosides from Strychnos spinosa

Dionaea muscipula

1 reference

Quercetin and kaempferol glycosides of Dionaea muscipula from in vitro cultures

Opuntia ficus-indica

1 reference

Secondary metabolites from Opuntia ficus-indica var. saboten.

Delphinium oliverianum

1 reference

Antileishmaniasis activity of flavonoids from Consolida oliveriana.

Ginkgo biloba

1 reference

High-Density Kinetic Analysis of the Metabolomic and Transcriptomic Response of Ginkgo biloba Flavonoids Biosynthesis to Selenium Treatments

Capsicum annuum

1 reference