Luteolin 7-rutinoside (Q104394905)

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

1 reference

luteolin 7-rutinoside

1 reference

mass

594.15847026 dalton

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3',4',5-Trihydroxy-7-[[6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-galactopyranosyl]oxy]flavone

stereoisomer of

2 references

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

2 references

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

1 reference

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

1 reference

chemical formula

C₂₇H₃₀O₁₅

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canonical SMILES

O=C1C=C(OC2=CC(OC3OC(COC4OC(C)C(O)C(O)C4O)C(O)C(O)C3O)=CC(O)=C12)C=5C=CC(O)=C(O)C5

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isomeric SMILES

C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](Oc3cc(O)c4c(=O)cc(-c5ccc(O)c(O)c5)oc4c3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O

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found in taxon

Sonchus luxurians

1 reference

A chemosystematic study of the phenolics of Sonchus

Cynara cardunculus var. scolymus

1 reference

Characterization of Violetto di Toscana, a typical Italian variety of artichoke (Cynara scolymus L.)

Mentha piperita piperita

2 references

Analysis and Distribution of Flavonoid Glycosides and Rosmarinic Acid in 40 Mentha x piperita Clones

Phenolic fingerprint of peppermint leaves

Ammoides pusilla

1 reference

Flavonoid Glycosides from Ammoides pusilla

Biebersteinia orphanidis

1 reference

A distinctive flavonoid chemistry for the anomalous genus Biebersteinia

Campanula persicifolia

2 references

Flavonoids ofCampanula persicifolia. I

Phenolic compounds of Campanula rotundifolia and C. persicifolia

Cremanthodium ellisii

1 reference

Nor-lignan and sesquiterpenes from Cremanthodium ellisii

Hieracium gymnocephalum

1 reference

A taraxasterol derivative and phenolic compounds from Hieracium gymnocephalum

Hololepis pedunculata

1 reference

Constituents of Hololepis pedunculata leaves and their trypanocidal activity

Lycianthes synanthera

1 reference

Three new furostanol saponins from the leaves of Lycianthes synanthera ("Chomte"), an edible Mesoamerican plant.

Meehania urticifolia

1 reference

New phenolic compounds from Meehania urticifolia

Phlomis nissolii

1 reference

Flavonoids from Phlomis nissolii

Pteris cretica

1 reference

A new flavone glycoside from the fern Pteris cretica

Saussurea medusa

1 reference

Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa

Setaria italica

1 reference

Flavone O- and C-glycosides from Setaria italica

Thymbra capitata

1 reference

A chemotaxonomic study of flavonoids in Thymbra capitata

Trachycarpus fortunei

2 references

Studies on the constituents of plamae plants. I. The constituents of Trachycarpus fortunei (Hook.) H. Wendl. 1.

Studies on the constituents of palmae plants. III. The constituents of Chamaerops humilis L. and Trachycarpus wagnerianus Becc.

Trachycarpus wagnerianus

1 reference

Studies on the constituents of palmae plants. III. The constituents of Chamaerops humilis L. and Trachycarpus wagnerianus Becc.

Cynara cardunculus scolymus

1 reference

Characterization of Violetto di Toscana, a typical Italian variety of artichoke (Cynara scolymus L.)

Sicyos edulis

1 reference

Study of flavonoids of Sechium edule (Jacq) Swartz (Cucurbitaceae) different edible organs by liquid chromatography photodiode array mass spectrometry

Artemisia argyi

1 reference

Extraction and identification of three major aldose reductase inhibitors from Artemisia montana.

Sechium edule

1 reference

Study of flavonoids of Sechium edule (Jacq) Swartz (Cucurbitaceae) different edible organs by liquid chromatography photodiode array mass spectrometry

Thymus capitatus

1 reference

A chemotaxonomic study of flavonoids in Thymbra capitata

Thymus martinezii

1 reference

A chemotaxonomic study of flavonoids in Thymbra capitata

Identifiers

InChI

InChI=1S/C27H30O15/c1-9-20(32)22(34)24(36)26(39-9)38-8-18-21(33)23(35)25(37)27(42-18)40-11-5-14(30)19-15(31)7-16(41-17(19)6-11)10-2-3-12(28)13(29)4-10/h2-7,9,18,20-30,32-37H,8H2,1H3/t9-,18+,20-,21+,22+,23-,24+,25+,26+,27+/m0/s1

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InChIKey

MGYBYJXAXUBTQF-FOBVWLSUSA-N

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CAS Registry Number

20633-84-5

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

1 reference

17 September 2022

SureChEMBL ID

SCHEMBL23870123

2 references