(Q3564258)

English

luteolin 7-O-neohesperidoside

chemical compound

Veronicastroside
Scolymoside
7-((2-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-5-hydroxy-4H-1-benzopyran-4-one
Luteoline-7-rhamnoglucoside
Luteolin-7-rutinoside
Luteolin-7-O-rhamnoside
Lonicerin
Luteolin 7-O-neohesperidoside

In more languages

Statements

type of chemical entity

0 references

7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one

1 reference

based on heuristic

inferred from SMILES

7-O-Neohesperidosylluteolin

1 reference

based on heuristic

inferred from SMILES

594.15847±0 dalton

1 reference

language of work or name

Lonicerin (English)

6 October 2016

stereoisomer of

7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₇H₃₀O₁₅

1 reference

language of work or name

Lonicerin (English)

6 October 2016

canonical SMILES

CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O

1 reference

language of work or name

Lonicerin (English)

6 October 2016

isomeric SMILES

C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H]([C@H](O[C@H]2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O

1 reference

language of work or name

Lonicerin (English)

6 October 2016

Oenothera macrocarpa

1 reference

The Flavonoids of Oenothera Sect. Megapterium (Onagraceae)

Carex fraseriana

1 reference

Taxonomic implications of the flavonoids of Cymophyllus fraseri (Cyperaceae)

Asyneuma campanuloides

1 reference

Flavones and their glycosides in some plants of the family Campanulaceae

Achillea fragrantissima

1 reference

Volatiles of Achillea fragrantissima (Forssk.) Sch. Bip.

Achillea pannonica

1 reference

Flavone glycosides of some species of the genus Thymus

Artemisia montana

1 reference

Isolation of luteolin 7-O-rutinoside and esculetin with potential antioxidant activity from the aerial parts of Artemisia montana

Biebersteinia multifida

1 reference

Flavonoids of Biebersteinia multifida

Campanula persicifolia

2 references

Flavonoids ofCampanula persicifolia. I

Flavonoids ofCampanula persicifolia. I

1 reference

Flavonoids of Carduus nutans and C. acanthoides

Cornulaca monacantha

1 reference

Polyphenols from Cornulaca monacantha.

Cynara cornigera

1 reference

The flavonoids of Cynara sibthorpiana

Cynara sibthorpiana

1 reference

The flavonoids of Cynara sibthorpiana

1 reference

Flavone glucosides and other constituents of the Egyptian variety of Daucus carota var. boissieri grown in Egypt

Genista transcaucasica

2 references

Flavonoids from Genista involucrata

Flavonoids ofGenista transcaucasica

Gonocytisus angulatus

1 reference

FLAVONOIDS FROM GONOCYTISUS PTEROCIADUS

Hylocomium splendens

1 reference

A New Biflavone and Further Flavonoids from the Moss Hylocomium splendens

Launaea arborescens

1 reference

Phenolics of Spanish Launaea species

Lonicera japonica

2 references

Antiinflammatory activity of Polygala japonica extract

Comparison of lonicerin and veronicastroside (author's transl)

Matricaria chamomilla

1 reference

Characterization ofMatricaria recutita L. Flower extracts by HPLC-MS and HPLC-DAD analysis

Mentha piperita

3 references

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

Antiallergic effect of flavonoid glycosides obtained from Mentha piperita L.

Flavonoids from Mentha piperita Leaves

Osmanthus × fortunei

1 reference

Studies on the Constituents of Osmanthus Species. IV. On the Components of the Leaves of Osmanthus fortunei CARR.

Ostericum viridiflorum

1 reference

Separation of Ostericum from Angelica on the Basis of Leaf and Mericarp Flavonoids

Phlomis nissolii

1 reference

Flavonoids from Phlomis nissolii

Phoenix loureiroi var. loureiroi

2 references

Neural cell protective compounds isolated from Phoenix hanceana var. formosana.

Neural cell protective compounds isolated from Phoenix hanceana var. formosana.

Pratia nummularia

1 reference

Secondary Metabolites in Cyanobacteria

1 reference

A new flavone glycoside from the fern Pteris cretica

Reichardia tingitana

1 reference

Phenolics of Reichardia and their taxonomic implications

Scutellaria albida

3 references

Iridoids from Scutellaria albida ssp. albida

Iridoids from Scutellaria albida ssp. albida

Iridoids from Scutellaria albida ssp. albida

Setaria italica

1 reference

Flavone O- and C-glycosides from Setaria italica

1 reference

Phytochemical and biological studies on the leaves of Tecoma mollis Humb. And Bonpl cultivated in Egypt

Teucrium gnaphalodes

1 reference

Flavonoid Aglycones and Glycosides from Teucrium gnaphalodes

Thymus membranaceus

1 reference

Flavonoid Glycosides from Thymus membranaceus

Trachelospermum asiaticum

1 reference

Comparison of lonicerin and veronicastroside (author's transl)

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.

Vellozia scoparia

1 reference

Variations in the lipophilic and vacuolar flavonoids of the genus Vellozia

1 reference

Systematic chemical profiling of Citrus grandis 'Tomentosa' by ultra-fast liquid chromatography/diode-array detector/quadrupole time-of-flight tandem mass spectrometry

Neocheiropteris fortunei

1 reference

Effects of eleven flavonoids from the osteoprotective fraction of Drynaria fortunei (KUNZE) J. SM. on osteoblastic proliferation using an osteoblast-like cell line

Hedysarum setigerum

1 reference

Dactylin and Lonicerin from the Aerial Part of Hedysarum setigerum

Genista dracunculoides

2 references

Flavonoids from Genista involucrata

Flavonoids ofGenista transcaucasica

Passiflora biflora

1 reference

o-and c-glycosylflavones from passiflora biflora

Frullania teneriffae

1 reference

Flavonoids from Some Frullania Species (Hepaticae)

1 reference

Flavone glycosides from Mentha longifolia

Mentha longifolia

1 reference

Flavone glycosides from Mentha longifolia

Verbena officinalis

1 reference

The flavonoid chemosystematics of Egyptian Verbena species.

Dicranum scoparium

1 reference

Antibacterial activity of pure flavonoids isolated from mosses

Bryum pseudotriquetrum

1 reference

New Flavonoids from the Moss Bryum pseudotriquetrum

Ptychostomum pseudotriquetrum

1 reference

New Flavonoids from the Moss Bryum pseudotriquetrum

Lepisorus fortunei

1 reference

Effects of eleven flavonoids from the osteoprotective fraction of Drynaria fortunei (KUNZE) J. SM. on osteoblastic proliferation using an osteoblast-like cell line

Cynara scolymus

3 references

Anti-hyperlipidemic sesquiterpenes and new sesquiterpene glycosides from the leaves of artichoke (Cynara scolymus L.): structure requirement and mode of action

The flavonoids of Cynara sibthorpiana

Developmental changes in leaf phenolics composition from three artichoke cvs. (Cynara scolymus) as determined via UHPLC-MS and chemometrics

Verbena officinalis var. officinalis

1 reference

The flavonoid chemosystematics of Egyptian Verbena species.

Cynara cardunculus

4 references

Developmental changes in leaf phenolics composition from three artichoke cvs. (Cynara scolymus) as determined via UHPLC-MS and chemometrics

The flavonoids of Cynara sibthorpiana

Anti-hyperlipidemic sesquiterpenes and new sesquiterpene glycosides from the leaves of artichoke (Cynara scolymus L.): structure requirement and mode of action

Metabolomics driven analysis of artichoke leaf and its commercial products via UHPLC-q-TOF-MS and chemometrics.

Chamomilla recutita

1 reference

Characterization ofMatricaria recutita L. Flower extracts by HPLC-MS and HPLC-DAD analysis

1 reference

Systematic chemical profiling of Citrus grandis 'Tomentosa' by ultra-fast liquid chromatography/diode-array detector/quadrupole time-of-flight tandem mass spectrometry

Identifiers

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

1 reference

language of work or name

Lonicerin (English)

6 October 2016

SHPPXMGVUDNKLV-KMFFXDMSSA-N

2 references

language of work or name

Lonicerin (English)

6 October 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

language of work or name

luteolin 7-O-neohesperidoside (English)

6 October 2016

SHPPXMGVUDNKLV-KMFFXDMSSA-N

CAS Common Chemistry

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=25694-72-8

1 reference

language of work or name

Veronicastroside (English)

6 October 2016

1 reference

language of work or name

Lonicerin (English)

6 October 2016

Reaxys registry number

1361176

1 reference

language of work or name

luteolin 7-O-neohesperidoside (English)

6 October 2016

mapping relation type

1 reference

language of work or name

luteolin 7-O-neohesperidoside (English)

6 October 2016

1 reference

language of work or name

LONICERIN (English)

6 October 2016

UniChem compound ID

1 reference

DSSTox substance ID

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

Human Metabolome Database ID

1 reference

based on heuristic

inferred from InChIKey

1 reference

language of work or name

luteolin 7-O-neohesperidoside (English)

6 October 2016

Probes And Drugs ID

0 references

1 reference

language of work or name

luteolin 7-O-neohesperidoside (English)

6 October 2016

0 references

Sitelinks

Wikipedia(2 entries)

enwiki Veronicastroside
frwiki Véronicastroside

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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