petiolaroside (Q23418292)

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chemical compound

7-((6-deoxy-alpha-L-mannopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-one
quercetin-3-O-beta-D-glucopyranoside-7-O-alpha-L-rhamnopyranoside
vincetoxicoside A

Language	Label	Description	Also known as
English	petiolaroside	chemical compound	7-((6-deoxy-alpha-L-mannopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-one quercetin-3-O-beta-D-glucopyranoside-7-O-alpha-L-rhamnopyranoside vincetoxicoside A

Statements

type of chemical entity

0 references

0 references

610.153385±0 dalton

1 reference

language of work or name

Vincetoxicoside A (English)

7 October 2016

stereoisomer of

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

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

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

1 reference

based on heuristic

inferred from InChI

2-(3,4-Dihydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-5-hydroxy-4-oxo-4H-chromen-7-yl 6-deoxy-alpha-L-altropyranoside

1 reference

based on heuristic

inferred from InChI

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

1 reference

based on heuristic

inferred from InChI

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

1 reference

based on heuristic

inferred from InChI

Quercetin 3-O-galactoside-7-O-rhamnoside

1 reference

based on heuristic

inferred from InChI

Quercetin 3-O-glucoside 7-O-rhamnoside

1 reference

based on heuristic

inferred from InChI

quercetin-3-O-glucoside-7-O-rhamnoside

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₇H₃₀O₁₆

1 reference

language of work or name

Vincetoxicoside A (English)

7 October 2016

canonical SMILES

CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O

1 reference

language of work or name

Vincetoxicoside A (English)

7 October 2016

isomeric SMILES

C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O

1 reference

language of work or name

Vincetoxicoside A (English)

7 October 2016

Asplenium trichomanes-ramosum

1 reference

New and rare flavonol glycosides from asplenium trichomanes-ramosum as stable chemotaxonomic markers

Aconitum lycoctonum

1 reference

Flavonol glycosides from Aconitum vulparia.

Androsace umbellata

1 reference

Two New Kaempferol Glycosides fromAndrosace umbellata

Arabidopsis thaliana

1 reference

Metabolomics-oriented isolation and structure elucidation of 37 compounds including two anthocyanins from Arabidopsis thaliana

Barbarea vulgaris

1 reference

Flavonoid glycosides of Barbarea vulgaris L. (Brassicaceae)

Elaeodendron xylocarpum

1 reference

ChemInform Abstract: FLAVONOIDVERBINDUNGEN IN DEN BLAETTERN VON CELASTRUS ORBICULATA THUNB.

Chrozophora plicata

1 reference

Phenylpropanoid glucosides from Chrozophora obliqua

Sinocrassula indica

3 references

Bioactive constituents from Chinese natural medicines. XXXII. aminopeptidase N and aldose reductase inhibitors from Sinocrassula indica: structures of sinocrassosides B(4), B(5), C(1), and D(1)-D(3).

Bioactive Constituents from Chinese Natural Medicines. XXXI. Hepatoprotective Principles from Sinocrassula indica: Structures of Sinocrassosides A8, A9, A10, A11, and A12

Bioactive constituents from chinese natural medicines. XXIV. Hypoglycemic effects of Sinocrassula indica in sugar-loaded rats and genetically diabetic KK-A(y) mice and structures of new acylated flavonol glycosides, sinocrassosides A(1), A(2), B(1),

Delphinium staphisagria

1 reference

In vitro and in vivo trypanocidal activity of flavonoids from Delphinium staphisagria against Chagas disease

Lathyrus chrysanthus

1 reference

Floral pigmentation in two yellow-flowered Lathyrus species and their hybrid

Ligustrum vulgare

1 reference

HPLC analysis of flavonoids and secoiridoids in leaves of Ligustrum vulgare L. (Oleaceae)

Potentilla erecta

1 reference

Flavonoids of Potentilla erecta

Scarlet firethorn

1 reference

Flavonoids from Pyracantha coccinea roots

1 reference

Activity-guided isolation and identification of free radical-scavenging components from various leaf extracts of Sorbus aria (L.) Crantz

1 reference

Coumarins ofVicia sativa

Staphisagria macrosperma

1 reference

In vitro and in vivo trypanocidal activity of flavonoids from Delphinium staphisagria against Chagas disease

Capsicum annuum var. annuum

1 reference

Metabolite biodiversity in pepper (Capsicum) fruits of thirty-two diverse accessions: variation in health-related compounds and implications for breeding.

1 reference

Activity-guided isolation and identification of free radical-scavenging components from various leaf extracts of Sorbus aria (L.) Crantz

Capsicum annuum

1 reference

Metabolite biodiversity in pepper (Capsicum) fruits of thirty-two diverse accessions: variation in health-related compounds and implications for breeding.

Asplenium viride

1 reference

New and rare flavonol glycosides from asplenium trichomanes-ramosum as stable chemotaxonomic markers

subject has role

1 reference

Identifiers

InChI=1S/C27H30O16/c1-8-17(32)20(35)22(37)26(39-8)40-10-5-13(31)16-14(6-10)41-24(9-2-3-11(29)12(30)4-9)25(19(16)34)43-27-23(38)21(36)18(33)15(7-28)42-27/h2-6,8,15,17-18,20-23,26-33,35-38H,7H2,1H3/t8-,15+,17-,18+,20+,21-,22+,23+,26-,27-/m0/s1

1 reference

language of work or name

Vincetoxicoside A (English)

7 October 2016

OTUCXMIQUNROBJ-JFNZIVIESA-N

2 references

language of work or name

Vincetoxicoside A (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

language of work or name

petiolaroside (English)

7 October 2016

OTUCXMIQUNROBJ-JFNZIVIESA-N

CAS Common Chemistry

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=18016-58-5

1 reference

language of work or name

Quercetin-3-O-beta-glucopyranosyl-7-O-alpha-rhamnopyranoside (English)

7 October 2016

2 references

language of work or name

Vincetoxicoside A (English)

7 October 2016

matched by identifier from

OTUCXMIQUNROBJ-JFNZIVIESA-N

Reaxys registry number

1339876

1 reference

language of work or name

petiolaroside (English)

7 October 2016

mapping relation type

2 references

language of work or name

petiolaroside (English)

7 October 2016

matched by identifier from

International Chemical Identifier

InChI=1S/C27H30O16/c1-8-17(32)20(35)22(37)26(39-8)40-10-5-13(31)16-14(6-10)41-24(9-2-3-11(29)12(30)4-9)25(19(16)34)43-27-23(38)21(36)18(33)15(7-28)42-27/h2-6,8,15,17-18,20-23,26-33,35-38H,7H2,1H3/t8-,15+,17-,18+,20+,21-,22+,23+,26-,27-/m0/s1

UniChem compound ID

1 reference

MassBank accession ID

MSBNK-RIKEN-PR100998

0 references

MSBNK-RIKEN-PR100999

0 references

MSBNK-RIKEN-PR101053

0 references

splash10-0udi-0009301000-2d828798151c6741ef34

0 references

DSSTox substance ID

1 reference

matched by identifier from

OTUCXMIQUNROBJ-JFNZIVIESA-N

DSSTOX compound identifier

DTXCID901365438

0 references

Sitelinks

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Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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