(Q104195901)

English

2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol

group of stereoisomers with the chemical formula C₁₇H₂₄O₉

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Statements

instance of

group of stereoisomers

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subclass of

eleutheroside

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mass

372.1420323479999 dalton

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₇H₂₄O₉

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canonical SMILES

OCC=CC1=CC(OC)=C(OC2OC(CO)C(O)C(O)C2O)C(OC)=C1

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found in taxon

Oplopanax elatus

1 reference

stated in

Studies on the anti-psoriasis constituents of Oplopanax elatus Nakai

rooibos

1 reference

stated in

Phytoestrogens from Aspalathus linearis

Daphne tangutica

1 reference

stated in

Chemical constituents investigation of Daphne tangutica.

Cuscuta reflexa

1 reference

stated in

Alpha-glucosidase inhibitory constituents from Cuscuta reflexa

tarragon

1 reference

stated in

Chemical constituents from the aerial parts of Artemisia minor.

Viscum coloratum

1 reference

stated in

Phenylpropanes and Lignans ofViscum albumCardioactive Drugs V1

Eleutherococcus nodiflorus

1 reference

stated in

Pharmacokinetics of isofraxidin in rat plasma after oral administration of the extract of Acanthopanax senticosus using HPLC with solid phase extraction method

Wedelia scaberrima

1 reference

stated in

Coumestans as the Main Active Principles of the Liver DrugsEclipta albaandWedelia calendulacea1

Panax ginseng

1 reference

stated in

Pharmacokinetics of isofraxidin in rat plasma after oral administration of the extract of Acanthopanax senticosus using HPLC with solid phase extraction method

Eleutherococcus giraldii

1 reference

stated in

Pharmacokinetics of isofraxidin in rat plasma after oral administration of the extract of Acanthopanax senticosus using HPLC with solid phase extraction method

Euodia

1 reference

stated in

Euodionosides A-G: megastigmane glucosides from leaves of Euodia meliaefolia

Piper cubeba

1 reference

stated in

Lirioresinol-C dimethyl ether, a diaxially substituted 3,7-dioxabicyclo[3,3,0]octane lignan from Macropiper excelsum(Forst.f.) Miq.

Syringa oblata

1 reference

stated in

Secoiridoid and iridoid glucosides from Syringa afghanica

Viscum angulatum

1 reference

stated in

Phenylpropanes and Lignans ofViscum albumCardioactive Drugs V1

Magnolia officinalis

3 references

stated in

Two new lignans from the stem bark of Magnolia obovata and their cytotoxic activity

stated in

Magnolialide: A novel eudesmanolide from the root bark of Magnolia grandiflora

stated in

Constituintes químicos isolados dos caules de Michelia champaca L. (Magnoliaceae)

Daphne feddei

1 reference

stated in

Terpenoids and aromatic compounds from Daphne oleoides ssp. oleoides

Syringa vulgaris

1 reference

stated in

Secoiridoid and iridoid glucosides from Syringa afghanica

Jasminum nudiflorum

1 reference

stated in

Two new flavanone glycosides of Jasminum lanceolarium and their anti-oxidant activities

Magnolia obovata

3 references

stated in

Cytotoxic lignans from the stem bark of Magnolia officinalis

stated in

Magnolialide: A novel eudesmanolide from the root bark of Magnolia grandiflora

stated in

Constituintes químicos isolados dos caules de Michelia champaca L. (Magnoliaceae)

Magnolia sieboldii

4 references

stated in

Cytotoxic lignans from the stem bark of Magnolia officinalis

stated in

Two new lignans from the stem bark of Magnolia obovata and their cytotoxic activity

stated in

Magnolialide: A novel eudesmanolide from the root bark of Magnolia grandiflora

stated in

Constituintes químicos isolados dos caules de Michelia champaca L. (Magnoliaceae)

Magnolia grandiflora

3 references

stated in

Cytotoxic lignans from the stem bark of Magnolia officinalis

stated in

Two new lignans from the stem bark of Magnolia obovata and their cytotoxic activity

stated in

Constituintes químicos isolados dos caules de Michelia champaca L. (Magnoliaceae)

Jasminum lanceolarium

1 reference

stated in

Nine new secoiridoid glucosides from Jasminum nudiflorum.

Wedelia calycina

1 reference

stated in

Coumestans as the Main Active Principles of the Liver DrugsEclipta albaandWedelia calendulacea1

Inga feuillei

1 reference

stated in

Secoiridoid glucosides and related compounds from Syringa reticulata and their antioxidant activities

Cistanche tubulosa

2 references

stated in

Iridoid and acyclic monoterpene glycosides, kankanosides L, M, N, O, and P from Cistanche tubulosa.

stated in

The constituents of Cistanche tubulosa (Schrenk) Hook. f. II. Isolation and structures of a new phenylethanoid glycoside and a new neolignan glycoside.

Globularia alypum

1 reference

stated in

In vitro antioxidant effect of Globularia alypum L. hydromethanolic extract

Cistanche phelypaea

2 references

stated in

The constituents of Cistanche tubulosa (Schrenk) Hook. f. II. Isolation and structures of a new phenylethanoid glycoside and a new neolignan glycoside.

stated in

Iridoid and acyclic monoterpene glycosides, kankanosides L, M, N, O, and P from Cistanche tubulosa.

Eleutherococcus senticosus

1 reference

stated in

Hypoglycemic effect of syringin from Eleutherococcus senticosus in streptozotocin-induced diabetic rats

Alniaria japonica

1 reference

stated in

Iridoid glucosides from Linaria japonica

Arabidopsis thaliana

1 reference

stated in

Metabolic changes in Arabidopsis thaliana expressing the feedback-resistant anthranilate synthase alpha subunit gene OASA1D

Identifiers

InChI

InChI=1S/C17H24O9/c1-23-10-6-9(4-3-5-18)7-11(24-2)16(10)26-17-15(22)14(21)13(20)12(8-19)25-17/h3-4,6-7,12-15,17-22H,5,8H2,1-2H3

0 references

InChIKey

QJVXKWHHAMZTBY-UHFFFAOYSA-N

0 references

2 references

26 December 2021

matched by identifier from

InChIKey

QJVXKWHHAMZTBY-UHFFFAOYSA-N

ChEBI ID

182936

mapping relation type

exact match

2 references

stated in

ChEBI release 2022-06-13

matched by identifier from

International Chemical Identifier

InChI

InChI=1S/C17H24O9/c1-23-10-6-9(4-3-5-18)7-11(24-2)16(10)26-17-15(22)14(21)13(20)12(8-19)25-17/h3-4,6-7,12-15,17-22H,5,8H2,1-2H3

1 reference

MassBank accession ID

MSBNK-RIKEN_ReSpect-PS113505

1 reference

InChIKey

QJVXKWHHAMZTBY-UHFFFAOYSA-N

stated in

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

matched by identifier from

InChIKey

QJVXKWHHAMZTBY-UHFFFAOYSA-N

Human Metabolome Database ID

HMDB0242525

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

InChIKey

QJVXKWHHAMZTBY-UHFFFAOYSA-N

Probes And Drugs ID

PD056612

0 references

(Q104195901)

2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol

Statements

Identifiers

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