(Q105167009)

English

phenylethyl beta-D-glucopyranoside

chemical compound

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instance of

type of chemical entity

0 references

subclass of

2-phenylethyl beta-D-glucopyranoside

1 reference

based on heuristic

inferred from SMILES

chemical structure

Phenethyl glucoside.svg
680 × 275; 22 KB

0 references

mass

284.12598836 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

Phenylethyl beta-D-galactopyranoside

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₁₄H₂₀O₆

0 references

canonical SMILES

OCC1OC(OCCC=2C=CC=CC2)C(O)C(O)C1O

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isomeric SMILES

OC[C@H]1O[C@@H](OCCc2ccccc2)[C@H](O)[C@@H](O)[C@@H]1O

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found in taxon

Rhodiola crenulata

2 references

stated in

Bioactive constituents from Chinese natural medicines. XXVIII. Chemical structures of acyclic alcohol glycosides from the roots of Rhodiola crenulata

stated in

Bioactive constituents from Chinese natural medicines. XXVIII. Chemical structures of acyclic alcohol glycosides from the roots of Rhodiola crenulata

Rhodiola sachalinensis

4 references

stated in

Bioactive constituents from Chinese natural medicines. XXVI. Chemical structures and hepatoprotective effects of constituents from roots of Rhodiola sachalinensis

stated in

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis

stated in

Neuroprotective effects of constituents of the oriental crude drugs, Rhodiola sacra, R. sachalinensis and Tokaku-joki-to, against beta-amyloid toxicity, oxidative stress and apoptosis.

stated in

Bioactive constituents from Chinese natural medicines. XXVI. Chemical structures and hepatoprotective effects of constituents from roots of Rhodiola sachalinensis

Buddleja officinalis

2 references

stated in

A new iridoid and effect on the rat aortic vascular smooth muscle cell proliferation of isolated compounds from Buddleja officinalis

stated in

A new iridoid and effect on the rat aortic vascular smooth muscle cell proliferation of isolated compounds from Buddleja officinalis

Moricandia arvensis

2 references

stated in

Antioxidant phenolic glycosides from Moricandia arvensis

stated in

Antioxidant phenolic glycosides from Moricandia arvensis

Epimedium sagittatum

1 reference

stated in

Lignan and terpene glycosides from Epimedium sagittatum

Artemisia gmelinii

1 reference

stated in

Seco- and Nor-sesquiterpene lactones with a new carbon skeleton from Artemisia santolinifolia

Artemisia santolinifolia

1 reference

stated in

Seco- and Nor-sesquiterpene lactones with a new carbon skeleton from Artemisia santolinifolia

Aster koraiensis

1 reference

stated in

Two New Sesquiterpene Glucosides from Gymnaster koraiensis

Breynia fruticosa

1 reference

stated in

Glycosides from Breynia fruticosa and Breynia rostrata

Carica papaya

1 reference

stated in

Aryl β-d-glucosides from Carica papaya fruit

mandarin orange

1 reference

stated in

Studies on the constituents of leaves of Citrus unshiu MARCOV.

Citrus unshiu

1 reference

stated in

Studies on the constituents of leaves of Citrus unshiu MARCOV.

Crocus sativus

1 reference

stated in

Identification of Novel Glycosidic Aroma Precursors in Saffron (CrocussativusL.)

Epimedium grandiflorum

1 reference

stated in

Studies on the glycosides of Epimedium grandiflorum Morr. var. thunbergianum (Miq.) Nakai. III

Equisetum ramosissimum

1 reference

stated in

Megastigmane glucosides from Equisetum debile and E. diffusum

Foeniculum vulgare

1 reference

stated in

Five New Monoterpene Glycosides and Other Compounds from Foeniculi Fructus (Fruit of Foeniculum vulgare MILLER).

Glehnia littoralis

1 reference

stated in

Water-soluble constituents of Glehnia littoralis fruit

Hydrangea macrophylla

1 reference

stated in

New Cyanoglycosides, Hydracyanosides D, E, and F, from the Leaves of Hydrangea macrophylla

Hylocereus undatus

1 reference

stated in

Three new glycosides from Hylocereus undatus

Hypericum sikokumontanum

1 reference

stated in

Chromone and chromanone glucosides from Hypericum sikokumontanum and their anti-Helicobacter pylori activities

Isatis tinctoria

1 reference

stated in

A Novel Anthranilic Acid Derivative from Isatis tinctoria

Campanula medium

1 reference

stated in

Studies on the glycosides of Epimedium grandiflorum Morr. var. thunbergianum (Miq.) Nakai. III

Mentha spicata

1 reference

stated in

Antihistaminic flavones and aliphatic glycosides from Mentha spicata

Mikania hirsutissima

1 reference

stated in

ent-Kaurenoic acids from Mikania hirsutissima (Compositae).

Ipomoea nil

1 reference

stated in

Bioactive phenolic constituents from the seeds of Pharbitis nil.

Pluchea indica

1 reference

stated in

Terpenic glycosides from Pluchea indica

Rhodiola chrysanthemifolia

2 references

stated in

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sacra S. H. Fu.

stated in

Neuroprotective effects of constituents of the oriental crude drugs, Rhodiola sacra, R. sachalinensis and Tokaku-joki-to, against beta-amyloid toxicity, oxidative stress and apoptosis.

Rhodiola sacra

2 references

stated in

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sacra S. H. Fu.

stated in

Neuroprotective effects of constituents of the oriental crude drugs, Rhodiola sacra, R. sachalinensis and Tokaku-joki-to, against beta-amyloid toxicity, oxidative stress and apoptosis.

Rosa × damascena

2 references

stated in

(S)-3,7-Dimethyl-5-octene-1,7-diol and Related Oxygenated Monoterpenoids from Petals ofRosadamascenaMill.

stated in

Recovery of polyphenols from rose oil distillation wastewater using adsorption resins--a pilot study

Rosa gallica

3 references

stated in

(S)-3,7-Dimethyl-5-octene-1,7-diol and Related Oxygenated Monoterpenoids from Petals ofRosadamascenaMill.

stated in

Phenethylβ-D-glucopyranoside from the flowers of Rosa gallica

stated in

Recovery of polyphenols from rose oil distillation wastewater using adsorption resins--a pilot study

Rosa rugosa

1 reference

stated in

Kaempferol and quercetin flavonoids from Rosa rugosa

Saussurea medusa

1 reference

stated in

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

Sedum sarmentosum

2 references

stated in

Bioactive constituents from Chinese natural medicines. XXII. Absolute structures of new megastigmane glycosides, sedumosides E1, E2, E3, F1, F2, and G, from Sedum sarmentosum (Crassulaceae)

stated in

Bioactive Constituents from Chinese Natural Medicines. XXV. New Flavonol Bisdesmosides, Sarmenosides I, II, III, and IV, with Hepatoprotective Activity from Sedum sarmentosum (Crassulaceae)

Ziziphora clinopodioides

1 reference

stated in

Monoterpene glucosides from Ziziphora clinopodioides (Labiatae).

Selenicereus undatus

1 reference

stated in

Three new glycosides from Hylocereus undatus

Equisetum giganteum

1 reference

stated in

Megastigmane glucosides from Equisetum debile and E. diffusum

Artemisia stechmanniana

1 reference

stated in

Seco- and Nor-sesquiterpene lactones with a new carbon skeleton from Artemisia santolinifolia

Citrus × deliciosa

1 reference

stated in

Studies on the constituents of leaves of Citrus unshiu MARCOV.

Mikania banisteriae

1 reference

stated in

ent-Kaurenoic acids from Mikania hirsutissima (Compositae).

Artemisia chamaemelifolia

1 reference

stated in

Seco- and Nor-sesquiterpene lactones with a new carbon skeleton from Artemisia santolinifolia

Rhodiola rosea

3 references

stated in

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis

stated in

Neuroprotective effects of constituents of the oriental crude drugs, Rhodiola sacra, R. sachalinensis and Tokaku-joki-to, against beta-amyloid toxicity, oxidative stress and apoptosis.

stated in

Bioactive constituents from Chinese natural medicines. XXVI. Chemical structures and hepatoprotective effects of constituents from roots of Rhodiola sachalinensis

Identifiers

InChI

InChI=1S/C14H20O6/c15-8-10-11(16)12(17)13(18)14(20-10)19-7-6-9-4-2-1-3-5-9/h1-5,10-18H,6-8H2/t10-,11-,12+,13-,14-/m1/s1

0 references

InChIKey

MLRIJUWUQTVDQE-RKQHYHRCSA-N

0 references

CAS Registry Number

18997-54-1

1 reference

stated in

CAS (formerly Chemical Abstracts Service)

25 January 2022

2 references

17 September 2022

inferred from InChIKey

matched by identifier from

InChIKey

MLRIJUWUQTVDQE-RKQHYHRCSA-N

ChEBI ID

182253

mapping relation type

exact match

2 references

stated in

ChEBI release 2022-06-13

matched by identifier from

International Chemical Identifier

InChI

InChI=1S/C14H20O6/c15-8-10-11(16)12(17)13(18)14(20-10)19-7-6-9-4-2-1-3-5-9/h1-5,10-18H,6-8H2/t10-,11-,12+,13-,14-/m1/s1

1 reference

1 reference

matched by identifier from

InChIKey

MLRIJUWUQTVDQE-RKQHYHRCSA-N

(Q105167009)

phenylethyl beta-D-glucopyranoside

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