benzyl β-D-glucoside (Q27268359)

inferred from SMILES

mass

270.11±0 dalton

1 reference

(2R,3R,4S,5S,6R)-2-(Benzyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (English)

beta-D-Galactopyranoside, phenylmethyl

14 October 2016

stereoisomer of

2 references

inferred from InChIKey

Benzyl beta-D-allopyranoside

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₁₃H₁₈O₆

1 reference

(2R,3R,4S,5S,6R)-2-(Benzyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (English)

14 October 2016

canonical SMILES

C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O

1 reference

(2R,3R,4S,5S,6R)-2-(Benzyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (English)

14 October 2016

isomeric SMILES

C1=CC=C(C=C1)CO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O

1 reference

Glycosidically bound aroma components from sour cherry

(2R,3R,4S,5S,6R)-2-(Benzyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (English)

14 October 2016

1 reference

Asystasia gangetica

2 references

Megastigmane glucoside from Asystasia gangetica (L.) T. Anderson

Aliphatic alcohol and iridoid glycosides from Asystasia intrusa

peach

1 reference

Anti-tumor promoting effect of glycosides from Prunus persica seeds

Camellia sinensis

4 references

Medicinal flowers. XXII. Structures of chakasaponins V and VI, chakanoside I, and chakaflavonoside A from flower buds of Chinese tea plant (Camellia sinensis).

Benzyl glucoside from tea leaves.

Bioactive saponins and glycosides. XXV. Acylated oleanane-type triterpene saponins from the seeds of tea plant (Camellia sinensis)

Acylated oleanane-type triterpene saponins with acceleration of gastrointestinal transit and inhibitory effect on pancreatic lipase from flower buds of chinese tea plant (Camellia sinensis).

Perilla frutescens

1 reference

A phenylpropanoid glucoside from Perilla frutescens

Pyrus bourgaeana

1 reference

New benzyl alcohol glycosides from Pyrus bourgaeana

Tabebuia aurea

1 reference

Phenolic glycosides from Tabebuia argentea and Catalpa bignonioides

Alpinia officinarum

1 reference

Isolation and structural elucidation of some glycosides from the rhizomes of smaller galanga (Alpinia officinarum Hance).

Baccharis dracunculifolia

1 reference

Studies on the constituents from the aerial part of Baccharis dracunculifolia DC.

Beaumontia grandiflora

1 reference

Chemical constituents of Duabanga grandiflora (Lythraceae)

Camellia japonica

2 references

New Noroleanane-Type Triterpene Saponins with Gastroprotective Effect and Platelet Aggregation Activity from the Flowers of Camellia japonica: Revised Structures of Camellenodiol and Camelledionol

Medicinal flowers. XV. The structures of noroleanane- and oleanane-type triterpene oligoglycosides with gastroprotective and platelet aggregation activities from flower buds of Camellia japonica

Carica papaya

2 references

Aryl β-d-glucosides from Carica papaya fruit

Cyanogenic allosides and glucosides from Passiflora edulis and Carica papaya.

Centaurea amanicola

1 reference

Chemical constituents of Centaurea cadmea

Cichorium intybus

1 reference

A new coumarin glucoside ester from Cichorium intybus

Wild Carrot

1 reference

Antioxidative and Antihyaluronidase Activities of Some Contituents from the Aerial Part of Daucus carota.

Lactuca tatarica

1 reference

Sesquiterpene lactones from Lactuca tatarica

Margyricarpus setosus

1 reference

Aryl and triterpenic glycosides from Margyricarpus setosus

Prunus mume

1 reference

New flavonol oligoglycosides and polyacylated sucroses with inhibitory effects on aldose reductase and platelet aggregation from the flowers of Prunus mume

Piper retrofractum

1 reference

A new phenylpropanoid and an alkylglycoside from Piper retrofractum leaves with their antioxidant and α-glucosidase inhibitory activity

Arnica mollis

1 reference

A 1,5-cis-guaianolide glucoside from flowers of Arnica mollis

Asystasia intrusa

1 reference

Aliphatic alcohol and iridoid glycosides from Asystasia intrusa

Breynia fruticosa

1 reference

Glycosides from Breynia fruticosa and Breynia rostrata

Agastache cana

1 reference

Chavicol β-d-glucoside, a phenylpropanoid heteroside, benzyl-β-d-glucoside and glycosidically bound volatiles from subspecies of Cedronella canariensis

Cedronella canariensis

1 reference

Chavicol β-d-glucoside, a phenylpropanoid heteroside, benzyl-β-d-glucoside and glycosidically bound volatiles from subspecies of Cedronella canariensis

Centella asiatica

1 reference

A new triterpene glycoside from Centella erecta

Centella erecta

1 reference

A new triterpene glycoside from Centella erecta

Chrozophora plicata

1 reference

Phenylpropanoid glucosides from Chrozophora obliqua

Citrullus colocynthis

1 reference

Bioactive saponins and glycosides. XXVII. Structures of new cucurbitane-type triterpene glycosides and antiallergic constituents from Citrullus colocynthis

Cotoneaster simonsii

1 reference

Flavonols and isoflavones from Cotoneaster simonsii

Crocus sativus

1 reference

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

Cucurbita pepo

1 reference

Phenolic plant growth inhibitors from the flowers of Cucurbita pepo

Epimedium grandiflorum

1 reference

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

Eupatorium chinense

1 reference

Chemical constituents from Eupatorium chinense

Foeniculum vulgare

1 reference

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

Glehnia littoralis

1 reference

Water-soluble constituents of Glehnia littoralis fruit

Gymnadenia conopsea

1 reference

Bioactive constituents from Chinese natural medicines. XVII. constituents with radical scavenging effect and new glucosyloxybenzyl 2-isobutylmalates from Gymnadenia conopsea

Houttuynia cordata

1 reference

The constituents and their bioactivities of Houttuynia cordata

Hylocereus undatus

1 reference

Three new glycosides from Hylocereus undatus

Collinsonia japonica

1 reference

Hyaluronidase inhibitors from Keiskea japonica

Laguncularia racemosa

1 reference

Phenolic compounds and their anti-oxidative properties and protein kinase inhibition from the Chinese mangrove plant Laguncularia racemosa

Linaria vulgaris

1 reference

A new pyrroloquinazoline alkaloid from Linaria vulgaris

tomato

1 reference

Aliphatic and aromatic glycosides from the cell cultures of Lycopersicon esculentum

Mallotus macrostachyus

1 reference

Chemical constituents of Mallotus macrostachyus growing in Vietnam and cytotoxic activity of some cycloartane derivatives

Campanula medium

1 reference

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

Mentha spicata

1 reference

Antihistaminic flavones and aliphatic glycosides from Mentha spicata

moringa

1 reference

Unusual glycosides of pyrrole alkaloid and 4'-hydroxyphenylethanamide from leaves of Moringa oleifera

Morus alba

1 reference

Studies on the constituents of the leaves of Morus alba L.

Phlomis grandiflora

1 reference

Phlomisethanoside, a phenylethanoid glycoside from Phlomis grandiflora var. grandiflora

Pluchea indica

1 reference

Terpenic glycosides from Pluchea indica

Rhodiola rosea

4 references

Phenylpropanoid glycosides from Rhodiola rosea

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis

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.

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

Rhodiola sachalinensis

3 references

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis

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.

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

Rosa × damascena

2 references

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

Isolation of a Glucosidic β-Damascenone Precursor from Rose Petals

Rosa gallica

2 references

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

Isolation of a Glucosidic β-Damascenone Precursor from Rose Petals

Salacia chinensis

1 reference

Chemical structures and hepatoprotective effects of constituents from the leaves of Salacia chinensis

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

Schefflera rotundifolia

1 reference

Cytotoxic saponins from Schefflera rotundifolia.

Scutellaria albida

1 reference

Iridoids from Scutellaria albida ssp. albida

Soroseris hookeriana

1 reference

New antimicrobial mono- and sesquiterpenes from Soroseris hookeriana subsp. erysimoides

Staphylea bumalda

1 reference

Bumaldosides A, B and C from the Leaves of Staphylea bumalda

Taraxacum alpinum

1 reference

A Guaianolide Sulfate Conjugate and Other Constituents from Taraxacum alpinum

Taraxacum obovatum

1 reference

Sesquiterpene lactones from Taraxacum obovatum.

Thunbergia laurifolia

1 reference

Iridoid glucosides from Thunbergia laurifolia

Trachelospermum jasminoides

1 reference

Chemical constituents of Trachelospermum jasminoides

Tridax procumbens

1 reference

Chemical-constituent diversity of Tridax procumbens

Vaccinium dunalianum

1 reference

Caffeoyl arbutin and related compounds from the buds of Vaccinium dunalianum

Ambassa hochstetteri

1 reference

Sesquiterpene lactones fromVernonia jugalis

Ziziphora clinopodioides

1 reference

Monoterpene glucosides from Ziziphora clinopodioides (Labiatae).

Cotoneaster symondsii

1 reference

Flavonols and isoflavones from Cotoneaster simonsii

Selenicereus undatus

1 reference

Three new glycosides from Hylocereus undatus

Dracocephalum ruyschiana

1 reference

Flavone tetraglycosides and benzyl alcohol glycosides from the Mongolian medicinal plant Dracocephalum ruyschiana.

Cotoneaster integrifolius

1 reference

Flavonols and isoflavones from Cotoneaster simonsii

Taraxacum apenninum

1 reference

A Guaianolide Sulfate Conjugate and Other Constituents from Taraxacum alpinum

Margyricarpus pinnatus

1 reference

Aryl and triterpenic glycosides from Margyricarpus setosus

Identifiers

InChI

InChI=1S/C13H18O6/c14-6-9-10(15)11(16)12(17)13(19-9)18-7-8-4-2-1-3-5-8/h1-5,9-17H,6-7H2/t9-,10-,11+,12-,13-/m1/s1

1 reference

(2R,3R,4S,5S,6R)-2-(Benzyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (English)

GKHCBYYBLTXYEV-UJPOAAIJSA-N

14 October 2016

InChIKey

2 references

(2R,3R,4S,5S,6R)-2-(Benzyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (English)

14 October 2016

ChEBI release 2020-09-01

CAS Registry Number

4304-12-5

1 reference

Global Substance Registration System

UNII

7ILL1IJM8R

benzyl β-D-glucoside (English)

14 October 2016

1 reference

Benzyl beta-D-glucopyranoside (English)

14 October 2016

2 references

(2R,3R,4S,5S,6R)-2-(Benzyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (English)

matched by identifier from

14 October 2016

InChIKey

GKHCBYYBLTXYEV-UJPOAAIJSA-N

ChEBI ID

141411

mapping relation type

exact match

2 references

matched by identifier from

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C13H18O6/c14-6-9-10(15)11(16)12(17)13(19-9)18-7-8-4-2-1-3-5-8/h1-5,9-17H,6-7H2/t9-,10-,11+,12-,13-/m1/s1

1 reference

splash10-000f-0960000000-2535bc03f569cb2a6fc6

CHEMBL2336738 (English)

14 October 2016

1 reference

0 references

DSSTox substance ID

DTXSID30962864

0 references

DSSTOX compound identifier

0 references

2 references

Global Substance Registration System

UNII

7ILL1IJM8R

benzyl β-D-glucoside (English)