oleuropein (Q402625)

inferred from SMILES

chemical structure

Oleuropein.png
992 × 732; 14 KB

0 references

mass

540.184 dalton

1 reference

methyl (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate

Oleuropein (English)

18 November 2016

0 references

2 references

methyl (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate

2 references

methyl (4S,5Z,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate

2 references

methyl (4S,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate

1 reference

methyl (4R,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate

1 reference

chemical formula

C₂₅H₃₂O₁₃

1 reference

Oleuropein (English)

18 November 2016

CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O

1 reference

Oleuropein (English)

18 November 2016

C/C=C/1\[C@@H](C(=CO[C@H]1O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O

1 reference

Secoiridoid glucosides from Fraxinus americana

Oleuropein (English)

18 November 2016

1 reference

Fraxinus ornus

1 reference

Secoiridoid glucosides from fraxinus ornus bark

Ligustrum japonicum

1 reference

Three secoiridoid glucosides from Ligustrum japonicum

Syringa vulgaris

5 references

Jasminidin, ein neues monoterpenalkaloid aus Syringa vulgaris

Biosynthesis of iridoids in Syringa and Fraxinus: Carbocyclic iridoid precursors

Two new phenolic glycosides from Syringa reticulata

Iridoids of the bark of Syringa vulgaris

TLC and HPLC analysis of syringin in Syringa vulgaris

borage

1 reference

Chemical composition and antioxidant activity of Borago officinalis L. leaf extract growing in Algeria

Olea europaea

29 references

Phenolic profile characterization of Chemlali olive stones by liquid chromatography-ion trap mass spectrometry

Analysis by liquid chromatography-tandem mass spectrometry of biophenolic compounds in olives and vegetation waters, Part I

Analysis by liquid chromatography-tandem mass spectrometry of biophenolic compounds in virgin olive oil, Part II

Biophenolic components of olives

Determination of antioxidant compounds and antioxidant activity in commercial oilseeds for food use

Effect of irrigation and lactic acid bacteria inoculants on the phenolic fraction, fermentation and sensory characteristics of olive (Olea europaea L. cv. Ascolana tenera) fruits

Effect of irrigation applied to olive trees (Olea europaea L.) on phenolic compound transfer during olive oil extraction

Phenolic compounds of virgin olive oil: influence of paste preparation techniques

Phenolic glucosides from Olea europaea subs. africana

Characterization of phenolic and secoiridoid aglycons present in virgin olive oil by gas chromatography-chemical ionization mass spectrometry

Quantitative determination of biologically active constituents in medicinal plant crude extracts by thin-layer chromatography—densitometry

Antioxidative activities of Olea europaea leaves and related phenolic compounds

Liquid chromatography with electrospray ionisation mass spectrometric detection of phenolic compounds from Olea europaea

Quantitation of oleuropein in virgin olive oil by ionspray mass spectrometry-selected reaction monitoring

Rapid high-performance liquid chromatography analysis for the quantitative determination of oleuropein in Olea europaea leaves

Recovery of phenolic compounds from Olea europaea

Molluscicides from olive Olea europaea and their efficient isolation by counter-current chromatographies

Hypoglycemic and antioxidant effect of oleuropein in alloxan-diabetic rabbits

A New Secoiridoid from Olive Wastewaters

1H NMR Study of Phenolics in the Vegetation Water of Three Cultivars ofOlea europaea: Similarities and Differences†

Isolation of cornoside from Olea europaea and its transformation into halleridone

Screening of nine vasoactive medicinal plants for their possible calcium antagonistic activity. Strategy of selection and isolation for the active principles ofOlea europaea andPeucedanum ostruthium

Oleuropein, a Secoiridoid Glucoside from Olive, as a Feeding Stimulant to the Olive Weevil (Dyscerus perforatus)

Secoiridoids from Olea europaea

Coumarin and secoiridoid glucosides from bark of Olea africana and Olea capensis.

A secoiridoid glucoside from Olea europaea

Direct Identification of Phenolic Glucosides from Olive Leaf Extracts by Atmospheric Pressure Ionization Tandem Mass Spectrometry

Oleuropein, a non-toxic olive iridoid, is an anti-tumor agent and cytoskeleton disruptor

Polyphenolic content in five tuscany cultivars of Olea europaea L

rapeseed

1 reference

Determination of antioxidant compounds and antioxidant activity in commercial oilseeds for food use

Fraxinus excelsior

4 references

Excelsioside, a secoiridoid glucoside from Fraxinus excelsior

Secoiridoids and hydroxycoumarins in Bulgarian Fraxinus species

Biosynthesis of iridoids in Syringa and Fraxinus: Carbocyclic iridoid precursors

Biosynthesis of secoiridoid glucosides in oleaceae

Fraxinus insularis

1 reference

Isolation of Oleayunnanoside from Fraxinus insularis and Revision of Its Structure to Insularoside-6'''-O-.BETA.-D-glucoside.

Jasminum officinale

1 reference

Structure Elucidation of Two Secoiridoid Glucosides from Jasminum officinale L. var. grandiflorum (L.) KOBUSKI.

Ligustrum vulgare

2 references

Polar constituents of Ligustrum vulgare L. and their effect on lipoxygenase activity

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

Osmanthus heterophyllus

2 references

Secoiridoid Di-glycosides from Osmanthus ilicifolius

Studies on the Constituents of Osmanthus Species. III. On the Components of the Leaves of Osmanthus ilicifolius (HASSK.) MOUILLEFERT

Osmanthus ilicifolius

2 references

Secoiridoid Di-glycosides from Osmanthus ilicifolius

Studies on the Constituents of Osmanthus Species. III. On the Components of the Leaves of Osmanthus ilicifolius (HASSK.) MOUILLEFERT

Syringa josikaea

2 references

Biosynthesis of iridoids in Syringa and Fraxinus: Carbocyclic iridoid precursors

Biosynthesis of secoiridoid glucosides in oleaceae

Inga feuillei

1 reference

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

Ligustrum obtusifolium

2 references

Studies on the Constituents of Ligustrum Species. IX. On the Components of the Fruits of Ligustrum obtusifolium SIEB. et ZUCC. (3)

Studies on the Constituents of Ligustrum Species. XIII. : Structures of Phenylethanoid Glycosides from the Leaves of Ligustrum obtusifolium SIEB. et ZUCC.

Osmanthus × fortunei

1 reference

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

Jasminum polyanthum

3 references

Two dimeric secoiridoid glucosides from Jasminum polyanthum

Jaspolyside, a secoiridoid glycoside from Jasminum polyanthum

Secoiridoid Glycosides fromJasminum Polyanthum

Phillyrea latifolia

1 reference

Biosynthesis of secoiridoid glucosides in oleaceae

Fraxinus pallisiae

1 reference

Secoiridoids and hydroxycoumarins in Bulgarian Fraxinus species

Osmanthus fragrans

1 reference

Studies on the Constituents of Osmanthus Species. I. On the Components of the Leaves of Osmanthus fragrans LOUR. var. aurantiacus MAKINO (1)

Olea capensis

1 reference

Coumarin and secoiridoid glucosides from bark of Olea africana and Olea capensis.

Inga feuilleei

1 reference

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

Fraxinus angustifolia

1 reference

Secoiridoids from Fraxinus angustifolia

Fraxinus chinensis

1 reference

Secoiridoid, coumarin and secoiridoid-coumarin glucosides from Fraxinus chinensis

Jasminum grandiflorum

2 references

Angiotensin converting enzyme (ACE) inhibitors from Jasminum azoricum and Jasminum grandiflorum

Secoiridoid glucosides from Jasminium azoricum L. and Jasminium grandiflorum L.

Ligustrum lucidum

2 references

Antioxidative glucosides from the fruits of Ligustrum lucidum

Three secoiridoid glucosides from Ligustrum japonicum

1 reference

antihypertensive drug

1 reference

15 March 2018

1 reference

15 March 2018

1 reference

2-(3,4-dihydroxyphenyl)ethyl 2-[(3E)-5-acetyloxy-3-ethylidene-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetate

15 March 2018

0 references

Commons category

Oleuropein

0 references

Identifiers

Bibliothèque nationale de France ID

1 reference

14 April 2018

1 reference

Integrated Authority File

14 April 2018

1 reference

14 April 2018

InChI=1S/C25H32O13/c1-3-13-14(9-19(29)35-7-6-12-4-5-16(27)17(28)8-12)15(23(33)34-2)11-36-24(13)38-25-22(32)21(31)20(30)18(10-26)37-25/h3-5,8,11,14,18,20-22,24-28,30-32H,6-7,9-10H2,1-2H3/b13-3+/t14-,18+,20+,21-,22+,24-,25-/m0/s1

1 reference

Oleuropein (English)

18 November 2016

2 references

Oleuropein (English)

18 November 2016

ChEBI release 2020-09-01

CAS Registry Number

32619-42-4

2 references

https://commonchemistry.cas.org/detail?cas_rn=32619-42-4

oleuropein (English)

18 November 2016

5 April 2021

1 reference

Oleuropein (English)

18 November 2016

2 references

Oleuropein (English)

18 November 2016

ChEBI ID

7747

mapping relation type

exact match

2 references

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C25H32O13/c1-3-13-14(9-19(29)35-7-6-12-4-5-16(27)17(28)8-12)15(23(33)34-2)11-36-24(13)38-25-22(32)21(31)20(30)18(10-26)37-25/h3-5,8,11,14,18,20-22,24-28,30-32H,6-7,9-10H2,1-2H3/b13-3+/t14-,18+,20+,21-,22+,24-,25-/m0/s1

1 reference

OLEUROPEIN (English)

18 November 2016

2 references

splash10-0ue9-0009600000-947c879bdb2058d41453

1 reference

0 references

splash10-0c00-0026950000-87e2892e14652b90374c

0 references

splash10-004i-0399000000-ddf8b0b19a4f3b7950a7

0 references

splash10-000i-0900000000-61db18e4286e83b02dde

0 references

splash10-002r-0795070000-44f113f7f78398bc643e

0 references

splash10-03di-0002390000-798eb1c83fcb3d0f9f7e

0 references

DSSTox substance ID

DTXSID60905103

1 reference

DSSTOX compound identifier

DTXCID401334206

0 references

EC number

251-129-6

1 reference

oleuropein (English)

ECHA Substance Infocard ID

18 November 2016

100.046.466

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.046.466

27 December 2018

Guide to Pharmacology Ligand ID

2-(3,4-dihydroxyphenyl)ethyl [2S-(2α,3E,4β)]-3-ethylidene-2-(β-D-glucopyranosyloxy)-3,4-dihydro-5-(methoxycarbonyl)-2H-pyran-4-acetate (English)

quotation

CAS no.: 32619-42-4 (English)

11027

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

5 February 2021

1 reference

MeSH descriptor ID

C002769

Human Metabolome Database ID

14 March 2018

HMDB0035872

2 references

2 references

oleuropein (English)

18 November 2016

NDF-RT ID

N0000182737

1 reference

Encyclopedia of China (Third Edition) ID

oleuropein (English)

18 November 2016

0 references

0 references

1 reference

28 October 2013

1 reference

10 September 2022

https://golden.com/wiki/Oleuropein-ZWZ8EP

Microsoft Academic ID

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

UMLS CUI

C0069413

1 reference

oleuropein (English)