ethyl gallate (Q4532976)

ETHYL GALLATE (English)

19 October 2016

chemical formula

C₉H₁₀O₅

1 reference

ETHYL GALLATE (English)

19 October 2016

canonical SMILES

CCOC(=O)C1=CC(=C(C(=C1)O)O)O

1 reference

ETHYL GALLATE (English)

19 October 2016

melting point

150.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Rhus chinensis

2 references

Chemical Constituents of Rhus chinensis

Phenolic Constituents of Rhus semialata Leaves

Acer negundo

1 reference

GALLOTANNIN AND FLAVONOID GLYCOSIDES FROM THE STEM BARK OF ACER NEGUNDO (L.)

Entada pervillei

1 reference

Antiplasmodial phenolic compounds from Piptadenia pervillei

Toxicodendron vernicifluum

1 reference

Inhibitory effect of the compounds isolated from Rhus verniciflua on aldose reductase and advanced glycation endproducts

Paeonia anomala

1 reference

A chemical study of the roots of Paeonia anomala

Acalypha hispida

1 reference

Antimicrobial constituents of the leaves ofAcalypha wilkesiana and Acalypha hispida

Limonium axillare

1 reference

A new flavonoid from Limonium axillare

Terminalia arjuna

1 reference

Antineoplastic agents 338. The cancer cell growth inhibitory. Constituents of Terminalia arjuna (Combretaceae)

Acer rubrum

1 reference

1-O-galloyl-α-l-rhamnose from Acer rubrum

Haematoxylum campechianum

3 references

Phenolics and flavonoids from Haematoxyloncampechianum

Gallotannins and flavonoids from Haematoxylon campechianum.

Flavonoids and other phenolics of Haematoxylon campechianum

Acer oblongum

1 reference

Ethyl brevifolin carboxylate and other constituents from Acer oblongum leaves

Ailanthus altissima

1 reference

Phenolic compounds from Ailanthus altissima Swingle

Alchornea glandulosa

1 reference

Biological activity of phenolic compounds from Alchornea glandulosa

Euphorbia ferganensis

1 reference

Phenolic compounds ofEuphorbia ferganensis

Euphorbia maculata

1 reference

Chemical constituents from Euphorbia lunulata

Koelreuteria paniculata

1 reference

Polyphenolic compounds from the leaves of Koelreuteria paniculata Laxm

Mabea fistulifera

1 reference

A bioactive naringenin coumaroyl glucoside from Mabea fistulifera subsp. robusta

Nymphaea alba

1 reference

Phenolic arids from the flowers of Nymphaea alba L.

Phyllanthus sellowianus

1 reference

A Triterpene and Phenolic Compounds from Leaves and Stems ofPhyllanthus sellowianus

Phyllanthus urinaria

1 reference

The mechanisms underlying the relaxant effect of methyl and ethyl gallates in the guinea pig trachea in vitro: contribution of potassium channels

Rhodiola crenulata

1 reference

Chemical constituents of Rhodiola kirilowii Maxim.

Rhodiola fastigiata

1 reference

Chemical constituents of Rhodiola kirilowii Maxim.

Terminalia chebula

3 references

Chemical Constituents of Terminalia chebula

Extraction and purification of effective antimicrobial constituents of Terminalia chebula RETS. against methicillin-resistant Staphylococcus aureus

Inhibition of cancer cell growth by crude extract and the phenolics of Terminalia chebula retz. fruit

Terminalia myriocarpa

1 reference

Pharmacologically active ellagitannins from Terminalia myriocarpa

Dimocarpus longan

1 reference

Antimicrobial activities of various fractions of longan (Dimocarpus longan Lour. Fen Ke) seed extract

Phyllanthus emblica

2 references

Progallin A isolated from the acetic ether part of the leaves of Phyllanthus emblica L. induces apoptosis of human hepatocellular carcinoma BEL-7404 cells by up-regulation of Bax expression and down-regulation of Bcl-2 expression

A New Ellagitannin from the Fruit ofPhyllanthus EmblicaL.

Phyfnnvik eyyfn

1 reference

Suppression of TNF-α induced NFκB activity by gallic acid and its semi-synthetic esters: possible role in cancer chemoprevention

Vitis vinifera

1 reference

Direct determination of phenolic compounds in Sicilian wines by liquid chromatography with PDA and MS detection

Acer truncatum

1 reference

Weight-reducing effect of Acer truncatum Bunge may be related to the inhibition of fatty acid synthase

Cashew

1 reference

Polyphenols of anacardium occidentale

Bombax malabaricum

1 reference

Chemical examination of the seeds of Bombax malabaricum

Canarium album

1 reference

Phenolic constituents of Canarium album

Elaeocarpus tuberculatus

1 reference

Chemical investigation of some Elaeocarpus species

Excoecaria agallocha

1 reference

Inhibitory effects of polyphenols toward HCV from the mangrove plant Excoecaria agallocha L.

Pistacia mexicana

1 reference

L'acide masticadienonique de Pistacia mexicana

Pulicaria wightiana

1 reference

A Benzofuranoid and Two Clerodane Diterpenoids fromPulicaria wightiana

Rhus coriaria

1 reference

Polyphenolic components of Rhus coriaria leaves

Syzygium cumini

1 reference

Chemical constituents of the seeds and bark of Syzygium cumini

Toona sinensis

2 references

Antioxidant activities of Toona Sinensis leaves extracts using different antioxidant models

α-glucosidase inhibitory constituents from Toona sinensis

Excoecaria acerifolia

1 reference

Chemical constituents of Excoecaria acerifolia and their bioactivities

Trewia nudiflora

1 reference

Chemical Constituents from the Pericarp ofTrewia nudiflora

Nephelium lappaceum

1 reference

Fatty acid synthase inhibitors from the hulls of Nephelium lappaceum L.

Distylium racemosum

1 reference

Compounds with tyrosinase inhibition, elastase inhibition and DPPH radical scavenging activities from the branches of Distylium racemosum Sieb. et Zucc

Acer ginnala

1 reference

1-O-galloyl-α-l-rhamnose from Acer rubrum

Punica granatum

1 reference

A comprehensive study of pomegranate flowers polyphenols and metabolites in rat biological samples by high-performance liquid chromatography quadrupole time-of-flight mass spectrometry

Ocimum tenuiflorum

1 reference

New Constituents from Ocimum sanctum

Bombax ceiba

1 reference

Chemical examination of the seeds of Bombax malabaricum

Archidendron clypearia

1 reference

Effects of Pithecellobium clypearia Benth extract and its main components on inflammation and allergy.

1 reference

0 references

Ethyl gallate

0 references

Identifiers

InChI

InChI=1S/C9H10O5/c1-2-14-9(13)5-3-6(10)8(12)7(11)4-5/h3-4,10-12H,2H2,1H3

1 reference

ETHYL GALLATE (English)

19 October 2016

2 references

ETHYL GALLATE (English)

19 October 2016

ChEBI release 2020-09-01

2 references

ethyl gallate (English)

19 October 2016

https://commonchemistry.cas.org/detail?cas_rn=831-61-8

10 April 2021

1 reference

Ethyl gallate (English)

19 October 2016

2 references

ETHYL GALLATE (English)

19 October 2016

Reaxys registry number

2116014

1 reference

ethyl gallate (English)

19 October 2016

ChEBI ID

87247

mapping relation type

2 references

ethyl gallate (English)

19 October 2016

International Chemical Identifier

InChI

InChI=1S/C9H10O5/c1-2-14-9(13)5-3-6(10)8(12)7(11)4-5/h3-4,10-12H,2H2,1H3

1 reference

ETHYLGALLATE (English)

19 October 2016

2 references

inferred from InChIKey

splash10-001i-0291200000-d1ec8193d3b49ff9e32e

1 reference

0 references

RTECS number

LW7700000

1 reference

imported from Wikimedia project

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

212-608-5

1 reference

Global Substance Registration System

UNII

235I6UDD3L

ethyl gallate (English)

ECHA Substance Infocard ID

19 October 2016

100.011.462

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.011.462

27 December 2018

AICS Chemical ID (BEING DELETED)

Ethyl 3,4,5-trihydroxybenzoate (English)

quotation

CAS no.: 831-61-8 (English)

0 references

1 reference

28 December 2019

ETHYL GALLATE (English)

quotation

CAS no.: 831-61-8 (English)

5743

0 references

Human Metabolome Database ID

HMDB0033836

2 references

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00030222

2 references

based on heuristic

inferred from InChIKey

UNII

235I6UDD3L

2 references

Global Substance Registration System

UNII

235I6UDD3L

ethyl gallate (English)

19 October 2016

0 references

0 references

1 reference

28 October 2013

Microsoft Academic ID

0 references

1 reference

4JUI (English)

19 October 2016

1 reference

4J0K (English)