(Q229987)

imported from Wikimedia project

Medical Subject Headings

15 March 2018

Methylparaben.svg
512 × 512; 12 KB

1 reference

German Wikipedia

mass

152.047 dalton

1 reference

Methyl 4-hydroxybenzoate (English)

19 October 2016

chemical formula

C₈H₈O₃

1 reference

Methyl 4-hydroxybenzoate (English)

19 November 2016

canonical SMILES

COC(=O)C1=CC=C(C=C1)O

1 reference

Methyl 4-hydroxybenzoate (English)

19 November 2016

melting point

127 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

safety classification and labelling

NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response

1

1

0

no value

1 reference

imported from Wikimedia project

2 references

Phytotoxic compounds from the new coprophilous fungus guanomyces polythrix

Phytotoxic naphthopyranone derivatives from the coprophilous fungus Guanomyces polythrix.

Securidaca longepedunculata

1 reference

Gas chromatographic/mass spectrometric investigation of the volatile main components from roots ofSecuridaca longipedunculata

Lessertia frutescens

1 reference

In vitro culture studies of Sutherlandia frutescens on human tumor cell lines

Oxalis tuberosa

1 reference

Exudation of fluorescent beta-carbolines from Oxalis tuberosa L roots

Lactuca indica

1 reference

Antioxidant properties and phytochemical characteristics of extracts from Lactuca indica

Hypericum ascyron

1 reference

Xanthones from Hypericum ascyron

Vitex agnus-castus

1 reference

Antiinflammatory and lipoxygenase inhibitory compounds from Vitex agnus-castus.

Houttuynia cordata

2 references

The constituents and their bioactivities of Houttuynia cordata

Constituents ofHouttuyniae Cordataand the Crystal Structure of Vomifoliol

Aristolochia kankauensis

1 reference

Aristolochic acids, aristolactam alkaloids and amides from Aristolochia kankauensis

Aristolochia zollingeriana

1 reference

Aristolochic acids, aristolactam alkaloids and amides from Aristolochia kankauensis

Stocksia brahuica

1 reference

Benzoic acid derivatives from Stocksia brahuica

moringa

1 reference

Hypotensive constituents from the pods of Moringa oleifera

Petasites formosanus

2 references

The bakkenolides from the root of Petasites formosanus and their cytotoxicity

Constituents of the Leaves of Petasites formosanus and Their Antioxidative Activity

Aristolochia cucurbitifolia

1 reference

Constituents of the Fresh Leaves of Aristolochia cucurbitifolia.

Aristolochia elegans

3 references

Constituents from the leaves of Aristolochia elegans

The alkaloids and other constituents from the root and stem of Aristolochia elegans

The constituents of the root and stem of Aristolochia heterophylla Hemsl

Aristolochia heterophylla

2 references

The constituents of the root and stem of Aristolochia heterophylla Hemsl

Constituents from the leaves of Aristolochia elegans

Lonicera angustifolia

1 reference

A new secoiridoid glycoside from Lonicera angustifolia

Annona purpurea

3 references

Four alkaloids from Annona cherimola.

New alkaloids from Annona purpurea

Tryptamine-derived amides and alkaloids from the seeds of Annona atemoya.

Gonocaryum calleryanum

2 references

A secoiridoid and other constituents of gonocaryum calleryanum

A secoiridoid and other constituents of Gonocaryum calleryanum

Annona cherimola

4 references

Cheritamine, A NewN-Fatty Acyl Tryptamine and Other Constituents from the Stems ofAnnona cherimola

Annocherine C, A New C-α Hydroxy Benzylisoquinoline and Other Constituents from the Leaves ofAnnona Cherimola

Tryptamine-derived amides and alkaloids from the seeds of Annona atemoya.

New alkaloids from Annona purpurea

Artemisia capillaris

1 reference

New constituents and antiplatelet aggregation and anti-HIV principles of Artemisia capillaris

Lindera glauca

2 references

Constituents of Lindera erythrocarpa

The Constituents ofLindera Glauca

Crocus sativus

5 references

Constituents of the pollen of Crocus sativus L. and their tyrosinase inhibitory activity

Antityrosinase principles and constituents of the petals of Crocus sativus

Constituents of the Pollen of Crocus sativus L. and Their Tyrosinase Inhibitory Activity.

Constituents of the stigmas of Crocus sativus and their tyrosinase inhibitory activity

Saffron. Crocus sativus L.

Peperomia leptostachya

1 reference

Chemical and cytotoxic constituents from Peperomia sui

Taraxacum formosanum

3 references

Chemical Constituents of Taraxacum formosanum.

Chemical constituents of Taraxacum formosanum

Chemical constituents from roots of Taraxacum formosanum

Begonia nantoensis

2 references

Cytotoxic and anti-HIV Principles from the Rhizomes of Begonia nantoensis.

Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensis

Tamarix aphylla

1 reference

Antimicrobial Activity and Phytochemical Constituents of Leaf Extracts of Cassia auriculata

Allium grayi

1 reference

Nematicidal and antimicrobial constituents from Allium grayi regel and Allium fistulosum L. var. caespitosum.

Tachigali paniculata

1 reference

Antioxidant and free-radical scavenging activity of constituents of the leaves of Tachigalia paniculata

Streptomyces xiamenensis

1 reference

Chemical constituents from the deep sea-derived Streptomyces xiamenensis MCCC 1A01570 and their effects on RXRα transcriptional regulation

Andrographis paniculata

1 reference

p-Hydroxybenzoic acid alkyl esters in Andrographis paniculata herbs, commercial extracts, and formulated products.

Nigrospora sphaerica

1 reference

Nigrosphaerin A a new isochromene derivative from the endophytic fungus Nigrospora sphaerica

Machilus zuihoensis

1 reference

Steryl epoxide, secobutanolide and butanolides from the stem wood of Machilus zuihoensis

Monascus pilosus

1 reference

Secondary metabolites from the mycelia of the fungus Monascus pilosus BCRC 38072.

Neolitsea acuminatissima

1 reference

Cytotoxic constituents of the stem bark of Neolitsea acuminatissima

Phellodendron amurense

3 references

Constituents from the leaves of Phellodendron amurense and their antioxidant activity

Constituents from the leaves of Phellodendron amurense var. wilsonii and their bioactivity

Constituents of leaves of Phellodendron japonicum MAXIM. and their antioxidant activity

Viscum articulatum

2 references

The inhibition of superoxide anion generation by neutrophils from Viscum articulactum

The inhibition of superoxide anion generation in human neutrophils by Viscum coloratum

Haplopteris anguste-elongata

1 reference

Constituents of Vittaria anguste-elongata and their biological activities

Zanthoxylum ailanthoides

2 references

Amides and benzenoids from Zanthoxylum ailanthoides with inhibitory activity on superoxide generation and elastase release by neutrophils

Chemical Constituents from the Root Bark of FormosanZanthoxylum Ailanthoides

Allium macrostemon

1 reference

Nematicidal and antimicrobial constituents from Allium grayi regel and Allium fistulosum L. var. caespitosum.

Schisandra

1 reference

Constituents ofSchisandra verruculosa. and Their Cytotoxic Effect on Human Cancer Cell Lines

Aster himalaicus

1 reference

Eudesmane sesquiterpenes and other constituents from Aster himalaicus

Cestrum parqui

1 reference

Low molecular weight phenols from the bioactive aqueous fraction of Cestrum parqui

Glebionis coronaria

1 reference

Novel Plant Growth Inhibitors and an Insect Antifeedant fromChrysanthemum coronarium(Japanese Name: Shungiku)

Glebionis coronarium

1 reference

Novel Plant Growth Inhibitors and an Insect Antifeedant fromChrysanthemum coronarium(Japanese Name: Shungiku)

Great diving beetle

1 reference

Zur Kenntnis der Pygidialblasensubstanzen vom Gelbrandkäfer (Dytiscus marginalis L.)

Gynura japonica

1 reference

Cerebrosides from the Rhizomes ofGynura Japonica

Illigera luzonensis

1 reference

Aporphine alkaloids and cytotoxic lignans from the roots of Illigera luzonensis

Leucaena leucocephala

1 reference

Secondary metabolites from Leucaena leucocephala

Litsea hypophaea

1 reference

Secondary metabolites from the roots of Litsea hypophaea and their antitubercular activity

Magnolia kachirachirai

1 reference

Secondary Metabolites from Magnolia kachirachirai

Marasmiellus ramealis

1 reference

Isolation and partial synthesis of 3-methoxycarbonyl-7-formyl-1-benzoxepin-5(2H)-one, the ester of a metabolite from shake cultures of the fungus Marasmiellus ramealis(Bull. ex Fr.) Singer

Magnolia compressa

1 reference

Chemical constituents from the leaves of Michelia compressa var. formosana

Muntingia calabura

1 reference

New dihydrochalcones and anti-platelet aggregation constituents from the leaves of Muntingia calabura

Common rose

1 reference

Aristolochic Acids as a Defensive Substance for the Aristolochiaceous Plant-Feeding Swallowtail Butterfly,Pachliopta aristolochiae interpositus

Peltostigma guatemalense

1 reference

Biological activity of secondary metabolites from Peltostigma guatemalense.

Phellodendron amurense var. wilsonii

1 reference

Constituents from the leaves of Phellodendron amurense var. wilsonii and their bioactivity

Phellodendron chinense var. glabriusculum

1 reference

Constituents from the leaves of Phellodendron amurense var. wilsonii and their bioactivity

Piper lolot

1 reference

Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot

Piper sarmentosum

1 reference

Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot

Rhizophora apiculata

1 reference

Phthalide and Isocoumarin Derivatives Produced by an Acremonium sp. Isolated from a Mangrove Rhizophora apiculata

Rodgersia sambucifolia

1 reference

Chemical Constituents from the Root Bark ofRodgersia Sambucifolia

Sambucus adnata

1 reference

Chemical Constituents from Sambucus adnata and Their Protein-Tyrosine Phosphatase 1B Inhibitory Activities

Synsepalum dulcificum

1 reference

Chemical constituents from the roots of Synsepalum dulcificum

Tetradium glabrifolium

1 reference

The heartwood constituents of Tetradium glabrifolium

Zanthoxylum beecheyanum

1 reference

Chemical and Antiplatelet Constituents from the Stem ofZanthoxylum Beecheyanum

Lipschitziella deltoidea

1 reference

Secondary Metabolites from Saussurea deltoidea and Their Inhibitory Activity on Lipopolysaccharide-Induced Tumor Necrosis Factor Production

Papaver rhoeas

1 reference

Depsides from the petals of Papaver rhoeas

Anisomeles indica

1 reference

Bioactive cembrane diterpenoids of Anisomeles indica

Daphne tangutica

1 reference

Chemical constituents investigation of Daphne tangutica.

Ocimum gratissimum

1 reference

Basil. The genus Ocimum

Cucurbita moschata

1 reference

Cucurbitane-type triterpenoids from the stems of Cucumis melo

Zanthoxylum rhoifolium

1 reference

Amides and benzenoids from Zanthoxylum ailanthoides with inhibitory activity on superoxide generation and elastase release by neutrophils

Moringa pterygosperma

1 reference

Hypotensive constituents from the pods of Moringa oleifera

Pueraria montana var. lobata

1 reference

Isoflavonoids and the other constituents in callus tissues of Pueraria lobata.

Cannabis sativa

2 references

Constituents of Cannabis Sativa

Chemical Constituents of Cannabis sativa L. Root

Mangifera indica

1 reference

Glycosidically-bound aroma volatile compounds in the skin and pulp of ‘Kensington Pride’ mango fruit at different stages of maturity

Saccharomyces cerevisiae

1 reference

Overproduction of squalene synergistically downregulates ethanol production in Saccharomyces cerevisiae

Thalictrum lucidum

2 references

Alkaloids of Thalictrum angustifolium

Alkaloids of Thalictrum angustifolium

Taraxacum mongolicum

3 references

Chemical constituents from roots of Taraxacum formosanum

Chemical Constituents of Taraxacum formosanum.

Chemical constituents of Taraxacum formosanum

Aristolochia littoralis

3 references

Constituents from the leaves of Aristolochia elegans

The alkaloids and other constituents from the root and stem of Aristolochia elegans

The constituents of the root and stem of Aristolochia heterophylla Hemsl

Aristolochia kaempferi

4 references

Constituents from the leaves of Aristolochia elegans

The constituents of the root and stem of Aristolochia heterophylla Hemsl

Constituents of the Leaves of Aristolochia kaempferi.

Constituents from the stem and root of Aristolochia kaempferi

Nigrospora oryzae

1 reference

Nigrosphaerin A a new isochromene derivative from the endophytic fungus Nigrospora sphaerica

Kadsura verrucosa

1 reference

Constituents ofSchisandra verruculosa. and Their Cytotoxic Effect on Human Cancer Cell Lines

Chelonanthus albus

1 reference

Chemical constituents from the leaves of Michelia alba

Peperomia humilis

1 reference

Chemical and cytotoxic constituents from Peperomia sui

physically interacts with

Transient receptor potential cation channel, subfamily A, member 1

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

6273

InChI=1S/C8H8O3/c1-11-8(10)6-2-4-7(9)5-3-6/h2-5,9H,1H3

17 August 2016

1 reference

27 February 2018

2918.29.22

0 references

0 references

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Methylparaben

0 references

Identifiers

InChI

1 reference

Methyl 4-hydroxybenzoate (English)

19 November 2016

2 references

Methyl 4-hydroxybenzoate (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

99-76-3

2 references

methylparaben (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=99-76-3

9 April 2021

1 reference

Methylparaben (English)

19 November 2016

1 reference

Methyl 4-hydroxybenzoate (English)

19 November 2016

ChEBI ID

31835

mapping relation type

2 references

METHYLPARABEN (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C8H8O3/c1-11-8(10)6-2-4-7(9)5-3-6/h2-5,9H,1H3

1 reference

METHYLPARABEN (English)

19 November 2016

2 references

inferred from InChIKey

MSBNK-Fac_Eng_Univ_Tokyo-JP000067

1 reference

MassBank accession ID

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP002806

0 references

MSBNK-Athens_Univ-AU237157

0 references

MSBNK-Athens_Univ-AU237158

0 references

MSBNK-Athens_Univ-AU237162

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP004566

0 references

SPLASH

splash10-00di-5900000000-f3eccc0d6c2c948bd57b

0 references

splash10-00di-4900000000-c5ef5603a5b5d1102f5a

0 references

splash10-00di-7900000000-42b2fb742e91f0c75f63

0 references

splash10-00di-6900000000-84c13ea1bb11717dde42

0 references

NMRShiftDB structure ID

10008850

1 reference

Hazardous Substances Data Bank

0 references

1 reference

28 October 2019

METHYLPARABEN (English)

10 May 2021

2 references

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

DSSTOX compound identifier

0 references

0 references

0 references

1 reference

methylparaben (English)

ECHA Substance Infocard ID

19 November 2016

100.002.532

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.002.532

27 December 2018

Open Food Facts food additive ID

Methyl 4-hydroxybenzoate (English)

quotation

CAS no.: 99-76-3 (English)

E number

E218

0 references

e218-methyl-p-hydroxybenzoate

0 references

1 reference

28 December 2019

METHYLPARABEN (English)

quotation

CAS no.: 99-76-3 (English)

PesticideInfo chemical ID

PRI4145

0 references

Nikkaji ID

J3.996I

0 references

Guide to Pharmacology Ligand ID

6273

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

6273

methyl p-hydroxybenzoate (English)

19 November 2016

1 reference

Medical Subject Headings

14 March 2018

1 reference

methylparaben (English)

19 November 2016

DrugBank ID

DB14212

1 reference

Human Metabolome Database ID

HMDB0032572

2 references

based on heuristic

inferred from InChIKey

1 reference

methylparaben (English)

19 October 2016

C00030751

2 references

based on heuristic

inferred from InChIKey

2 references

methylparaben (English)

19 November 2016

NDF-RT ID

N0000146196

1 reference

methylparaben (English)

19 November 2016

1 reference

26 February 2018

0 references

1 reference

1 reference

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

methylparaben (English)

19 October 2016

0 references

1 reference

6 April 2020

1 reference

28 October 2013

0 references

Microsoft Academic ID

0 references

1 reference

26 January 2022

1 reference

2VK0 (English)

19 October 2016

1 reference

3MTH (English)

19 October 2016

1 reference

1 reference

methylparaben (English)