(E)-cinnamaldehyde (Q204036)

Gene Ontology release 2020-05-02

Rhea release 113

cinnamyl-alcohol dehydrogenase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

chemical structure

Zimtaldehyd - cinnamaldehyde.svg
214 × 129; 3 KB

1 reference

German Wikipedia

mass

132.057515 dalton

1 reference

cinnamaldehyde (English)

3 October 2016

chemical formula

C₉H₈O

1 reference

cinnamaldehyde (English)

19 November 2016

canonical SMILES

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

1 reference

cinnamaldehyde (English)

19 November 2016

isomeric SMILES

C1=CC=C(C=C1)/C=C/C=O

1 reference

cinnamaldehyde (English)

19 November 2016

density

1.05 gram per cubic centimetre

25 degree Celsius

1 reference

30 March 2020

−8 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

boiling point

253 degree Celsius

under pressure

760 torr

1 reference

30 March 2020

120 degree Celsius

1 reference

30 March 2020

safety classification and labelling

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

no value

1 reference

Miscellaneous contributions to the essential oils of plants from various territories. XLVII. On the components of essential oils of Cinnamomum sieboldii Meisn

1 reference

Chaerophyllum bulbosum

1 reference

Essential oil of turnip-root chervil

Litchi chinensis

1 reference

Volatile constituents of litchi (Litchi chinesis Sonn.)

Swertia japonica

1 reference

Semburins and Swertiols, Novel 2,8-Dioxabicyclo[3.3.1]nonanes and Their Precursory Alcohols, from Swertia japonica Makino

starfruit

1 reference

Volatile constituents of carambola (Averrhoa carambola L.)

Cinnamomum cassia

14 references

In vivo cytokine modulatory effects of cinnamaldehyde, the major constituent of leaf essential oil from Cinnamomum osmophloeum Kaneh

Determination of cinnamaldehyde, coumarin and cinnamyl alcohol in cinnamon and cassia by high-performance liquid chromatography

Determination of Cinnamomi Cortex by high-performance liquid chromatography

Cinnamaldehyde inhibits lymphocyte proliferation and modulates T-cell differentiation.

Growth-Inhibiting Effects of Cinnamomum cassia Bark-Derived Materials on Human Intestinal Bacteria

A fluorometric assay of trans-cinnamaldehyde in cinnamon

Potent inhibition of human phosphodiesterase-5 by icariin derivatives.

Tyrosinase-inhibitory constituents from the twigs of Cinnamomum cassia

Effects of cinnamaldehyde on PGE2 release and TRPV4 expression in mouse cerebral microvascular endothelial cells induced by interleukin-1beta

Suppression effect of Cinnamomum cassia bark-derived component on nitric oxide synthase

The Major Constituents of the Essential Oils of Cinnamomum Cassia BLUME Growing in Nigeria

Cinnamaldehyde and 2-methoxycinnamaldehyde as NF-kappaB inhibitors from Cinnamomum cassia

Tyrosinase-inhibitory constituents from the twigs of Cinnamomum cassia

Anti-Inflammatory Activities of Cinnamomum cassia Constituents In Vitro and In Vivo

Cinnamomum yabunikkei

1 reference

In vivo cytokine modulatory effects of cinnamaldehyde, the major constituent of leaf essential oil from Cinnamomum osmophloeum Kaneh

Cinnamomum tamala

2 references

In vivo cytokine modulatory effects of cinnamaldehyde, the major constituent of leaf essential oil from Cinnamomum osmophloeum Kaneh

Cinnamon Leaf Oil from Cinnamomum tamala Grown in Nepal.

Cinnamomum zeylanicum

8 references

In vivo cytokine modulatory effects of cinnamaldehyde, the major constituent of leaf essential oil from Cinnamomum osmophloeum Kaneh

The antibacterial component from Cinnamomi Cortex against a cariogenic bacteriumStreptococcus mutans OMZ 176

Determination of cinnamaldehyde, coumarin and cinnamyl alcohol in cinnamon and cassia by high-performance liquid chromatography

Volatile constituents of cinnamon (Cinnamomum zeylanicum) oils

A fluorometric assay of trans-cinnamaldehyde in cinnamon

In vitro antibacterial activity of some plant essential oils

Quality control of traditional chinese drugs by high performance liquid chromatography.

Studies on Cinnamomum zeylanicum

Lauraceae

1 reference

Cinnamaldehyde inhibits pro-inflammatory cytokines secretion from monocytes/macrophages through suppression of intracellular signaling

Rhodiola rosea

1 reference

Volatiles from rhizomes of Rhodiola rosea L.

Heteranthemis viscidehirta

1 reference

Antibacterial and molluscicidal activities of the essential oil of Chrysanthemum viscidehirtum

Alpinia chinensis

1 reference

Chemical Composition of the Flower Oil ofAlpinia chinensisRosc, from Vietnam

Alpinia katsumadai

2 references

Studies on the constituents of the seeds of Alpinia katsumadai Hayata.

Studies on the constituents of the seeds of Alpinia katsumadai Hayata.

Apium graveolens

1 reference

GC/MS and GC/FTIR Analysis of the Essential Oil of Celery Seed

Alpinia latilabris

1 reference

Volatile Constituents of the Seed and Fruit Skin Oils of Catimbium latilabre (Ridl.) Holtt. from Vietnam

Cinnamomum osmophloeum

1 reference

Antibacterial activity of leaf essential oils and their constituents from Cinnamomum osmophloeum

Cryptocarya amygdalina

2 references

The Constituents and Synthesis of Cryptamygin-A from the Stem Bark ofCryptocarya Amygadalina

The Constituents and Synthesis of Cryptamygin-A from the Stem Bark ofCryptocarya Amygadalina

Cucurbita maxima

1 reference

The composition of the floral odor of Cucurbita maxima Duchesne (Cucurbitaceae)

Curcuma xanthorrhiza

1 reference

Three non-phenolic diarylheptanoids with anti-inflammatory activity from Curcuma xanthorrhiza

Ficus carica

1 reference

Volatile compounds from extracts of figs of Ficus carica

Illicium verum

1 reference

Effects of p-Methoxycinnamaldehyde from Star Anise and Related Cinnamic Acid Derivatives on Velvetleaf Germination

Ocotea quixos

1 reference

Ocotea quixos, American cinnamon

Polygala senega

1 reference

Volatile compounds ofPolygala senega L. var.latifolia Torrey et Gray roots

Rhanterium epapposum

1 reference

Volatile components ofRhanterium epapposum oliv

Rosa × damascena

1 reference

Contact dermatitis from geraniol in Bulgarian rose oil.

Rosa gallica

1 reference

Contact dermatitis from geraniol in Bulgarian rose oil.

Syzygium jambos

1 reference

Volatile Constituents of the Jamrosa AromaSyzygium jambosL. Aston from Reunion Island

Kaempferia galanga

1 reference

Repellent and insecticidal effects of the essential oil of Kaempferia galanga rhizomes to Liposcelis bostrychophila (Psocoptera: Liposcelidae).

Centaurea benedicta

1 reference

CONSTITUTION ET PROPRIETES ANTIBACTERIENNES DE L'HUILE ESSENTIELLE DECNICUS BENEDICTUS

Coespeletia timotensis

1 reference

Essential oil of Coespeletia timotensis Cuatrec

Espeletia timotensis

1 reference

Essential oil of Coespeletia timotensis Cuatrec

Alpinia hainanensis

1 reference

Studies on the constituents of the seeds of Alpinia katsumadai Hayata.

Mangifera indica

1 reference

Volatile components from mango (Mangifera indica L.) cultivars

Arabidopsis thaliana

1 reference

Characterization of two novel aldo-keto reductases from Arabidopsis: expression patterns, broad substrate specificity, and an open active-site structure suggest a role in toxicant metabolism following stress

Nicotiana tabacum

1 reference

A Chemical Study of Burley Tobacco Flavour (Nicotiana tabacum L.). I. Volatile to medium-volatile constituents (b.p. ≦ 84°/0.001 Torr

clove

1 reference

The chemical composition and biological activity of clove essential oil, Eugenia caryophyllata (Syzigium aromaticum L. Myrtaceae): a short review

Mimusops elengi

1 reference

Volatile Components of Mimusops elengi L. Flowers

Cinnamon

8 references

Volatile constituents of cinnamon (Cinnamomum zeylanicum) oils

Studies on Cinnamomum zeylanicum

Determination of cinnamaldehyde, coumarin and cinnamyl alcohol in cinnamon and cassia by high-performance liquid chromatography

In vitro antibacterial activity of some plant essential oils

Quality control of traditional chinese drugs by high performance liquid chromatography.

The antibacterial component from Cinnamomi Cortex against a cariogenic bacteriumStreptococcus mutans OMZ 176

In vivo cytokine modulatory effects of cinnamaldehyde, the major constituent of leaf essential oil from Cinnamomum osmophloeum Kaneh

A fluorometric assay of trans-cinnamaldehyde in cinnamon

Malus pumila

1 reference

Headspace and essential oil analysis of apple flowers

Vachellia rigidula

1 reference

Volatile components of Acacia sp. blossoms

Cinnamomum burmanni

13 references

Determination of Cinnamomi Cortex by high-performance liquid chromatography

Suppression effect of Cinnamomum cassia bark-derived component on nitric oxide synthase

Tyrosinase-inhibitory constituents from the twigs of Cinnamomum cassia

Anti-Inflammatory Activities of Cinnamomum cassia Constituents In Vitro and In Vivo

Determination of cinnamaldehyde, coumarin and cinnamyl alcohol in cinnamon and cassia by high-performance liquid chromatography

Cinnamaldehyde and 2-methoxycinnamaldehyde as NF-kappaB inhibitors from Cinnamomum cassia

The Major Constituents of the Essential Oils of Cinnamomum Cassia BLUME Growing in Nigeria

In vivo cytokine modulatory effects of cinnamaldehyde, the major constituent of leaf essential oil from Cinnamomum osmophloeum Kaneh

Growth-Inhibiting Effects of Cinnamomum cassia Bark-Derived Materials on Human Intestinal Bacteria

A fluorometric assay of trans-cinnamaldehyde in cinnamon

Potent inhibition of human phosphodiesterase-5 by icariin derivatives.

Effects of cinnamaldehyde on PGE2 release and TRPV4 expression in mouse cerebral microvascular endothelial cells induced by interleukin-1beta

Cinnamaldehyde inhibits lymphocyte proliferation and modulates T-cell differentiation.

Malus domestica

1 reference

Headspace and essential oil analysis of apple flowers

Matsutake

1 reference

Volatile flavor compounds of Matsutake-Tricholomam atsutake (Ito et Imai) Sing.

Thymus

1 reference

ANTIBACTERIAL AND CHEMICAL PROPERTIES OF THYMUS PERSICUS ESSENTIAL OILS AT PRE AND FLOWERING STAGES

physically interacts with

Transient receptor potential cation channel, subfamily A, member 1

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Transient receptor potential cation channel, subfamily V, member 3

17 August 2016

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

phytogenic antineoplastic agents

17 August 2016

subject has role

1 reference

15 March 2018

1 reference

15 March 2018

1 reference

MeSH descriptor ID

C012843

xanthine oxidase inhibitor

15 March 2018

1 reference

InChI=1S/C9H8O/c10-8-4-7-9-5-2-1-3-6-9/h1-8H/b7-4+

20 August 2019

0 references

0 references

Cinnamaldehyde

0 references

Identifiers

InChI

1 reference

cinnamaldehyde (English)

19 November 2016

2 references

cinnamaldehyde (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

14371-10-9

2 references

Global Substance Registration System

cinnamaldehyde (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=14371-10-9

10 April 2021

1 reference

Cinnamaldehyde (English)

19 November 2016

2 references

cinnamaldehyde (English)

19 November 2016

Reaxys registry number

1071571

1 reference

cinnamaldehyde (English)

3 October 2016

ChEBI ID

16731

mapping relation type

2 references

CINNAMALDEHYDE (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C9H8O/c10-8-4-7-9-5-2-1-3-6-9/h1-8H/b7-4+

1 reference

CINNAMALDEHYDE (English)

19 November 2016

2 references

SCHEMBL3441

2 references

MSBNK-Fac_Eng_Univ_Tokyo-JP002122

1 reference

MassBank accession ID

0 references

MSBNK-RIKEN-PR100059

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP004930

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP005392

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP005393

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP007347

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP007433

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP008083

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP008705

0 references

SPLASH

splash10-0f89-5900000000-482f8b5c30c53689d8eb

0 references

splash10-001i-3900000000-9d274f5e3981ab662650

0 references

splash10-001i-0900000000-4f0ad7748ac21b7320c9

0 references

splash10-0f89-6900000000-ecaba4b9d657020c3f4c

0 references

splash10-001i-0900000000-c02b7869dea8f1113cb4

0 references

splash10-001i-2900000000-d89aa99ef7a6ae16b942

0 references

splash10-0ugi-8900000000-14f14e29c81360ebdd4b

0 references

splash10-067i-2900000000-76d2db81f3822a698f0a

0 references

splash10-000f-9000000000-1f1780c664d76621d665

0 references

splash10-0059-3900000000-52db83b595237437ab08

0 references

splash10-056r-9300000000-043ea317ed08a1cbacfb

0 references

splash10-0a59-5900000000-a125425df0f09bb01129

0 references

splash10-004i-9000000000-39ab07ef5d737e851671

0 references

NMRShiftDB structure ID

10005746

1 reference

RTECS number

GD6475000

1 reference

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

2 references

DSSTOX compound identifier

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.111.079

27 December 2018

ECHA Substance Infocard ID

(2E)-3-phenylprop-2-enal (English)

quotation

CAS no.: 14371-10-9 (English)

100.111.079

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.111.079

27 December 2018

PesticideInfo chemical ID

(2E)-3-phenylprop-2-enal (English)

quotation

CAS no.: 14371-10-9 (English)

PRI6288

0 references

Nikkaji ID

J43.393D

0 references

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

cinnamaldehyde (English)

19 November 2016

1 reference

Global Substance Registration System

14 March 2018

1 reference

cinnamaldehyde (English)

19 November 2016

DrugBank ID

DB14184

1 reference

Human Metabolome Database ID

HMDB0003441

2 references

3 references

cinnamaldehyde (English)

3 October 2016

C00002725

2 references

2 references

Global Substance Registration System

cinnamaldehyde (English)

19 November 2016

0 references

1 reference

Immune Epitope Database and Analysis Resource

1 reference

1 March 2022

0 references

1 reference

28 October 2013

Great Russian Encyclopedia portal ID

korichnyi-al-degid-0d810d

0 references

J-GLOBAL ID

200907090358617998

0 references

Microsoft Academic ID

0 references

1 reference

26 January 2022

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

Store norske leksikon ID

kanelaldehyd

mapping relation type

0 references

1 reference

inferred by common MeSH mappings on source and on Wikidata

UMLS 2023