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Details

Stereochemistry ACHIRAL
Molecular Formula C10H16
Molecular Weight 136.234
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MYRCENE

SMILES

CC(C)=CCCC(=C)C=C

InChI

InChIKey=UAHWPYUMFXYFJY-UHFFFAOYSA-N
InChI=1S/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7H,1,4,6,8H2,2-3H3

HIDE SMILES / InChI

Molecular Formula C10H16
Molecular Weight 136.234
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Isotope ratio by HRGC-MS of citrus Junos tanaka (yuzu) essential oils: m/z 137/136 of terpene hydrocarbons.
2001 Dec
Fungitoxic activity of 12 essential oils against four postharvest citrus pathogens: chemical analysis of thymus capitatus oil and its effect in subatmospheric pressure conditions.
2001 Jul
Practical synthesis of myrcene derivatives possessing oxidized methyl groups.
2001 Jun 15
Degradation of monoterpenes in orange juice by gamma radiation.
2001 May
Isolation and functional analysis of a cDNA encoding a myrcene synthase from holm oak (Quercus ilex L.).
2001 Nov
Volatile compounds of Psidium salutare (H.B.K.) Berg. fruit.
2002 Aug 28
Acaricidal activity of pine essential oils and their main components against Tyrophagus putrescentiae, a stored food mite.
2002 Jul 31
Effect of the essential oil from the flowers of Magnolia sieboldii on the lipopolysaccharide-induced production of nitric oxide and prostaglandin E2 by rat peritoneal macrophages.
2002 May
Anticonflict effects of rose oil and identification of its active constituents.
2002 Nov 22
Investigation on the supercritical CO(2) extraction of the volatile constituents from Juniperus communis obtained under different treatments of the "berries" (cones).
2002 Sep
Volatile chemicals identified in extracts from newly hybrid citrus, dekopon (Shiranuhi mandarin Suppl. J.).
2002 Sep 11
A cDNA clone for 3-carene synthase from Salvia stenophylla.
2003 Apr
Bacterial susceptibility to and chemical composition of essential oils from Thymus kotschyanus and Thymus persicus.
2003 Apr 9
Analysis of some Italian lemon liquors (limoncello).
2003 Aug 13
Antispasmodic effect of the essential oil of Plectranthus barbatus and some major constituents on the guinea-pig ileum.
2003 Dec
Monoterpenes produced by Cupressus lusitanica cultured cells including a novel monoterpene (1R, 2S, 6S)-(+)-1,6-epoxy-4(8)-p-menthen-2-ol [corrected].
2003 Dec
Analysis of volatile compounds of taperebá (Spondias mombin L.) and cajá (Spondias mombin L.) by simultaneous distillation and extraction (SDE) and solid phase microextraction (SPME).
2003 Feb 26
Changes of the volatile profile and artifact formation in Daidai (Citrus aurantium) cold-pressed peel oil on storage.
2003 Jul 2
Isolation of halogenated monoterpenes from bioreactor-cultured microplantlets of the macrophytic red algae Ochtodes secundiramea and Portieria hornemannii.
2003 Jun
Functional identification of AtTPS03 as (E)-beta-ocimene synthase: a monoterpene synthase catalyzing jasmonate- and wound-induced volatile formation in Arabidopsis thaliana.
2003 Mar
Halogenated monoterpene production by microplantlets of the marine red alga Ochtodes secundiramea within an airlift photobioreactor under nutrient medium perfusion.
2003 May 20
Composition and antimicrobial activity of Achillea clavennae L. essential oil.
2003 Nov
Content and composition of the essential oil of Thymus serpyllum L. growing wild in Estonia.
2004
[The crop-producing power and chemical composition of the essential oil of the cones of hop cultivars].
2004
Behavioral response of Lygus hesperus to conspecifics and headspace volatiles of alfalfa in a Y-tube olfactometer.
2004 Aug
Characterization of a root-specific Arabidopsis terpene synthase responsible for the formation of the volatile monoterpene 1,8-cineole.
2004 Aug
cDNA isolation and functional expression of myrcene synthase from Perilla frutescens.
2004 Dec
Composition of the essential oil of leaves, galls, and ripe and unripe fruits of Jordanian Pistacia palaestina Boiss.
2004 Feb 11
Analysis of volatile secondary metabolites from Colombian Xylopia aromatica (Lamarck) by different extraction and headspace methods and gas chromatography.
2004 Jan 30
Differences in the volatile components and their odor characteristics of green and ripe fruits and dried pericarp of Japanese pepper (Xanthoxylum piperitum DC.).
2004 Jun 30
Chemical composition and anticancer activity of leaf essential oil of Myrica gale L.
2005 Apr
Application of artificial neural network on mono- and sesquiterpenes compounds determined by headspace solid-phase microextraction-gas chromatography-mass spectrometry for the Piedmont ricotta cheese traceability.
2005 Apr 15
In vivo antimalarial activity of essential oils from Cymbopogon citratus and Ocimum gratissimum on mice infected with Plasmodium berghei.
2005 Jan
The effect of terpenoid extracts from 15 pine species on the feeding behavioural sequence of the late instars of the pine processionary caterpillar Thaumetopoea pityocampa.
2005 Jun 30
The essential oils from Zanthoxylum schinifolium pericarp induce apoptosis of HepG2 human hepatoma cells through increased production of reactive oxygen species.
2005 May
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 20:24:39 GMT 2023
Edited
by admin
on Fri Dec 15 20:24:39 GMT 2023
Record UNII
3M39CZS25B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MYRCENE
FCC   FHFI   HSDB  
INCI  
Official Name English
.BETA.-MYRCENE [IARC]
Common Name English
NSC-406264
Code English
1,6-OCTADIENE, 7-METHYL-3-METHYLENE-
Systematic Name English
.BETA.-GERANIOLENE
Common Name English
7-METHYL-3-METHYLENE-1,6-OCTADIENE
Systematic Name English
MYRCENE [FCC]
Common Name English
MYRCENE [INCI]
Common Name English
.BETA.-MYRCENE
MI  
Systematic Name English
DECATRIENE
Systematic Name English
MYRCENE [FHFI]
Common Name English
FEMA NO. 2762
Code English
MYRCENE [HSDB]
Common Name English
.BETA.-MYRCENE [MI]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 125901
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
DSLD 4190 (Number of products:2)
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
JECFA EVALUATION MYRCENE
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
Code System Code Type Description
NSC
406264
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
HSDB
1258
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
DAILYMED
3M39CZS25B
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
FDA UNII
3M39CZS25B
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
RXCUI
2166047
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
CAS
123-35-3
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
WIKIPEDIA
MYRCENE
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
MESH
C509595
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
PUBCHEM
31253
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
JECFA MONOGRAPH
1326
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
EPA CompTox
DTXSID6025692
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
CHEBI
17221
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
EVMPD
SUB62723
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
SMS_ID
100000134489
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-622-5
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY
MERCK INDEX
m7686
Created by admin on Fri Dec 15 20:24:39 GMT 2023 , Edited by admin on Fri Dec 15 20:24:39 GMT 2023
PRIMARY Merck Index
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