Page last updated: 2024-12-05

gamma-terpinene

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Gamma-terpinene is a monoterpene hydrocarbon found in a variety of essential oils, particularly those derived from plants like tea tree, thyme, and marjoram. It is a colorless liquid with a pleasant, citrus-like odor.

While research on gamma-terpinene is ongoing, it has shown potential in several areas, including:

* **Antioxidant Properties:** Gamma-terpinene has demonstrated antioxidant activity, suggesting potential benefits in protecting against oxidative stress and related health issues.
* **Anti-Inflammatory Effects:** Studies have indicated that gamma-terpinene may possess anti-inflammatory properties, potentially contributing to the relief of inflammation-related conditions.
* **Anticancer Activity:** Some research suggests that gamma-terpinene may exhibit anticancer activity, though further investigation is needed to confirm its potential therapeutic applications.
* **Antimicrobial Activity:** Gamma-terpinene has demonstrated antimicrobial activity against a range of bacteria and fungi, potentially contributing to its use in natural remedies and personal care products.

Its synthesis is typically achieved through various methods, including the dehydration of terpineol, the isomerization of other terpenes, and the use of biocatalysts.

The study of gamma-terpinene is driven by its potential applications in various fields, such as:

* **Food Industry:** As a natural flavoring agent and potential preservative.
* **Pharmaceutical Industry:** For its possible therapeutic properties in treating various diseases.
* **Cosmetics Industry:** In skin care products for its potential antioxidant and antimicrobial effects.

Further research is needed to fully understand the mechanisms and potential applications of gamma-terpinene in various fields. Its diverse activities and potential benefits make it an interesting subject of study.'

gamma-terpinene: RN given refers to gamma-terpinene; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

gamma-terpinene : One of three isomeric monoterpenes differing in the positions of their two double bonds (alpha- and beta-terpinene being the others). In gamma-terpinene the double bonds are at the 1- and 4-positions of the p-menthane skeleton. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID7461
CHEMBL ID449693
CHEBI ID10577
MeSH IDM0070425

Synonyms (73)

Synonym
AKOS015840812
.gamma.-terpinen
nsc-21448
wln: l6u cutj ay1&1 d1
1-methyl-4-isopropylcyclohexadiene-1,4
moslene
1-methyl-4-isopropyl-1,4-cyclohexadiene
crithmene
.gamma.-terpinene
terpinene, alpha
1, 1-methyl-4-isopropyl-
nsc21448
1,4-p-menthadiene
p-mentha-1,4-diene
gamma-terpinene (natural)
ai3-26468
gamma-terpinen
nsc 21448
fema no. 3559
1,4-cyclohexadiene, 1-methyl-4-isopropyl-
einecs 202-794-6
1-methyl-4-propan-2-ylcyclohexa-1,4-diene
1-methyl-4-(1-methylethyl)-1,4-cyclohexadiene
CHEBI:10577 ,
1-isopropyl-4-methyl-1,4-cyclohexadiene
4-isopropyl-1-methyl-1,4-cyclohexadiene
1-methyl-4-(propan-2-yl)cyclohexa-1,4-diene
1,4-cyclohexadiene, 1-methyl-4-(1-methylethyl)-
inchi=1/c10h16/c1-8(2)10-6-4-9(3)5-7-10/h4,7-8h,5-6h2,1-3h
1-isopropyl-4-methylcyclohexa-1,4-diene
gamma-terpinene
99-85-4
C09900
gamma-terpinene, >=95%, fg
gamma-terpinene, 97%
LMPR0102090027
CHEMBL449693
BMSE000778
M0318
NCGC00248232-01
dtxsid6041210 ,
NCGC00254865-01
tox21_300963
dtxcid4021210
cas-99-85-4
unii-4ygf4pqp49
4ygf4pqp49 ,
|a-tpn
FT-0626623
gamma-terpinene [fcc]
p-mentha-1,4-diene [fhfi]
1-isopropyl-4-methyl-cyclohexa-1,4-diene
W-100015
1-isopropyl-4-methyl-1,4-cyclohexadiene #
terpinene, .gamma.-
mfcd00001537
gamma-terpinene, analytical standard
gamma-terpinene, purum, >=97.0% (gc)
gamma-terpinene, primary pharmaceutical reference standard
gamma terpinene
alpha terpinene
gamma-terpinene, natural, 95%, fg
-terpinene
Q423975
gamma-terpinene gamma-terpinene
crithmene; moslene; nsc 21448; gamma-terpinene
9NI ,
EN300-211578
BS-23574
E80754
HY-W020183
gamma -terpinene
Z1255382936

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" However, the irritant effect of the essential oil was linked to thymol in a dose-response fashion, up to 10 microg/pellet, where it was still showing irritation."( Investigation of the Origanum onites L. essential oil using the chorioallantoic membrane (CAM) assay.
Başer, KH; Demirci, F; Franz, G; Paper, DH, 2004
)
0.32
" In the Rotarod test, Kabuchii did not affect the motor performance, even at the highest dosage tested (3 mg/cage), whereas diazepam decreased it dose- dependently."( Enhancement of Pentobarbital-induced Sleep by the Vaporized Essential Oil of Citrus keraji var. kabuchii and its Characteristic Component, y-Terpinene.
Fua, Z; Kinjo, Y; Kobayashi, Y; Shimizu, E; Takemoto, H, 2016
)
0.43
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (4)

RoleDescription
antioxidantA substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
volatile oil componentAny plant metabolite that is found naturally as a component of a volatile oil.
human xenobiotic metaboliteAny human metabolite produced by metabolism of a xenobiotic compound in humans.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
monoterpeneA C10 terpene.
cyclohexadiene
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Bioassays (24)

Assay IDTitleYearJournalArticle
AID338302Acaricidal activity against Psoroptes cuniculi at 1 uL after 24 hrs by inhalation assay1995Journal of natural products, Aug, Volume: 58, Issue:8
Structure/activity relationship of some natural monoterpenes as acaricides against Psoroptes cuniculi.
AID338300Acaricidal activity against Psoroptes cuniculi at 6 uL after 24 hrs by inhalation assay1995Journal of natural products, Aug, Volume: 58, Issue:8
Structure/activity relationship of some natural monoterpenes as acaricides against Psoroptes cuniculi.
AID334992Antimicrobial activity against Staphylococcus aureus ATCC 12598 after 2 days by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID334994Antimicrobial activity against Escherichia coli ATCC 9637 after 2 days by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID334999Antimicrobial activity against Pityrosporum ovale ATCC 14521 by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID338297Acaricidal activity against Psoroptes cuniculi at 1% dilution in physiological saline after 48 hrs by direct contact assay1995Journal of natural products, Aug, Volume: 58, Issue:8
Structure/activity relationship of some natural monoterpenes as acaricides against Psoroptes cuniculi.
AID334998Antimicrobial activity against Candida utilis ATCC 9226 after 2 days by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID360503Antioxidant activity assessed as DPPH radical scavenging activity1995Journal of natural products, Nov, Volume: 58, Issue:11
Santolindiacetylene, a polyacetylene derivative isolated from the essential oil of Santolina canescens.
AID334990Antimicrobial activity against Brevibacterium ammoniagenes ATCC 6872 after 2 days by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID335000Antimicrobial activity against Penicillium chrysogenum ATCC 10106 after 5 days by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID334993Antimicrobial activity against Streptococcus mutans ATCC 25175 after 2 days by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID334995Antimicrobial activity against Pseudomonas aeruginosa ATCC 10145 after 2 days by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID334989Antimicrobial activity against Bacillus subtilis ATCC 9372 after 2 days by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID338299Acaricidal activity against Psoroptes cuniculi at 0.125% dilution in physiological saline after 48 hrs by direct contact assay1995Journal of natural products, Aug, Volume: 58, Issue:8
Structure/activity relationship of some natural monoterpenes as acaricides against Psoroptes cuniculi.
AID338301Acaricidal activity against Psoroptes cuniculi at 3 uL after 24 hrs by inhalation assay1995Journal of natural products, Aug, Volume: 58, Issue:8
Structure/activity relationship of some natural monoterpenes as acaricides against Psoroptes cuniculi.
AID1090744Antifungal activity against Aspergillus flavus assessed as mycelial growth at 60 uL after 4 to 12 days by agar disk diffusion method relative to untreated control2007Journal of agricultural and food chemistry, Aug-22, Volume: 55, Issue:17
Characterization of the volatile constituents in the essential oil of Pistacia lentiscus L. from different origins and its antifungal and antioxidant activity.
AID334996Antimicrobial activity against Enterobacter aerogenes ATCC 13048 after 2 days by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID1090745Antifungal activity against Aspergillus flavus assessed as mycelial growth at 20 uL after 4 to 12 days by agar disk diffusion method relative to untreated control2007Journal of agricultural and food chemistry, Aug-22, Volume: 55, Issue:17
Characterization of the volatile constituents in the essential oil of Pistacia lentiscus L. from different origins and its antifungal and antioxidant activity.
AID334991Antimicrobial activity against Propionibacterium acnes ATCC 11827 after 2 days by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID334997Antimicrobial activity against Saccharomyces cerevisiae ATCC 7754 after 2 days by twofold serial broth dilution method1992Journal of natural products, May, Volume: 55, Issue:5
Antimicrobial agents from Licaria puchuri-major and their synergistic effect with polygodial.
AID338298Acaricidal activity against Psoroptes cuniculi at 0.25% dilution in physiological saline after 48 hrs by direct contact assay1995Journal of natural products, Aug, Volume: 58, Issue:8
Structure/activity relationship of some natural monoterpenes as acaricides against Psoroptes cuniculi.
AID1347083qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: Viability assay - alamar blue signal for LASV Primary Screen2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347082qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: LASV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347086qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lymphocytic Choriomeningitis Arenaviruses (LCMV): LCMV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (197)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (2.03)18.7374
1990's10 (5.08)18.2507
2000's50 (25.38)29.6817
2010's109 (55.33)24.3611
2020's24 (12.18)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 42.89

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index42.89 (24.57)
Research Supply Index5.33 (2.92)
Research Growth Index5.33 (4.65)
Search Engine Demand Index65.76 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (42.89)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (0.49%)5.53%
Reviews4 (1.96%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other199 (97.55%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]