U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry MIXED
Molecular Formula C10H16
Molecular Weight 136.234
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAMPHENE

SMILES

CC1(C)C2CCC(C2)C1=C

InChI

InChIKey=CRPUJAZIXJMDBK-UHFFFAOYSA-N
InChI=1S/C10H16/c1-7-8-4-5-9(6-8)10(7,2)3/h8-9H,1,4-6H2,2-3H3

HIDE SMILES / InChI

Molecular Formula C10H16
Molecular Weight 136.234
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Camphene is a bicyclic monoterpene, a Plant Derived Monoterpene, which possessed antitumor activity. This was found in vivo by inhibiting subcutaneous tumor growth of highly aggressive melanoma cells in a syngeneic model, suggesting a promising role of this compound in cancer therapy. In addition was shown, that camphene lowered cholesterol and triglycerides (TG) in the plasma of hyperlipidemic rats without affecting HMG-CoA reductase activity. And was suggested, that camphene upregulated Sterol regulatory element-binding proteins (SREBP-1) expression and microsomal triglyceride transfer protein (MTP) inhibition was likely to be a probable mechanism whereby camphene exerts its hypolipidemic effect.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P36956|||Q6PJ36
Gene ID: 6720.0
Gene Symbol: SREBF1
Target Organism: Homo sapiens (Human)
Target ID: P55157
Gene ID: 4547.0
Gene Symbol: MTTP
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Formaldehyde in the indoor environment.
2010-04-14
Comparative chemical composition and antiproliferative activity of aerial parts of Salvia leriifolia Benth. and Salvia acetabulosa L. essential oils against human tumor cell in vitro models.
2010-02
Cannabinoid receptor 1 binding activity and quantitative analysis of Cannabis sativa L. smoke and vapor.
2010-02
Rosmarinus officinalis L.: chemical modifications of the essential oil and evaluation of antioxidant and antimicrobial activity.
2009-12
Chemical composition of hydrodistilled essential oil of Artemisia incana (L.) Druce and antimicrobial activity against foodborne microorganisms.
2009-12
Influence of growth phase and geographic origin on the essential oil composition of Pituranthos chloranthus from Tunisia.
2009-11
Multiple ultrafast, broadband 2D NMR spectra of hyperpolarized natural products.
2009-10-07
Fingerprint of selected Salvia species by HS-GC-MS analysis of their volatile fraction.
2009-08
Temperature-dependent release of volatile organic compounds of eucalypts by direct analysis in real time (DART) mass spectrometry.
2009-08
Tissue engineering polymeric microcarriers with macroporous morphology and bone-bioactive surface.
2009-07-07
Formation and stability of secondary ozonides from monoterpenes studied by mass spectrometry.
2009-07
Composition and seasonal variation of the essential oil from Abies sachalinensis from Hokkaido, Japan.
2009-06
Terpenoid emissions from Quercus robur. A case study of Galicia (NW Spain).
2009-06
Preparation of porous bioactive ceramic microspheres and in vitro osteoblastic culturing for tissue engineering application.
2009-06
Effects of a thiosemicarbazide camphene derivative on Trichophyton mentagrophytes.
2009-05-13
Radical Scavenging Activity of the Essential Oil of Silver Fir (Abies alba).
2009-05
Fumigant and contact toxicities of monoterpenes to Sitophilus oryzae (L.) and Tribolium castaneum (Herbst) and their inhibitory effects on acetylcholinesterase activity.
2009-05
Fabrication of HA/TCP scaffolds with a graded and porous structure using a camphene-based freeze-casting method.
2009-05
Comparative analysis of chemical compositions and antimicrobial activities of essential oils from Abies holophylla and Abies koreana activities of essential oils from Abies holophylla and Abies koreana.
2009-04
Antinociceptive effect and GC/MS analysis of Rosmarinus officinalis L. essential oil from its aerial parts.
2009-04
Plant derived antioxidants - Geraniol and camphene protect rat alveolar macrophages against t-BHP induced oxidative stress.
2009-03
Composition and antibacterial activity of essential oils of Artemisia fragrans Willd. leaves and roots from Iran.
2009-02
Essential oil variability in natural populations of Picea omorika, a rare European conifer.
2009-02
Comparative analysis of essential oils from eight herbal medicines with pungent flavor and cool nature by GC-MS and chemometric resolution methods.
2009-02
In vitro biological activity of Salvia leriifolia benth essential oil relevant to the treatment of Alzheimer's disease.
2009
The oil-dispersion bath in anthroposophic medicine--an integrative review.
2008-12-04
Anti-inflammation activity of fruit essential oil from Cinnamomum insularimontanum Hayata.
2008-12
[Analysis of volatile oil in pre and post processed pieces of Eriobotrya japonica by GC-MS].
2008-11
[Characterization of chemical components of essential oil from flowers of Chrysanthemum morifolium produced in Anhui province].
2008-10
The essential oil qualitative and quantitative composition in the needles of Pinus sylvestris L. growing along industrial transects.
2008-10
Activity of essential oils and individual components against acetyl- and butyrylcholinesterase.
2008-09-25
Variability of the needle essential oils of Pinus peuce from different populations in Montenegro and Serbia.
2008-07
Effects of cis-beta-ocimene, cis-sabinene hydrate, and monoterpene and sesquiterpene mixtures on alfalfa pellet intake by lambs.
2008-06
Speedy component resolution: an improved tool for processing diffusion-ordered spectroscopy data.
2008-05-15
Mass propagation and essential oil analysis of Artemisia vulgaris.
2008-03
Chemical composition and antimicrobial activity of essential oil from cones of Pinus koraiensis.
2008-03
Bimolecular and unimolecular contributions to the disparate self-chemical ionizations of alpha-pinene and camphene isomers.
2007-11
Chemical compositions of the essential oils of stems, leaves and flowers of Prangos acaulis (Dc) Bornm.
2007-08-15
Essential oil composition of terminal branches, cones and roots of Tetraclinis articulata from Tunisia.
2007-08-01
Variability of the needle essential oils of Pinus heldreichii from different populations in Montenegro and Serbia.
2007-05
Temperature dependence of the optical rotation in six bicyclic organic molecules calculated by vibrational averaging.
2007-03-12
Volatile chemical constituents of Piper aduncum L and Piper gibbilimbum C. DC (Piperaceae) from Papua New Guinea.
2007-03-09
Analysis by gas chromatography-mass spectrometry of essential oil from seeds and aerial parts of Ferulago angulata (Schlecht.) Boiss gathered in Nevakoh and Shahoo, Zagross mountain, West of Iran.
2007-03-01
Volatile organic compounds of Angelica gigas Nakai, Korean medicinal herb.
2007-03
Assessment and implications of intraspecific and phenological variability in monoterpenes of Scots pine (Pinus sylvestris) foliage.
2007-03
Plant coexistence alters terpene emission and content of Mediterranean species.
2007-03
Chemical composition of the essential oil of Pelargonium quercetorum Agnew. of Iran.
2007-01
Anticonflict effects of lavender oil and identification of its active constituents.
2006-12
Baseline isotopic data of polyhalogenated compounds.
2006-09-08
Biotransformation of terpenoids by mammals, microorganisms, and plant-cultured cells.
2005-05
Patents

Patents

Sample Use Guides

Unknown
Route of Administration: Other
In Vitro Use Guide
Curator's Comment: Camphene induced apoptosis by the intrinsic pathway in melanoma cells mainly by causing endoplasmic reticulum (ER) stress, with release of Ca(2+) together with HmgB1 and calreticulin, loss of mitochondrial membrane potential and up regulation of caspase-3 activity.
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:42:43 GMT 2025
Edited
by admin
on Mon Mar 31 18:42:43 GMT 2025
Record UNII
G3VG94Z26E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CAMPHENE
FCC   FHFI   HSDB   INCI   MART.   MI   WHO-DD  
INCI  
Official Name English
FEMA NO. 2229
Preferred Name English
CAMPHENE [FCC]
Common Name English
2,2-DIMETHYL-3-METHYLENENORBORNANE
Systematic Name English
CAMPHENE, D,L-
Common Name English
CAMPHENE [HSDB]
Common Name English
Camphene [WHO-DD]
Common Name English
CAMPHENE, (±)-
Systematic Name English
CAMPHENE, DL-
Common Name English
CAMPHENE [MI]
Common Name English
NSC-4165
Code English
CAMPHENE [MART.]
Common Name English
DL-CAMPHENE
Common Name English
CAMPHENE [FHFI]
Common Name English
(±)-CAMPHENE
Systematic Name English
BICYCLO(2.2.1)HEPTANE, 2,2-DIMETHYL-3-METHYLENE-
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
JECFA EVALUATION CAMPHENE
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
Code System Code Type Description
RXCUI
2395761
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
HSDB
900
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
SMS_ID
100000076601
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-234-8
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
NSC
4165
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
WIKIPEDIA
CAMPHENE
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
DAILYMED
G3VG94Z26E
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
EVMPD
SUB13212MIG
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
PUBCHEM
6616
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
CHEBI
3830
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
JECFA MONOGRAPH
1322
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
MERCK INDEX
m3002
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY Merck Index
CAS
79-92-5
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
EPA CompTox
DTXSID8026488
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
FDA UNII
G3VG94Z26E
Created by admin on Mon Mar 31 18:42:43 GMT 2025 , Edited by admin on Mon Mar 31 18:42:43 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
Monoterpene Class
PARENT -> CONSTITUENT MAY BE PRESENT