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ActivityReference
(-)-Chronotropic Hansel, R., Keller, K., Rimpler, H., and Schneider, G. eds. 1992. Hager's Handbuch der Pharmazeutischen Praxis, Drogen (A-D), 1209 pp., 1993 (E-O), 970 pp., 1994 (P-Z), 1196 pp. Springer-Verlag, Berlin.
Chemicals (2)
1,8-CINEOLE 87 nl/ml
BORNYL-ACETATE 933 nl/ml
(-)-Inotropic Hansel, R., Keller, K., Rimpler, H., and Schneider, G. eds. 1992. Hager's Handbuch der Pharmazeutischen Praxis, Drogen (A-D), 1209 pp., 1993 (E-O), 970 pp., 1994 (P-Z), 1196 pp. Springer-Verlag, Berlin.
Chemicals (2)
1,8-CINEOLE 87 nl/ml
BORNYL-ACETATE 933 nl/ml
Acaricide
Chemicals (3)
1,8-CINEOLE LC100=6 uM
GAMMA-TERPINENE
LIMONENE LC100=8 uM
ACE-Inhibitor
Chemicals (3)
ALPHA-TERPINEOL 100 ug/ml (weak activity)
GAMMA-TERPINENE 100 ug/ml (weak activity)
MYRCENE 100 ug/ml
AChE-Inhibitor Grundy, D. L. and Still, C. C., Inhibition of acetylcholinesterases by pulegone-1,2-epoxide, Oest. Biochem. & Physiol., 23, 1985, 383-8.
Chemicals (1)
LIMONENE
Aldose-Reductase-Inhibitor Okamura, K., Iwakami, S., Matsunaga, T. 1992. Biological Activity of Monoterpenes from Trees. Toyama-Ken Yakuji Kenkyusho Nenpo, (20): 95-101.
Chemicals (3)
ALPHA-TERPINEOL 100 ug/ml
GAMMA-TERPINENE 100 ug/ml
MYRCENE 100 ug/ml
Allelochemic
Chemicals (2)
ALPHA-PINENE
LIMONENE
Allelopathic Wright,C.W.(Ed)2002.Medicinal&Aromatic Plants-Industrial Profiles.Artemisia.344pp.Maffei,M.(Ed)2002.Vetiveria.The Genus Vetiveria.Taylor&Francis.NY,NY.191pp.Southwell,I.,Lowe,R.(Eds)1999.Tea Tree.The Genus Melaleuca.Harwood Acad.Pub.Amsterdam,Netherlands.
Chemicals (3)
1,8-CINEOLE
ALPHA-TERPINEOL
CAMPHENE
Allergenic
Chemicals (5)
1,8-CINEOLE
ALPHA-PINENE
CARVACROL
LIMONENE 1/20th carene
MYRCENE
Analgesic Kauderer, B., Zamith, H., Paumgartten, F.J.R., and Speit, G. Evaluation of the Mutagenicity of B-Myrcene in Mammalian Cells In Vitro. Environmental and Molecular Mutagenesis 18: 28-34, 1991.
Chemicals (2)
MYRCENE
P-CYMENE
Anesthetic
Chemicals (2)
1,8-CINEOLE
CARVACROL
Anthelmintic Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Chemicals (2)
1,8-CINEOLE
CARVACROL
Antiacetylcholinesterase
Chemicals (5)
1,8-CINEOLE IC50=41 ug/ml
GAMMA-TERPINENE IC23=1.2 mM
ISOMENTHONE IC50=1.6 mM
LIMONENE IC22-26=1.2 mM
P-CYMENE IC40=1.2 mM
Antiacne
Chemicals (2)
ALPHA-PINENE
ALPHA-TERPINEOL
Antiadenomic
Chemicals (1)
LIMONENE
Antiallergic J. Food Hyg. Soc. Jap. 33(6): 569.
Chemicals (1)
1,8-CINEOLE
Antialzheimeran? L. Gracza (1985) as cited by Buchbauer re antiacetylcholinesterase.
Chemicals (2)
CARVACROL
LIMONENE
Antiasthmatic
Chemicals (1)
LIMONENE
Antiatherosclerotic
Chemicals (1)
CARVACROL IC50=5.53 uM
Antibacillary
Chemicals (1)
P-CYMENE
Antibacterial Revista Itiliana Eppos, 12: 5, 1994.
Chemicals (8)
1,8-CINEOLE 50 ppm
ALPHA-PINENE
ALPHA-TERPINEOL MIC=800-1,600 ug/ml
BORNYL-ACETATE
CARVACROL MIC 170-290
LIMONENE
MYRCENE
P-CYMENE
Antibronchitic
Chemicals (1)
1,8-CINEOLE
Anticancer Joseph, J., Nadeau, D. and Underwood, A. 2001. The Color Code. Hyperion, NY.
Chemicals (2)
ALPHA-TERPINEOL
LIMONENE
Anticariogenic
Chemicals (2)
1,8-CINEOLE
ALPHA-TERPINEOL MIC=800-1,600 ug/ml
Anticatarrh Martindale's 29th
Chemicals (1)
1,8-CINEOLE
Anticholinesterase
Chemicals (1)
1,8-CINEOLE IC50=50-70
Anticholinesterase? L. Gracza (1985) as cited by Buchbauer re antiacetylcholinesterase.
Chemicals (1)
CARVACROL
Anticonvulsant
Chemicals (1)
MYRCENE
Antidiuretic Lawrence Review of Natural Products, Mar-92.
Chemicals (1)
CARVACROL
Antiesophagitic
Chemicals (1)
LIMONENE
Antifatigue
Chemicals (1)
1,8-CINEOLE
Antifeedant Jacobson, M., Glossary of Plant-Derived Insect Deterrents, CRC Press, Inc., Boca Raton, FL, 213 p, 1990.
Chemicals (4)
ALPHA-PINENE
BORNYL-ACETATE
GAMMA-TERPINENE
LIMONENE
Antiflu Economic & Medicinal Plant Research, 5: 195.
Chemicals (3)
ALPHA-PINENE
LIMONENE
P-CYMENE
Antihalitosic American Health, 12(4): 17, 1993.
Chemicals (1)
1,8-CINEOLE
Antiinflammatory
Chemicals (5)
1,8-CINEOLE
ALPHA-PINENE 500 mg/kg
ALPHA-TERPINEOL
CARVACROL IC50=4 uM
LIMONENE
Antilaryngitic
Chemicals (1)
1,8-CINEOLE
Antilithic
Chemicals (1)
LIMONENE
Antilithic? Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Chemicals (1)
CAMPHENE
Antilymphomic
Chemicals (1)
LIMONENE
Antimelanomic
Chemicals (1)
CARVACROL IC50=120 uM/l
Antimetastatic (Stomach)
Chemicals (1)
LIMONENE
Antimutagenic Kauderer, B., Zamith, H., Paumgartten, F.J.R., and Speit, G. Evaluation of the Mutagenicity of B-Myrcene in Mammalian Cells In Vitro. Environmental and Molecular Mutagenesis 18: 28-34, 1991.
Chemicals (2)
LIMONENE
MYRCENE
Antinitrosaminic
Chemicals (1)
MYRCENE
Antinociceptive Rao, V.S.N., Menezes, A.M.S., Viana, G.S.B. 1990. Effect of myrcene on nociception in mice. J. Pharm. Pharmacol. 42: 877-878, 1990.
Chemicals (2)
1,8-CINEOLE
MYRCENE 10-20 mg/kg ipr mus
Antiobesity
Chemicals (1)
LIMONENE
Antioxidant Jim Duke's personal files.
Chemicals (5)
CAMPHENE
CARVACROL
GAMMA-TERPINENE
ISOMENTHONE
MYRCENE
Antioxidant (LDL)
Chemicals (1)
CARVACROL IC50=5.53 uM
Antipharyngitic
Chemicals (1)
1,8-CINEOLE
Antiplaque Osawa, K., Matsumoto, T., Maruyama, T., Takiguchi, T., Okuda, K., and Takazoe, I., Studies of the antibacterial activity of plant extracts and their constituents against periodontopathic bacteria, Bull Tokyo Dent. Coll., 31 (1), 1990, 17-21
Chemicals (2)
1,8-CINEOLE
CARVACROL MIC=39-625 ug/ml
Antipneumonic
Chemicals (1)
ALPHA-PINENE
Antiproliferant
Chemicals (1)
ALPHA-TERPINEOL
Antiprostaglandin
Chemicals (1)
CARVACROL
Antiradicular
Chemicals (2)
CARVACROL 600 x thymol
ISOMENTHONE
Antirheumatalgic Martindale's 28th
Chemicals (1)
P-CYMENE
Antirheumatic
Chemicals (1)
1,8-CINEOLE
Antirhinitic
Chemicals (1)
1,8-CINEOLE
Antiseptic Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Chemicals (5)
1,8-CINEOLE
ALPHA-PINENE
ALPHA-TERPINEOL
CARVACROL 1.5 x phenol
LIMONENE
Antisinusitic
Chemicals (1)
1,8-CINEOLE
Antispasmodic Jim Duke's personal files.
Chemicals (6)
1,8-CINEOLE
ALPHA-PINENE
BORNYL-ACETATE ED50=0.09 mg/ml
CARVACROL
LIMONENE ED50=0.197 mg/ml
MYRCENE
Antistaphylococcic
Chemicals (3)
1,8-CINEOLE 50 ppm
ALPHA-PINENE
CARVACROL
Antistreptococcic
Chemicals (1)
CARVACROL
Antitumor
Chemicals (1)
LIMONENE
Antitumor (Breast)
Chemicals (1)
LIMONENE
Antitumor (Colon)
Chemicals (1)
LIMONENE
Antitumor (Pancreas)
Chemicals (1)
LIMONENE
Antitumor (Prostate)
Chemicals (1)
LIMONENE
Antitumor (Stomach)
Chemicals (1)
LIMONENE
Antitussive Newall, C. A., Anderson, L. A. and Phillipson, J. D. 1996. Herbal Medicine - A Guide for Health-care Professionals. The Pharmaceutical Press, London. 296pp.
Chemicals (2)
1,8-CINEOLE
CARVACROL
Antiulcer
Chemicals (1)
1,8-CINEOLE
Antiviral Economic & Medicinal Plant Research, 5: 195.
Chemicals (4)
ALPHA-PINENE
BORNYL-ACETATE
LIMONENE
P-CYMENE
Apoptotic
Chemicals (1)
LIMONENE
Bronchoprotectant
Chemicals (1)
LIMONENE
Cancer-Preventive Stitt, P. A. Why George Should Eat Broccoli. Dougherty Co, Milwaukee, WI, 1990, 399 pp.
Chemicals (2)
ALPHA-PINENE
LIMONENE
Candidicide
Chemicals (2)
1,8-CINEOLE
CARVACROL MIC<0.1 ug/ml
Candidistat
Chemicals (1)
LIMONENE
Carcinogenic Zebovitz, T. C. Ed. 1989. Part VII. Flavor and Fragrance Substances, in Keith L. H. and Walters, D.B., eds. Compendium of Safety Data Sheets for Research and Industrial Chemicals. VCH Publishers, New York. 3560-4253.
Chemicals (1)
1,8-CINEOLE
Carminative Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp.
Chemicals (1)
CARVACROL
Chemopreventive
Chemicals (2)
LIMONENE
MYRCENE
Choleretic
Chemicals (1)
1,8-CINEOLE
Cholesterolytic
Chemicals (1)
LIMONENE
Cicatrizant
Chemicals (1)
ALPHA-TERPINEOL ED50=240 ug/g mus
CNS-Stimulant
Chemicals (1)
1,8-CINEOLE
Coleoptophile
Chemicals (1)
ALPHA-PINENE
Convulsant
Chemicals (1)
1,8-CINEOLE
Counterirritant Martindale's 29th
Chemicals (1)
1,8-CINEOLE
Cyclooxygenase-Inhibitor
Chemicals (1)
CARVACROL #NAME?
Cytochrome-P450-Inducer
Chemicals (1)
1,8-CINEOLE
Decongestant
Chemicals (1)
1,8-CINEOLE
Degranulant
Chemicals (1)
1,8-CINEOLE 0.3 ul/ml
Dentifrice Martindale's 29th
Chemicals (1)
1,8-CINEOLE
Detoxicant
Chemicals (1)
LIMONENE
Edemagenic
Chemicals (1)
1,8-CINEOLE inj
Enterocontractant J. Aromatherapy 4: 22.
Chemicals (1)
LIMONENE
Enterorelaxant J. Aromatherapy 4: 22.
Chemicals (1)
CARVACROL
Expectorant
Chemicals (6)
1,8-CINEOLE
ALPHA-PINENE
BORNYL-ACETATE
CAMPHENE
CARVACROL
LIMONENE
FLavor Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry
Chemicals (11)
1,8-CINEOLE FEMA 1-200
3-OCTANOL FEMA
ALPHA-PINENE FEMA 15-150
ALPHA-TERPINEOL FEMA 5-40
BORNYL-ACETATE FEMA 70-80
CAMPHENE FEMA 15-175
CARVACROL FEMA 10-125
GAMMA-TERPINENE FEMA 1-40
LIMONENE
MYRCENE FEMA 0.5-9
P-CYMENE FEMA 12-250
Fungicide Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Chemicals (4)
1,8-CINEOLE
CARVACROL
MYRCENE
P-CYMENE
Fungiphilic J. Agric. Food Chem. 43: 2283.
Chemicals (1)
LIMONENE
Fungistat
Chemicals (1)
LIMONENE
Gastroprotective
Chemicals (1)
1,8-CINEOLE
Gram(+)icide
Chemicals (1)
1,8-CINEOLE
Gram(-)icide
Chemicals (1)
1,8-CINEOLE
GST-Inducer
Chemicals (1)
LIMONENE
Hepatotonic
Chemicals (1)
1,8-CINEOLE
Herbicide Keeler, R.F. and Tu, A.T. eds. 1991. Toxicology of Plant and Fungal Compounds. (Handbook of Natural Toxins Vol. 6) Marcel Dekker, Inc. NY. 665 pp.
Chemicals (4)
1,8-CINEOLE IC50=78 uM
ALPHA-PINENE IC50=30 uM
LIMONENE IC50=45 uM
P-CYMENE IC50=50 uM
Histaminic
Chemicals (1)
LIMONENE
Hypocholesterolemic? Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Chemicals (1)
CAMPHENE
Hypotensive
Chemicals (1)
1,8-CINEOLE
Hypothermic
Chemicals (1)
MYRCENE
Immunomodulator
Chemicals (1)
LIMONENE
Inflammatory
Chemicals (1)
1,8-CINEOLE inj
Insecticide
Chemicals (3)
ALPHA-PINENE 0.82 uM/fly
ALPHA-TERPINEOL 1.29 uM/fly
LIMONENE 0.37 uM/fly
Insectifuge Blaschek, W., Hansel, R., Keller, K., Reichling, J., Rimpler, H., and Schneider, G. eds. 1998. Hager's Handbuch der Pharmazeutischen Praxis, Auflage Band 2 (A-K), 909 pp., (L-Z), 858 pp. Springer-Verlag, Berlin.
Chemicals (9)
1,8-CINEOLE
ALPHA-PINENE 50 ppm
BORNYL-ACETATE
CAMPHENE
CARVACROL
GAMMA-TERPINENE
LIMONENE
MYRCENE
P-CYMENE
Insectiphile J. Stored. Prod. Res., 22:141, 1986.
Chemicals (1)
ALPHA-PINENE
Interleukin-6-Inhibitor
Chemicals (2)
ALPHA-TERPINEOL
LIMONENE
Irritant Zebovitz, T. C. Ed. 1989. Part VII. Flavor and Fragrance Substances, in Keith L. H. and Walters, D.B., eds. Compendium of Safety Data Sheets for Research and Industrial Chemicals. VCH Publishers, New York. 3560-4253.
Chemicals (7)
1,8-CINEOLE
ALPHA-PINENE
CARVACROL
GAMMA-TERPINENE
LIMONENE
MYRCENE
P-CYMENE
Laxative Zebovitz, T. C. Ed. 1989. Part VII. Flavor and Fragrance Substances, in Keith L. H. and Walters, D.B., eds. Compendium of Safety Data Sheets for Research and Industrial Chemicals. VCH Publishers, New York. 3560-4253.
Chemicals (1)
P-CYMENE
Lipolytic
Chemicals (1)
LIMONENE
Mosquitofuge
Chemicals (1)
ALPHA-TERPINEOL > Deet
Motor-Depressant Buchbauer et al, e.g.Buchbauer et al,1993.Therapeutic properties of essential oils and fragrances. Chap.12 in Teranishi,R, Buttery,R.G and Sugisawa,H. Eds. Bioactive Volatile Compounds from Plants. ACS Symposium Series 525. Amer. Chem. Soc., Washington DC
Chemicals (1)
ALPHA-TERPINEOL
Myorelaxant Newall, C. A., Anderson, L. A. and Phillipson, J. D. 1996. Herbal Medicine - A Guide for Health-care Professionals. The Pharmaceutical Press, London. 296pp.
Chemicals (4)
1,8-CINEOLE
BORNYL-ACETATE
LIMONENE 50 mg/kg
MYRCENE 100-200 mg/kg
Nematicide Nigg, H.N. and Seigler, D.S., eds. 1992. Phytochemical Resources for Medicine and Agriculture. Plenum Press, New York. 445 pp.
Chemicals (4)
1,8-CINEOLE
ALPHA-TERPINEOL MLC=1 mg/ml
CARVACROL MLC=1 mg/ml
LIMONENE IC=100 ug/ml
Neurotoxic
Chemicals (1)
1,8-CINEOLE
NO-Genic
Chemicals (1)
LIMONENE
Ornithine-Decarboxylase-Inhibitor
Chemicals (1)
LIMONENE ~750 mg/kg (diet)
Ozone-Scavenger
Chemicals (1)
LIMONENE
P450-2B1-Inhibitor
Chemicals (2)
ALPHA-PINENE IC50=0.087 uM
MYRCENE IC50=0.14 uM
P450-Inducer
Chemicals (2)
1,8-CINEOLE
LIMONENE
Pediculicide
Chemicals (1)
1,8-CINEOLE 2.3 x pyrethrin
Perfume Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry
Chemicals (1)
1,8-CINEOLE
Perfumery Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Chemicals (5)
3-OCTANOL
ALPHA-PINENE
ALPHA-TERPINEOL
GAMMA-TERPINENE
MYRCENE
Peristaltic
Chemicals (1)
LIMONENE
Pesticide
Chemicals (10)
1,8-CINEOLE
ALPHA-PINENE
ALPHA-TERPINEOL
BORNYL-ACETATE
CAMPHENE
CARVACROL
GAMMA-TERPINENE
LIMONENE
MYRCENE
P-CYMENE
Photosensitizer Rinzler, C. A. 1990. The Complete Book of Herbs, Spices and Condiments. Facts on File, New York. 199 pp.
Chemicals (1)
LIMONENE
Prostaglandin-Inhibitor
Chemicals (1)
CARVACROL
Rubefacient Martindale's 29th
Chemicals (1)
1,8-CINEOLE
Secretogogue
Chemicals (1)
1,8-CINEOLE
Sedative Zebovitz, T. C. Ed. 1989. Part VII. Flavor and Fragrance Substances, in Keith L. H. and Walters, D.B., eds. Compendium of Safety Data Sheets for Research and Industrial Chemicals. VCH Publishers, New York. 3560-4253.
Chemicals (6)
1,8-CINEOLE
ALPHA-PINENE
ALPHA-TERPINEOL
BORNYL-ACETATE
LIMONENE ED=1-32 mg/kg
P-CYMENE
Spasmogenic Fitoterapia No.59-1984.
Chemicals (3)
1,8-CINEOLE
ALPHA-PINENE
CAMPHENE
Surfactant
Chemicals (1)
1,8-CINEOLE
Termiticide
Chemicals (1)
ALPHA-TERPINEOL IC100=5 mg/g
Testosterone-Hydroxylase-Inducer
Chemicals (1)
1,8-CINEOLE
Tracheorelaxant
Chemicals (1)
CARVACROL
Tranquilizer Lawrence Review of Natural Products, Jun-90.
Chemicals (1)
ALPHA-PINENE
Transdermal
Chemicals (4)
1,8-CINEOLE
ALPHA-PINENE
ALPHA-TERPINEOL
LIMONENE
Trichomonicide
Chemicals (3)
1,8-CINEOLE LD100=1,000 ug/ml
CARVACROL LD100=150 ug/ml
P-CYMENE LD100=50 ug/ml
Vermifuge
Chemicals (1)
CARVACROL
Vulnerary
Chemicals (1)
ALPHA-TERPINEOL ED50=240 ug/g mus
*Unless otherwise noted all references are to Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.