Data Views

Activities: 179
  CSV  Excel  PDF
Click on column headings to sort table by that column
ActivityReference
Vulnerary
Chemicals (2)
ALPHA-TERPINEOL ED50=240 ug/g mus
TERPINEN-4-OL
Vibriocide Wealth of India.
Chemicals (1)
CAMPHOR 500 ug/ml
Verrucolytic Nigg, H.N. and Seigler, D.S., eds. 1992. Phytochemical Resources for Medicine and Agriculture. Plenum Press, New York. 445 pp.
Chemicals (1)
CAMPHOR
Ulcerogenic 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)
CUMINALDEHYDE
Tyrosinase-Inhibitor
Chemicals (1)
CUMINALDEHYDE ID50=0.05 mM
Trichomonicide
Chemicals (2)
1,8-CINEOLE LD100=1,000 ug/ml
P-CYMENE LD100=50 ug/ml
Transdermal
Chemicals (6)
1,8-CINEOLE
ALPHA-PINENE
ALPHA-TERPINEOL
BETA-PINENE
CAMPHOR
LIMONENE
Tranquilizer
Chemicals (2)
ALPHA-PINENE
BORNEOL
Testosterone-Hydroxylase-Inducer
Chemicals (1)
1,8-CINEOLE
Termiticide
Chemicals (1)
ALPHA-TERPINEOL IC100=5 mg/g
Surfactant
Chemicals (1)
1,8-CINEOLE
Stomachic
Chemicals (1)
BETA-BISABOLENE
Stimulant R.J. Hixtable (Huxtable, R.J. (as T. Max). 1992. This and That:The Essential Pharmacology of Herbs and Spices. Tips 13:15-20 Huxtable, R.J. 1992b. The Myth of Benficent Nature. The Risk of Herbal Preparations. Anns. Intern. Med. 117(2):165-6; Huxtable, R.
Chemicals (1)
CAMPHOR
Spermicide
Chemicals (1)
TERPINEN-4-OL ED100=0.015
Spasmogenic
Chemicals (5)
1,8-CINEOLE
ALPHA-PINENE
ALPHA-TERPINENE
BETA-PINENE
CAMPHENE
Sedative Lawrence Review of Natural Products, Jun-90.
Chemicals (8)
1,8-CINEOLE
ALPHA-PINENE
ALPHA-TERPINEOL
BORNEOL
CUMINALDEHYDE
LIMONENE ED=1-32 mg/kg
LINALYL-ACETATE
P-CYMENE
Secretogogue
Chemicals (1)
1,8-CINEOLE
Rubefacient Martindale's 29th
Chemicals (2)
1,8-CINEOLE
CAMPHOR
Respirastimulant Huang, K. C. 1993. The Pharmacology of Chinese Herbs. CRC Press, Boca Raton, FL 388 pp.
Chemicals (1)
CAMPHOR
Respirainhibitor Merck 11th Edition
Chemicals (1)
CAMPHOR
Renoirritant 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 (1)
TERPINEN-4-OL
Photosensitizer Rinzler, C. A. 1990. The Complete Book of Herbs, Spices and Condiments. Facts on File, New York. 199 pp.
Chemicals (1)
LIMONENE
Pheromone
Chemicals (1)
GERMACRENE-D
Pesticide
Chemicals (18)
1,8-CINEOLE
ALPHA-PINENE
ALPHA-TERPINENE
ALPHA-TERPINEOL
BETA-PINENE
BORNEOL
CAMPHENE
CAMPHOR
CARYOPHYLLENE-OXIDE
CUMINALDEHYDE
GAMMA-TERPINENE
GERMACRENE-D
LIMONENE
MYRCENE
MYRTENAL
P-CYMENE
TERPINEN-4-OL
TERPINOLENE
Peristaltic
Chemicals (1)
LIMONENE
Perfumery Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry
Chemicals (14)
ALPHA-PINENE
ALPHA-TERPINENE
ALPHA-TERPINEOL
BETA-BISABOLENE
BETA-PINENE
BORNEOL
CUMINALDEHYDE
GAMMA-TERPINENE
LINALYL-ACETATE
MYRCENE
MYRTENAL
PINOCARVONE
SABINENE
TERPINOLENE
Perfume Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry
Chemicals (1)
1,8-CINEOLE
Pediculicide
Chemicals (1)
1,8-CINEOLE 2.3 x pyrethrin
P450-Inducer
Chemicals (2)
1,8-CINEOLE
LIMONENE
P450-2B1-Inhibitor
Chemicals (4)
ALPHA-PINENE IC50=0.087 uM
ALPHA-TERPINENE IC50=0.76 uM
CAMPHOR IC50=7.89 uM
MYRCENE IC50=0.14 uM
Ozone-Scavenger
Chemicals (1)
LIMONENE
Ornithine-Decarboxylase-Inhibitor
Chemicals (1)
LIMONENE ~750 mg/kg (diet)
Occuloirritant
Chemicals (1)
CAMPHOR
NO-Genic
Chemicals (1)
LIMONENE
Neurotoxic
Chemicals (1)
1,8-CINEOLE
Nematicide Shoyakugaku Zasshi, 44: 183.
Chemicals (6)
1,8-CINEOLE
ALPHA-TERPINEOL MLC=1 mg/ml
BORNEOL MLC=1 mg/ml
CAMPHOR MLC=1 mg/ml
LIMONENE IC=100 ug/ml
TERPINEN-4-OL MLC=1 mg/ml
Myorelaxant
Chemicals (4)
1,8-CINEOLE
BORNEOL
LIMONENE 50 mg/kg
MYRCENE 100-200 mg/kg
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 (2)
ALPHA-TERPINEOL
LINALYL-ACETATE
Mosquitofuge
Chemicals (1)
ALPHA-TERPINEOL > Deet
Lipolytic
Chemicals (1)
LIMONENE
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
Larvicide Leung, A.Y., Encyclopedia of Common Natural Ingredients Used in Food, Drugs, and Cosmetics, John Wiley & Sons, New York, 1980.
Chemicals (1)
CUMINALDEHYDE
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 (11)
1,8-CINEOLE
ALPHA-PINENE
BETA-PINENE
BORNEOL
CAMPHOR
CUMINALDEHYDE
GAMMA-TERPINENE
LIMONENE
MYRCENE
P-CYMENE
TERPINEN-4-OL
Interleukin-6-Inhibitor
Chemicals (2)
ALPHA-TERPINEOL
LIMONENE
Insectiphile J. Stored. Prod. Res., 22:141, 1986.
Chemicals (1)
ALPHA-PINENE
Insectifuge Jacobson, M., Glossary of Plant-Derived Insect Deterrents, CRC Press, Inc., Boca Raton, FL, 213 p, 1990.
Chemicals (12)
1,8-CINEOLE
ALPHA-PINENE 50 ppm
ALPHA-TERPINENE
BETA-PINENE
BORNEOL
CAMPHENE
CAMPHOR
GAMMA-TERPINENE
LIMONENE
MYRCENE
P-CYMENE
TERPINEN-4-OL
Insecticide
Chemicals (5)
ALPHA-PINENE 0.82 uM/fly
ALPHA-TERPINENE 0.86 uM/fly
ALPHA-TERPINEOL 1.29 uM/fly
CARYOPHYLLENE-OXIDE
LIMONENE 0.37 uM/fly
Insect-Repellent
Chemicals (2)
BORNEOL
CAMPHOR
Inhalant Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Chemicals (1)
BORNEOL
Inflammatory
Chemicals (1)
1,8-CINEOLE inj
Immunomodulator
Chemicals (1)
LIMONENE
Hypothermic
Chemicals (1)
MYRCENE
Hypotensive
Chemicals (1)
1,8-CINEOLE
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
Histaminic
Chemicals (1)
LIMONENE
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 (9)
1,8-CINEOLE IC50=78 uM
ALPHA-PINENE IC50=30 uM
BETA-PINENE
BORNEOL IC50=470 mM
CAMPHOR IC50=3.3-180 mM
LIMONENE IC50=45 uM
MYRTENAL
P-CYMENE IC50=50 uM
TERPINEN-4-OL IC50=200 mM
Hepatotonic
Chemicals (1)
1,8-CINEOLE
Hepatoprotective
Chemicals (1)
BORNEOL
GST-Inducer
Chemicals (1)
LIMONENE
Gram(-)icide
Chemicals (1)
1,8-CINEOLE
Gram(+)icide
Chemicals (1)
1,8-CINEOLE
Gastroprotective
Chemicals (1)
1,8-CINEOLE
Fungistat
Chemicals (1)
LIMONENE
Fungiphilic J. Agric. Food Chem. 43: 2283.
Chemicals (1)
LIMONENE
Fungicide 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 (9)
1,8-CINEOLE
BORNEOL
CAMPHOR ED50=2.7 mM
CARYOPHYLLENE-OXIDE
CUMINALDEHYDE
MYRCENE
P-CYMENE
TERPINEN-4-OL
TERPINOLENE
FLavor Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry
Chemicals (15)
1,8-CINEOLE FEMA 1-200
ALPHA-PINENE FEMA 15-150
ALPHA-TERPINENE FEMA 1-40
ALPHA-TERPINEOL FEMA 5-40
BETA-PINENE FEMA 15-600
BORNEOL FEMA<1
CAMPHENE FEMA 15-175
CUMINALDEHYDE FEMA <1
GAMMA-TERPINENE FEMA 1-40
HEXYL-BUTYRATE FEMA 2-10
LIMONENE
LINALYL-ACETATE FEMA 2-15
MYRCENE FEMA 0.5-9
P-CYMENE FEMA 12-250
TERPINOLENE FEMA 15-60
Expectorant 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
CAMPHENE
CAMPHOR
LIMONENE
Epileptigenic 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 (1)
CAMPHOR
Enterocontractant J. Aromatherapy 4: 22.
Chemicals (1)
LIMONENE
Emetic
Chemicals (1)
CAMPHOR
Edemagenic
Chemicals (1)
1,8-CINEOLE inj
Ecbolic
Chemicals (1)
CAMPHOR
Diuretic
Chemicals (1)
TERPINEN-4-OL 0.1 ml/rat
Detoxicant
Chemicals (1)
LIMONENE
Deodorant Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Chemicals (1)
TERPINOLENE
Dentifrice Martindale's 29th
Chemicals (1)
1,8-CINEOLE
Deliriant Merck 11th Edition
Chemicals (1)
CAMPHOR
Degranulant
Chemicals (1)
1,8-CINEOLE 0.3 ul/ml
Decongestant Nigg, H.N. and Seigler, D.S., eds. 1992. Phytochemical Resources for Medicine and Agriculture. Plenum Press, New York. 445 pp.
Chemicals (2)
1,8-CINEOLE
CAMPHOR
Cytochrome-P450-Inducer
Chemicals (1)
1,8-CINEOLE
Counterirritant Martindale's 28th
Chemicals (2)
1,8-CINEOLE
CAMPHOR
Cosmetic Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Chemicals (1)
CAMPHOR
Convulsant R.J. Hixtable (Huxtable, R.J. (as T. Max). 1992. This and That:The Essential Pharmacology of Herbs and Spices. Tips 13:15-20 Huxtable, R.J. 1992b. The Myth of Benficent Nature. The Risk of Herbal Preparations. Anns. Intern. Med. 117(2):165-6; Huxtable, R.
Chemicals (2)
1,8-CINEOLE
CAMPHOR
Coleoptophile
Chemicals (1)
ALPHA-PINENE
CNS-Toxic Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Chemicals (1)
BORNEOL
CNS-Stimulant List, P.H. and Horhammer, L., Hager's Handbuch der Pharmazeutischen Praxis, Vols. 2-6, Springer-Verlag, Berlin, 1969-1979.
Chemicals (3)
1,8-CINEOLE
BORNEOL
CAMPHOR
Cicatrizant
Chemicals (1)
ALPHA-TERPINEOL ED50=240 ug/g mus
Cholesterolytic
Chemicals (1)
LIMONENE
Choleretic
Chemicals (2)
1,8-CINEOLE
BORNEOL
Chemopreventive Stitt, P. A. Why George Should Eat Broccoli. Dougherty Co, Milwaukee, WI, 1990, 399 pp.
Chemicals (2)
LIMONENE
MYRCENE
Carminative Yamamoto, A., Umemori, S., and Muranishi, S. 1993. Absorption Enhancement of Intrapulmonary Administered Insulin by Various Absorption Enhancers and Protease Inhibitors in Rats. J. Pharm. Pharmacol. 46: 14-18, 1994.
Chemicals (1)
CAMPHOR
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
Candidistat
Chemicals (1)
LIMONENE
Candidicide
Chemicals (3)
1,8-CINEOLE
BETA-PINENE
BORNEOL MIC=250 ug/ml
Cancer-Preventive Stitt, P. A. Why George Should Eat Broccoli. Dougherty Co, Milwaukee, WI, 1990, 399 pp.
Chemicals (3)
ALPHA-PINENE
CAMPHOR
LIMONENE
Calcium-Antagonist
Chemicals (1)
CARYOPHYLLENE-OXIDE ED50=32 uM gpg
Bronchoprotectant
Chemicals (1)
LIMONENE
Bacteriostatic Chin. J. Tuber. Respir. Dis.
Chemicals (1)
TERPINEN-4-OL
Apoptotic
Chemicals (1)
LIMONENE
Antiyeast
Chemicals (1)
BORNEOL MIC=250 ug/ml
Antiviral Economic & Medicinal Plant Research, 5: 195.
Chemicals (4)
ALPHA-PINENE
BETA-BISABOLENE IC50=1,800?
LIMONENE
P-CYMENE
Antiulcer
Chemicals (4)
1,8-CINEOLE
BETA-BISABOLENE IC57=100 mg/kg
SABINENE
TERPINEN-4-OL
Antitussive Chin. J. Tuber. Respir. Dis.
Chemicals (2)
1,8-CINEOLE
TERPINEN-4-OL
Antitumor (Stomach)
Chemicals (1)
LIMONENE
Antitumor (Prostate)
Chemicals (1)
LIMONENE
Antitumor (Pancreas)
Chemicals (1)
LIMONENE
Antitumor (Colon)
Chemicals (1)
LIMONENE
Antitumor (Breast)
Chemicals (1)
LIMONENE
Antitumor
Chemicals (2)
CARYOPHYLLENE-OXIDE
LIMONENE
Antistaphylococcic
Chemicals (3)
1,8-CINEOLE 50 ppm
ALPHA-PINENE
BORNEOL MIC=250 ug/ml
Antispasmodic
Chemicals (10)
1,8-CINEOLE
ALPHA-PINENE
ALPHA-TERPINENE
BETA-PINENE
BORNEOL ED50=0.008 mg/ml
CAMPHOR ED50=0.075 mg/ml
LIMONENE ED50=0.197 mg/ml
LINALYL-ACETATE ED50=0.21 mg/ml
MYRCENE
TERPINEN-4-OL
Antisinusitic
Chemicals (1)
1,8-CINEOLE
Antiseptic
Chemicals (8)
1,8-CINEOLE
ALPHA-PINENE
ALPHA-TERPINEOL
BETA-PINENE
CAMPHOR
LIMONENE
SABINENE
TERPINEN-4-OL
Antisalmonella
Chemicals (1)
BORNEOL MIC=125 ug/ml
Antirhinoviral Denyer, C.V., Jackson, P., Loakes, D.M., Ellis, M.R., and Yound, D.A.B. Isolation of Antirhinoviral Sesquiterpenes From Ginger (Zingiber officinale). Journal of Natural Products, 57(5): 658-662, 1994.
Chemicals (1)
BETA-BISABOLENE IC50=1,800?
Antirhinitic
Chemicals (1)
1,8-CINEOLE
Antirheumatic
Chemicals (1)
1,8-CINEOLE
Antirheumatalgic Martindale's 28th
Chemicals (1)
P-CYMENE
Antipyretic
Chemicals (1)
BORNEOL
Antipruritic Merck 11th Edition
Chemicals (1)
CAMPHOR
Antiproliferant
Chemicals (1)
ALPHA-TERPINEOL
Antipneumonic
Chemicals (1)
ALPHA-PINENE
Antiplasmodial Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
Chemicals (2)
MYRTENAL IC50=5-50 ug/ml
TRANS-PINOCARVEOL IC50=5-50 ug/ml
Antiplaque
Chemicals (1)
1,8-CINEOLE
Antipharyngitic
Chemicals (1)
1,8-CINEOLE
Antioxidant
Chemicals (6)
CAMPHENE
GAMMA-TERPINENE
LINALYL-ACETATE 400 ppm
MYRCENE
TERPINEN-4-OL
TERPINOLENE
Antiotitic
Chemicals (1)
BORNEOL
Antiobesity
Chemicals (1)
LIMONENE
Antinociceptive
Chemicals (2)
1,8-CINEOLE
MYRCENE 10-20 mg/kg ipr mus
Antinitrosaminic
Chemicals (3)
ALPHA-TERPINENE
MYRCENE
TERPINOLENE
Antineuralgic Martindale's 28th
Chemicals (1)
CAMPHOR
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
Antimetastatic (Stomach)
Chemicals (1)
LIMONENE
Antimalarial Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
Chemicals (2)
MYRTENAL IC50=5-50 ug/ml
TRANS-PINOCARVEOL IC50=5-50 ug/ml
Antilymphomic
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
Antilithic
Chemicals (1)
LIMONENE
Antilaryngitic
Chemicals (1)
1,8-CINEOLE
Antiinflammatory Shimizu,*M., et al. 1990. Anti-inflammatory Constituents of Topically Applied Crude Drugs. IV.1) Constituents and Anti-inflammatory Effect of Paraguayan Crude Drug 'Alhucema' (Lavandula latifolia Vill.)2). Chem. Pharm. Bull. 38(8): 2283-2284, 1990.
Chemicals (7)
1,8-CINEOLE
ALPHA-PINENE 500 mg/kg
ALPHA-TERPINEOL
BETA-PINENE
BORNEOL
CARYOPHYLLENE-OXIDE
LIMONENE
Antihelicobacter
Chemicals (1)
SABINENE
Antihalitosic American Health, 12(4): 17, 1993.
Chemicals (1)
1,8-CINEOLE
Antiflu Economic & Medicinal Plant Research, 5: 195.
Chemicals (3)
ALPHA-PINENE
LIMONENE
P-CYMENE
Antifibrositic Martindale's 28th
Chemicals (1)
CAMPHOR
Antifeedant
Chemicals (7)
ALPHA-PINENE
BORNEOL
CAMPHOR IC50=5,000 ppm diet
CARYOPHYLLENE-OXIDE
GAMMA-TERPINENE
LIMONENE
TERPINOLENE
Antifatigue
Chemicals (1)
1,8-CINEOLE
Antiesophagitic
Chemicals (1)
LIMONENE
Antiescherichic
Chemicals (1)
BORNEOL MIC=125 ug/ml
Antiemetic Huang, K. C. 1993. The Pharmacology of Chinese Herbs. CRC Press, Boca Raton, FL 388 pp.
Chemicals (1)
CAMPHOR 100-200 mg man orl
Antiedemic Shimizu,*M., et al. 1990. Anti-inflammatory Constituents of Topically Applied Crude Drugs. IV.1) Constituents and Anti-inflammatory Effect of Paraguayan Crude Drug 'Alhucema' (Lavandula latifolia Vill.)2). Chem. Pharm. Bull. 38(8): 2283-2284, 1990.
Chemicals (1)
CARYOPHYLLENE-OXIDE
Antidysenteric Wealth of India.
Chemicals (1)
CAMPHOR 500 ug/ml
Antidiarrheic Wealth of India.
Chemicals (1)
CAMPHOR 500 ug/ml
Anticonvulsant
Chemicals (1)
MYRCENE
Anticholinesterase
Chemicals (1)
1,8-CINEOLE IC50=50-70
Anticatarrh Martindale's 29th
Chemicals (1)
1,8-CINEOLE
Anticariogenic Muroi, H. and Kubo, I. 1993. Combination Effects of Antibacterial Compounds in Green Tea Flavor against Streptococcus mutans. J. Agric. Food Chem. 41: 1102-1105.
Chemicals (2)
1,8-CINEOLE
ALPHA-TERPINEOL MIC=800-1,600 ug/ml
Anticancer
Chemicals (2)
ALPHA-TERPINEOL
LIMONENE
Antibronchitic
Chemicals (2)
1,8-CINEOLE
BORNEOL
Antibacterial
Chemicals (10)
1,8-CINEOLE 50 ppm
ALPHA-PINENE
ALPHA-TERPINEOL MIC=800-1,600 ug/ml
BORNEOL MIC=125-250 ug/ml
CUMINALDEHYDE
LIMONENE
MYRCENE
P-CYMENE
SABINENE
TERPINEN-4-OL
Antibacillary
Chemicals (1)
P-CYMENE
Antiasthmatic
Chemicals (2)
LIMONENE
TERPINEN-4-OL
Antialzheimeran? 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
Antiallergic J. Food Hyg. Soc. Jap. 33(6): 569.
Chemicals (2)
1,8-CINEOLE
TERPINEN-4-OL
Antiadenomic
Chemicals (1)
LIMONENE
Antiacne Nigg, H.N. and Seigler, D.S., eds. 1992. Phytochemical Resources for Medicine and Agriculture. Plenum Press, New York. 445 pp.
Chemicals (4)
ALPHA-PINENE
ALPHA-TERPINEOL
CAMPHOR
TERPINEN-4-OL
Antiacetylcholinesterase
Chemicals (6)
1,8-CINEOLE IC50=41 ug/ml
ALPHA-TERPINENE IC50=1.0 mM
GAMMA-TERPINENE IC23=1.2 mM
LIMONENE IC22-26=1.2 mM
P-CYMENE IC40=1.2 mM
TERPINEN-4-OL IC21-24=1.2 mM
Antiacetylcholine 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 (1)
BORNEOL
Anthelmintic Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Chemicals (1)
1,8-CINEOLE
Anesthetic
Chemicals (3)
1,8-CINEOLE
CAMPHOR
LINALYL-ACETATE 0.01-1 ug/ml
Analgesic
Chemicals (4)
BORNEOL
CAMPHOR
MYRCENE
P-CYMENE
Allergenic
Chemicals (5)
1,8-CINEOLE
ALPHA-PINENE
BETA-PINENE
LIMONENE 1/20th carene
MYRCENE
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 (5)
1,8-CINEOLE
ALPHA-TERPINEOL
CAMPHENE
CAMPHOR
TERPINEN-4-OL
Allelochemic
Chemicals (4)
ALPHA-PINENE
BORNEOL
LIMONENE
TERPINOLENE
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 (4)
ALPHA-TERPINENE 100 ug/ml
ALPHA-TERPINEOL 100 ug/ml
GAMMA-TERPINENE 100 ug/ml
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
ACE-Inhibitor
Chemicals (4)
ALPHA-TERPINENE 100 ug/ml (weak activity)
ALPHA-TERPINEOL 100 ug/ml (weak activity)
GAMMA-TERPINENE 100 ug/ml (weak activity)
MYRCENE 100 ug/ml
Acaricide
Chemicals (4)
1,8-CINEOLE LC100=6 uM
ALPHA-TERPINENE
GAMMA-TERPINENE
LIMONENE LC100=8 uM
Abortifacient
Chemicals (1)
BETA-BISABOLENE
(-)-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
BORNEOL 29 ug/ml
(-)-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
BORNEOL 29 ug/ml
*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.