Observations placeholder
Dr Duke's list of Chemicals and their Biological Activities in: Pinus mugo TURRA (Pinaceae) -- Dwarf Pine, Swiss Mountain Pine
Identifier
019037
Type of Spiritual Experience
Background
A description of the experience
Chemicals and their Biological Activities in: Pinus mugo TURRA (Pinaceae) -- Dwarf Pine, Swiss Mountain Pine
Chemicals
ALPHA-PHELLANDRENE Leaf: GEO
Antibacterial CWW ; Antistaphylococcic CWW ; Dermal JBH ; Emetic PJB1(1) ; FLavor FEMA 10-130 ARC ; Fungicide HH2 ; Insectiphile PEP ; Irritant JBH ; Laxative PJB1(1) ; Perfumery JBH ; Pesticide DUKE1992B
ANISALDEHYDE Leaf: GEO
Antimutagenic EMP6:235 ; Fungicide PJB1(2):261 ; Insecticide CAN ; Pesticide DUKE1992B ; Tyrosinase-Inhibitor ID50=0.32 mM JAF47:4574 ID50=320 uM JAF46:1268 ID50=380-970 uM
ARABINOGALACTAN Plant: HHB
Anticomplementary EMP1:145 ; Antileishmanic 250 ug/ml EMP5:305 ; Immunostimulant 3.7-500 ug/ml EMP5:305 ; Interferonogenic EMP5:305 ; Mitogenic EMP1:145 ; Phagocytotic EMP5:304
ARABINOSE Plant: HHB
No activity reported.
BETA-PHELLANDRENE Leaf: GEO
Expectorant JBH ; Fungicide HH2 ; Perfumery M11
BETA-PINENE Leaf: GEO
Allergenic M&R618 ; Antiinflammatory FT63(1):3 ; Antiseptic LAF ; Antispasmodic; Candidicide LAF337 ; FLavor FEMA 15-600 ARC ; Herbicide TOX ; Insectifuge 382 ; Irritant ZEB ; Perfumery ARC ; Pesticide DUKE1992B ; Spasmogenic CAN ; Transdermal X10408241
BORNYL-ACETATE Leaf: GEO
(-)-Chronotropic 933 nl/ml HH2 ; (-)-Inotropic HH2 ; Antibacterial LAF ; Antifeedant 382 ; Antispasmodic ED50=0.09 mg/ml FT59:465 ; Antiviral LAF ; Expectorant JBH ; FLavor FEMA 70-80 ARC ; Insectifuge HH3 ; Myorelaxant CAN ; Pesticide DUKE1992B ; Sedative
BORNYL-CAPROATE Leaf: GEO
No activity reported.
BORNYL-PROPIONATE Leaf: GEO
No activity reported.
CADINENE Leaf: GEO
Antifeedant 382 ; FLavor FEMA 400-4,000 ARC ; Perfumery JBH ; Pesticide DUKE1992B
CAMPHENE Leaf: AYL
Allelopathic CWW ; Antilithic? JBH ; Antioxidant JA6(4):33 ; Expectorant HH2 ; FLavor FEMA 15-175 ARC ; Hypocholesterolemic? JBH ; Insectifuge 382 ; Pesticide DUKE1992B ; Spasmogenic FT59:465
CAPROALDEHYDE Leaf: GEO
No activity reported.
CRYPTONE Leaf: GEO
No activity reported.
CUMINALDEHYDE Leaf: GEO
Antibacterial DUKE1992B ; FLavor FEMA <1 ARC ; Fungicide FT62:86 ; Irritant ZEB ; Larvicide AYL ; Perfumery JBH ; Pesticide DUKE1992B ; Sedative ZEB ; Tyrosinase-Inhibitor ID50=0.05 mM JAF47:4574 ; Ulcerogenic ZEB
D-LIMONENE Leaf: AYL
Antiacetylcholinesterase IC22=1.2 mM JAF45:677 ; Anticancer (Breast) 8,000 mg/kg; Anticancer (Gastric) JAR9(4):182 ; Antimelanomic IC50=450 uM/l JN127:668 ; Antitumor (Breast) 8,000 mg/kg; Antitumor (Gastric) JAR9(4):182 ; Antitumor-Promoter HH2(2):12 ; Apoptotic BO2 ; Cancer-Preventive HH2(2):12 ; Chemopreventive JAR9(4):182 ; Differentiator BO2 ; FLavor FEMA 30-2,300 ARC ; Hypocholesterolemic HH2(2):12 ; Insecticide DUKE1992B ; Insectifuge 382 ; Litholytic MAR ; Nephrotoxic X8449457 ; P450-2B1-Inhibitor IC50=0.19 uM X9242356 ; Pesticide DUKE1992B
DELTA-3-CARENE Leaf: GEO
Allergenic? M&R184 ; Antibacterial RIE12:5 ; Antiinflammatory ipr IJO15(4):194 ; Dermatitigenic M&R520 ; FLavor FEMA ARC ; Insectifuge 382 ; Irritant PJB1(2):263 ; Pesticide DUKE1992B
DIPENTENE Leaf: GEO
Allergenic M&R618 ; Antibacterial LAF ; Antiviral LAF ; Expectorant JBH ; Irritant JBH ; Pesticide DUKE1992B ; Sedative JBH
EO Leaf 1,200 - 6,100 ppm GEO
No activity reported.
ESTERS Leaf 62 - 564 ppm GEO
No activity reported.
FUCOSE Plant: HHB
No activity reported.
GALACTOSE Plant: HHB
Sweetener 0.32 x sucrose MAR
GLUCOSE Plant: HHB
Acetylcholinergic DUKE1992B ; Antiedemic JBH ; Antihepatotoxic M11 ; Antiketotic M11 ; Antivaricose JBH ; Hyperglycemic M11 ; Memory-Enhancer SN138:189.1990
HEXANAL Leaf: AYL
Antibacterial MBC=800 ug/ml JNP49:5750 ; Antisalmonella MIC=400 ug/ml JNP49:5750 ; Antiseptic 400-800 ug/ml; FLavor FEMA <1-5 ARC ; Pesticide DUKE1992B
KAEMPFEROL Wood: HHB
11B-HSD-Inhibitor CPT59:62 ; 5-Lipoxygenase-Inhibitor IC50 (uM)=20; Aldose-Reductase-Inhibitor 100 uM JBC8:211 ; Antiaflatoxin IC50=3.28 ppm X11714299 IC50=8.73 uM X11714299 ; Antiaggregant 30 uM; Antiallergic RWG122 ; Antibacterial 20 ug/ml; Anticancer JAF47:397 ; Antifertility 250 mg/kg/day/60 days/orl rat PMP23:193 ; Antigingivitic 20 ug/ml JNP59:987 ; Antiherpetic 23-92 ug/ml JNP55:1732 ; Antihistaminic 411 ; Antiimplantation JE32:175 ; Antiinflammatory 20 mg/kg DUKE1992B 200 mg/kg ipr rat DUKE1992B ; Antileukemic IC50=3.1 ug/ml LS55:1061 ; Antilymphocytic JBH ; Antimutagenic ID50=10-40 nM PCF ; Antioxidant 3/4 quercetin JAF49:3653 IC50=1.2 ug/ml JAF50:3150 IC50=40 uM PC27:972 ; Antiperiodontic 20 ug/ml JNP59:987 ; Antiplaque JNP59:987 ; Antiradicular 7 x quercetin; Antiseptic 20 ug/ml JNP59:987 ; Antiserotonin 200 mg/kg ipr rat FT63(1):3 ; Antispasmodic 411 ; Antistaphylococcic PR14:561 ; Antitumor JAF47:397 ; Antitumor-Promoter CPB38:774 ; Antiulcer 50-200 mg/kg ipr rat; Antiviral 23-92 ug/ml; Apoptotic 60 uM X10673981 ; Aromatase-Inhibitor IC12=1 uM/l JMF2:235 ; cAMP-Phosphodiesterase-Inhibitor AFR27:180 ; Cancer-Preventive 525 ; Carcinogenic ZUL ; Choleretic LAF ; Copper-Chelator X10976523 ; COX-2-Inhibitor COX:50 ; Cyclooxygenase-Inhibitor IC50 (uM) =20; Cytotoxic JAF50:850 ; Diaphoretic? LRN-DEC90 ; Diuretic BJP3:10 ; Estrogenic EC50=0.1-25 uM/l JMF2:227 EC50=0.56 uM X10923837 ; Fungicide 20 ug/ml FNF ; Hepatoprotective IC50=1.30 ppm X11714299 IC50=5.46 uM X11714299 ; HIV-RT-Inhibitor IC50=50-150 ug/ml JNP54:142 ; Hypotensive FT1990:508 ; ICAM-1-Inhibitor X15322261 ; iNOS-Inhibitor IC50=13.9 uM X15832817 IC50=<15 uM X10506109 ; Inotropic X10404425 ; Iodothyronine-Deiodinase-Inhibitor JBH ; JNK-Inhibitor X15322261 ; Lipoxygenase-Inhibitor JBH ; MAO-Inhibitor X10813558 ; Mutagenic; Natriuretic BJP3:10 ; Neuroprotective X10813558 ; NO-Inhibitor IC50=13.9 uM X15832817 ; PAF-Inhibitor FT67:548 ; Pesticide DUKE1992B ; Protisticide PR13:102 ; Quinone-Reductase-Inducer 3 uM; Teratologic DUKE1992B ; TNF-alpha-Inhibitor IC50=3.99 uM JMF6:365 ; Topoisomerase-I-Inhibitor TIH14:223 ; Topoisomerase-II-Inhibitor IC50=8.1 ug/ml JNP58:217 ; Tyrosinase-Inhibitor ID50=230 uM; Uterotrophic EC50=0.1-25 uM/l JMF2:227 ; Vasodilator JAFC48:220
L-ALPHA-PINENE Leaf: GEO
No activity reported.
L-LIMONENE Leaf: GEO
Antiacetylcholinesterase IC25=1.2 mM JAF45:677 IC27=164 ug/ml JAF46:3434
MYRCENE Leaf: AYL
ACE-Inhibitor 100 ug/ml K26575 ; Aldose-Reductase-Inhibitor TYK1992:95 ; Allergenic M&R154 ; Analgesic EMM18:28 ; Antibacterial DUKE1992B ; Anticonvulsant X11085358 ; Antimutagenic EMM18:28 ; Antinitrosaminic X10606544 ; Antinociceptive 10-20 mg/kg ipr mus JPP42:877 20-40 mg/kg scu mus JPP42:877 ; Antioxidant JA6(4):33 ; Antispasmodic PM&T20:213.1986 ; Chemopreventive 525 ; FLavor FEMA 0.5-9 ARC ; Fungicide TOX ; Hypothermic X11085358 ; Insectifuge DUKE1992B ; Irritant ZEB ; Myorelaxant 100-200 mg/kg X12587690 ; P450-2B1-Inhibitor IC50=0.14 uM X9242356 ; Perfumery JBH ; Pesticide DUKE1992B
PINOCEMBRIN Wood: HHB
Anesthetic PC29(5):1667 ; Antibacterial IC 3 ug/ml JBH ; Antileukemic DUKE1992B ; Antiseptic DUKE1992B ; Artemicide LC50=12 ppm PC29(5):1667 ; Candidicide IC 0.1-3 mg/ml JBH ; Cytotoxic ED50=21 DUKE1992B ; Fungicide PMP24:117 ; Pesticide DUKE1992B
PINOSYLVIN Wood: HHB
Antibacterial DUKE1992B ; Antifeedant JCE12:2117.86 ; Fungicide DUKE1992B ; Pesticide DUKE1992B ; Phytoalexin 450
PINOSYLVINMONOMETHYLETHER Wood: HHB
No activity reported.
PUMILIOL Leaf: GEO
No activity reported.
PUMILONE Leaf: GEO
No activity reported.
QUERCETIN Wood: HHB
11B-HSD-Inhibitor CPT59:62 ; 5-Lipoxygenase-Inhibitor IC50 (uM)=4; Aldehyde-Oxidase-Inhibitor IC70-96=10 uM X16394541 ; Aldose-Reductase-Inhibitor 100 uM 4 ug/ml SKN43:99 IC50=0.344 uM ZZZ18:623 IC50=0.84 ug/ml cow CPB43:1385 ; Allelochemic IC82=1 mM 438 ; Allergenic JBH ; Analgesic FT63(3):197 ; Antiaflatoxin IC50=25 uM X11714299 IC50=7.5 ppm X11714299 ; Antiaggregant 30 uM JAF45:4505 IC50=55 uM EMP5:333 ; Antiaging PM69:1125 ; Antiallergic IC50=14 uM JIM127:546 ; Antialzheimeran COX ; Antianaphylactic PR4(5):201 ; Antiangiogenic EJP459:255 ; Antiarthritic COX ; Antiasthmatic; Antiatherosclerotic X11020457 ; Antibacterial JBH ; Anticarcinomic (Breast) IC50=1.5 uM MED ; Anticariogenic ID50=120 ug/ml JAF48:5666 ; Anticataract PM56(3):258 ; Anticolitic 400 mg/man/3x/day PAM ; Anticomplementary JNP65:1457 ; AntiCrohn's PAM ; Anticystitic 1,000 mg/day/4 weeks X11272677 ; Antidepressant JMF6:391 ; Antidermatitic PAM ; Antidiabetic; Antielastase IC50=0.8 ug/ml DUKE1992B ; Antiencephalitic EMP5:199 ; Antiescherichic X10857921 ; Antiestrogenic; Antifeedant IC52=<1,000 ppm diet 438 ; Antifibrosarcomic JAF45:4505 ; Antiflu V&D ; Antigastric RR21:85 ; Antigonadotropic JBH ; AntiGTF ID50=120 ug/ml JAF48:5666 ; Antihepatotoxic PM56(2):171 ; Antiherpetic 48-150 ug/ml; Antihistaminic IC50=<10 uM; AntiHIV JNP60(9):884 ; Antihydrophobic V&D ; Antihypertensive KCH ; Antiinflammatory 20-150 mg/kg FT5:1990 ; Antileishmanic IC50=64 JNP65:1457 ; Antileukemic 5.5-60 uM BO2 IC50=10 uM EMP5:225 IC50=>10 ug/ml LS55:1061 ; Antileukotriene PAM ; Antilipoperoxidant IC67=50; Antimalarial IC50=1-6.4 ug/ml MPT ; Antimelanomic; Antimetastatic BO2 ; Antimutagenic ID50=0.62 ug/ml X14586095 ID50=2-5 nM PCF ; Antimyocarditic EMP5:199 ; Antinitrosaminic PAL:339 ; Antinociceptive PR14:40 ; Antioxidant 4.7 x Vit. E BO2 ED50=2.3 uM PR14:93 IC47=10 uM JMF5:1 IC96=300 ppm PCF ; Antipancreatitic JNU ; Antiperiodontal PAM ; Antiperistaltic X14646351 ; Antipermeability DUKE1992B ; Antiperoxidant PM57:A110 ; Antipharyngitic PAM ; Antiplaque PAM ; Antiplasmodial IC50=13-64 JNP65:1457 ; AntiPMS 500 mg/2x/day/wmn PAM ; Antipodriac; Antipolio PAM ; Antiproliferant 10 nM; Antiprostanoid PCF:51 ; Antiprostatitic JNU ; Antipsoriac PAM ; Antiradicular IC50=4.6 uM PM56(6):695 ; Antispasmodic; Antistreptococcic ID50=120 ug/ml JAF48:5666 ; Antithiamin PCF:69 ; Antithrombic PAL:339 ; Antitrypanosomic IC50=13 JNP65:1457 ; Antitumor 10 uM; Antitumor (Bladder) JNM7:51 ; Antitumor (Breast) JNM7:51 ; Antitumor (Colon) JAF45:4505 ; Antitumor (Lung) X10918203 ; Antitumor (Ovary) JNM7:51 ; Antitumor (Skin) 20 uM BO2 ; Antitumor-Promoter PAM ; Antiulcer PR14:581 ; Antiviral 48-150 ug/ml JNP55:1732 IC50=10 uM EMP5:225 ; Apoptotic 20-60 uM; ATPase-Inhibitor NIG ; Bacteristat 10 mg/ml QRNM(SUMMER):91 ; Bradycardiac KCH ; Calmodulin-Antagonist PAM ; cAMP-Phosphodiesterase-Inhibitor PAM ; Cancer-Preventive 525 ; Candidicide X10857921 ; Capillariprotective M11 ; Carcinogenic 40,000 ppm (diet) mus NIG ; Catabolic AFR27:173 ; COMT-Inhibitor QRNM1997:293 ; Copper-Chelator; COX-2-Inhibitor <40 uM BO2 ; Cyclooxygenase-Inhibitor PCF:49 ; Cytochrome-P450-1A2-Inhibitor X11752233 ; Cytotoxic ED50=70 ug/ml PM56(6):677 IC82=100 ug/ml PM57:A113 ; Deiodinase-Inhibitor JNM1:10 ; Diaphoretic? LRN-DEC90 ; Differentiator 5.5 uM BO2 ; Estrogenic 10% genistein B02 ; Fungicide X10857921 ; Glucosyl-Transferase-Inhibitor ID50=120 ug/ml JAF48:5666 ; Hemostat KCH ; Hepatomagenic 5,000 ppm (diet) rat PCF ; Hepatoprotective FT67:200 ; HIV-RT-Inhibitor IC50=<1 ug/ml JNP53(5):1239 ; Hypoglycemic 100 mg/kg orl rat JE27:243 ; iNOS-Inhibitor IC50=20 uM; Inotropic X10404425 ; Insulinogenic PAM ; Juvabional 438 ; Larvistat 8,000 ppm diet 438 ; Lipoxygenase-Inhibitor IC11=1.25 mM JAF38:688 IC50=0.1-5 uM DFN:154 ; MAO-A-Inhibitor QRNM1997:293 ; Mast-Cell-Stabilizer DUKE1992B ; Metal-Chelator (Copper) PR14:93 ; Metalloproteinase-Inhibitor IC50=>42 uM X10723772 ; MMP-9-Inhibitor 20 uM BO2 ; Mutagenic HG22:27 ; NADH-Oxidase-Inhibitor BJP3:10 ; NEP-Inhibitor IC50=>42 uM X10723772 ; Neuroprotective 5-25 uM; NF-kB-Inhibitor X15180920 ; NO-Inhibitor IC50=20 uM X15832817 IC>50=125 uM JAF50:850 ; NO-Synthase-Inhibitor 5-50 uM; Ornithine-Decarboxylase-Inhibitor <10 uM; P450-Inducer 5 uM FNF ; P450-Inhibitor 50-100 uM FNF ; Pesticide DUKE1992B ; PGE2-Inhibitor X12144868 ; Phospholipase-Inhibitor BJP3:10 ; Plasmodicide HDN ; Proliferant X12224631 ; Prostaglandin-Synthesis-Inhibitor 40 ug/ml PR11:281 ; Protein-Kinase-C-Inhibitor PCF:14 ; PTK-Inhibitor 0.4-24 uM BO2 ; Quinone-Reductase-Inducer 13 uM 6 uM CLE120:213 ; Teratologic DUKE1992B ; TNF-alpha-Inhibitor IC50=3.11 uM JMF6:365 ; Topoisomerase-I-Inhibitor IC50=12.8 ug/ml IC50=42 uM BO2 ; Topoisomerase-II-Inhibitor IC50=1-6.9 ug/ml IC50=23-40 uM BO2 ; Tumorigenic 0.1% diet orl rat/yr 505 ; Tyrosinase-Inhibitor ID50=70 uM; Tyrosine-Kinase-Inhibitor EMP6:170 ; Vasodilator; VEGF-Inhibitor X16737615 ; Xanthine-Oxidase-Inhibitor 3.1 uM PM69:1125 IC50=10.6 ug/ml X12591129 IC50=>0.4 ug/ml CPB38:1772
XYLOGALACTURONANE Plant: HHB
No activity reported.
XYLOSE Plant: HHB
Antidiabetic; Diagnostic MAR ; Dye M11
The source of the experience
Dr Dukes plant databaseConcepts, symbols and science items
Concepts
Symbols
Science Items
Activities and commonsteps
Commonsteps
References
382: Jacobson, M., Glossary of Plant-Derived Insect Deterrents, CRC Press, Inc., Boca Raton, FL, 213 p, 1990.
411: Williamson, E. M. and Evans, F. J., Potter's New Cyclopaedia of Botanical Drugs and Preparations, Revised Ed., Saffron Walden, the C. W. Daniel Co., Ltd., Essex UK, 362 pp, 1988, reprint 1989.
438: Lydon, J. & Duke, S., The potential of pesticides from plants, pp. 1-41 in Craker, L. & Simon, J., eds, Herbs, Spices & Medicinal Plants: Recent Advances in Botany, Horticulture, & Pharmacology, v. 4, Oryx Press, Phoenix, 1989, 267pp.
450: Russell, G. B., Phytochemical resources for crop protection, N. Z. J. Technol., 2, 1986, 127-134.
505: Jim Duke's personal files.
525: Stitt, P. A. Why George Should Eat Broccoli. Dougherty Co, Milwaukee, WI, 1990, 399 pp.
AFR27:173: Jim Duke's personal files
AFR27:180: Jim Duke's personal files
ARC: Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry Note: Most ARC numerical data were in mg/dl. I know of no other plant where zinc is more prevalent than other minerals and protein. These data should be viewed as suspect.
AYL: Leung, A.Y., Encyclopedia of Common Natural Ingredients Used in Food, Drugs, and Cosmetics, John Wiley & Sons, New York, 1980.
B02: Jim Duke's personal files
BJP3:10: Jim Duke's personal files
BO2: Jim Duke's personal files
CAN: Newall, C. A., Anderson, L. A. and Phillipson, J. D. 1996. Herbal Medicine - A Guide for Health-care Professionals. The Pharmaceutical Press, London. 296pp.
CLE120:213: Uda, Y., Price, K. R., Williamson, G., Rhodes, M. J. C. 1997. Induction of the Anticarcinogenic Marker Enzyme, Quinone Reductase, in Murine Hepatoma Cells In Vitro by Flavonoids. Cancer Lett., 120 (2): 213-216.
COX: Jim Duke's personal files
COX:50: Jim Duke's personal files
CPB38:1772: Chem. & Pharm. Bull. 38: 1772.
CPB38:774: Yasukawa, K., Takido, M., Takeuchi, M., Sato, Y., Nitta, K., and Nakagawa, S. 1989. Inhibitory Effects of Flavonol Glycosides on 12-O-Tetradecanoylphorbol-13-acetate-Induced Tumor Promotion. Chem. Pharm. Bull. 38(3): 774-776, 1990.
CPB43:1385: Okada,Y,et al.1995.Search for Naturally Occurring Substances to Prevent the Complications of Diabetes.II.Inhibitory Effect of Coumarin and Flavonoid Derivatives on Bovine Lens Aldose Reductase and Rabbit Platelet Aggregation.Chem Pharm Bull43(8):1385-1387
CPT59:62: Jim Duke's personal files
CWW: 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.
DFN:154: Jim Duke's personal files
DUKE1992B: Duke, James A. 1992. Handbook of biologically active phytochemicals and their activities. Boca Raton, FL. CRC Press.
EJP459:255: Jim Duke's personal files
EMM18:28: 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.
EMP1:145: Jim Duke's personal files
EMP5:199: Economic & Medicinal Plant Research, 5: 199.
EMP5:225: Economic & Medicinal Plant Research, 5: 225.
EMP5:304: Jim Duke's personal files
EMP5:305: Jim Duke's personal files
EMP5:333: Economic & Medicinal Plant Research, 5: 333.
EMP6:170: Economic & Medicinal Plant Research, 6: 170.
EMP6:235: Economic & Medicinal Plant Research, 6: 235.
FNF: Father Nature's Farmacy: The aggregate of all these three-letter citations.
FT1990:508: Jim Duke's personal files
FT59:465: Fitoterapia No.59-1984.
FT5:1990: Fitoterapia No.5-1990.
FT62:86: Singh*, G., Upadhyay, R.K. 1990. Fungitoxic Activity of Cumaldehyde, Main Constituent of the Cuminum cyminum Oil. Fitoterapia 62(1): 86, 1991.
FT63(1):3: Jim Duke's personal files
FT63(3):197: Jim Duke's personal files
FT67:200: Jim Duke's personal files
FT67:548: Jim Duke's personal files
GEO: Guenther, E., The Essential Oils, 6 volumes, D. van Nostrand, New York, 1948-1952.
HDN: Neuwinger, H. D. 1996. African Ethnobotany - Poisons and Drugs. Chapman & Hall, New York. 941 pp.
HG22:27: Jim Duke's personal files
HH2: 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.
HH2(2):12: Jim Duke's personal files
HH3: 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.
HHB: List, P.H. and Horhammer, L., Hager's Handbuch der Pharmazeutischen Praxis, Vols. 2-6, Springer-Verlag, Berlin, 1969-1979.
IJO15(4):194: Internat. J. Oriental Med. 15(4): 194, 1990+
JA6(4):33: Jim Duke's personal files.
JAF38:688: Oszmianski, J. and Lee, C.Y. 1990. Inhibitory Effect of Phenolics on Carotene Bleaching in Vegetables. J. Agric. Food Chem. 38: 688-690.
JAF45:4505: Jim Duke's personal files
JAF45:677: Jim Duke's personal files
JAF46:1268: Jim Duke's personal files
JAF46:3434: Jim Duke's personal files
JAF47:397: Jim Duke's personal files
JAF47:4574: Jim Duke's personal files
JAF48:5666: Jim Duke's personal files
JAF49:3653: Jim Duke's personal files
JAF50:3150: Jim Duke's personal files
JAF50:850: Jim Duke's personal files
JAFC48:220: Jim Duke's personal files
JAR9(4):182: Jim Duke's personal files
JBC8:211: Oliveira, T. T., Nagem, T. J., Miranda, L. C. G., Paula, V. F., Teixeira, M. A. 1997. Inhibitory Action on Aldose Reductase by Soybean Flavonoids. J Braz Chem Soc, 8(3): 211-213.
JBH: Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
JCE12:2117.86: Jim Duke's personal files
JE27:243: Ivorra, M.D., Paya, M., and Villar, A. 1989. A Review of Natural Products and Plants as Potential Antidiabetic Drugs. Journal of Ethnopharmacology, 27: 243-275, 1989.
JE32:175: Jim Duke's personal files
JIM127:546: Jim Duke's personal files.
JMF2:227: Journal of Medicinal Food 2: 227.1999.
JMF2:235: Journal of Medicinal Food 2: 235.1999.
JMF5:1: Jim Duke's personal files
JMF6:365: Jim Duke's personal files
JMF6:391: Jim Duke's personal files
JN127:668: Jim Duke's personal files
JNM1:10: Jim Duke's personal files.
JNM7:51: Jim Duke's personal files
JNP49:5750: Jim Duke's personal files
JNP53(5):1239: Nakane, H., Fukushima, M., and Ono*, K. Differential Inhibition Of Reverse Transcriptase And Various DNA Polymerases By Digallic Acid And Its Derivatives. Journal of Natural Products, 53(5): 1234-1240, 1990.
JNP54:142: Garcia, J., Morin,* C., Nyasse, B., Sondengam, B-L., Tchouankeu, J-C., and Tsamo, E. Complete Structural Assignments Of An Ergosterol Derivative From Entandrophragma utile. Journal of Natural Products, 54(1): 136-142, 1991.
JNP55:1732: Amoros, M., Simoes, C.M.O., Girre, L., et al. Synergistic Effect Of Flavones And Flavonols Against Herpes Simplex Virus Type 1 In Cell Culture. Comparison With The Antiviral Activity Of Propolis. J. of Natural Products 55(12):1732-1740, 1992.
JNP58:217: Constantinou, A., Mehta, R., Runyan, C., Rao, K., Vaughan, A., Moon, R. 1995. Flavonoids as DNA Topoisomerase Antagonists and Poisons: Structure-Activity Relationships. J Natural Products, 58: 217-225.
JNP59:987: Jim Duke's personal files
JNP60(9):884: Jim Duke's personal files
JNP65:1457: Jim Duke's personal files
JNU: Joseph, J., Nadeau, D. and Underwood, A. 2001. The Color Code. Hyperion, NY.
JPP42:877: 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.
K26575: Jim Duke's personal files
KCH: Huang, K. C. 1993. The Pharmacology of Chinese Herbs. CRC Press, Boca Raton, FL 388 pp.
LAF: Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp.
LAF337: Jim Duke's personal files
LRN-DEC90: Lawrence Review of Natural Products, Dec-90.
LS55:1061: Life Sciences 55: 1061.
M&R154: Jim Duke's personal files
M&R184: Jim Duke's personal files
M&R520: Jim Duke's personal files
M&R618: Jim Duke's personal files
M11: Merck 11th Edition
MAR: Martindale's 28th
MED: Medline (post 1990 searches filed in my computer)
MPT: Medicinal and Poisonous Plants of the Tropics. Leeuwenberg, A.J.M., ed. Pudoc, Wageningen. 1987.
NIG: Nigg, H.N. and Seigler, D.S., eds. 1992. Phytochemical Resources for Medicine and Agriculture. Plenum Press, New York. 445 pp.
PAL:339: Jim Duke's personal files
PAM: Pizzorno, J.E. and Murray, M.T. 1985. A Textbook of Natural Medicine. John Bastyr College Publications, Seattle, Washington (Looseleaf).
PC27:972: Jim Duke's personal files
PC29(5):1667: Jung, J.H., Pummangura, S., Chaichantipyuth, c., Patarapanich, C., and McLaughlin, J.L. 1989. Bioactive Constituents of Melodorum fruticosum. Phytochemistry. 29(5): 1667-1670. 1990.
PCF: Phenolic Compounds in Food and Their Effects on Health. Antioxidants & Cancer Prevention. Huang, M.T., Ho, C.T. and Lee, C.Y. eds. 1992. ACS Symposium Series 507.ACS, Washington 402 pp.
PCF:14: Naim, M., Zehavi, U., Nagy, S., and Rouseff, R.L. Hydroxycinnamic Acids as Off-Flavor Precursors in Citrus Fruits and Their Products. Phenolic Compounds in Food and Their Effects on Health, Ch.14.
PCF:49: Jim Duke's personal files
PCF:51: Jim Duke's personal files
PCF:69: Phenolic Compounds in Food and Their Effects on Health, 69.
PEP: Pakistan Encyclopedia Planta Medica. 1986.
PJB1(1): Jim Duke's personal files
PJB1(2):261: Jim Duke's personal files
PJB1(2):263: Jim Duke's personal files
PM&T20:213.1986: Jim Duke's personal files.
PM56(2):171: Joyeux, M., Rolland, A., Fleurentin, J., Mortier, F., and Dorfman, P. 1989. Tert-Butyl Hydroperoxide-Induced Injury in Isolated Rat Hepatocytes: A Model for Studying Anti-Hepatotoxic Crude Drugs. Planta Medica 56(2): 171-173, 1990.
PM56(3):258: Jim Duke's personal files
PM56(6):677: Matsukawa, Y., et al. The Effect of Quercetin and Other Flavonoids on Cell Cycle Progresssion and Growth of Human Gastric Cancer Cells. Planta Medica, 56(6): 677, 1990.
PM56(6):695: Planta Medica, 56(6): 695, 1990.
PM57:A110: Planta Medica, 57: A110, 1991.
PM57:A113: Planta Medica, 57: A113, 1991.
PM69:1125: Jim Duke's personal files
PMP23:193: Kumar, P., Dixit*, V.P., and Khanna, P. Antifertility Studies of Kaempferol: Isolation and Identification from Tissue Culture of some Medicinally Important Plant Species. Plantes medicinales et phytotherapie, 23: 193-201, 1989.
PMP24:117: Jim Duke's personal files
PR11:281: Ibewuike, J. C., Ogungbamila, F. O., Ogundaini, A. O., Okeke, I. N., Bohlin, L. 1997. Antiinflammatory and Antibacterial Activities of C-methylflavonol from Piliostigma thonningii. Phytotherapy Research, 11(4): 281-284.
PR13:102: Meckes, M., Calzada, F., Tapia-Contreras, A., Cedillo-Rivera, R. 1999. Antiprotozoal Properties of Helianthemum glomeratum. Phytotherapy Research, 13(2): 102-105.
PR14:40: Jim Duke's personal files
PR14:561: Jim Duke's personal files
PR14:581: Jim Duke's personal files
PR14:93: Seidel, V., Verholle, M., Malard, Y., Tillequin, F., Fruchart, J-C., Duriez, P., Bailleul, F., Teissier, E. 2000. Phenylpropanoids from Ballota nigra L. Inhibit in vitro LDL Peroxidation. Phytotherapy Research, 14(2): 93-98.
PR4(5):201: Meli, R., Autore, G., Di Carlo, G., Capasso, F. Inhibitory Action of Quercetin on Intestinal Transit in Mice. Phytotherapy Research 4(5): 201, 1990.
QRNM(SUMMER):91: Jim Duke's personal files
QRNM1997:293: Jim Duke's personal files
RIE12:5: Revista Itiliana Eppos, 12: 5, 1994.
RR21:85: Rastitel'nye Resursy, 21: 85.
RWG122: Jim Duke's personal files
SKN43:99: Ichikawa, K., et al. 1991. Isolation and Structure Determination of Aldose Reductase Inhibitors from Traditional Thai Medicine, and Syntheses of Their Derivatives. Sankyo Kenkyusho Nempo, 43: 99-110.
SN138:189.1990: Science News, 138: 189, 1990.
TIH14:223: Santti, R., Makela, S., Strauss, L., Korman, J., Kostian, M. L. 1998. Phytoestrogens: Potential Endocrine Disruptors in Males. Toxicol Ind Health, 14: 223-237.
TOX: 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.
TYK1992:95: Okamura, K., Iwakami, S., Matsunaga, T. 1992. Biological Activity of Monoterpenes from Trees. Toyama-Ken Yakuji Kenkyusho Nenpo, (20): 95-101.
V&D: Vlietinck, A.J. and Dommisse, R.A. eds. 1985. Advances in Medicinal Plant Research. Wiss. Verlag. Stuttgart.
X10404425: Jim Duke's personal files
X10408241: Jim Duke's personal files
X10506109: Jim Duke's personal files
X10606544: Jim Duke's personal files
X10673981: Jim Duke's personal files
X10723772: Jim Duke's personal files
X10813558: Jim Duke's personal files
X10857921: Jim Duke's personal files
X10918203: Jim Duke's personal files
X10923837: Jim Duke's personal files
X10976523: Jim Duke's personal files
X11020457: Jim Duke's personal files
X11085358: Jim Duke's personal files
X11272677: Jim Duke's personal files
X11714299: Jim Duke's personal files
X11752233: Jim Duke's personal files
X12144868: Jim Duke's personal files
X12224631: Jim Duke's personal files
X12587690: Jim Duke's personal files
X12591129: Jim Duke's personal files
X14586095: Jim Duke's personal files
X14646351: Jim Duke's personal files
X15180920: Jim Duke's personal files
X15322261: Jim Duke's personal files
X15832817: Jim Duke's personal files
X16394541: Jim Duke's personal files
X16737615: Jim Duke's personal files
X8449457: Jim Duke's personal files
X9242356: Jim Duke's personal files
ZEB: 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.
ZUL: Hutchings, A, Scott, AH, Lewis, G, and Cunningham, A. 1996. Zulu Medicinal Plants. An inventory. University of Natal Press, Pietermaritzburg. 450 pp.
ZZZ18:623: Mao, X. M., Zhang, J. Q. 1993. Inhibition of Aldose Reductase by Extracts of Chinese Herbal Medicine. Zhongguo Zhongyao Zazhi , 18(10): 623-624.
ppm = parts per million
tr = trace