A giant canopy tree growing to 90 feet, Azucar Huayo, or Jatoba, is a toning and energising bark. It also finds use as an antibacterial, antifungal, antiinflammatory, expectorant, antiyeast and hepatoprotector (liver tonic). It is loaded with nearly 40 phytochemicals, making it useful for many more conditions throughout South America as well as a general tonic.
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Jatoba (Bark) Options
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$14.99
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Suggested Use: Liquids: Use 15-20 drops mixed with water two to three times daily or as recommended by a practitioner.
Cautions: Jatoba has a natural stimulating effect. Use under care/advice of a medical practitioner. Not intended for long term therapy. Not intended for pregnant or nursing women. Keep out of the reach of children
Contraindications: Take early in the day to prevent insomnia.
Ingredients: Extracted in distilled water and 40% organic grain alcohol.
More About Jatoba:
1. Screening Brazilian plant species for in vitro inhibition of 5-lipoxygenase.
Braga FC, Wagner H, Lombardi JA, de Oliveira AB.
Faculdade de Farmacia, UFMG, Belo Horizonte, Brazil. fernao@dedalus.lcc.ufmg.br
Phytomedicine. 2000 Jan;6(6):447-52.
PMID: 10715848 [PubMed - indexed for MEDLINE]
2. Isolation and absolute configuration of ent-Halimane diterpenoids from Hymenaea courbaril from the Suriname rain forest.
Abdel-Kader M, Berger JM, Slebodnick C, Hoch J, Malone S, Wisse JH, Werkhoven MC, Mamber S, Kingston DG.
Department of Chemistry, M/C 0212, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.
J Nat Prod. 2002 Jan;65(1):11-5.
PMID: 11809056 [PubMed - indexed for MEDLINE]
3. In vitro antiplasmodial investigation of medicinal plants from El Salvador.
Kohler I, Jenett-Siems K, Siems K, Hernandez MA, Ibarra RA, Berendsohn WG, Bienzle U, Eich E.
Institut fur Pharmazie, Freie Universitat Berlin, Germany.
Z Naturforsch [C]. 2002 Mar-Apr;57(3-4):277-81.
PMID: 12064726 [PubMed - indexed for MEDLINE]
4. In vitro antiplasmodial investigation of medicinal plants from El Salvador.
Kohler I, Jenett-Siems K, Siems K, Hernandez MA, Ibarra RA, Berendsohn WG, Bienzle U, Eich E.
Institut fur Pharmazie, Freie Universitat Berlin, Germany.
Z Naturforsch [C]. 2002 Mar-Apr;57(3-4):277-81.
PMID: 12064726 [PubMed - indexed for MEDLINE]
5. Isolation and absolute configuration of ent-Halimane diterpenoids from Hymenaea courbaril from the Suriname rain forest.
Abdel-Kader M, Berger JM, Slebodnick C, Hoch J, Malone S, Wisse JH, Werkhoven MC, Mamber S, Kingston DG.
Department of Chemistry, M/C 0212, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.
J Nat Prod. 2002 Jan;65(1):11-5.
PMID: 11809056 [PubMed - indexed for MEDLINE]
6. Screening Brazilian plant species for in vitro inhibition of 5-lipoxygenase.
Braga FC, Wagner H, Lombardi JA, de Oliveira AB.
Faculdade de Farmacia, UFMG, Belo Horizonte, Brazil. fernao@dedalus.lcc.ufmg.br
Phytomedicine. 2000 Jan;6(6):447-52.
PMID: 10715848 [PubMed - indexed for MEDLINE]
1. Screening Brazilian plant species for in vitro inhibition of 5-lipoxygenase.
Braga FC, Wagner H, Lombardi JA, de Oliveira AB.
Faculdade de Farmacia, UFMG, Belo Horizonte, Brazil. fernao@dedalus.lcc.ufmg.br
Phytomedicine. 2000 Jan;6(6):447-52.
Plants from the Brazilian flora were evaluated for the inhibition of 5-lipoxygenase. The species were selected based on their traditional use and on a chemosystematic approach. In total, 19 species belonging to 13 families have been investigated. Hedychium coronarium J. Koenig (Zingiberaceae), Xylopia frutescens Aubl. (Annonaceae) and Hymenaea courbaril L. (Leguminosae) presented a high 5-lipoxygenase inhibitory activity. Some hypothesis about the nature of the active compounds are discussed, based on reports of the chemical constitution of these species or other species from the same botanical family.
PMID: 10715848 [PubMed - indexed for MEDLINE]
2. Isolation and absolute configuration of ent-Halimane diterpenoids from Hymenaea courbaril from the Suriname rain forest.
Abdel-Kader M, Berger JM, Slebodnick C, Hoch J, Malone S, Wisse JH, Werkhoven MC, Mamber S, Kingston DG.
Department of Chemistry, M/C 0212, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.
J Nat Prod. 2002 Jan;65(1):11-5.
Bioactivity-directed fractionation of a methanol extract of Hymenaea courbaril afforded the three new diterpenoids (13R)-13-hydroxy-1(10),14-ent-halimadien-18-oic acid (1), (2S,13R)-2,13-dihydroxy-1(10),14-ent-halimadien-18-oic acid (2), and (13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid (3). The configurations of these compounds were determined from X-ray crystallography of 1, circular dichroism of 2 and 3, and spectral studies of prepared derivatives. Compound 1 exhibited weak cytotoxicity toward the 1138 mutant yeast strain and the A2780 human ovarian cancer cell line.
PMID: 11809056 [PubMed - indexed for MEDLINE]
3. In vitro antiplasmodial investigation of medicinal plants from El Salvador.
Kohler I, Jenett-Siems K, Siems K, Hernandez MA, Ibarra RA, Berendsohn WG, Bienzle U, Eich E.
Institut fur Pharmazie, Freie Universitat Berlin, Germany.
Z Naturforsch [C]. 2002 Mar-Apr;57(3-4):277-81.
In vitro antiplasmodial activities of extracts from Albizia saman, Fabaceae, Calea tenuifolia (C. zacatechichi), Asteraceae, Hymenaea courbaril, Fabaceae, Jatropha curcas, Euphorbiaceae, Momordica charantia, Cucurbitaceae, and Moringa oleifera, Moringaceae were evaluated. From the lipophilic extract of C tenuifolia five active flavones were obtained. 4’,5-Dihydroxy-7-methoxyflavone [genkwanin] and 5-hydroxy-4’,7-dimethoxyflavone [apigenin 4’,7-dimethylether] exhibited the strongest antiplasmodial activity against a chloroquine-sensitive strain (poW) and a chloroquine-resistant strain (Dd2) of Plasmodium falciparum [IC50 values: 17.1-28.5 microM). Furthermore octadeca-9,12-dienoic acid [linoleic acid] [IC50] values of 21.8 microM (poW) and 31.1 microM (Dd2)] and octadeca-9,12,15-trienoic acid (alpha-linolenic acid) were isolated.
PMID: 12064726 [PubMed - indexed for MEDLINE]
4. In vitro antiplasmodial investigation of medicinal plants from El Salvador.
Kohler I, Jenett-Siems K, Siems K, Hernandez MA, Ibarra RA, Berendsohn WG, Bienzle U, Eich E.
Institut fur Pharmazie, Freie Universitat Berlin, Germany.
Z Naturforsch [C]. 2002 Mar-Apr;57(3-4):277-81.
In vitro antiplasmodial activities of extracts from Albizia saman, Fabaceae, Calea tenuifolia (C. zacatechichi), Asteraceae, Hymenaea courbaril, Fabaceae, Jatropha curcas, Euphorbiaceae, Momordica charantia, Cucurbitaceae, and Moringa oleifera, Moringaceae were evaluated. From the lipophilic extract of C tenuifolia five active flavones were obtained. 4’,5-Dihydroxy-7-methoxyflavone [genkwanin] and 5-hydroxy-4’,7-dimethoxyflavone [apigenin 4’,7-dimethylether] exhibited the strongest antiplasmodial activity against a chloroquine-sensitive strain (poW) and a chloroquine-resistant strain (Dd2) of Plasmodium falciparum [IC50 values: 17.1-28.5 microM). Furthermore octadeca-9,12-dienoic acid [linoleic acid] [IC50] values of 21.8 microM (poW) and 31.1 microM (Dd2)] and octadeca-9,12,15-trienoic acid (alpha-linolenic acid) were isolated.
PMID: 12064726 [PubMed - indexed for MEDLINE]
5. Isolation and absolute configuration of ent-Halimane diterpenoids from Hymenaea courbaril from the Suriname rain forest.
Abdel-Kader M, Berger JM, Slebodnick C, Hoch J, Malone S, Wisse JH, Werkhoven MC, Mamber S, Kingston DG.
Department of Chemistry, M/C 0212, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.
J Nat Prod. 2002 Jan;65(1):11-5.
Bioactivity-directed fractionation of a methanol extract of Hymenaea courbaril afforded the three new diterpenoids (13R)-13-hydroxy-1(10),14-ent-halimadien-18-oic acid (1), (2S,13R)-2,13-dihydroxy-1(10),14-ent-halimadien-18-oic acid (2), and (13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid (3). The configurations of these compounds were determined from X-ray crystallography of 1, circular dichroism of 2 and 3, and spectral studies of prepared derivatives. Compound 1 exhibited weak cytotoxicity toward the 1138 mutant yeast strain and the A2780 human ovarian cancer cell line.
PMID: 11809056 [PubMed - indexed for MEDLINE]
6. Screening Brazilian plant species for in vitro inhibition of 5-lipoxygenase.
Braga FC, Wagner H, Lombardi JA, de Oliveira AB.
Faculdade de Farmacia, UFMG, Belo Horizonte, Brazil. fernao@dedalus.lcc.ufmg.br
Phytomedicine. 2000 Jan;6(6):447-52.
Plants from the Brazilian flora were evaluated for the inhibition of 5-lipoxygenase. The species were selected based on their traditional use and on a chemosystematic approach. In total, 19 species belonging to 13 families have been investigated. Hedychium coronarium J. Koenig (Zingiberaceae), Xylopia frutescens Aubl. (Annonaceae) and Hymenaea courbaril L. (Leguminosae) presented a high 5-lipoxygenase inhibitory activity. Some hypothesis about the nature of the active compounds are discussed, based on reports of the chemical constitution of these species or other species from the same botanical family.
PMID: 10715848 [PubMed - indexed for MEDLINE]
Disclaimer: Statements on this page have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease. Information on this publication should not be used as medical advice. Data prvided for research and professional use only.
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