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Reassessment of the polar fraction of .

Journal of intercultural ethnopharmacology

Venditti A, Frezza C, Lorenzetti LM, Maggi F, Serafini M, Bianco A.
PMID: 28512595
J Intercult Ethnopharmacol. 2017 Apr 12;6(2):144-153. doi: 10.5455/jice.20170327073801. eCollection 2017.

BACKGROUND: The phytochemical analysis of MATERIALS AND METHODS: Chromatographic techniques were used for the isolation of constituents while spectroscopic and spectrometric techniques were applied for the structures elucidation.RESULTS: Besides the known constituents, all of them reconfirmed, ajugoside (1), reptoside...

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Venditti A, Frezza C, Lorenzetti LM, et al. Reassessment of the polar fraction of . J Intercult Ethnopharmacol. 2017;6(2):144-153doi: 10.5455/jice.20170327073801.
Venditti, A., Frezza, C., Lorenzetti, L. M., Maggi, F., Serafini, M., & Bianco, A. (2017). Reassessment of the polar fraction of . Journal of intercultural ethnopharmacology, 6(2), 144-153. https://doi.org/10.5455/jice.20170327073801
Venditti, Alessandro, et al. "Reassessment of the polar fraction of ." Journal of intercultural ethnopharmacology vol. 6,2 (2017): 144-153. doi: https://doi.org/10.5455/jice.20170327073801
Venditti A, Frezza C, Lorenzetti LM, Maggi F, Serafini M, Bianco A. Reassessment of the polar fraction of . J Intercult Ethnopharmacol. 2017 Apr 12;6(2):144-153. doi: 10.5455/jice.20170327073801. eCollection 2017. PMID: 28512595; PMCID: PMC5429073.
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Pharmacognostic outlooks on medical herbs of Sasang typology.

Integrative medicine research

Lim SH, Jeon ES, Lee J, Han SY, Chae H.
PMID: 28951836
Integr Med Res. 2017 Sep;6(3):231-239. doi: 10.1016/j.imr.2017.06.005. Epub 2017 Jul 08.

The purpose of this study was to review the pharmacognostic characteristics of Sasang type-specific medical herbs and suggest biological mechanisms that might be related to the personalized treatment of the East. Major compounds and their pharmacological activities of medical...

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Lim SH, Jeon ES, Lee J, et al. Pharmacognostic outlooks on medical herbs of Sasang typology. Integr Med Res. 2017;6(3):231-239doi: 10.1016/j.imr.2017.06.005.
Lim, S. H., Jeon, E. S., Lee, J., Han, S. Y., & Chae, H. (2017). Pharmacognostic outlooks on medical herbs of Sasang typology. Integrative medicine research, 6(3), 231-239. https://doi.org/10.1016/j.imr.2017.06.005
Lim, Su Hye, et al. "Pharmacognostic outlooks on medical herbs of Sasang typology." Integrative medicine research vol. 6,3 (2017): 231-239. doi: https://doi.org/10.1016/j.imr.2017.06.005
Lim SH, Jeon ES, Lee J, Han SY, Chae H. Pharmacognostic outlooks on medical herbs of Sasang typology. Integr Med Res. 2017 Sep;6(3):231-239. doi: 10.1016/j.imr.2017.06.005. Epub 2017 Jul 08. PMID: 28951836; PMCID: PMC5605368.
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Traditional Uses, Phytochemistry, and Pharmacology of Olea europaea (Olive).

Evidence-based complementary and alternative medicine : eCAM

Hashmi MA, Khan A, Hanif M, Farooq U, Perveen S.
PMID: 25802541
Evid Based Complement Alternat Med. 2015;2015:541591. doi: 10.1155/2015/541591. Epub 2015 Feb 23.

Aim of the Review. To grasp the fragmented information available on the botany, traditional uses, phytochemistry, pharmacology, and toxicology of Olea europaea to explore its therapeutic potential and future research opportunities. Material and Methods. All the available information on...

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Hashmi MA, Khan A, Hanif M, et al. Traditional Uses, Phytochemistry, and Pharmacology of Olea europaea (Olive). Evid Based Complement Alternat Med. 2015;2015:541591doi: 10.1155/2015/541591.
Hashmi, M. A., Khan, A., Hanif, M., Farooq, U., & Perveen, S. (2015). Traditional Uses, Phytochemistry, and Pharmacology of Olea europaea (Olive). Evidence-based complementary and alternative medicine : eCAM, 2015541591. https://doi.org/10.1155/2015/541591
Hashmi, Muhammad Ali, et al. "Traditional Uses, Phytochemistry, and Pharmacology of Olea europaea (Olive)." Evidence-based complementary and alternative medicine : eCAM vol. 2015 (2015): 541591. doi: https://doi.org/10.1155/2015/541591
Hashmi MA, Khan A, Hanif M, Farooq U, Perveen S. Traditional Uses, Phytochemistry, and Pharmacology of Olea europaea (Olive). Evid Based Complement Alternat Med. 2015;2015:541591. doi: 10.1155/2015/541591. Epub 2015 Feb 23. PMID: 25802541; PMCID: PMC4352757.
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Interactions betweenAlloxysta brevis (Hymenoptera, Cynipoidea, Alloxystidae) and honeydew-collecting ants: How an aphid hyperparasitoid overcomes ant aggression by chemical defense.

Journal of chemical ecology

Völkl W, Hübner G, Dettner K.
PMID: 24241923
J Chem Ecol. 1994 Nov;20(11):2901-15. doi: 10.1007/BF02098397.

Foraging females of the aphid hyperparasitoidAlloxysta brevis were attacked by honeydew-collecting workers of the antLasius niger at the first encounter. However, ants abandoned their attacks quickly, and foragingA. brevis remained unmolested for a subsequent time interval of approximately 5...

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Völkl W, Hübner G, Dettner K. Interactions betweenAlloxysta brevis (Hymenoptera, Cynipoidea, Alloxystidae) and honeydew-collecting ants: How an aphid hyperparasitoid overcomes ant aggression by chemical defense. J Chem Ecol. 1994;20(11):2901-15doi: 10.1007/BF02098397.
Völkl, W., Hübner, G., & Dettner, K. (1994). Interactions betweenAlloxysta brevis (Hymenoptera, Cynipoidea, Alloxystidae) and honeydew-collecting ants: How an aphid hyperparasitoid overcomes ant aggression by chemical defense. Journal of chemical ecology, 20(11), 2901-15. https://doi.org/10.1007/BF02098397
Völkl, W, et al. "Interactions betweenAlloxysta brevis (Hymenoptera, Cynipoidea, Alloxystidae) and honeydew-collecting ants: How an aphid hyperparasitoid overcomes ant aggression by chemical defense." Journal of chemical ecology vol. 20,11 (1994): 2901-15. doi: https://doi.org/10.1007/BF02098397
Völkl W, Hübner G, Dettner K. Interactions betweenAlloxysta brevis (Hymenoptera, Cynipoidea, Alloxystidae) and honeydew-collecting ants: How an aphid hyperparasitoid overcomes ant aggression by chemical defense. J Chem Ecol. 1994 Nov;20(11):2901-15. doi: 10.1007/BF02098397. PMID: 24241923.
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Monoterpenol Oxidative Metabolism: Role in Plant Adaptation and Potential Applications.

Frontiers in plant science

Ilc T, Parage C, Boachon B, Navrot N, Werck-Reichhart D.
PMID: 27200002
Front Plant Sci. 2016 Apr 26;7:509. doi: 10.3389/fpls.2016.00509. eCollection 2016.

Plants use monoterpenols as precursors for the production of functionally and structurally diverse molecules, which are key players in interactions with other organisms such as pollinators, flower visitors, herbivores, fungal, or microbial pathogens. For humans, many of these monoterpenol...

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Ilc T, Parage C, Boachon B, et al. Monoterpenol Oxidative Metabolism: Role in Plant Adaptation and Potential Applications. Front Plant Sci. 2016;7:509doi: 10.3389/fpls.2016.00509.
Ilc, T., Parage, C., Boachon, B., Navrot, N., & Werck-Reichhart, D. (2016). Monoterpenol Oxidative Metabolism: Role in Plant Adaptation and Potential Applications. Frontiers in plant science, 7509. https://doi.org/10.3389/fpls.2016.00509
Ilc, Tina, et al. "Monoterpenol Oxidative Metabolism: Role in Plant Adaptation and Potential Applications." Frontiers in plant science vol. 7 (2016): 509. doi: https://doi.org/10.3389/fpls.2016.00509
Ilc T, Parage C, Boachon B, Navrot N, Werck-Reichhart D. Monoterpenol Oxidative Metabolism: Role in Plant Adaptation and Potential Applications. Front Plant Sci. 2016 Apr 26;7:509. doi: 10.3389/fpls.2016.00509. eCollection 2016. PMID: 27200002; PMCID: PMC4844611.
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A general approach to iridoids by applying a new Julia olefination and a tandem anion-radical-carbocation crossover reaction.

Organic & biomolecular chemistry

Řehová L, Dračínský M, Jahn U.
PMID: 27714288
Org Biomol Chem. 2016 Oct 12;14(40):9612-9621. doi: 10.1039/c6ob01599a.

A unified, asymmetric approach to the total synthesis of naturally occurring iridoids is presented. The synthesis features a recently discovered ortho → α transmetalation of alkyl aryl sulfone carbanions, thus enabling Julia reactions, by which so far hardly accessible...

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Řehová L, Dračínský M, Jahn U. A general approach to iridoids by applying a new Julia olefination and a tandem anion-radical-carbocation crossover reaction. Org Biomol Chem. 2016;14(40):9612-9621doi: 10.1039/c6ob01599a.
Řehová, L., Dračínský, M., & Jahn, U. (2016). A general approach to iridoids by applying a new Julia olefination and a tandem anion-radical-carbocation crossover reaction. Organic & biomolecular chemistry, 14(40), 9612-9621. https://doi.org/10.1039/c6ob01599a
Řehová, Lucie, et al. "A general approach to iridoids by applying a new Julia olefination and a tandem anion-radical-carbocation crossover reaction." Organic & biomolecular chemistry vol. 14,40 (2016): 9612-9621. doi: https://doi.org/10.1039/c6ob01599a
Řehová L, Dračínský M, Jahn U. A general approach to iridoids by applying a new Julia olefination and a tandem anion-radical-carbocation crossover reaction. Org Biomol Chem. 2016 Oct 12;14(40):9612-9621. doi: 10.1039/c6ob01599a. PMID: 27714288.
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Noni juice reduces lipid peroxidation-derived DNA adducts in heavy smokers.

Food science & nutrition

Wang MY, Peng L, Jensen CJ, Deng S, West BJ.
PMID: 24804023
Food Sci Nutr. 2013 Mar;1(2):141-9. doi: 10.1002/fsn3.21. Epub 2013 Jan 07.

Food plants provide important phytochemicals which help improve or maintain health through various biological activities, including antioxidant effects. Cigarette smoke-induced oxidative stress leads to the formation of lipid hydroperoxides (LOOHs) and their decomposition product malondialdehyde (MDA), both of which...

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Wang MY, Peng L, Jensen CJ, et al. Noni juice reduces lipid peroxidation-derived DNA adducts in heavy smokers. Food Sci Nutr. 2013;1(2):141-9doi: 10.1002/fsn3.21.
Wang, M. Y., Peng, L., Jensen, C. J., Deng, S., & West, B. J. (2013). Noni juice reduces lipid peroxidation-derived DNA adducts in heavy smokers. Food science & nutrition, 1(2), 141-9. https://doi.org/10.1002/fsn3.21
Wang, Mian-Ying, et al. "Noni juice reduces lipid peroxidation-derived DNA adducts in heavy smokers." Food science & nutrition vol. 1,2 (2013): 141-9. doi: https://doi.org/10.1002/fsn3.21
Wang MY, Peng L, Jensen CJ, Deng S, West BJ. Noni juice reduces lipid peroxidation-derived DNA adducts in heavy smokers. Food Sci Nutr. 2013 Mar;1(2):141-9. doi: 10.1002/fsn3.21. Epub 2013 Jan 07. PMID: 24804023; PMCID: PMC3967752.
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Phylogeny and classification of Oleaceae based on rps16 and trnL-F sequence data.

American journal of botany

Wallander E, Albert VA.
PMID: 11118421
Am J Bot. 2000 Dec;87(12):1827-41.

Phylogenetic relationships among 76 species of Oleaceae, representing all 25 recognized genera of the family, were assessed by a cladistic analysis of DNA sequences from two noncoding chloroplast loci, the rps16 intron and the trnL-F region. Consensus trees from...

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Wallander E, Albert VA. Phylogeny and classification of Oleaceae based on rps16 and trnL-F sequence data. Am J Bot. 2000;87(12):1827-41
Wallander, E., & Albert, V. A. (2000). Phylogeny and classification of Oleaceae based on rps16 and trnL-F sequence data. American journal of botany, 87(12), 1827-41.
Wallander, E, and Albert, V A. "Phylogeny and classification of Oleaceae based on rps16 and trnL-F sequence data." American journal of botany vol. 87,12 (2000): 1827-41.
Wallander E, Albert VA. Phylogeny and classification of Oleaceae based on rps16 and trnL-F sequence data. Am J Bot. 2000 Dec;87(12):1827-41. PMID: 11118421.
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Iridoids from Carbohydrates via Pauson-Khand Reaction: Synthesis of Advanced Highly Oxygenated Cyclopentane-Annulated Pyranosides from D-Glucal Derivatives.

The Journal of organic chemistry

Marco-Contelles J, Ruiz-Caro J.
PMID: 11674752
J Org Chem. 1999 Oct 29;64(22):8302-8310. doi: 10.1021/jo991044x.

The Pauson-Khand reaction on suitable 4-oxa-hept-1-en-6-ynes (1, 17) obtained from 3,4,6-tri-O-acetyl-D-glucal gives the cyclopentane-annulated pyranosides (2, 18) that can be efficiently and stereoselectivelly transformed into chiral, advanced, highly oxygenated intermediates (10, 16, 24) for the synthesis of iridoid aglycones.

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Marco-Contelles J, Ruiz-Caro J. Iridoids from Carbohydrates via Pauson-Khand Reaction: Synthesis of Advanced Highly Oxygenated Cyclopentane-Annulated Pyranosides from D-Glucal Derivatives. J Org Chem. 1999;64(22):8302-8310doi: 10.1021/jo991044x.
Marco-Contelles, J., & Ruiz-Caro, J. (1999). Iridoids from Carbohydrates via Pauson-Khand Reaction: Synthesis of Advanced Highly Oxygenated Cyclopentane-Annulated Pyranosides from D-Glucal Derivatives. The Journal of organic chemistry, 64(22), 8302-8310. https://doi.org/10.1021/jo991044x
Marco-Contelles, José, and Ruiz-Caro, Juliana. "Iridoids from Carbohydrates via Pauson-Khand Reaction: Synthesis of Advanced Highly Oxygenated Cyclopentane-Annulated Pyranosides from D-Glucal Derivatives." The Journal of organic chemistry vol. 64,22 (1999): 8302-8310. doi: https://doi.org/10.1021/jo991044x
Marco-Contelles J, Ruiz-Caro J. Iridoids from Carbohydrates via Pauson-Khand Reaction: Synthesis of Advanced Highly Oxygenated Cyclopentane-Annulated Pyranosides from D-Glucal Derivatives. J Org Chem. 1999 Oct 29;64(22):8302-8310. doi: 10.1021/jo991044x. PMID: 11674752.
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Hydrogenation of iridoid glucosides with exocyclic double bond.

Planta medica

Junior P.
PMID: 17342604
Planta Med. 1985 Oct;51(5):434-6. doi: 10.1055/s-2007-969541.

Catalytic hydrogenation of two iridoids of unusual type with an exocyclic double bond, namely serrulatoloside and gardoside methyl ester, over PtO (2) catalyst to give 10-desoxypatrinoside and 8-epiloganin, respectively, is described.

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Junior P. Hydrogenation of iridoid glucosides with exocyclic double bond. Planta Med. 1985;51(5):434-6doi: 10.1055/s-2007-969541.
Junior, P. (1985). Hydrogenation of iridoid glucosides with exocyclic double bond. Planta medica, 51(5), 434-6. https://doi.org/10.1055/s-2007-969541
Junior, P. "Hydrogenation of iridoid glucosides with exocyclic double bond." Planta medica vol. 51,5 (1985): 434-6. doi: https://doi.org/10.1055/s-2007-969541
Junior P. Hydrogenation of iridoid glucosides with exocyclic double bond. Planta Med. 1985 Oct;51(5):434-6. doi: 10.1055/s-2007-969541. PMID: 17342604.
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Iridoids from Scaevola racemigera1.

Planta medica

Skaltsounis AL, Tillequin F, Koch M, Pusset J, Chauvière G.
PMID: 17262339
Planta Med. 1989 Apr;55(2):191-2. doi: 10.1055/s-2006-961922.

Five iridoids have been isolated from the aerial parts of SCAEVOLA RACEMIGERA Däniker, namely, loganin, loganic acid, sylvestroside III, cantleyoside, and scaevoloside. This latter is a novel compound whose structure 1 has been elucidated on the basis of its...

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Skaltsounis AL, Tillequin F, Koch M, et al. Iridoids from Scaevola racemigera1. Planta Med. 1989;55(2):191-2doi: 10.1055/s-2006-961922.
Skaltsounis, A. L., Tillequin, F., Koch, M., Pusset, J., & Chauvière, G. (1989). Iridoids from Scaevola racemigera1. Planta medica, 55(2), 191-2. https://doi.org/10.1055/s-2006-961922
Skaltsounis, A L, et al. "Iridoids from Scaevola racemigera1." Planta medica vol. 55,2 (1989): 191-2. doi: https://doi.org/10.1055/s-2006-961922
Skaltsounis AL, Tillequin F, Koch M, Pusset J, Chauvière G. Iridoids from Scaevola racemigera1. Planta Med. 1989 Apr;55(2):191-2. doi: 10.1055/s-2006-961922. PMID: 17262339.
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Evaluation of the antioxidant activity of five endemic Ligustrum species leaves from Taiwan flora in vitro.

Food chemistry

Wu CR, Lin WH, Hseu YC, Lien JC, Lin YT, Kuo TP, Ching H.
PMID: 23140701
Food Chem. 2011 Jul 15;127(2):564-71. doi: 10.1016/j.foodchem.2011.01.041. Epub 2011 Jan 18.

Leaves from the plant species belonging to the genus Ligustrum are widely used as tea or herbal medicine in Europe, China, and Japan. The antioxidant properties of five Ligustrum species from Taiwan were compared using in vitro antioxidant methods...

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Wu CR, Lin WH, Hseu YC, et al. Evaluation of the antioxidant activity of five endemic Ligustrum species leaves from Taiwan flora in vitro. Food Chem. 2011;127(2):564-71doi: 10.1016/j.foodchem.2011.01.041.
Wu, C. R., Lin, W. H., Hseu, Y. C., Lien, J. C., Lin, Y. T., Kuo, T. P., & Ching, H. (2011). Evaluation of the antioxidant activity of five endemic Ligustrum species leaves from Taiwan flora in vitro. Food chemistry, 127(2), 564-71. https://doi.org/10.1016/j.foodchem.2011.01.041
Wu, Chi-Rei, et al. "Evaluation of the antioxidant activity of five endemic Ligustrum species leaves from Taiwan flora in vitro." Food chemistry vol. 127,2 (2011): 564-71. doi: https://doi.org/10.1016/j.foodchem.2011.01.041
Wu CR, Lin WH, Hseu YC, Lien JC, Lin YT, Kuo TP, Ching H. Evaluation of the antioxidant activity of five endemic Ligustrum species leaves from Taiwan flora in vitro. Food Chem. 2011 Jul 15;127(2):564-71. doi: 10.1016/j.foodchem.2011.01.041. Epub 2011 Jan 18. PMID: 23140701.
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Showing 1 to 12 of 147 entries