| CA01156 Sorgomol An allelochemical - germination stimulant for root parasitic plants Striga and Orobanche (Ref.617), chemical signal for Arbuscular Mycorrhizal fungi during presymbiotic stages (Ref.594).
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| CA01151 5-Deoxystrigol An allelochemical - plant branching factor, one of the major germination stimulants produced by gramineous plants such as maize, pearl millet, and sorghum after the end of the branching factor (Ref.594).
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| CA01021 Annuionone C An allelochemical - stimulates the root growth of barely (Hordeum vulgare) (Ref.401).
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| CA01022 Annuionone D An allelochemical - stimulates the root elongation of onion (Allium cepa), and barely.: Hordeum vulgare (Ref.401, Ref.469).
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| CA01019 Annuionone A An allelochemical - inhibites the germination, but stimulates the root growth of onion (Allium cepa) (Ref.401).
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| CA00998 (3R)-3-Hydroxy-β-ionone An allelochemical - an endogenous growth inhibitor which may play an important role in the inhibition by light of internode growth of bean seedlings (Ref.613).
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| CA01020 Annuionone B An allelochemical - stimulates the root growth of garden cress (Lepidium sativum) (Ref.401).
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| CA00799 β-Cyclocitral An allelochemical - non enzymatically induced by strong high-light , and induce changes in the expression of a large set of genes that have been identified as singlet oxygen responsive genes (Ref.612).
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| CA00868 Abscisate A plant hormone (Ref.653) Promotes developmental processes such as seed maturation and dormancy (Ref.653). An allelochemical (Ref.655), Inhibitory effects on radicle growth in lettuce and weeds (Ref.655).
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| CA00806 Blumenol B An allelochemical (Ref.469). Inhibitory effects on radicle growth in lettuce and weeds (Ref.655).
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| CA00805 Blumenol A An allelochemical (Ref.469). Cytotoxic against human solid tumor cells, but not significantly potent (Ref.654). Inhibitory effects on radicle growth in lettuce and weeds (Ref.655).
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| CA01209 (6S,9R)-Roseoside An allelochemical. Inhibit the histamine release from rat peritoneal exudate cells induced by antigen-antibody reaction (Ref.656).
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Ref.619 : Abe S., Sado A., Tanaka K., Kisugi T., Asami K., Ota S., Kim H. II., Yoneyama K., Xiaonan Xie, Ohnishi T., Seto Y., Yamaguchi S., Akiyama K., Yoneyama K., Nomura T. (2014), Carlactone is converted to carlactonoic acid by MAX1 in Arabidopsis and its methyl ester can directly interact with AtD14 in vitro, PNAS, December 16, 2014, vol. 111, no. 50, pp.18084–18089, www.pnas.org/cgi/doi/10.1073/pnas.1410801111. Ref.617 : Xiaonan X., Yoneyama K., Kusumoto D., Yamada Y., Takeuchi Y., Sugimoto Y., Yoneyama K., Sorgomol, germination stimulant for root parasitic plants, produced by Sorghum bicolor., Tetrahedron Letters 49 (2008) pp. 2066–2068. Ref.594 : Kohki AKIYAMA, Bioscience, Biotechnology, and Biochemistry, 71:6, 1405-1414, DOI: 10.1271/bbb.70023, "Chemical Identification and Functional Analysis of Apocarotenoids Involved in the Development of Arbuscular Mycorrhizal Symbiosis". Ref.469 : Francisco A. Macíasa, Rodney Lacreta, Rosa M. Varelaa, Clara Nogueirasb, Jose M.G. Molinillo, Phytochemistry, Volume 69, Issue 15, November 2008, Pages 2708–2715, "Bioactive apocarotenoids from Tectona grandis". Ref.401 : Luiz Cláudio Almeida Barbosa, Róbson Ricardo Teixeira, Ricardo Marques Montanari, 2009, "PHYTOTOXIC NATURAL PRODUCTS AS MODELS FOR THE DEVELOPMENT OF CROP PROTECTION AGENTS". Ref.613 : Kato-Noguchi, H. (1996) An endogenous growth inhibitor, 3- hydroxy-b-ionone. III. Its longitudinal gradients in the first internode of Phaseolus vulgaris. Physiol. Plant. 98, 241–244. Ref.767 : Mika Murata, Tetsuya Kobayashi and Shigemi Seo, Molecules 2020, 25, 17; doi:10.3390/molecules25010017, “α-Ionone, an Apocarotenoid, Induces Plant Resistance to Western Flower Thrips, Frankliniella occidentalis, Independently of Jasmonic Acid”. Ref.612 : Ramel, F. et al. (2012) Carotenoid oxidation products are stress signals that mediate gene responses to singlet oxygen in plants. Proc. Natl Acad. Sci. U.S.A. 109, 5535–5540. Ref.653 : Mitsunori Seo and Tomokazu Koshiba, Trends in Plant Science, Volume 7, Issue 1, 1 January 2002, Pages 41-48, "Complex regulation of ABA biosynthesis in plants", https://doi.org/10.1016/S1360-1385(01)02187-2. Ref.655 : Manoel Albuquerque, Roseane Santos, Liziane Lima, Péricles Melo Filho, Rejane Nogueira, Claudio Câmara, Ramos, Agronomy for Sustainable Development, April 2011, Volume 31, Issue 2, pp 379–395, "Allelopathy, an alternative tool to improve cropping systems. A review", https://doi.org/10.1051/agro/2010031. Ref.654 : Xiaoxi Liu , Feifei Tian , Hong-Bing Zhang , Elsa Pilarinou, and Jerry L. McLaughlin, Natural Product Letters Volume 14, 1999 - Issue 1, Pages 77-81, "Biologically Active Blumenol A from the Leaves of Annona Glabra", https://doi.org/10.1080/10575639908045437. Ref.656 : Murai Y., Kashimura S., Tamezawa S., Hashimoto T., Takaoka S., Asakawa Y., Kiguchi K., Murai F., Tagawa M., Planta Med., 67, 480—481 (2001), "Absolute configuration of (6S, 9S)-roseoside from Polygonum hydropiper".
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