Strigol (BioDeep_00000007225)

 

Secondary id: BioDeep_00000364689

human metabolite PANOMIX_OTCML-2023 Endogenous natural product


代谢物信息卡片


5-{[(3E)-5-hydroxy-8,8-dimethyl-2-oxo-2H,3H,3aH,4H,5H,6H,7H,8H,8bH-indeno[1,2-b]furan-3-ylidene]methoxy}-3-methyl-2,5-dihydrofuran-2-one

化学式: C19H22O6 (346.1416)
中文名称:
谱图信息: 最多检出来源 Viridiplantae(plant) 10.36%

分子结构信息

SMILES: CC1=CC(OC1=O)OC=C2C3CC4=C(C3OC2=O)C(CCC4O)(C)C
InChI: InChI=1S/C19H22O6/c1-9-6-14(24-17(9)21)23-8-12-10-7-11-13(20)4-5-19(2,3)15(11)16(10)25-18(12)22/h6,8,10,13-14,16,20H,4-5,7H2,1-3H3/b12-8+

描述信息

Strigol is found in corn. Strigol is a constituent of the root of Gossypium hirsutum (cotton) Strigolactones are plant hormones that have been implicated in inhibition of shoot branching. Strigolactones are carotenoid-derived and trigger germination of parasitic plant seeds (for example striga from which they gained their name) and stimulate symbiotic mycorrhizal fungi. Strigolactones contain a labile ether bond that is easily hydrolysed in the rhizosphere meaning that there is a large concentration gradient between areas near the root and those further away.
Constituent of the root of Gossypium hirsutum (cotton)

同义名列表

6 个代谢物同义名

5-{[(3E)-5-hydroxy-8,8-dimethyl-2-oxo-2H,3H,3aH,4H,5H,6H,7H,8H,8bH-indeno[1,2-b]furan-3-ylidene]methoxy}-3-methyl-2,5-dihydrofuran-2-one; (3E)-5-hydroxy-8,8-dimethyl-3-[(4-methyl-5-oxo-2H-furan-2-yl)oxymethylidene]-3a,4,5,6,7,8b-hexahydroindeno[1,2-b]furan-2-one; 5-{[(3E)-5-hydroxy-8,8-dimethyl-2-oxo-3aH,4H,5H,6H,7H,8bH-indeno[1,2-b]furan-3-ylidene]methoxy}-3-methyl-5H-furan-2-one; Strigol; (+)-Strigol; Strigol



数据库引用编号

20 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

22 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 5 ALB, ARHGAP45, CNP, HDAC1, HDAC2
Peripheral membrane protein 1 CYP1B1
Endoplasmic reticulum membrane 1 CYP1B1
Nucleus 4 ALB, GABPA, HDAC1, HDAC2
cytosol 5 ALB, ARHGAP45, GSR, HDAC1, LIPE
centrosome 1 ALB
nucleoplasm 3 GABPA, HDAC1, HDAC2
Cell membrane 1 LIPE
Lipid-anchor 1 CNP
ruffle membrane 1 ARHGAP45
Synapse 1 CNP
cell surface 1 C3
Golgi apparatus 1 ALB
mitochondrial inner membrane 1 CNP
neuronal cell body 1 HDAC1
Cytoplasm, cytosol 1 LIPE
plasma membrane 3 ARHGAP45, C3, C8B
Membrane 6 ARHGAP45, C8B, CNP, CYP1B1, HDAC2, LIPE
caveola 1 LIPE
extracellular exosome 5 ALB, C3, C8B, CNP, GSR
endoplasmic reticulum 1 ALB
extracellular space 4 ALB, C3, C8B, CNP
perinuclear region of cytoplasm 1 CNP
mitochondrion 2 CYP1B1, GSR
protein-containing complex 4 ALB, C3, HDAC1, HDAC2
intracellular membrane-bounded organelle 1 CYP1B1
Microsome membrane 1 CYP1B1
ESC/E(Z) complex 1 HDAC2
Secreted 3 ALB, C3, C8B
extracellular region 4 ALB, ARHGAP45, C3, C8B
mitochondrial outer membrane 1 CNP
mitochondrial matrix 1 GSR
anchoring junction 1 ALB
external side of plasma membrane 1 GSR
Extracellular vesicle 1 C8B
Cell projection, ruffle membrane 1 ARHGAP45
heterochromatin 1 HDAC1
microtubule 1 CNP
ciliary basal body 1 ALB
chromatin 3 GABPA, HDAC1, HDAC2
centriole 1 ALB
spindle pole 1 ALB
chromosome, telomeric region 1 HDAC2
blood microparticle 2 ALB, C3
microvillus 1 CNP
Lipid droplet 1 LIPE
Membrane, caveola 1 LIPE
Melanosome 1 CNP
pseudopodium 1 CNP
secretory granule lumen 2 ARHGAP45, C3
endoplasmic reticulum lumen 2 ALB, C3
transcription repressor complex 1 HDAC1
platelet alpha granule lumen 1 ALB
histone deacetylase complex 2 HDAC1, HDAC2
azurophil granule lumen 2 ARHGAP45, C3
NuRD complex 2 HDAC1, HDAC2
Sin3-type complex 2 HDAC1, HDAC2
membrane attack complex 1 C8B
myelin sheath abaxonal region 1 CNP
myelin sheath adaxonal region 1 CNP
ciliary transition fiber 1 ALB


文献列表

  • Sheng Wu, Anqi Zhou, Kozue Hiugano, Akiyoshi Yoda, Xiaonan Xie, Kenji Yamane, Kenji Miura, Takahito Nomura, Yanran Li. Identification of a Prunus MAX1 homolog as a unique strigol synthase. The New phytologist. 2023 Jun; ?(?):. doi: 10.1111/nph.19052. [PMID: 37292030]
  • Satoshi Ogawa, Ken Shirasu. Strigol induces germination of the facultative parasitic plant Phtheirospermum japonicum in the absence of nitrate ions. Plant signaling & behavior. 2022 12; 17(1):2114647. doi: 10.1080/15592324.2022.2114647. [PMID: 35993137]
  • Tao Yang, Yuke Lian, Chongying Wang. Comparing and Contrasting the Multiple Roles of Butenolide Plant Growth Regulators: Strigolactones and Karrikins in Plant Development and Adaptation to Abiotic Stresses. International journal of molecular sciences. 2019 Dec; 20(24):. doi: 10.3390/ijms20246270. [PMID: 31842355]
  • Laura Ravazzolo, Sara Trevisan, Alessandro Manoli, Stï Phanie Boutet-Mercey, Franï Ois Perreau, Silvia Quaggiotti. The Control of Zealactone Biosynthesis and Exudation is Involved in the Response to Nitrogen in Maize Root. Plant & cell physiology. 2019 Sep; 60(9):2100-2112. doi: 10.1093/pcp/pcz108. [PMID: 31147714]
  • Melissa Van Overtveldt, Lukas Braem, Sylwia Struk, Anna M Kaczmarek, François-Didier Boyer, Rik Van Deun, Kris Gevaert, Sofie Goormachtig, Thomas S A Heugebaert, Christian V Stevens. Design and visualization of second-generation cyanoisoindole-based fluorescent strigolactone analogs. The Plant journal : for cell and molecular biology. 2019 04; 98(1):165-180. doi: 10.1111/tpj.14197. [PMID: 30552776]
  • Le Luo, Megumu Takahashi, Hiromu Kameoka, Ruyi Qin, Toshihide Shiga, Yuri Kanno, Mitsunori Seo, Masaki Ito, Guohua Xu, Junko Kyozuka. Developmental analysis of the early steps in strigolactone-mediated axillary bud dormancy in rice. The Plant journal : for cell and molecular biology. 2019 03; 97(6):1006-1021. doi: 10.1111/tpj.14266. [PMID: 30740793]
  • Han Wu, Huihui Li, Hong Chen, Qi Qi, Qiangqiang Ding, Juan Xue, Jing Ding, Xiangning Jiang, Xilin Hou, Yi Li. Identification and expression analysis of strigolactone biosynthetic and signaling genes reveal strigolactones are involved in fruit development of the woodland strawberry (Fragaria vesca). BMC plant biology. 2019 Feb; 19(1):73. doi: 10.1186/s12870-019-1673-6. [PMID: 30764758]
  • Natalia M Moreno-Pachon, Marie-Chantal Mutimawurugo, Eveline Heynen, Lidiya Sergeeva, Anne Benders, Ikram Blilou, Henk W M Hilhorst, Richard G H Immink. Role of Tulipa gesneriana TEOSINTE BRANCHED1 (TgTB1) in the control of axillary bud outgrowth in bulbs. Plant reproduction. 2018 06; 31(2):145-157. doi: 10.1007/s00497-017-0316-z. [PMID: 29218597]
  • Le Luo, Hongxuan Wang, Xiaohong Liu, Jinqi Hu, Xueli Zhu, Shou Pan, Ruyi Qin, Yifeng Wang, Pingping Zhao, Xiaorong Fan, Guohua Xu. Strigolactones affect the translocation of nitrogen in rice. Plant science : an international journal of experimental plant biology. 2018 May; 270(?):190-197. doi: 10.1016/j.plantsci.2018.02.020. [PMID: 29576072]
  • Fang Liu, Pandi Wang, Xiaobo Zhang, Xiaofei Li, Xiaohong Yan, Donghui Fu, Gang Wu. The genetic and molecular basis of crop height based on a rice model. Planta. 2018 Jan; 247(1):1-26. doi: 10.1007/s00425-017-2798-1. [PMID: 29110072]
  • Shuo Lv, Yonghong Zhang, Chen Li, Zhijun Liu, Nan Yang, Lixia Pan, Jinbin Wu, Jiajing Wang, Jingwei Yang, Yanting Lv, Yutao Zhang, Wenqian Jiang, Xiaoping She, Guodong Wang. Strigolactone-triggered stomatal closure requires hydrogen peroxide synthesis and nitric oxide production in an abscisic acid-independent manner. The New phytologist. 2018 Jan; 217(1):290-304. doi: 10.1111/nph.14813. [PMID: 28940201]
  • Duncan Holbrook-Smith, Peter McCourt. Chemical Screening for Strigolactone Receptor Antagonists Using Arabidopsis thaliana. Methods in molecular biology (Clifton, N.J.). 2018; 1795(?):117-126. doi: 10.1007/978-1-4939-7874-8_10. [PMID: 29846923]
  • Marek Marzec. Strigolactones and Gibberellins: A New Couple in the Phytohormone World?. Trends in plant science. 2017 10; 22(10):813-815. doi: 10.1016/j.tplants.2017.08.001. [PMID: 28844847]
  • Xiaoyu Yang, Lei Chen, Junxian He, Weichang Yu. Knocking out of carotenoid catabolic genes in rice fails to boost carotenoid accumulation, but reveals a mutation in strigolactone biosynthesis. Plant cell reports. 2017 Oct; 36(10):1533-1545. doi: 10.1007/s00299-017-2172-6. [PMID: 28676963]
  • Peter V Minorsky. On the Inside. Plant physiology. 2017 Jun; 174(2):843-844. doi: 10.1104/pp.17.00635. [PMID: 28584066]
  • Javier Agusti. Strigolactone-mediated Stimulation of Secondary Xylem Proliferation in Stems. Methods in molecular biology (Clifton, N.J.). 2017; 1544(?):21-26. doi: 10.1007/978-1-4939-6722-3_2. [PMID: 28050825]
  • Angela Boari, Biancamaria Ciasca, Rocío Pineda-Martos, Veronica Mt Lattanzio, Koichi Yoneyama, Maurizio Vurro. Parasitic weed management by using strigolactone-degrading fungi. Pest management science. 2016 Nov; 72(11):2043-2047. doi: 10.1002/ps.4226. [PMID: 26757233]
  • Claudio Screpanti, Koichi Yoneyama, Harro J Bouwmeester. Strigolactones and parasitic weed management 50 years after the discovery of the first natural strigolactone strigol: status and outlook. Pest management science. 2016 Nov; 72(11):2013-2015. doi: 10.1002/ps.4436. [PMID: 27700003]
  • Narumi Mori, Kenta Nishiuma, Takuya Sugiyama, Hideo Hayashi, Kohki Akiyama. Carlactone-type strigolactones and their synthetic analogues as inducers of hyphal branching in arbuscular mycorrhizal fungi. Phytochemistry. 2016 Oct; 130(?):90-8. doi: 10.1016/j.phytochem.2016.05.012. [PMID: 27264641]
  • Lu Wang, Steven M Smith. Strigolactones redefine plant hormones. Science China. Life sciences. 2016 Oct; 59(10):1083-1085. doi: 10.1007/s11427-016-0259-5. [PMID: 27658783]
  • Stefano Pavan, Adalgisa Schiavulli, Angelo Raffaele Marcotrigiano, Nicoletta Bardaro, Valentina Bracuto, Francesca Ricciardi, Tatsiana Charnikhova, Concetta Lotti, Harro Bouwmeester, Luigi Ricciardi. Characterization of Low-Strigolactone Germplasm in Pea (Pisum sativum L.) Resistant to Crenate Broomrape (Orobanche crenata Forsk.). Molecular plant-microbe interactions : MPMI. 2016 Oct; 29(10):743-749. doi: 10.1094/mpmi-07-16-0134-r. [PMID: 27558842]
  • Kun-Peng Jia, Boubacar A Kountche, Muhammad Jamil, Xiujie Guo, Valentine O Ntui, Andreas Rüfenacht, Soizic Rochange, Salim Al-Babili. Nitro-Phenlactone, a Carlactone Analog with Pleiotropic Strigolactone Activities. Molecular plant. 2016 09; 9(9):1341-1344. doi: 10.1016/j.molp.2016.05.017. [PMID: 27288318]
  • Philip B Brewer, Kaori Yoneyama, Fiona Filardo, Emma Meyers, Adrian Scaffidi, Tancred Frickey, Kohki Akiyama, Yoshiya Seto, Elizabeth A Dun, Julia E Cremer, Stephanie C Kerr, Mark T Waters, Gavin R Flematti, Michael G Mason, Georg Weiller, Shinjiro Yamaguchi, Takahito Nomura, Steven M Smith, Koichi Yoneyama, Christine A Beveridge. LATERAL BRANCHING OXIDOREDUCTASE acts in the final stages of strigolactone biosynthesis in Arabidopsis. Proceedings of the National Academy of Sciences of the United States of America. 2016 May; 113(22):6301-6. doi: 10.1073/pnas.1601729113. [PMID: 27194725]
  • Syusaku Tsuzuki, Yoshihiro Handa, Naoya Takeda, Masayoshi Kawaguchi. Strigolactone-Induced Putative Secreted Protein 1 Is Required for the Establishment of Symbiosis by the Arbuscular Mycorrhizal Fungus Rhizophagus irregularis. Molecular plant-microbe interactions : MPMI. 2016 Apr; 29(4):277-86. doi: 10.1094/mpmi-10-15-0234-r. [PMID: 26757243]
  • Xue-Guang Sun, Paola Bonfante, Ming Tang. Effect of volatiles versus exudates released by germinating spores of Gigaspora margarita on lateral root formation. Plant physiology and biochemistry : PPB. 2015 Dec; 97(?):1-10. doi: 10.1016/j.plaphy.2015.09.010. [PMID: 26397199]
  • Hiroaki Ueda, Makoto Kusaba. Strigolactone Regulates Leaf Senescence in Concert with Ethylene in Arabidopsis. Plant physiology. 2015 Sep; 169(1):138-47. doi: 10.1104/pp.15.00325. [PMID: 25979917]
  • Yuichiro Tsuchiya, Masahiko Yoshimura, Yoshikatsu Sato, Keiko Kuwata, Shigeo Toh, Duncan Holbrook-Smith, Hua Zhang, Peter McCourt, Kenichiro Itami, Toshinori Kinoshita, Shinya Hagihara. PARASITIC PLANTS. Probing strigolactone receptors in Striga hermonthica with fluorescence. Science (New York, N.Y.). 2015 Aug; 349(6250):864-8. doi: 10.1126/science.aab3831. [PMID: 26293962]
  • Marc-Marie Lechat, Guillaume Brun, Grégory Montiel, Christophe Véronési, Philippe Simier, Séverine Thoiron, Jean-Bernard Pouvreau, Philippe Delavault. Seed response to strigolactone is controlled by abscisic acid-independent DNA methylation in the obligate root parasitic plant, Phelipanche ramosa L. Pomel. Journal of experimental botany. 2015 Jun; 66(11):3129-40. doi: 10.1093/jxb/erv119. [PMID: 25821070]
  • Joëlle Sasse, Sibu Simon, Christian Gübeli, Guo-Wei Liu, Xi Cheng, Jiří Friml, Harro Bouwmeester, Enrico Martinoia, Lorenzo Borghi. Asymmetric localizations of the ABC transporter PaPDR1 trace paths of directional strigolactone transport. Current biology : CB. 2015 Mar; 25(5):647-55. doi: 10.1016/j.cub.2015.01.015. [PMID: 25683808]
  • Shelley Urquhart, Eloise Foo, James B Reid. The role of strigolactones in photomorphogenesis of pea is limited to adventitious rooting. Physiologia plantarum. 2015 Mar; 153(3):392-402. doi: 10.1111/ppl.12246. [PMID: 24962787]
  • Shinsaku Ito, Tomoko Nozoye, Eriko Sasaki, Misaki Imai, Yuh Shiwa, Mari Shibata-Hatta, Taichiro Ishige, Kosuke Fukui, Ken Ito, Hiromi Nakanishi, Naoko K Nishizawa, Shunsuke Yajima, Tadao Asami. Strigolactone regulates anthocyanin accumulation, acid phosphatases production and plant growth under low phosphate condition in Arabidopsis. PloS one. 2015; 10(3):e0119724. doi: 10.1371/journal.pone.0119724. [PMID: 25793732]
  • Jinfeng Zhao, Tao Wang, Minxia Wang, Yuanyuan Liu, Shoujiang Yuan, Yanan Gao, Liang Yin, Wei Sun, Lixiang Peng, Wenhui Zhang, Jianmin Wan, Xueyong Li. DWARF3 participates in an SCF complex and associates with DWARF14 to suppress rice shoot branching. Plant & cell physiology. 2014 Jun; 55(6):1096-109. doi: 10.1093/pcp/pcu045. [PMID: 24616269]
  • Claire B Pollock, Sara McDonough, Victor S Wang, Hyojung Lee, Lymor Ringer, Xin Li, Cristina Prandi, Richard J Lee, Adam S Feldman, Hinanit Koltai, Yoram Kapulnik, Olga C Rodriguez, Richard Schlegel, Christopher Albanese, Ronit I Yarden. Strigolactone analogues induce apoptosis through activation of p38 and the stress response pathway in cancer cell lines and in conditionally reprogrammed primary prostate cancer cells. Oncotarget. 2014 Mar; 5(6):1683-98. doi: 10.18632/oncotarget.1849. [PMID: 24742967]
  • Sneha Bhogale, Ameya S Mahajan, Bhavani Natarajan, Mohit Rajabhoj, Hirekodathakallu V Thulasiram, Anjan K Banerjee. MicroRNA156: a potential graft-transmissible microRNA that modulates plant architecture and tuberization in Solanum tuberosum ssp. andigena. Plant physiology. 2014 Feb; 164(2):1011-27. doi: 10.1104/pp.113.230714. [PMID: 24351688]
  • Yoshiya Seto, Aika Sado, Kei Asami, Atsushi Hanada, Mikihisa Umehara, Kohki Akiyama, Shinjiro Yamaguchi. Carlactone is an endogenous biosynthetic precursor for strigolactones. Proceedings of the National Academy of Sciences of the United States of America. 2014 Jan; 111(4):1640-5. doi: 10.1073/pnas.1314805111. [PMID: 24434551]
  • Chien Van Ha, Marco Antonio Leyva-González, Yuriko Osakabe, Uyen Thi Tran, Rie Nishiyama, Yasuko Watanabe, Maho Tanaka, Motoaki Seki, Shinjiro Yamaguchi, Nguyen Van Dong, Kazuko Yamaguchi-Shinozaki, Kazuo Shinozaki, Luis Herrera-Estrella, Lam-Son Phan Tran. Positive regulatory role of strigolactone in plant responses to drought and salt stress. Proceedings of the National Academy of Sciences of the United States of America. 2014 Jan; 111(2):851-6. doi: 10.1073/pnas.1322135111. [PMID: 24379380]
  • Alexandre de Saint Germain, Sandrine Bonhomme, François-Didier Boyer, Catherine Rameau. Novel insights into strigolactone distribution and signalling. Current opinion in plant biology. 2013 Oct; 16(5):583-9. doi: 10.1016/j.pbi.2013.06.007. [PMID: 23830996]
  • Mark T Waters, Adrian Scaffidi, Gavin R Flematti, Steven M Smith. The origins and mechanisms of karrikin signalling. Current opinion in plant biology. 2013 Oct; 16(5):667-73. doi: 10.1016/j.pbi.2013.07.005. [PMID: 23954000]
  • Carlo Sorce, Alessio Giovannelli, Luca Sebastiani, Tommaso Anfodillo. Hormonal signals involved in the regulation of cambial activity, xylogenesis and vessel patterning in trees. Plant cell reports. 2013 Jun; 32(6):885-98. doi: 10.1007/s00299-013-1431-4. [PMID: 23553557]
  • Saki Nomura, Hitomi Nakashima, Masaharu Mizutani, Hirosato Takikawa, Yukihiro Sugimoto. Structural requirements of strigolactones for germination induction and inhibition of Striga gesnerioides seeds. Plant cell reports. 2013 Jun; 32(6):829-38. doi: 10.1007/s00299-013-1429-y. [PMID: 23563521]
  • C B Pollock, H Koltai, Y Kapulnik, C Prandi, R I Yarden. Strigolactones: a novel class of phytohormones that inhibit the growth and survival of breast cancer cells and breast cancer stem-like enriched mammosphere cells. Breast cancer research and treatment. 2012 Aug; 134(3):1041-55. doi: 10.1007/s10549-012-1992-x. [PMID: 22476848]
  • Dina Plakhine, Yaakov Tadmor, Hammam Ziadne, Daniel M Joel. Maternal tissue is involved in stimulant reception by seeds of the parasitic plant Orobanche. Annals of botany. 2012 Apr; 109(5):979-86. doi: 10.1093/aob/mcs016. [PMID: 22378837]
  • Kinga Chojnacka, Stefano Santoro, Radi Awartani, Nigel G J Richards, Fahmi Himo, Aaron Aponick. Synthetic studies on the solanacol ABC ring system by cation-initiated cascade cyclization: implications for strigolactone biosynthesis. Organic & biomolecular chemistry. 2011 Aug; 9(15):5350-3. doi: 10.1039/c1ob05751k. [PMID: 21706088]
  • Alinanuswe S Mwakaboko, Binne Zwanenburg. Strigolactone analogs derived from ketones using a working model for germination stimulants as a blueprint. Plant & cell physiology. 2011 Apr; 52(4):699-715. doi: 10.1093/pcp/pcr031. [PMID: 21421570]
  • Evgenia Dor, Koichi Yoneyama, Smadar Wininger, Yoram Kapulnik, Kaori Yoneyama, Hinanit Koltai, Xiaonan Xie, Joseph Hershenhorn. Strigolactone deficiency confers resistance in tomato line SL-ORT1 to the parasitic weeds Phelipanche and Orobanche spp. Phytopathology. 2011 Feb; 101(2):213-22. doi: 10.1094/phyto-07-10-0184. [PMID: 20942651]
  • Shinsaku Ito, Mikihisa Umehara, Atsushi Hanada, Nobutaka Kitahata, Hiroki Hayase, Shinjiro Yamaguchi, Tadao Asami. Effects of triazole derivatives on strigolactone levels and growth retardation in rice. PloS one. 2011; 6(7):e21723. doi: 10.1371/journal.pone.0021723. [PMID: 21760901]
  • Hinanit Koltai, Sivarama P LekKala, Chaitali Bhattacharya, Einav Mayzlish-Gati, Nathalie Resnick, Smadar Wininger, Evgenya Dor, Kaori Yoneyama, Koichi Yoneyama, Joseph Hershenhorn, Daniel M Joel, Yoram Kapulnik. A tomato strigolactone-impaired mutant displays aberrant shoot morphology and plant interactions. Journal of experimental botany. 2010 Jun; 61(6):1739-49. doi: 10.1093/jxb/erq041. [PMID: 20194924]
  • Chaitali Bhattacharya, Paola Bonfante, Annamaria Deagostino, Yoram Kapulnik, Paolo Larini, Ernesto G Occhiato, Cristina Prandi, Paolo Venturello. A new class of conjugated strigolactone analogues with fluorescent properties: synthesis and biological activity. Organic & biomolecular chemistry. 2009 Sep; 7(17):3413-20. doi: 10.1039/b907026e. [PMID: 19675895]
  • Caiyan Chen, Junhuang Zou, Shuying Zhang, David Zaitlin, Lihuang Zhu. Strigolactones are a new-defined class of plant hormones which inhibit shoot branching and mediate the interaction of plant-AM fungi and plant-parasitic weeds. Science in China. Series C, Life sciences. 2009 Aug; 52(8):693-700. doi: 10.1007/s11427-009-0104-6. [PMID: 19727586]
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  • Koichi Yoneyama, Xiaonan Xie, Kaori Yoneyama, Yasutomo Takeuchi. Strigolactones: structures and biological activities. Pest management science. 2009 May; 65(5):467-70. doi: 10.1002/ps.1726. [PMID: 19222028]
  • Juan A López-Ráez, Radoslava Matusova, Catarina Cardoso, Muhammad Jamil, Tatsiana Charnikhova, Wouter Kohlen, Carolien Ruyter-Spira, Francel Verstappen, Harro Bouwmeester. Strigolactones: ecological significance and use as a target for parasitic plant control. Pest management science. 2009 May; 65(5):471-7. doi: 10.1002/ps.1692. [PMID: 19115242]
  • Binne Zwanenburg, Alinanuswe S Mwakaboko, Anat Reizelman, Gopinathan Anilkumar, Divakaramenon Sethumadhavan. Structure and function of natural and synthetic signalling molecules in parasitic weed germination. Pest management science. 2009 May; 65(5):478-91. doi: 10.1002/ps.1706. [PMID: 19222046]
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