3-Methyl-2h-Furo[2,3-C]pyran-2-One (BioDeep_00000291757)

   


代谢物信息卡片


3-Methyl-2h-Furo[2,3-C]pyran-2-One

化学式: C8H6O3 (150.03169259999999)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: Cc1c2ccocc-2oc1=O
InChI:

描述信息

同义名列表

1 个代谢物同义名

3-Methyl-2h-Furo[2,3-C]pyran-2-One



数据库引用编号

2 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)

0 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。



文献列表

  • Young-Joon Park, Bo Eun Nam, Chung-Mo Park. Environmentally adaptive reshaping of plant photomorphogenesis by karrikin and strigolactone signaling. Journal of integrative plant biology. 2024 May; 66(5):865-882. doi: 10.1111/jipb.13602. [PMID: 38116738]
  • Shannon A Stirling, Angelica M Guercio, Ryan M Patrick, Xing-Qi Huang, Matthew E Bergman, Varun Dwivedi, Ruy W J Kortbeek, Yi-Kai Liu, Fuai Sun, W Andy Tao, Ying Li, Benoît Boachon, Nitzan Shabek, Natalia Dudareva. Volatile communication in plants relies on a KAI2-mediated signaling pathway. Science (New York, N.Y.). 2024 Mar; 383(6689):1318-1325. doi: 10.1126/science.adl4685. [PMID: 38513014]
  • Pingping Fang, Minxuan Li, Qinwei Guo, Xinyang Wu, Yannan Hu, Yusu Cheng, Pei Xu. Genome-wide analysis of the SMXL gene family in common bean and identification of karrikin-responsive PvSMXL2 as a negative regulator of PEG-induced drought stress. Gene. 2023 Dec; 887(?):147741. doi: 10.1016/j.gene.2023.147741. [PMID: 37634881]
  • Muhammad Kamran, Kim T Melville, Mark T Waters. Karrikin signalling: impacts on plant development and abiotic stress tolerance. Journal of experimental botany. 2023 Nov; ?(?):. doi: 10.1093/jxb/erad476. [PMID: 38001035]
  • Kiyoshi Mashiguchi, Ryo Morita, Kai Tanaka, Kyoichi Kodama, Hiromu Kameoka, Junko Kyozuka, Yoshiya Seto, Shinjiro Yamaguchi. Activation of Strigolactone Biosynthesis by the DWARF14-LIKE/KARRIKIN-INSENSITIVE2 Pathway in Mycorrhizal Angiosperms, but Not in Arabidopsis, a Non-mycorrhizal Plant. Plant & cell physiology. 2023 Sep; 64(9):1066-1078. doi: 10.1093/pcp/pcad079. [PMID: 37494415]
  • Hiromu Kameoka, Shota Shimazaki, Kiyoshi Mashiguchi, Bunta Watanabe, Aino Komatsu, Akiyoshi Yoda, Yohei Mizuno, Kyoichi Kodama, Masanori Okamoto, Takahito Nomura, Shinjiro Yamaguchi, Junko Kyozuka. DIENELACTONE HYDROLASE LIKE PROTEIN1 negatively regulates the KAI2-ligand pathway in Marchantia polymorpha. Current biology : CB. 2023 08; 33(16):3505-3513.e5. doi: 10.1016/j.cub.2023.06.083. [PMID: 37480853]
  • Kartikye Varshney, Caroline Gutjahr. KAI2 can do: Karrikin Receptor Function in Plant Development and Response to Abiotic and Biotic Factors. Plant & cell physiology. 2023 Jul; ?(?):. doi: 10.1093/pcp/pcad077. [PMID: 37548562]
  • Kyoichi Kodama, Xiaonan Xie, Junko Kyozuka. The D14 and KAI2 Orthologs of Gymnosperms Sense Strigolactones and KL Mimics, Respectively, and the Signals Are Transduced to Control Downstream Genes. Plant & cell physiology. 2023 Jul; ?(?):. doi: 10.1093/pcp/pcad072. [PMID: 37489639]
  • Minghui Liu, Qing Shan, Erqiao Ding, Tingting Gu, Biao Gong. Karrikin increases tomato cold tolerance via strigolactone and the abscisic acid signaling network. Plant science : an international journal of experimental plant biology. 2023 Jul; 332(?):111720. doi: 10.1016/j.plantsci.2023.111720. [PMID: 37120034]
  • Mark T Waters, David C Nelson. Karrikin perception and signalling. The New phytologist. 2023 03; 237(5):1525-1541. doi: 10.1111/nph.18598. [PMID: 36333982]
  • Mostafa Abdelrahman, Mohammad Golam Mostofa, Cuong Duy Tran, Magdi El-Sayed, Weiqiang Li, Saad Sulieman, Maho Tanaka, Motoaki Seki, Lam-Son Phan Tran. The Karrikin Receptor Karrikin Insensitive2 Positively Regulates Heat Stress Tolerance in Arabidopsis thaliana. Plant & cell physiology. 2023 Jan; 63(12):1914-1926. doi: 10.1093/pcp/pcac112. [PMID: 35880749]
  • Mohammad Golam Mostofa, Mostafa Abdelrahman, Md Mezanur Rahman, Cuong Duy Tran, Kien Huu Nguyen, Yasuko Watanabe, Misao Itouga, Weiqiang Li, Zhe Wang, Keiichi Mochida, Lam-Son Phan Tran. Karrikin Receptor KAI2 Coordinates Salt Tolerance Mechanisms in Arabidopsis thaliana. Plant & cell physiology. 2023 Jan; 63(12):1927-1942. doi: 10.1093/pcp/pcac121. [PMID: 35997763]
  • Fang Ni, Faheem Afzal Shah, Jie Ren. Identification and characterization of the karrikins signaling gene SsSMAX1 in Sapium sebiferum. PeerJ. 2023; 11(?):e16610. doi: 10.7717/peerj.16610. [PMID: 38089914]
  • Peipei Xu, Hu Jinbo, Weiming Cai. Karrikin signaling regulates hypocotyl shade avoidance response by modulating auxin homeostasis in Arabidopsis. The New phytologist. 2022 12; 236(5):1748-1761. doi: 10.1111/nph.18459. [PMID: 36068957]
  • Hongtao Tian, Yasuko Watanabe, Kien Huu Nguyen, Cuong Duy Tran, Mostafa Abdelrahman, Xiaohan Liang, Kun Xu, Claudia Sepulveda, Mohammad Golam Mostofa, Chien Van Ha, David C Nelson, Keiichi Mochida, Chunjie Tian, Maho Tanaka, Motoaki Seki, Yuchen Miao, Lam-Son Phan Tran, Weiqiang Li. KARRIKIN UPREGULATED F-BOX 1 negatively regulates drought tolerance in Arabidopsis. Plant physiology. 2022 11; 190(4):2671-2687. doi: 10.1093/plphys/kiac336. [PMID: 35822606]
  • Marieke Dubois. KUFfed by drought: A KARRIKIN-upregulated F-box protein compromises plant growth and survival under drought. Plant physiology. 2022 11; 190(4):2087-2089. doi: 10.1093/plphys/kiac413. [PMID: 36063030]
  • Stephanie E Martinez, Caitlin E Conn, Angelica M Guercio, Claudia Sepulveda, Christopher J Fiscus, Daniel Koenig, Nitzan Shabek, David C Nelson. A KARRIKIN INSENSITIVE2 paralog in lettuce mediates highly sensitive germination responses to karrikinolide. Plant physiology. 2022 Sep; 190(2):1440-1456. doi: 10.1093/plphys/kiac328. [PMID: 35809069]
  • Jae Young Kim, Young-Joon Park, June-Hee Lee, Chung-Mo Park. SMAX1 Integrates Karrikin and Light Signals into GA-Mediated Hypocotyl Growth during Seedling Establishment. Plant & cell physiology. 2022 Jul; 63(7):932-943. doi: 10.1093/pcp/pcac055. [PMID: 35477800]
  • Maxime Hamon-Josse, José Antonio Villaécija-Aguilar, Karin Ljung, Ottoline Leyser, Caroline Gutjahr, Tom Bennett. KAI2 regulates seedling development by mediating light-induced remodelling of auxin transport. The New phytologist. 2022 07; 235(1):126-140. doi: 10.1111/nph.18110. [PMID: 35313031]
  • Qia Wang, Steven M Smith, Jinling Huang. Origins of strigolactone and karrikin signaling in plants. Trends in plant science. 2022 05; 27(5):450-459. doi: 10.1016/j.tplants.2021.11.009. [PMID: 34876337]
  • Claudia Sepulveda, Michael A Guzmán, Qingtian Li, José Antonio Villaécija-Aguilar, Stephanie E Martinez, Muhammad Kamran, Aashima Khosla, Wei Liu, Joshua M Gendron, Caroline Gutjahr, Mark T Waters, David C Nelson. KARRIKIN UP-REGULATED F-BOX 1 (KUF1) imposes negative feedback regulation of karrikin and KAI2 ligand metabolism in Arabidopsis thaliana. Proceedings of the National Academy of Sciences of the United States of America. 2022 03; 119(11):e2112820119. doi: 10.1073/pnas.2112820119. [PMID: 35254909]
  • Yongjie Meng, Kartikye Varshney, Norbert Incze, Eszter Badics, Muhammad Kamran, Sabrina F Davies, Larissa M F Oppermann, Kévin Magne, Marion Dalmais, Abdel Bendahmane, Richard Sibout, John Vogel, Debbie Laudencia-Chingcuanco, Charles S Bond, Vilmos Soós, Caroline Gutjahr, Mark T Waters. KARRIKIN INSENSITIVE2 regulates leaf development, root system architecture and arbuscular-mycorrhizal symbiosis in Brachypodium distachyon. The Plant journal : for cell and molecular biology. 2022 03; 109(6):1559-1574. doi: 10.1111/tpj.15651. [PMID: 34953105]
  • José Antonio Villaécija-Aguilar, Caroline Körösy, Lukas Maisch, Maxime Hamon-Josse, Andrea Petrich, Sonja Magosch, Philipp Chapman, Tom Bennett, Caroline Gutjahr. KAI2 promotes Arabidopsis root hair elongation at low external phosphate by controlling local accumulation of AUX1 and PIN2. Current biology : CB. 2022 01; 32(1):228-236.e3. doi: 10.1016/j.cub.2021.10.044. [PMID: 34758285]
  • Katharina Bursch, Ella T Niemann, David C Nelson, Henrik Johansson. Karrikins control seedling photomorphogenesis and anthocyanin biosynthesis through a HY5-BBX transcriptional module. The Plant journal : for cell and molecular biology. 2021 09; 107(5):1346-1362. doi: 10.1111/tpj.15383. [PMID: 34160854]
  • Amir Arellano-Saab, Michael Bunsick, Hasan Al Galib, Wenda Zhao, Stefan Schuetz, James Michael Bradley, Zhenhua Xu, Claresta Adityani, Asrinus Subha, Hayley McKay, Alexandre de Saint Germain, François-Didier Boyer, Christopher S P McErlean, Shigeo Toh, Peter McCourt, Peter J Stogios, Shelley Lumba. Three mutations repurpose a plant karrikin receptor to a strigolactone receptor. Proceedings of the National Academy of Sciences of the United States of America. 2021 07; 118(30):. doi: 10.1073/pnas.2103175118. [PMID: 34301902]
  • Dóra Oláh, Árpád Molnár, Vilmos Soós, Zsuzsanna Kolbert. Nitric oxide is associated with strigolactone and karrikin signal transduction in Arabidopsis roots. Plant signaling & behavior. 2021 03; 16(3):1868148. doi: 10.1080/15592324.2020.1868148. [PMID: 33446007]
  • Anis Ali Shah, Waheed Ullah Khan, Nasim Ahmad Yasin, Waheed Akram, Aqeel Ahmad, Muhammad Abbas, Aamir Ali, Muhammad Naeem Safdar. Butanolide alleviated cadmium stress by improving plant growth, photosynthetic parameters and antioxidant defense system of brassica oleracea. Chemosphere. 2020 Dec; 261(?):127728. doi: 10.1016/j.chemosphere.2020.127728. [PMID: 32731022]
  • Samy Carbonnel, Salar Torabi, Maximilian Griesmann, Elias Bleek, Yuhong Tang, Stefan Buchka, Veronica Basso, Mitsuru Shindo, François-Didier Boyer, Trevor L Wang, Michael Udvardi, Mark T Waters, Caroline Gutjahr. Lotus japonicus karrikin receptors display divergent ligand-binding specificities and organ-dependent redundancy. PLoS genetics. 2020 12; 16(12):e1009249. doi: 10.1371/journal.pgen.1009249. [PMID: 33370251]
  • Ji-Long Zhang, Xiaoting Liu, Hong-Xing Zhang. Interaction Mechanism of the Germination Stimulants Karrikins and Their Receptor ShKAI2iB. The journal of physical chemistry. B. 2020 11; 124(44):9812-9819. doi: 10.1021/acs.jpcb.0c06734. [PMID: 33089685]
  • Amana Khatoon, Shafiq Ur Rehman, Muhammad Mudasar Aslam, Muhammad Jamil, Setsuko Komatsu. Plant-Derived Smoke Affects Biochemical Mechanism on Plant Growth and Seed Germination. International journal of molecular sciences. 2020 Oct; 21(20):. doi: 10.3390/ijms21207760. [PMID: 33092218]
  • Jianshu Zheng, Kai Hong, Longjun Zeng, Lei Wang, Shujing Kang, Minghao Qu, Jiarong Dai, Linyuan Zou, Lixin Zhu, Zhanpeng Tang, Xiangbing Meng, Bing Wang, Jiang Hu, Dali Zeng, Yonghui Zhao, Peng Cui, Quan Wang, Qian Qian, Yonghong Wang, Jiayang Li, Guosheng Xiong. Karrikin Signaling Acts Parallel to and Additively with Strigolactone Signaling to Regulate Rice Mesocotyl Elongation in Darkness. The Plant cell. 2020 09; 32(9):2780-2805. doi: 10.1105/tpc.20.00123. [PMID: 32665307]
  • Stéphanie M Swarbreck, Amirah Mohammad-Sidik, Julia M Davies. Common Components of the Strigolactone and Karrikin Signaling Pathways Suppress Root Branching in Arabidopsis. Plant physiology. 2020 09; 184(1):18-22. doi: 10.1104/pp.19.00687. [PMID: 32690756]
  • Weiqiang Li, Aarti Gupta, Hongtao Tian, Kien Huu Nguyen, Cuong Duy Tran, Yasuko Watanabe, Chunjie Tian, Kun Li, Yong Yang, Jinggong Guo, Yin Luo, Yuchen Miao, Lam-Son Phan Tran. Different strategies of strigolactone and karrikin signals in regulating the resistance of Arabidopsis thaliana to water-deficit stress. Plant signaling & behavior. 2020 09; 15(9):1789321. doi: 10.1080/15592324.2020.1789321. [PMID: 32669036]
  • Aashima Khosla, Nicholas Morffy, Qingtian Li, Lionel Faure, Sun Hyun Chang, Jiaren Yao, Jiameng Zheng, Mei L Cai, John Stanga, Gavin R Flematti, Mark T Waters, David C Nelson. Structure-Function Analysis of SMAX1 Reveals Domains That Mediate Its Karrikin-Induced Proteolysis and Interaction with the Receptor KAI2. The Plant cell. 2020 08; 32(8):2639-2659. doi: 10.1105/tpc.19.00752. [PMID: 32434855]
  • Lei Wang, Qian Xu, Hong Yu, Haiyan Ma, Xiaoqiang Li, Jun Yang, Jinfang Chu, Qi Xie, Yonghong Wang, Steven M Smith, Jiayang Li, Guosheng Xiong, Bing Wang. Strigolactone and Karrikin Signaling Pathways Elicit Ubiquitination and Proteolysis of SMXL2 to Regulate Hypocotyl Elongation in Arabidopsis. The Plant cell. 2020 07; 32(7):2251-2270. doi: 10.1105/tpc.20.00140. [PMID: 32358074]
  • Jeongmin Choi, Tak Lee, Jungnam Cho, Emily K Servante, Boas Pucker, William Summers, Sarah Bowden, Mehran Rahimi, Kyungsook An, Gynheung An, Harro J Bouwmeester, Emma J Wallington, Giles Oldroyd, Uta Paszkowski. The negative regulator SMAX1 controls mycorrhizal symbiosis and strigolactone biosynthesis in rice. Nature communications. 2020 04; 11(1):2114. doi: 10.1038/s41467-020-16021-1. [PMID: 32355217]
  • Abdul Sami, Muhammad Waheed Riaz, Xiangyu Zhou, Zonghe Zhu, Kejin Zhou. Alleviating dormancy in Brassica oleracea seeds using NO and KAR1 with ethylene biosynthetic pathway, ROS and antioxidant enzymes modifications. BMC plant biology. 2019 Dec; 19(1):577. doi: 10.1186/s12870-019-2118-y. [PMID: 31870301]
  • 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]
  • Guillaume Brun, Séverine Thoiron, Lukas Braem, Jean-Bernard Pouvreau, Grégory Montiel, Marc-Marie Lechat, Philippe Simier, Kris Gevaert, Sofie Goormachtig, Philippe Delavault. CYP707As are effectors of karrikin and strigolactone signalling pathways in Arabidopsis thaliana and parasitic plants. Plant, cell & environment. 2019 09; 42(9):2612-2626. doi: 10.1111/pce.13594. [PMID: 31134630]
  • Devashan Naidoo, Martin Pošta, Ayan Roy, Manoj Kulkarni, Johannes Van Staden. Synthesis of potent neuroprotective butenolides based on plant smoke derived 3,4,5-Trimethylfuran-2(5H)-one and 3-methyl-2H-furo[2,3-c]pyrone-2-one. Phytochemistry. 2019 Jul; 163(?):187-194. doi: 10.1016/j.phytochem.2019.03.014. [PMID: 31014820]
  • Jie Zhou, Zi-Xin Xu, Hui Sun, Lan-Ping Guo. Smoke-Isolated Karrikins Stimulated Tanshinones Biosynthesis in Salvia miltiorrhiza through Endogenous Nitric Oxide and Jasmonic Acid. Molecules (Basel, Switzerland). 2019 Mar; 24(7):. doi: 10.3390/molecules24071229. [PMID: 30934811]
  • Izabela Ruduś, Danuta Cembrowska-Lech, Anna Jaworska, Jan Kępczyński. Involvement of ethylene biosynthesis and perception during germination of dormant Avena fatua L. caryopses induced by KAR1 or GA3. Planta. 2019 Mar; 249(3):719-738. doi: 10.1007/s00425-018-3032-5. [PMID: 30370496]
  • Inhye Lee, Soobin Choi, Sumin Lee, Moon-Soo Soh. KAI2-KL signaling intersects with light-signaling for photomorphogenesis. Plant signaling & behavior. 2019; 14(4):e1588660. doi: 10.1080/15592324.2019.1588660. [PMID: 30829108]
  • Yuqun Xu, Takuya Miyakawa, Shohei Nosaki, Akira Nakamura, Ying Lyu, Hidemitsu Nakamura, Umeharu Ohto, Hanako Ishida, Toshiyuki Shimizu, Tadao Asami, Masaru Tanokura. Structural analysis of HTL and D14 proteins reveals the basis for ligand selectivity in Striga. Nature communications. 2018 09; 9(1):3947. doi: 10.1038/s41467-018-06452-2. [PMID: 30258184]
  • Lu Wang, Mark T Waters, Steven M Smith. Karrikin-KAI2 signalling provides Arabidopsis seeds with tolerance to abiotic stress and inhibits germination under conditions unfavourable to seedling establishment. The New phytologist. 2018 07; 219(2):605-618. doi: 10.1111/nph.15192. [PMID: 29726620]
  • Ewa Krawczyk, Marek Koprowski, Danuta Cembrowska-Lech, Agata Wójcik, Jan Kępczyński. Synthesis of tricyclic butenolides and comparison their effects with known smoke-butenolide, KAR1. Journal of plant physiology. 2017 Aug; 215(?):91-99. doi: 10.1016/j.jplph.2017.04.021. [PMID: 28618259]
  • Jutiporn Thussagunpanit, Yuko Nagai, Miyu Nagae, Kiyoshi Mashiguchi, Nobutaka Mitsuda, Masaru Ohme-Takagi, Takeshi Nakano, Hidemitsu Nakamura, Tadao Asami. Involvement of STH7 in light-adapted development in Arabidopsis thaliana promoted by both strigolactone and karrikin. Bioscience, biotechnology, and biochemistry. 2017 Feb; 81(2):292-301. doi: 10.1080/09168451.2016.1254536. [PMID: 27858514]
  • Nicholas Morffy, Lionel Faure, David C Nelson. Smoke and Hormone Mirrors: Action and Evolution of Karrikin and Strigolactone Signaling. Trends in genetics : TIG. 2016 Mar; 32(3):176-188. doi: 10.1016/j.tig.2016.01.002. [PMID: 26851153]
  • Yongjie Meng, Feng Chen, Haiwei Shuai, Xiaofeng Luo, Jun Ding, Shengwen Tang, Shuanshuan Xu, Jianwei Liu, Weiguo Liu, Junbo Du, Jiang Liu, Feng Yang, Xin Sun, Taiwen Yong, Xiaochun Wang, Yuqi Feng, Kai Shu, Wenyu Yang. Karrikins delay soybean seed germination by mediating abscisic acid and gibberellin biogenesis under shaded conditions. Scientific reports. 2016 Feb; 6(?):22073. doi: 10.1038/srep22073. [PMID: 26902640]
  • Caroline Gutjahr, Enrico Gobbato, Jeongmin Choi, Michael Riemann, Matthew G Johnston, William Summers, Samy Carbonnel, Catherine Mansfield, Shu-Yi Yang, Marina Nadal, Ivan Acosta, Makoto Takano, Wen-Biao Jiao, Korbinian Schneeberger, Krystyna A Kelly, Uta Paszkowski. Rice perception of symbiotic arbuscular mycorrhizal fungi requires the karrikin receptor complex. Science (New York, N.Y.). 2015 Dec; 350(6267):1521-4. doi: 10.1126/science.aac9715. [PMID: 26680197]
  • Ishwarya Soundappan, Tom Bennett, Nicholas Morffy, Yueyang Liang, John P Stanga, Amena Abbas, Ottoline Leyser, David C Nelson. SMAX1-LIKE/D53 Family Members Enable Distinct MAX2-Dependent Responses to Strigolactones and Karrikins in Arabidopsis. The Plant cell. 2015 Nov; 27(11):3143-59. doi: 10.1105/tpc.15.00562. [PMID: 26546447]
  • Mark T Waters, Adrian Scaffidi, Solène L Y Moulin, Yueming K Sun, Gavin R Flematti, Steven M Smith. A Selaginella moellendorffii Ortholog of KARRIKIN INSENSITIVE2 Functions in Arabidopsis Development but Cannot Mediate Responses to Karrikins or Strigolactones. The Plant cell. 2015 Jul; 27(7):1925-44. doi: 10.1105/tpc.15.00146. [PMID: 26175507]
  • Jana Baldrianová, Martin Černý, Jan Novák, Petr L Jedelský, Eva Divíšková, Břetislav Brzobohatý. Arabidopsis proteome responses to the smoke-derived growth regulator karrikin. Journal of proteomics. 2015 Apr; 120(?):7-20. doi: 10.1016/j.jprot.2015.02.011. [PMID: 25746380]
  • Yoshiya Seto, Shinjiro Yamaguchi. Strigolactone biosynthesis and perception. Current opinion in plant biology. 2014 Oct; 21(?):1-6. doi: 10.1016/j.pbi.2014.06.001. [PMID: 24981923]
  • Steven M Smith, Jiayang Li. Signalling and responses to strigolactones and karrikins. Current opinion in plant biology. 2014 Oct; 21(?):23-29. doi: 10.1016/j.pbi.2014.06.003. [PMID: 24996032]
  • Shigeo Toh, Duncan Holbrook-Smith, Michael E Stokes, Yuichiro Tsuchiya, Peter McCourt. Detection of parasitic plant suicide germination compounds using a high-throughput Arabidopsis HTL/KAI2 strigolactone perception system. Chemistry & biology. 2014 Aug; 21(8):988-98. doi: 10.1016/j.chembiol.2014.07.005. [PMID: 25126711]
  • Mark T Waters, Adrian Scaffidi, Yueming K Sun, Gavin R Flematti, Steven M Smith. The karrikin response system of Arabidopsis. The Plant journal : for cell and molecular biology. 2014 Aug; 79(4):623-31. doi: 10.1111/tpj.12430. [PMID: 24433542]
  • Aviad Mandabi, Hadas Ganin, Pnina Krief, Josep Rayo, Michael M Meijler. Karrikins from plant smoke modulate bacterial quorum sensing. Chemical communications (Cambridge, England). 2014 May; 50(40):5322-5. doi: 10.1039/c3cc47501h. [PMID: 24327106]
  • 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]
  • Li-Hua Zhao, X Edward Zhou, Zhong-Shan Wu, Wei Yi, Yong Xu, Suling Li, Ting-Hai Xu, Yue Liu, Run-Ze Chen, Amanda Kovach, Yangyong Kang, Li Hou, Yuanzheng He, Cen Xie, Wanling Song, Dafang Zhong, Yechun Xu, Yonghong Wang, Jiayang Li, Chenghai Zhang, Karsten Melcher, H Eric Xu. Crystal structures of two phytohormone signal-transducing α/β hydrolases: karrikin-signaling KAI2 and strigolactone-signaling DWARF14. Cell research. 2013 Mar; 23(3):436-9. doi: 10.1038/cr.2013.19. [PMID: 23381136]
  • Megumi Kagiyama, Yoshinori Hirano, Tomoyuki Mori, Sun-Yong Kim, Junko Kyozuka, Yoshiya Seto, Shinjiro Yamaguchi, Toshio Hakoshima. Structures of D14 and D14L in the strigolactone and karrikin signaling pathways. Genes to cells : devoted to molecular & cellular mechanisms. 2013 Feb; 18(2):147-60. doi: 10.1111/gtc.12025. [PMID: 23301669]
  • Gavin R Flematti, Mark T Waters, Adrian Scaffidi, David J Merritt, Emilio L Ghisalberti, Kingsley W Dixon, Steven M Smith. Karrikin and cyanohydrin smoke signals provide clues to new endogenous plant signaling compounds. Molecular plant. 2013 Jan; 6(1):29-37. doi: 10.1093/mp/sss132. [PMID: 23180672]
  • Mark T Waters, Steven M Smith. KAI2- and MAX2-mediated responses to karrikins and strigolactones are largely independent of HY5 in Arabidopsis seedlings. Molecular plant. 2013 Jan; 6(1):63-75. doi: 10.1093/mp/sss127. [PMID: 23142794]
  • Cristina Prandi, Helèna Rosso, Beatrice Lace, Ernesto G Occhiato, Alberto Oppedisano, Silvia Tabasso, Gabriele Alberto, Marco Blangetti. Strigolactone analogs as molecular probes in chasing the (SLs) receptor/s: design and synthesis of fluorescent labeled molecules. Molecular plant. 2013 Jan; 6(1):113-27. doi: 10.1093/mp/sss133. [PMID: 23180673]
  • Mark T Waters, Adrian Scaffidi, Gavin R Flematti, Steven M Smith. Karrikins force a rethink of strigolactone mode of action. Plant signaling & behavior. 2012 Aug; 7(8):969-72. doi: 10.4161/psb.20977. [PMID: 22827937]
  • Adrian Scaffidi, Mark T Waters, Charles S Bond, Kingsley W Dixon, Steven M Smith, Emilio L Ghisalberti, Gavin R Flematti. Exploring the molecular mechanism of karrikins and strigolactones. Bioorganic & medicinal chemistry letters. 2012 Jun; 22(11):3743-6. doi: 10.1016/j.bmcl.2012.04.016. [PMID: 22542018]
  • Mark T Waters, David C Nelson, Adrian Scaffidi, Gavin R Flematti, Yueming K Sun, Kingsley W Dixon, Steven M Smith. Specialisation within the DWARF14 protein family confers distinct responses to karrikins and strigolactones in Arabidopsis. Development (Cambridge, England). 2012 Apr; 139(7):1285-95. doi: 10.1242/dev.074567. [PMID: 22357928]
  • David C Nelson, Gavin R Flematti, Emilio L Ghisalberti, Kingsley W Dixon, Steven M Smith. Regulation of seed germination and seedling growth by chemical signals from burning vegetation. Annual review of plant biology. 2012; 63(?):107-30. doi: 10.1146/annurev-arplant-042811-105545. [PMID: 22404467]
  • David C Nelson, Adrian Scaffidi, Elizabeth A Dun, Mark T Waters, Gavin R Flematti, Kingsley W Dixon, Christine A Beveridge, Emilio L Ghisalberti, Steven M Smith. F-box protein MAX2 has dual roles in karrikin and strigolactone signaling in Arabidopsis thaliana. Proceedings of the National Academy of Sciences of the United States of America. 2011 May; 108(21):8897-902. doi: 10.1073/pnas.1100987108. [PMID: 21555559]
  • Vilmos Soós, Endre Sebestyén, Angéla Juhász, Marnie E Light, Ladislav Kohout, Gabriella Szalai, Júlia Tandori, Johannes Van Staden, Ervin Balázs. Transcriptome analysis of germinating maize kernels exposed to smoke-water and the active compound KAR1. BMC plant biology. 2010 Nov; 10(?):236. doi: 10.1186/1471-2229-10-236. [PMID: 21044315]
  • Gavin R Flematti, Adrian Scaffidi, Ethan D Goddard-Borger, Charles H Heath, David C Nelson, Lucy E Commander, Robert V Stick, Kingsley W Dixon, Steven M Smith, Emilio L Ghisalberti. Structure-activity relationship of karrikin germination stimulants. Journal of agricultural and food chemistry. 2010 Aug; 58(15):8612-7. doi: 10.1021/jf101690a. [PMID: 20617827]
  • Rowena L Long, Kimberlyn Williams, Erin M Griffiths, Gavin R Flematti, David J Merritt, Jason C Stevens, Shane R Turner, Stephen B Powles, Kingsley W Dixon. Prior hydration of Brassica tournefortii seeds reduces the stimulatory effect of karrikinolide on germination and increases seed sensitivity to abscisic acid. Annals of botany. 2010 Jun; 105(6):1063-70. doi: 10.1093/aob/mcq061. [PMID: 20348089]
  • David C Nelson, Gavin R Flematti, Julie-Anne Riseborough, Emilio L Ghisalberti, Kingsley W Dixon, Steven M Smith. Karrikins enhance light responses during germination and seedling development in Arabidopsis thaliana. Proceedings of the National Academy of Sciences of the United States of America. 2010 Apr; 107(15):7095-100. doi: 10.1073/pnas.0911635107. [PMID: 20351290]
  • Marnie E Light, Ben V Burger, Dan Staerk, Ladislav Kohout, Johannes Van Staden. Butenolides from plant-derived smoke: natural plant-growth regulators with antagonistic actions on seed germination. Journal of natural products. 2010 Feb; 73(2):267-9. doi: 10.1021/np900630w. [PMID: 20078110]
  • David C Nelson, Julie-Anne Riseborough, Gavin R Flematti, Jason Stevens, Emilio L Ghisalberti, Kingsley W Dixon, Steven M Smith. Karrikins discovered in smoke trigger Arabidopsis seed germination by a mechanism requiring gibberellic acid synthesis and light. Plant physiology. 2009 Feb; 149(2):863-73. doi: 10.1104/pp.108.131516. [PMID: 19074625]
  • Gavin R Flematti, Ethan D Goddard-Borger, David J Merritt, Emilio L Ghisalberti, Kingsley W Dixon, Robert D Trengove. Preparation of 2H-furo[2,3-c]pyran-2-one derivatives and evaluation of their germination-promoting activity. Journal of agricultural and food chemistry. 2007 Mar; 55(6):2189-94. doi: 10.1021/jf0633241. [PMID: 17316021]
  • Luc Verschaeve, Jef Maes, Marnie E Light, Johannes van Staden. Genetic toxicity testing of 3-methyl-2H-furo[2,3-c]pyran-2-one, an important biologically active compound from plant-derived smoke. Mutation research. 2006 Dec; 611(1-2):89-95. doi: 10.1016/j.mrgentox.2006.07.005. [PMID: 16990045]
  • Marnie E Light, Barend V Burger, Johannes van Staden. Formation of a seed germination promoter from carbohydrates and amino acids. Journal of agricultural and food chemistry. 2005 Jul; 53(15):5936-42. doi: 10.1021/jf050710u. [PMID: 16028977]
  • Gavin R Flematti, Emilio L Ghisalberti, Kingsley W Dixon, Robert D Trengove. A compound from smoke that promotes seed germination. Science (New York, N.Y.). 2004 Aug; 305(5686):977. doi: 10.1126/science.1099944. [PMID: 15247439]