Fludioxonil (BioDeep_00000002250)

 

Secondary id: BioDeep_00000397714

human metabolite blood metabolite


代谢物信息卡片


4-(2,2-difluoro-2H-1,3-benzodioxol-4-yl)-1H-pyrrole-3-carbonitrile

化学式: C12H6F2N2O2 (248.0397)
中文名称: 咯菌腈
谱图信息: 最多检出来源 Homo sapiens(blood) 7.88%

分子结构信息

SMILES: C1=CC(=C2C(=C1)OC(O2)(F)F)C3=CNC=C3C#N
InChI: InChI=1S/C12H6F2N2O2/c13-12(14)17-10-3-1-2-8(11(10)18-12)9-6-16-5-7(9)4-15/h1-3,5-6,16H

描述信息

CONFIDENCE standard compound; INTERNAL_ID 49; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4715; ORIGINAL_PRECURSOR_SCAN_NO 4711
CONFIDENCE standard compound; INTERNAL_ID 49; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4759; ORIGINAL_PRECURSOR_SCAN_NO 4755
CONFIDENCE standard compound; INTERNAL_ID 49; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4745; ORIGINAL_PRECURSOR_SCAN_NO 4740
CONFIDENCE standard compound; INTERNAL_ID 49; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4750; ORIGINAL_PRECURSOR_SCAN_NO 4747
CONFIDENCE standard compound; INTERNAL_ID 49; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4753; ORIGINAL_PRECURSOR_SCAN_NO 4751
CONFIDENCE standard compound; INTERNAL_ID 49; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4731; ORIGINAL_PRECURSOR_SCAN_NO 4728

同义名列表

3 个代谢物同义名

4-(2,2-difluoro-2H-1,3-benzodioxol-4-yl)-1H-pyrrole-3-carbonitrile; Fludioxonil; Fludioxonil



数据库引用编号

18 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)

1 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 10 AHR, ANXA5, AR, ARHGAP45, ATF7, CAT, CCND1, CCNE1, FRZB, MAPK14
Peripheral membrane protein 3 ANXA5, HK1, SDHB
Nucleus 8 AHR, AR, ATF1, ATF7, CCND1, CCNE1, HAMP, MAPK14
cytosol 10 AHR, ANXA5, AR, ARHGAP45, CAT, CCND1, CCNE1, GSR, HK1, MAPK14
dendrite 1 KCNB1
mitochondrial membrane 1 SDHB
centrosome 2 CCND1, CCNE1
nucleoplasm 8 AHR, AR, ATF1, ATF7, CCND1, CCNE1, MAPK14, SDHB
RNA polymerase II transcription regulator complex 2 ATF1, ATF7
Cell membrane 1 KCNB1
ruffle membrane 1 ARHGAP45
Cell projection, axon 1 KCNB1
Multi-pass membrane protein 4 KCNB1, MT-CYB, SDHC, SDHD
Synapse 1 KCNB1
cell surface 1 KCNB1
glutamatergic synapse 1 MAPK14
mitochondrial inner membrane 4 MT-CYB, SDHB, SDHC, SDHD
sarcolemma 2 ANXA5, KCNB1
Cytoplasm, cytosol 1 HK1
plasma membrane 4 AR, ARHGAP45, KCNB1, SDHB
Membrane 8 ANXA5, AR, ARHGAP45, CAT, FRZB, KCNB1, MT-CYB, SDHC
apical plasma membrane 1 KCNB1
axon 1 KCNB1
extracellular exosome 3 ANXA5, CAT, GSR
extracellular space 2 FRZB, HAMP
perinuclear region of cytoplasm 1 KCNB1
bicellular tight junction 1 CCND1
mitochondrion 8 CAT, GSR, HK1, MAPK14, MT-CYB, SDHB, SDHC, SDHD
protein-containing complex 3 AHR, AR, CAT
intracellular membrane-bounded organelle 1 CAT
Secreted 2 FRZB, HAMP
extracellular region 6 ANXA5, ARHGAP45, CAT, FRZB, HAMP, MAPK14
Mitochondrion outer membrane 1 HK1
mitochondrial outer membrane 1 HK1
neuronal cell body membrane 1 KCNB1
mitochondrial matrix 3 CAT, GSR, SDHB
transcription regulator complex 1 AHR
Nucleus membrane 1 CCND1
nuclear membrane 1 CCND1
external side of plasma membrane 2 ANXA5, GSR
perikaryon 1 KCNB1
postsynaptic membrane 1 KCNB1
Cell membrane, sarcolemma 1 KCNB1
Cell projection, ruffle membrane 1 ARHGAP45
Mitochondrion inner membrane 4 MT-CYB, SDHB, SDHC, SDHD
Matrix side 1 SDHB
Membrane raft 1 HK1
focal adhesion 2 ANXA5, CAT
Peroxisome 1 CAT
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
collagen-containing extracellular matrix 1 ANXA5
lateral plasma membrane 1 KCNB1
nuclear speck 2 AR, MAPK14
Postsynaptic cell membrane 1 KCNB1
Zymogen granule membrane 1 ANXA5
chromatin 4 AHR, AR, ATF1, ATF7
[Isoform 5]: Cytoplasm 1 ATF7
spindle pole 1 MAPK14
Chromosome, telomere 1 ATF7
chromosome, telomeric region 1 ATF7
aryl hydrocarbon receptor complex 1 AHR
Nucleus, nucleoplasm 1 ATF7
Cell projection, dendrite 1 KCNB1
voltage-gated potassium channel complex 1 KCNB1
ficolin-1-rich granule lumen 2 CAT, MAPK14
secretory granule lumen 3 ARHGAP45, CAT, MAPK14
transcription repressor complex 1 CCND1
azurophil granule lumen 1 ARHGAP45
mitochondrial envelope 1 SDHD
respiratory chain complex II (succinate dehydrogenase) 3 SDHB, SDHC, SDHD
vesicle membrane 1 ANXA5
respiratory chain complex III 1 MT-CYB
Synapse, synaptosome 1 KCNB1
Lateral cell membrane 1 KCNB1
postsynaptic specialization membrane 1 KCNB1
dendrite membrane 1 KCNB1
cyclin-dependent protein kinase holoenzyme complex 1 CCND1
cholinergic synapse 1 KCNB1
cyclin E1-CDK2 complex 1 CCNE1
catalase complex 1 CAT
endothelial microparticle 1 ANXA5
proximal dendrite 1 KCNB1
cyclin D1-CDK4 complex 1 CCND1
ATF4-CREB1 transcription factor complex 1 ATF1
ATF1-ATF4 transcription factor complex 1 ATF1
cyclin D1-CDK6 complex 1 CCND1
nuclear aryl hydrocarbon receptor complex 1 AHR
cytosolic aryl hydrocarbon receptor complex 1 AHR


文献列表

  • Lingling Wei, Bin Chen, Jiawei Li, Pengcheng Zhang, Wenchan Chen, Wenwu Ye, Changjun Chen. Resistance mechanism of Phomopsis longicolla to fludioxonil is associated with modifications in PlOS1, PlOS4 and PlOS5. Pesticide biochemistry and physiology. 2024 May; 201(?):105862. doi: 10.1016/j.pestbp.2024.105862. [PMID: 38685239]
  • Xueru Yin, Pengfei Li, Zongwei Wang, Jing Wang, Anfei Fang, Binnian Tian, Yuheng Yang, Yang Yu, Chaowei Bi. Binding Mode and Molecular Mechanism of the Two-Component Histidine Kinase Bos1 of Botrytis cinerea to Fludioxonil and Iprodione. Phytopathology. 2024 Apr; 114(4):770-779. doi: 10.1094/phyto-07-23-0241-r. [PMID: 38598410]
  • Ziyue Wen, Yueqi Zhang, Yun Chen, Youfu Zhao, Wenyong Shao, Zhonghua Ma. Characterization of the fludioxonil and phenamacril dual resistant mutants of Fusarium graminearum. Pesticide biochemistry and physiology. 2024 Mar; 200(?):105815. doi: 10.1016/j.pestbp.2024.105815. [PMID: 38582573]
  • Weichao Ren, Wenjiao Han, Tinghua Huan, Meiqi Zhu, Yihan Zhang, Baohua Li, Na Liu. A new point mutation (D1158N) in histidine kinase Bos1 confers high-level resistance to fludioxonil in field gray mold disease. Pesticide biochemistry and physiology. 2024 Jan; 198(?):105750. doi: 10.1016/j.pestbp.2023.105750. [PMID: 38225093]
  • Yunyan Deng, Tao Wang, Ying Du, LuLu Zhang, Jiaxin Wang, Zhiqiu Qi, Mingshan Ji. Risk assessment for resistance to fludioxonil in Corynespora cassiicola in Liaoning China. Pesticide biochemistry and physiology. 2023 Dec; 197(?):105622. doi: 10.1016/j.pestbp.2023.105622. [PMID: 38072516]
  • Dongya Shi, Jin Wang, Yingying Cao, Zhihui Zhang, Xin Li, Jane Ifunanya Mbadianya, Changjun Chen. Overexpression of FgPtp3 Is Involved in Fludioxonil Resistance in Fusarium graminearum by Inhibiting the Phosphorylation of FgHog1. Journal of agricultural and food chemistry. 2023 Aug; 71(34):12807-12818. doi: 10.1021/acs.jafc.3c02663. [PMID: 37585613]
  • Tao Li, Na Li, Ziyang Lei, Chuanqing Zhang. Sensitivity and resistance risk of Botryosphaeria dothidea causing Chinese hickory trunk canker to fludioxonil. Pesticide biochemistry and physiology. 2023 Aug; 194(?):105500. doi: 10.1016/j.pestbp.2023.105500. [PMID: 37532358]
  • Na Zhang, Yiying Xu, Qi Zhang, Le Zhao, Yanan Zhu, Yanhui Wu, Zhen Li, Wenxiang Yang. Detection of fungicide resistance to fludioxonil and tebuconazole in Fusarium pseudograminearum, the causal agent of Fusarium crown rot in wheat. PeerJ. 2023; 11(?):e14705. doi: 10.7717/peerj.14705. [PMID: 36721780]
  • Ping-Hu Wu, Min-Nan Tseng, Ying-Hong Lin, Chang-Hsin Kuo, Hao-Xun Chang. Identification of Cyprodinil+Fludioxonil to Manage Soybean Red Crown Rot using the Microplate-based High Throughput Screening and Pot Assay. Plant disease. 2022 Oct; ?(?):. doi: 10.1094/pdis-08-22-1976-re. [PMID: 36302731]
  • Xiang Liu, Xueting Wang, Fengwen Zhang, Xiangfeng Yao, Zhihua Qiao, Jiahui Deng, Qin Jiao, Luo Gong, Xingyin Jiang. Toxic effects of fludioxonil on the growth, photosynthetic activity, oxidative stress, cell morphology, apoptosis, and metabolism of Chlorella vulgaris. The Science of the total environment. 2022 Sep; 838(Pt 2):156069. doi: 10.1016/j.scitotenv.2022.156069. [PMID: 35605851]
  • Feng Zhou, Ye-Xian Cui, Bing-Li Wang, Yu-Dong Zhou, Shi-Wang Li, Yan-Tong Zhang, Ke Zhang, Ze-Yuan Chen, Hai-Yan Hu, Cheng-Wei Li. Baseline Sensitivity and Potential Resistance Mechanisms for Fusarium pseudograminearum to Fludioxonil. Plant disease. 2022 Aug; 106(8):2138-2144. doi: 10.1094/pdis-12-21-2626-re. [PMID: 35100030]
  • Le Chen, Baixin Sun, Yang Zhao, Peng Xiang, Zeyan Miao. Comparison of the Biological Characteristics and Molecular Mechanisms of Fludioxonil-Resistant Isolates of Botrytis cinerea from Tomato in Liaoning Province of China. Plant disease. 2022 Jul; 106(7):1959-1970. doi: 10.1094/pdis-07-21-1446-re. [PMID: 35678566]
  • Ziyue Wen, Jingrui Wang, Chen Jiao, Wenyong Shao, Zhonghua Ma. Biological and molecular characterizations of field fludioxonil-resistant isolates of Fusarium graminearum. Pesticide biochemistry and physiology. 2022 Jun; 184(?):105101. doi: 10.1016/j.pestbp.2022.105101. [PMID: 35715040]
  • Ζografina Mavriou, Ioanna Alexandropoulou, Paraschos Melidis, Dimitrios G Karpouzas, Spyridon Ntougias. Bioprocess performance, transformation pathway, and bacterial community dynamics in an immobilized cell bioreactor treating fludioxonil-contaminated wastewater under microaerophilic conditions. Environmental science and pollution research international. 2022 Apr; 29(20):29597-29612. doi: 10.1007/s11356-021-16452-3. [PMID: 34542817]
  • Hafiz Muhammad Usman, Qin Tan, Fei Fan, Mohammad Mazharul Karim, Wei-Xiao Yin, Fu-Xing Zhu, Chao-Xi Luo. Sensitivity of Colletotrichum nymphaeae to Six Fungicides and Characterization of Fludioxonil-Resistant Isolates in China. Plant disease. 2022 Jan; 106(1):165-173. doi: 10.1094/pdis-05-21-0993-re. [PMID: 34406787]
  • Miao Song, Siqi Fang, Zhigang Li, Na Wang, Xiao Li, Wenbo Liu, Yu Zhang, Chunhua Lin, Weiguo Miao. CsAtf1, a bZIP transcription factor, is involved in fludioxonil sensitivity and virulence in the rubber tree anthracnose fungus Colletotrichum siamense. Fungal genetics and biology : FG & B. 2022 01; 158(?):103649. doi: 10.1016/j.fgb.2021.103649. [PMID: 34921997]
  • Sayoko Oiki, Takashi Yaguchi, Syun-Ichi Urayama, Daisuke Hagiwara. Wide distribution of resistance to the fungicides fludioxonil and iprodione in Penicillium species. PloS one. 2022; 17(1):e0262521. doi: 10.1371/journal.pone.0262521. [PMID: 35100282]
  • Matthew Brown, Dasuni P Jayaweera, Annabel Hunt, James W Woodhall, Rumiana V Ray. Yield Losses and Control by Sedaxane and Fludioxonil of Soilborne Rhizoctonia, Microdochium, and Fusarium Species in Winter Wheat. Plant disease. 2021 Sep; 105(9):2521-2530. doi: 10.1094/pdis-11-20-2401-re. [PMID: 33439039]
  • Liana C Arnaud, Thierry Gauthier, Augustin Le Naour, Saleha Hashim, Nathalie Naud, Jerry W Shay, Fabrice H Pierre, Elisa Boutet-Robinet, Laurence Huc. Short-Term and Long-Term Carcinogenic Effects of Food Contaminants (4-Hydroxynonenal and Pesticides) on Colorectal Human Cells: Involvement of Genotoxic and Non-Genomic Mechanisms. Cancers. 2021 Aug; 13(17):. doi: 10.3390/cancers13174337. [PMID: 34503147]
  • Xiao-Xu Li, Li-Fei He, Xiu-Yu Pang, Yang-Yang Gao, Yang Liu, Peng Zhang, Guang Wei, Wei Mu, Bei-Xing Li, Feng Liu. Tank-mixing adjuvants enhanced the efficacy of fludioxonil on cucumber anthracnose by ameliorating the penetration ability of active ingredients on target interface. Colloids and surfaces. B, Biointerfaces. 2021 Aug; 204(?):111804. doi: 10.1016/j.colsurfb.2021.111804. [PMID: 33940521]
  • F Zhou, H Y Hu, D X Li, L G Tan, Q Zhang, H T Gao, H L Sun, X L Tian, M W Shi, F L Zhang, C W Li. Exploring the Biological and Molecular Characteristics of Resistance to Fludioxonil in Sclerotinia sclerotiorum From Soybean in China. Plant disease. 2021 Jul; 105(7):1936-1941. doi: 10.1094/pdis-07-20-1621-re. [PMID: 33044139]
  • Xiaolian Wang, Dongxiao Lu, Chengming Tian. CgEnd3 Regulates Endocytosis, Appressorium Formation, and Virulence in the Poplar Anthracnose Fungus Colletotrichum gloeosporioides. International journal of molecular sciences. 2021 Apr; 22(8):. doi: 10.3390/ijms22084029. [PMID: 33919762]
  • Hanxiang Wu, Pengtong Hu, Ye Xu, Chunxia Xiao, Zhibin Chen, Xiaojing Liu, Jinliang Jia, Hanhong Xu. Phloem Delivery of Fludioxonil by Plant Amino Acid Transporter-Mediated Polysuccinimide Nanocarriers for Controlling Fusarium Wilt in Banana. Journal of agricultural and food chemistry. 2021 Mar; 69(9):2668-2678. doi: 10.1021/acs.jafc.0c07028. [PMID: 33629581]
  • Madeline Dowling, Jhulia Gelain, Louise Larissa May De Mio, Guido Schnabel. Characterization of High Fludioxonil Resistance in Botrytis cinerea Isolates from Calibrachoa Flowers. Phytopathology. 2021 Mar; 111(3):478-484. doi: 10.1094/phyto-07-20-0268-r. [PMID: 33044131]
  • Tao Li, Qian Xiu, Jianxin Wang, Yabing Duan, Mingguo Zhou. A Putative MAPK Kinase Kinase Gene Ssos4 is Involved in Mycelial Growth, Virulence, Osmotic Adaptation, and Sensitivity to Fludioxonil and is Essential for SsHog1 Phosphorylation in Sclerotinia sclerotiorum. Phytopathology. 2021 Mar; 111(3):521-530. doi: 10.1094/phyto-07-20-0292-r. [PMID: 33044134]
  • Guido Schnabel, Qin Tan, Verena Schneider, Hideo Ishii. Inherent tolerance of Colletotrichum gloeosporioides to fludioxonil. Pesticide biochemistry and physiology. 2021 Feb; 172(?):104767. doi: 10.1016/j.pestbp.2020.104767. [PMID: 33518054]
  • Akeem O Taiwo, Lincoln A Harper, Mark C Derbyshire. Impacts of fludioxonil resistance on global gene expression in the necrotrophic fungal plant pathogen Sclerotinia sclerotiorum. BMC genomics. 2021 Jan; 22(1):91. doi: 10.1186/s12864-021-07402-x. [PMID: 33516198]
  • Zografina Mavriou, Ioanna Alexandropoulou, Paraschos Melidis, Dimitrios G Karpouzas, Spyridon Ntougias. Biotreatment and bacterial succession in an upflow immobilized cell bioreactor fed with fludioxonil wastewater. Environmental science and pollution research international. 2021 Jan; 28(4):3774-3786. doi: 10.1007/s11356-020-09231-z. [PMID: 32418094]
  • F Zhou, D X Li, H Y Hu, Y L Song, Y C Fan, Y Y Guan, P W Song, Q C Wei, H F Yan, C W Li. Biological Characteristics and Molecular Mechanisms of Fludioxonil Resistance in Fusarium graminearum in China. Plant disease. 2020 Sep; 104(9):2426-2433. doi: 10.1094/pdis-01-20-0079-re. [PMID: 32658633]
  • Feng Zhou, Hai-Yan Hu, Yu-Lu Song, Yu-Qing Gao, Qi-Li Liu, Pu-Wen Song, Er-Yong Chen, Yong-Ang Yu, Dong-Xiao Li, Cheng-Wei Li. Biological Characteristics and Molecular Mechanism of Fludioxonil Resistance in Botrytis cinerea From Henan Province of China. Plant disease. 2020 Apr; 104(4):1041-1047. doi: 10.1094/pdis-08-19-1722-re. [PMID: 31999220]
  • Wenwen Gong, Mengyun Jiang, Tingting Zhang, Wei Zhang, Gang Liang, Bingru Li, Bin Hu, Ping Han. Uptake and dissipation of metalaxyl-M, fludioxonil, cyantraniliprole and thiamethoxam in greenhouse chrysanthemum. Environmental pollution (Barking, Essex : 1987). 2020 Feb; 257(?):113499. doi: 10.1016/j.envpol.2019.113499. [PMID: 31706771]
  • Yangfan Li, Puhuizhong He, Chengming Tian, Yonglin Wang. CgHog1 controls the adaptation to both sorbitol and fludioxonil in Colletotrichum gloeosporioides. Fungal genetics and biology : FG & B. 2020 02; 135(?):103289. doi: 10.1016/j.fgb.2019.103289. [PMID: 31704368]
  • Eder Jorge de Oliveira, Saulo Alves Santos de Oliveira, Caroline Otto, Titus Alicai, Juan Paulo Xavier de Freitas, Diego Fernando Marmolejo Cortes, Anthony Pariyo, Charles Liri, Gerald Adiga, Andrea Balmer, Dominik Klauser, Mike Robinson. A novel seed treatment-based multiplication approach for cassava planting material. PloS one. 2020; 15(3):e0229943. doi: 10.1371/journal.pone.0229943. [PMID: 32142527]
  • Arne Haegerbaeumer, Ricarda Raschke, Nicola Reiff, Walter Traunspurger, Sebastian Höss. Comparing the effects of fludioxonil on non-target soil invertebrates using ecotoxicological methods from single-species bioassays to model ecosystems. Ecotoxicology and environmental safety. 2019 Nov; 183(?):109596. doi: 10.1016/j.ecoenv.2019.109596. [PMID: 31454750]
  • Stefan Bohnert, Luis Antelo, Christiane Grünewald, Alexander Yemelin, Karsten Andresen, Stefan Jacob. Rapid adaptation of signaling networks in the fungal pathogen Magnaporthe oryzae. BMC genomics. 2019 Oct; 20(1):763. doi: 10.1186/s12864-019-6113-3. [PMID: 31640564]
  • Jennifer N Apell, Nicholas C Pflug, Kristopher McNeill. Photodegradation of Fludioxonil and Other Pyrroles: The Importance of Indirect Photodegradation for Understanding Environmental Fate and Photoproduct Formation. Environmental science & technology. 2019 Oct; 53(19):11240-11250. doi: 10.1021/acs.est.9b03948. [PMID: 31486641]
  • A Chechi, J Stahlecker, M E Dowling, G Schnabel. Diversity in species composition and fungicide resistance profiles in Colletotrichum isolates from apples. Pesticide biochemistry and physiology. 2019 Jul; 158(?):18-24. doi: 10.1016/j.pestbp.2019.04.002. [PMID: 31378355]
  • Jian Hu, Yuxin Zhou, Tao Gao, Jiamei Geng, Yuan Dai, Haiyan Ren, Kurt Lamour, Xili Liu. Resistance risk assessment for fludioxonil in Sclerotinia homoeocarpa in China. Pesticide biochemistry and physiology. 2019 May; 156(?):123-128. doi: 10.1016/j.pestbp.2019.02.011. [PMID: 31027571]
  • Meng-Jun Hu, Scott Cosseboom, Guido Schnabel. atrB-Associated Fludioxonil Resistance in Botrytis fragariae Not Linked to Mutations in Transcription Factor mrr1. Phytopathology. 2019 May; 109(5):839-846. doi: 10.1094/phyto-09-18-0341-r. [PMID: 30543488]
  • Stefan Bohnert, Larissa Heck, Christoph Gruber, Hendrik Neumann, Ute Distler, Stefan Tenzer, Alexander Yemelin, Eckhard Thines, Stefan Jacob. Fungicide resistance toward fludioxonil conferred by overexpression of the phosphatase gene MoPTP2 in Magnaporthe oryzae. Molecular microbiology. 2019 03; 111(3):662-677. doi: 10.1111/mmi.14179. [PMID: 30537256]
  • S Saito, C L Xiao. Fungicide Resistance in Botrytis cinerea Populations in California and its Influence on Control of Gray Mold on Stored Mandarin Fruit. Plant disease. 2018 12; 102(12):2545-2549. doi: 10.1094/pdis-05-18-0766-re. [PMID: 30328758]
  • W X Yin, M Adnan, Y Shang, Y Lin, C X Luo. Sensitivity of Botrytis cinerea From Nectarine/Cherry in China to Six Fungicides and Characterization of Resistant Isolates. Plant disease. 2018 12; 102(12):2578-2585. doi: 10.1094/pdis-02-18-0244-re. [PMID: 30299208]
  • Leiming He, Kaidi Cui, Yufei Song, Zhengqun Zhang, Beixing Li, Wei Mu, Feng Liu. A precisely targeted application strategy of dipping young cucumber fruit in fungicide to control cucumber gray mold. Pest management science. 2018 Nov; 74(11):2432-2437. doi: 10.1002/ps.5055. [PMID: 29704289]
  • Stacey E Haack, Kelly L Ivors, Gerald J Holmes, Helga Förster, James E Adaskaveg. Natamycin, a New Biofungicide for Managing Crown Rot of Strawberry Caused by QoI-Resistant Colletotrichum acutatum. Plant disease. 2018 Sep; 102(9):1687-1695. doi: 10.1094/pdis-12-17-2033-re. [PMID: 30125151]
  • J B Qiu, M Z Yu, Q Yin, J H Xu, J R Shi. Molecular Characterization, Fitness, and Mycotoxin Production of Fusarium asiaticum Strains Resistant to Fludioxonil. Plant disease. 2018 Sep; 102(9):1759-1765. doi: 10.1094/pdis-11-17-1772-re. [PMID: 30125190]
  • Yingying Song, Lili Li, Chao Li, Zengbin Lu, Xingyuan Men, Fajun Chen. Evaluating the Sensitivity and Efficacy of Fungicides with Different Modes of Action Against Botryosphaeria dothidea. Plant disease. 2018 Sep; 102(9):1785-1793. doi: 10.1094/pdis-01-18-0118-re. [PMID: 30125189]
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