1-Naphthaleneacetic acid (BioDeep_00000002116)

 

Secondary id: BioDeep_00000408787, BioDeep_00000858412

human metabolite PANOMIX_OTCML-2023 Endogenous Plant Hormones


代谢物信息卡片


1-Naphthaleneacetic acid, plant cell culture tested, BioReagent, >=95\\%, crystalline

化学式: C12H10O2 (186.06807600000002)
中文名称: 1-萘乙酸(NAA), 1-萘基乙酸, α-萘乙酸, α-萘醋酸, 1-萘乙酸, 萘乙酸
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 8.2%

分子结构信息

SMILES: C1=CC=C2C(=C1)C=CC=C2CC(=O)O
InChI: InChI=1S/C12H10O2/c13-12(14)8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8H2,(H,13,14)

描述信息

Plant growth regulator. 1-Naphthaleneacetic acid is used for control of preharvest fruit drop, flower induction and fruit thinning in various crops such as apples, potatoes, olives and citrus fruits.1-Naphthaleneacetic acid (NAA) is a plant hormone in the auxin family. It is a rooting agent and used for the vegetative propagation of plants from stem and leaf cutting. It is also used for plant tissue culture. NAA does not occur naturally. Under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), products containing NAA require registration with the Environmental Protection Agency (EPA) as pesticides. (Wikipedia
1-naphthaleneacetic acid is a naphthylacetic acid substituted by a carboxymethyl group at position 1. It has a role as a synthetic auxin. It is a conjugate acid of a 1-naphthaleneacetate.
1-Naphthylacetic acid is a natural product found in Cocos nucifera, Humulus lupulus, and other organisms with data available.
1-Naphthaleneacetic acid (1-Naphthylacetic acid), a auxin, can promote plant growth. 1-Naphthaleneacetic acid is also an inhibitor of PLA2, with an IC50 of 13.16 μM[1][2].
1-Naphthaleneacetic acid (1-Naphthylacetic acid), a auxin, can promote plant growth. 1-Naphthaleneacetic acid is also an inhibitor of PLA2, with an IC50 of 13.16 μM[1][2].

同义名列表

155 个代谢物同义名

1-Naphthaleneacetic acid, plant cell culture tested, BioReagent, >=95\\%, crystalline; 3-(3-tert-Butoxycarbonylamino-piperidin-1-yl)-2-methyl-propionicacidmethylester; 1-Naphthylacetic acid, 1 mg/mL, BioReagent, plant cell culture tested; 1-Naphthaleneacetic acid, PESTANAL(R), analytical standard; (Naphthalen-1-yl)acetic Acid (1-Naphthylacetic Acid); NAPHAZOLINE HYDROCHLORIDE IMPURITY B [EP IMPURITY]; 2-(1-naphthyl)acetate;1-Naphthylacetic acid; 1-Naphthaleneacetic acid, technical grade; 1-naphthaleneacetic acid, potassium salt; 1-naphthaleneacetic acid, ammonium salt; 1-Naphthaleneacetic acid (7CI,8CI,9CI); 1-naphthaleneacetic acid, sodium salt; 1-Naphthalene-4-t-acetic acid (9CI); alpha-Naphthylessigsaeure [German]; Acide naphtylacetique [ISO-French]; (1-Naphthyl)acetic acid, BSI, ISO; 2-(.ALPHA.-NAPHTHYL)ETHANOIC ACID; 1-NAPHTHALENEACETIC ACID [WHO-DD]; ALPHA-NAPHTHYLACETIC ACID [HSDB]; 1-Naphthaleneacetic acid (solid); Kyselina 1-naftyloctova [Czech]; Naphthyl-1-essigsaeure [German]; 1-NAPHTHALENEACETIC ACID [INCI]; Acide naphthylacetique [French]; 2-(alpha-naphthyl)ethanoic acid; 2-(alpha-Naphthyl)ethanoic aid; 2-(naphthalen-1-yl)acetic acid; 1-Naphthaleneacetic acid, 97\\%; .alpha.-Naphthaleneacetic acid; Acide naphtylacetique [French]; .alpha.-Naphthyleneacetic acid; potassium 1-naphthaleneacetate; 1-NAPHTHALENEACETIC ACID [MI]; Naphyl-1-essigsaeure [German]; (Naphthalen-1-yl)acetic acid; 2-naphthalen-1-ylacetic acid; Naphthaleneacetic acid (VAN); alpha-Naphthyleneacetic acid; alpha-naphthaleneacetic acid; sodium 1-naphthaleneacetate; .alpha.-Naphthylacetic acid; 1-NAPHTHYLACETIC ACID [JAN]; .alpha.-Naphthylessigsaeure; 1-Naphthylacetic acid (JAN); NAPHTHYLACETIC ACID [MART.]; NAPHTHALEN-1-YL-ACETIC ACID; naphthalen-1-ylacetic acid; 1-naphthaleneethanoic acid; alpha-naphthyl acetic acid; Naphthalene-1-acetic acid; alpha-Naphthylessigsaeure; 1-Naphthtaleneacetic acid; alpha-Naphthylacetic acid; 1-Naphthalene acetic acid; 2-(1-naphthyl)acetic acid; Naphtalene-1-acetic acid; 2-naphthalyl acetic acid; 1-naphtalene acetic acid; a-naphthaleneacetic acid; Α-naphthaleneacetic acid; 1-Naphthaleneacetic acid; (naphth-1-yl)acetic acid; I+/--Naphthylacetic acid; (Naphthalen-1-yl)acetate; 2-(1-naphtyl)acetic acid; alpha-Naphthaleneacetate; (1-naphthyl)acetic acid; NAPHTHALEN-1-yl-acetate; Kyselina 1-naftyloctova; 1-naphthyl acetic acid; Acide naphthylacetique; Naphthyl-1-essigsaeure; NAPHTHALENEACETIC ACID; Naphthalene-1-acetate; 1-Naphthylessigsaeure; alpha-Naphthylacetate; Acide naphtylacetique; 1-Naphthylacetic acid; a-Naphthylacetic acid; Α-naphthylacetic acid; Naphyl-1-essigsaeure; a-Naphthaleneacetate; 1-Naphthaleneacetate; naphthyl acetic acid; Α-naphthaleneacetate; Naphthylacetic acid; Fruitone (Salt/Mix); a-Naphthylacetate; 1-Naphthylacetate; Α-naphthylacetate; UNII-33T7G7757C; Stimolante 66f; WLN: L66J B1VQ; Tox21_111051_1; Transplantone; Oprea1_374703; Tox21_111051; Tox21_400007; Niagara-Stik; NAA (auxin); Galle-Donau; CAS-86-87-3; .alpha.-NAA; Pimacol-Sol; 33T7G7757C; Liqui-stik; Fruitone N; Rhizopon B; Stop-Drop; Fruit Fix; Planofixe; alpha-NAA; AI3-16113; RAIZON 05; Fruitofix; Klingtite; Alphaspra; Regenasol; Primacol; Planofix; Phyomone; Hormofix; Nafusaku; Rhodofix; Appl-set; Tre-hold; Floramon; [3H]-NAA; Pomoxon; Plucker; Vardhak; Celmone; Stafast; Tip-Off; Nu-Tone; Agronaa; Phymone; NAFTAL; Etifix; Biokor; Germon; Tekkam; Α-naa; Rasin; a-NAA; 1-NAA; Alman; N 10; 1lrh; N 40; STIK; ANU; NAA; NLA; 1-Naphthylacetic acid



数据库引用编号

24 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)

3 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

  • Hongling Zeng, Kaiwei He, Qin He, Liting Xu, Wei Zhang, Xiang Lu, Yongyan Tang, Xiaobo Zhu, Junjie Yin, Min He, Xuewei Chen, Weitao Li. Exogenous Indole-3-Acetic Acid Suppresses Rice Infection of Magnaporthe oryzae by Affecting Plant Resistance and Fungal Growth. Phytopathology. 2024 May; 114(5):1050-1056. doi: 10.1094/phyto-10-23-0365-kc. [PMID: 38709298]
  • Zhongyi Wang, Fengqi Li, Chunjing Feng, Dongpeng Zheng, Zhaojun Pang, Yue Ma, Ying Xu, Ce Yang, Xueren Li, Shouchun Peng, Zichuan Liu, Xin Mu. 1-Naphthaleneacetic Acid Improved the In Vitro Cell Culturing by Inhibiting Apoptosis. Advanced biology. 2024 Mar; 8(3):e2300593. doi: 10.1002/adbi.202300593. [PMID: 38221687]
  • Mebrahtom Welehaweria, Desta Berhe Sbhatu. In vitro micropropagation of Aloe elegans Tod. using offshoot cuttings. BMC research notes. 2023 Sep; 16(1):215. doi: 10.1186/s13104-023-06490-0. [PMID: 37700378]
  • Xinghua Xing, Chunxin Cao, Simeng Li, Haorang Wang, Zejun Xu, Yujun Qi, Fei Tong, Haidong Jiang, Xing Wang. α-naphthaleneacetic acid positively regulates soybean seed germination and seedling establishment by increasing antioxidant capacity, triacylglycerol mobilization and sucrose transport under drought stress. Plant physiology and biochemistry : PPB. 2023 Jul; 201(?):107890. doi: 10.1016/j.plaphy.2023.107890. [PMID: 37454467]
  • Yuping Xiong, Shuangyan Chen, Teng Wu, Kunlin Wu, Yuan Li, Xinhua Zhang, Jaime A Teixeira da Silva, Songjun Zeng, Guohua Ma. Shoot organogenesis and somatic embryogenesis from leaf and petiole explants of endangered Euryodendron excelsum. Scientific reports. 2022 11; 12(1):20506. doi: 10.1038/s41598-022-24744-y. [PMID: 36443391]
  • Chen Chen, Xuan-Min Wu, Liu Pan, Ya-Ting Yang, Hai-Bo Dai, Bing Hua, Min-Min Miao, Zhi-Ping Zhang. Effects of Exogenous α-Naphthaleneacetic Acid and 24-Epibrassinolide on Fruit Size and Assimilate Metabolism-Related Sugars and Enzyme Activities in Giant Pumpkin. International journal of molecular sciences. 2022 Oct; 23(21):. doi: 10.3390/ijms232113157. [PMID: 36361943]
  • Kaniz Wahida Sultana, Sumanta Das, Indrani Chandra, Anindita Roy. Efficient micropropagation of Thunbergia coccinea Wall. and genetic homogeneity assessment through RAPD and ISSR markers. Scientific reports. 2022 01; 12(1):1683. doi: 10.1038/s41598-022-05787-7. [PMID: 35102225]
  • Bushra Asad, Taimoor Khan, Faiza Zareen Gul, Muhammad Asad Ullah, Samantha Drouet, Sara Mikac, Laurine Garros, Manon Ferrier, Shankhamala Bose, Thibaut Munsch, Duangjai Tungmunnithum, Arnaud Lanoue, Nathalie Giglioli-Guivarc'h, Christophe Hano, Bilal Haider Abbasi. Scarlet Flax Linum grandiflorum (L.) In Vitro Cultures as a New Source of Antioxidant and Anti-Inflammatory Lignans. Molecules (Basel, Switzerland). 2021 Jul; 26(15):. doi: 10.3390/molecules26154511. [PMID: 34361665]
  • Natalia Nikonorova, Evan Murphy, Cassio Flavio Fonseca de Lima, Shanshuo Zhu, Brigitte van de Cotte, Lam Dai Vu, Daria Balcerowicz, Lanxin Li, Xiangpei Kong, Gieljan De Rop, Tom Beeckman, Jiří Friml, Kris Vissenberg, Peter C Morris, Zhaojun Ding, Ive De Smet. The Arabidopsis Root Tip (Phospho)Proteomes at Growth-Promoting versus Growth-Repressing Conditions Reveal Novel Root Growth Regulators. Cells. 2021 07; 10(7):. doi: 10.3390/cells10071665. [PMID: 34359847]
  • Mark J Henderson, Kathleen A Trychta, Shyh-Ming Yang, Susanne Bäck, Adam Yasgar, Emily S Wires, Carina Danchik, Xiaokang Yan, Hideaki Yano, Lei Shi, Kuo-Jen Wu, Amy Q Wang, Dingyin Tao, Gergely Zahoránszky-Kőhalmi, Xin Hu, Xin Xu, David Maloney, Alexey V Zakharov, Ganesha Rai, Fumihiko Urano, Mikko Airavaara, Oksana Gavrilova, Ajit Jadhav, Yun Wang, Anton Simeonov, Brandon K Harvey. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. Cell reports. 2021 04; 35(4):109040. doi: 10.1016/j.celrep.2021.109040. [PMID: 33910017]
  • Alelegne Yeshamebel Adugna, Tileye Feyissa, Fikresilasie Samuel Tasew. Optimization of growth regulators on in vitro propagation of Moringa stenopetala from shoot explants. BMC biotechnology. 2020 11; 20(1):60. doi: 10.1186/s12896-020-00651-w. [PMID: 33198744]
  • Ayane Moriyama, Chiho Yamaguchi, Shinichi Enoki, Yoshinao Aoki, Shunji Suzuki. Crosstalk Pathway between Trehalose Metabolism and Cytokinin Degradation for the Determination of the Number of Berries per Bunch in Grapes. Cells. 2020 10; 9(11):. doi: 10.3390/cells9112378. [PMID: 33138306]
  • Maryam Dehestani-Ardakani, Mohadeseh Hejazi, Kazem Kamali Aliabad. Indirect somatic embryogenesis of purple coneflower (Echinacea purpurea (L.) Moench): a medicinal-ornamental plant: evaluation of antioxidant enzymes activity and histological study. Molecular biology reports. 2020 Sep; 47(9):6621-6633. doi: 10.1007/s11033-020-05713-y. [PMID: 32803508]
  • Li Han, Xuan Zhou, Yiting Zhao, Shusheng Zhu, Lixia Wu, Yunlu He, Xiangrui Ping, Xinqi Lu, Wuying Huang, Jie Qian, Lina Zhang, Xi Jiang, Dan Zhu, Chongyu Luo, Saijie Li, Qian Dong, Qijing Fu, Kaiyuan Deng, Xin Wang, Lei Wang, Sheng Peng, Jinsong Wu, Weimin Li, Jiří Friml, Youyong Zhu, Xiahong He, Yunlong Du. Colonization of endophyte Acremonium sp. D212 in Panax notoginseng and rice mediated by auxin and jasmonic acid. Journal of integrative plant biology. 2020 Sep; 62(9):1433-1451. doi: 10.1111/jipb.12905. [PMID: 31912615]
  • Shuangyan Chen, Yuping Xiong, Teng Wu, Kunlin Wu, Jaime A Teixeira da Silva, Youhua Xiong, Songjun Zeng, Guohua Ma. Axillary shoot proliferation and plant regeneration in Euryodendron excelsum H. T. Chang, a critically endangered species endemic to China. Scientific reports. 2020 09; 10(1):14402. doi: 10.1038/s41598-020-71360-9. [PMID: 32873835]
  • Yanke Lu, Pengfei Li, Chunliu Yang, Yehong Han, Hongyuan Yan. One pot green synthesis of m-aminophenol-urea-glyoxal resin as pipette tip solid-phase extraction adsorbent for simultaneous determination of four plant hormones in watermelon juice. Journal of chromatography. A. 2020 Jul; 1623(?):461214. doi: 10.1016/j.chroma.2020.461214. [PMID: 32505267]
  • Narongpol Kaewchangwat, Eknarin Thanayupong, Suwatchai Jarussophon, Nakorn Niamnont, Teerapong Yata, Sagaw Prateepchinda, Onuma Unger, Bao-Hang Han, Khomson Suttisintong. Coumarin-Caged Compounds of 1-Naphthaleneacetic Acid as Light-Responsive Controlled-Release Plant Root Stimulators. Journal of agricultural and food chemistry. 2020 Jun; 68(23):6268-6279. doi: 10.1021/acs.jafc.0c00138. [PMID: 32396350]
  • Gaojie Li, Shiqi Hu, Jingjing Yang, Xuyao Zhao, Seisuke Kimura, Elizabeth A Schultz, Hongwei Hou. Establishment of an Agrobacterium mediated transformation protocol for the detection of cytokinin in the heterophyllous plant Hygrophila difformis (Acanthaceae). Plant cell reports. 2020 Jun; 39(6):737-750. doi: 10.1007/s00299-020-02527-x. [PMID: 32146519]
  • Teresa Hazubska-Przybył, Ewelina Ratajczak, Agata Obarska, Emilia Pers-Kamczyc. Different Roles of Auxins in Somatic Embryogenesis Efficiency in Two Picea Species. International journal of molecular sciences. 2020 May; 21(9):. doi: 10.3390/ijms21093394. [PMID: 32403374]
  • Silvia Dal Santo, Matthew R Tucker, Hwei-Ting Tan, Crista A Burbidge, Marianna Fasoli, Christine Böttcher, Paul K Boss, Mario Pezzotti, Christopher Davies. Auxin treatment of grapevine (Vitis vinifera L.) berries delays ripening onset by inhibiting cell expansion. Plant molecular biology. 2020 May; 103(1-2):91-111. doi: 10.1007/s11103-020-00977-1. [PMID: 32043226]
  • Hao Huang, Ying Wei, Yongjin Zhai, Kunxi Ouyang, Xiaoyang Chen, Longhua Bai. High frequency regeneration of plants via callus-mediated organogenesis from cotyledon and hypocotyl cultures in a multipurpose tropical tree (Neolamarkia Cadamba). Scientific reports. 2020 03; 10(1):4558. doi: 10.1038/s41598-020-61612-z. [PMID: 32165694]
  • Yafei Wang, Wenwen Liu, Hongqiu Wang, Qingguo Du, Zhiyuan Fu, Wen-Xue Li, Jihua Tang. ZmEHD1 Is Required for Kernel Development and Vegetative Growth through Regulating Auxin Homeostasis. Plant physiology. 2020 03; 182(3):1467-1480. doi: 10.1104/pp.19.01336. [PMID: 31857426]
  • Yanqing Liu, Li Tang, Can Wang, Jinting Li. NAA and 6-BA promote accumulation of oleanolic acid by JA regulation in Achyranthes bidentata Bl. PloS one. 2020; 15(2):e0229490. doi: 10.1371/journal.pone.0229490. [PMID: 32107496]
  • Ke-Dong Xu, Wei Wang, De-Shui Yu, Xiao-Li Li, Jia-Min Chen, Bo-Jin Feng, Ya-Wen Zhao, Meng-Jia Cheng, Xin-Xin Liu, Cheng-Wei Li. NAA at a high concentration promotes efficient plant regeneration via direct somatic embryogenesis and SE-mediated transformation system in Ranunculus sceleratus. Scientific reports. 2019 12; 9(1):18321. doi: 10.1038/s41598-019-54538-8. [PMID: 31797961]
  • Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular pharmacology. 2019 11; 96(5):629-640. doi: 10.1124/mol.119.115964. [PMID: 31515284]
  • Samuel Tuhaise, Jesca L Nakavuma, John Adriko, Kenneth Ssekatawa, Andrew Kiggundu. In vitro regeneration of Ugandan passion fruit cultivars from leaf discs. BMC research notes. 2019 Jul; 12(1):425. doi: 10.1186/s13104-019-4469-8. [PMID: 31311592]
  • Raif Ilktaç, Zinar Pınar Gümüş, Nur Aksuner. Development of rapid, sensitive and selective fluorimetric method for determination of 1-naphthalene acetic acid in cucumber by using magnetite-molecularly imprinted polymer. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2019 Jul; 218(?):62-68. doi: 10.1016/j.saa.2019.03.061. [PMID: 30954798]
  • Faïza Masmoudi-Allouche, Walid Kriaa, Noureddine Drira. Staminodes evolution and in vitro development innovation in date palm (Phoenix dactylifera L.). Comptes rendus biologies. 2019 Jun; 342(5-6):220-229. doi: 10.1016/j.crvi.2019.06.001. [PMID: 31400945]
  • Aseesh Pandey, Tarun Belwal, Sushma Tamta, I D Bhatt, R S Rawal. Phenolic compounds, antioxidant capacity and antimutagenic activity in different growth stages of in vitro raised plants of Origanum vulgare L. Molecular biology reports. 2019 Apr; 46(2):2231-2241. doi: 10.1007/s11033-019-04678-x. [PMID: 30756335]
  • Nathan A Snyder, Adam Kim, Louis Kester, Andrew N Gale, Christian Studer, Dominic Hoepfner, Silvio Roggo, Stephen B Helliwell, Kyle W Cunningham. Auxin-Inducible Depletion of the Essentialome Suggests Inhibition of TORC1 by Auxins and Inhibition of Vrg4 by SDZ 90-215, a Natural Antifungal Cyclopeptide. G3 (Bethesda, Md.). 2019 03; 9(3):829-840. doi: 10.1534/g3.118.200748. [PMID: 30670608]
  • Li An, Jingwei Ma, Dongmei Qin, Hong Wang, Yongliang Yuan, Honglian Li, Risong Na, Xujin Wu. Novel Strategy to Decipher the Regulatory Mechanism of 1-Naphthaleneacetic Acid in Strawberry Maturation. Journal of agricultural and food chemistry. 2019 Jan; 67(4):1292-1301. doi: 10.1021/acs.jafc.8b05233. [PMID: 30629884]
  • Qixun Nian, Lianfeng Ai, Dongmei Li, Xuelei Chen, Lei Zhang, Manman Wang, Xuesheng Wang. Rapid monitoring of plant growth regulators in bean sprouts via automated on-line polymeric monolith solid-phase extraction coupled with liquid chromatography tandem mass spectrometry. Analytical and bioanalytical chemistry. 2018 Nov; 410(27):7239-7247. doi: 10.1007/s00216-018-1334-x. [PMID: 30151683]
  • Yaoxia Chen, Xinjing Li, Jing Bai, Fang Shi, Tengyan Xu, Qingqiu Gong, Zhimou Yang. A supramolecular hydrogel for spatial-temporal release of auxin to promote plant root growth. Chemical communications (Cambridge, England). 2018 Oct; 54(83):11721-11724. doi: 10.1039/c8cc05999c. [PMID: 30272064]
  • Sijie Zheng, Man He, Beibei Chen, Bin Hu. Melamine-based porous organic polymers inline solid phase extraction coupled with high performance liquid chromatography for the analysis of phytohormones in juice samples. Journal of chromatography. A. 2018 Sep; 1567(?):64-72. doi: 10.1016/j.chroma.2018.07.003. [PMID: 30100016]
  • Xiao-Fei Han, Juan Chen, Yan-Ping Shi. N-doped carbon nanotubes-reinforced hollow fiber solid-phase microextraction coupled with high performance liquid chromatography for the determination of phytohormones in tomatoes. Talanta. 2018 Aug; 185(?):132-140. doi: 10.1016/j.talanta.2018.03.063. [PMID: 29759179]
  • Maolin Zhang, Xiaoduo Lu, Cuiling Li, Bing Zhang, Chunyi Zhang, Xian-Sheng Zhang, Zhaojun Ding. Auxin Efflux Carrier ZmPGP1 Mediates Root Growth Inhibition under Aluminum Stress. Plant physiology. 2018 06; 177(2):819-832. doi: 10.1104/pp.17.01379. [PMID: 29720555]
  • Mariana Sánchez-Ramos, Silvia Marquina Bahena, Antonio Romero-Estrada, Antonio Bernabé-Antonio, Francisco Cruz-Sosa, Judith Gonzálesssz-Christen, Juan José Acevedo-Fernández, Irene Perea-Arango, Laura Alvarez. Establishment and Phytochemical Analysis of a Callus Culture from Ageratina pichinchensis (Asteraceae) and Its Anti-Inflammatory Activity. Molecules (Basel, Switzerland). 2018 May; 23(6):. doi: 10.3390/molecules23061258. [PMID: 29799442]
  • Xing Hua Xing, Ze Jun Xui, Yu Jun Qi, Xiao Jun Wang, Dong Lei Sun, Neng Fei Bian, Xing Wang. [Effect of exogenous α-naphthaleneacetic acid on carbon metabolism of soybean under drought stress at flowering stage]. Ying yong sheng tai xue bao = The journal of applied ecology. 2018 Apr; 29(4):1215-1224. doi: 10.13287/j.1001-9332.201804.022. [PMID: 29726231]
  • Nadeem Muhammad, Qamar Subhani, Fenglian Wang, Chaoyan Lou, Junwei Liu, Yan Zhu. Simultaneous determination of two plant growth regulators in ten food samples using ion chromatography combined with QuEChERS extraction method (IC-QuEChERS) and coupled with fluorescence detector. Food chemistry. 2018 Feb; 241(?):308-316. doi: 10.1016/j.foodchem.2017.08.112. [PMID: 28958533]
  • Tingting Liu, Fei Luo, Zhenyao Wang, Yuqin Li. The enhanced biomass and lipid accumulation in Coccomyxa subellipsoidea with an integrated treatment strategy initiated by brewery effluent and phytohormones. World journal of microbiology & biotechnology. 2018 Jan; 34(2):25. doi: 10.1007/s11274-018-2408-9. [PMID: 29330693]
  • Yanrong Liu, Kexin Wang, Dayong Li, Jianping Yan, Wanjun Zhang. Enhanced Cold Tolerance and Tillering in Switchgrass (Panicum virgatum L.) by Heterologous Expression of Osa-miR393a. Plant & cell physiology. 2017 Dec; 58(12):2226-2240. doi: 10.1093/pcp/pcx157. [PMID: 29069481]
  • Qionghui Fei, Shaodong Wei, Zhaoyang Zhou, Huanhuan Gao, Xiaofeng Li. Adaptation of root growth to increased ambient temperature requires auxin and ethylene coordination in Arabidopsis. Plant cell reports. 2017 Sep; 36(9):1507-1518. doi: 10.1007/s00299-017-2171-7. [PMID: 28660363]
  • Christopher P Keller. Leaf expansion in Phaseolus: transient auxin-induced growth increase. Physiologia plantarum. 2017 Aug; 130(4):580-589. doi: 10.1111/j.1399-3054.2007.00916.x. [PMID: 29200506]
  • Paweł Kubica, Agnieszka Szopa, Halina Ekiert. Production of verbascoside and phenolic acids in biomass of Verbena officinalis L. (vervain) cultured under different in vitro conditions. Natural product research. 2017 Jul; 31(14):1663-1668. doi: 10.1080/14786419.2017.1286477. [PMID: 28278649]
  • Misaki Ishibashi, Hiroki Yoshikawa, Yuichi Uno. Expression Profiling of Strawberry Allergen Fra a during Fruit Ripening Controlled by Exogenous Auxin. International journal of molecular sciences. 2017 Jun; 18(6):. doi: 10.3390/ijms18061186. [PMID: 28574483]
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