Статті в журналах з теми "Functions and Indoles"
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Moldvai, István, Eszter Gács-Baitz, and Csaba Szántay. "Chemistry of indoles carrying basic functions. I. Transformation of hydroxyindolones into indoles." Recueil des Travaux Chimiques des Pays-Bas 110, no. 11 (September 2, 2010): 437–40. http://dx.doi.org/10.1002/recl.19911101102.
Повний текст джерелаMOLDVAI, I., E. GACS-BAITZ, and C. SZANTAY. "ChemInform Abstract: Chemistry of Indoles Carrying Basic Functions. Part 1. Transformation of Hydroxyindolones into Indoles." ChemInform 23, no. 14 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199214194.
Повний текст джерелаChang, Chieh-Yu, Yu-Huan Lin, and Yen-Ku Wu. "Palladium-catalyzed N1-selective allylation of indoles with allylic alcohols promoted by titanium tetraisopropoxide." Chemical Communications 55, no. 8 (2019): 1116–19. http://dx.doi.org/10.1039/c8cc09817d.
Повний текст джерелаZhai, Yizhan, Xue Zhang, and Shengming Ma. "Stereoselective rhodium-catalyzed 2-C–H 1,3-dienylation of indoles: dual functions of the directing group." Chemical Science 12, no. 34 (2021): 11330–37. http://dx.doi.org/10.1039/d1sc02167b.
Повний текст джерелаSz�tay, Csaba, Istv� Moldval, Csaba Sz�tay Jr., and Csaba Sz�tay. "Chemistry of Indoles Carrying Basic Functions. Part II. Synthesis of 4-Substituted Cyclohept[c.d]indoles. A New Entry into the Ring System." HETEROCYCLES 34, no. 2 (1992): 219. http://dx.doi.org/10.3987/com-91-5803.
Повний текст джерелаVadaq, Nadira, Yue Zhang, Elise Meeder, Lisa Van de Wijer, Muhammad Hussein Gasem, Leo AB Joosten, Mihai G. Netea, et al. "Microbiome-Related Indole and Serotonin Metabolites are Linked to Inflammation and Psychiatric Symptoms in People Living with HIV." International Journal of Tryptophan Research 15 (January 2022): 117864692211268. http://dx.doi.org/10.1177/11786469221126888.
Повний текст джерелаMOLDVAI, I., C. JUN SZANTAY, and C. SZANTAY. "ChemInform Abstract: Chemistry of Indoles Carrying Basic Functions. Part 2. Synthesis of 4- Substituted Cyclohept(c,d)indoles. A New Entry into the Ring System." ChemInform 23, no. 27 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199227169.
Повний текст джерелаBock, Karl Walter. "Human and rodent aryl hydrocarbon receptor (AHR): from mediator of dioxin toxicity to physiologic AHR functions and therapeutic options." Biological Chemistry 398, no. 4 (April 1, 2017): 455–64. http://dx.doi.org/10.1515/hsz-2016-0303.
Повний текст джерелаDuvauchelle, Valentin, David Bénimélis, Patrick Meffre та Zohra Benfodda. "Catalyst-Free Site Selective Hydroxyalkylation of 5-Phenylthiophen-2-amine with α-Trifluoromethyl Ketones through Electrophilic Aromatic Substitution". Molecules 27, № 3 (29 січня 2022): 925. http://dx.doi.org/10.3390/molecules27030925.
Повний текст джерелаBershtein, L. M. "E. J. Pavlik, ed. Estrogens, progestins and their antagonists. - Vol. 2. Functions and mechanisms of action. - Boston, Basel, Berlin: Bikhauser, 1996 .-- 632 p." Problems of Endocrinology 44, no. 2 (September 23, 2019): 53–54. http://dx.doi.org/10.14341/probl199844253-54.
Повний текст джерелаRizwan, Komal, Ismat Majeed, Muhammad Bilal, Tahir Rasheed, Ahmad Shakeel, and Shahid Iqbal. "Phytochemistry and Diverse Pharmacology of Genus Mimosa: A Review." Biomolecules 12, no. 1 (January 5, 2022): 83. http://dx.doi.org/10.3390/biom12010083.
Повний текст джерелаBhargava, Shruti, Erik Merckelbach, Heidi Noels, Ashima Vohra, and Joachim Jankowski. "Homeostasis in the Gut Microbiota in Chronic Kidney Disease." Toxins 14, no. 10 (September 20, 2022): 648. http://dx.doi.org/10.3390/toxins14100648.
Повний текст джерелаTang, Jintian, Yukang Li, Leilei Zhang, Jintao Mu, Yangyang Jiang, Huilan Fu, Yafen Zhang, Haifeng Cui, Xiaoping Yu, and Zihong Ye. "Biosynthetic Pathways and Functions of Indole-3-Acetic Acid in Microorganisms." Microorganisms 11, no. 8 (August 12, 2023): 2077. http://dx.doi.org/10.3390/microorganisms11082077.
Повний текст джерелаMuyzhnek, E. L., S. V. Nikulin, A. D. Kaprin, L. A. Ashrafyan, N. I. Rozhkova, P. G. Labazanova, and V. I. Kiselev. "Antitumor Activity of Indole-3-carbinol in Breast Cancer Cells: Phenotype, Genetic Pattern, DNA Methylation Inversion." Biotekhnologiya 36, no. 2 (2020): 43–55. http://dx.doi.org/10.21519/0234-2758-2020-36-2-43-55.
Повний текст джерелаMayo, Juan C., and Rosa M. Sainz. "Melatonin from an Antioxidant to a Classic Hormone or a Tissue Factor: Experimental and Clinical Aspects 2019." International Journal of Molecular Sciences 21, no. 10 (May 21, 2020): 3645. http://dx.doi.org/10.3390/ijms21103645.
Повний текст джерелаLebrini, M., F. Robert, and C. Roos. "Adsorption Properties and Inhibition of C38 Steel Corrosion in Hydrochloric Solution by Some Indole Derivates: Temperature Effect, Activation Energies, and Thermodynamics of Adsorption." International Journal of Corrosion 2013 (2013): 1–13. http://dx.doi.org/10.1155/2013/139798.
Повний текст джерелаSouth, J. H. Exon, E. H. "DIETARY INDOLE-3-CARBINOL ALTERS IMMUNE FUNCTIONS IN RATS." Journal of Toxicology and Environmental Health, Part A 59, no. 4 (February 25, 2000): 271–79. http://dx.doi.org/10.1080/009841000156934.
Повний текст джерелаMueller, Carrie, Madhu Katepalli, Shelby Steinmeyer, Arul Jayaraman, and Robert Alaniz. "A role for microbiota metabolites in generation of mucosal dendritic cells (P3160)." Journal of Immunology 190, no. 1_Supplement (May 1, 2013): 61.5. http://dx.doi.org/10.4049/jimmunol.190.supp.61.5.
Повний текст джерелаTsuchiya, Hironori. "Comparative Effects ofα-,β-, andγ-Carbolines on Platelet Aggregation and Lipid Membranes". Journal of Toxicology 2011 (2011): 1–9. http://dx.doi.org/10.1155/2011/151596.
Повний текст джерелаPirog, T. P., D. V. Piatetska, N. O. Klymenko, and G. O. Iutynska. "Ways of Auxin Biosynthesis in Microorganisms." Mikrobiolohichnyi Zhurnal 84, no. 2 (November 28, 2022): 57–72. http://dx.doi.org/10.15407/microbiolj84.02.057.
Повний текст джерелаGwon, Seon-Yeong, Sue-Yeon Lee, Young-A. Son, and Sung-Hoon Kim. "Benzothiazole and indole based dye sensor: Optical switching functions with pH stimuli." Fibers and Polymers 13, no. 9 (November 2012): 1101–4. http://dx.doi.org/10.1007/s12221-012-1101-0.
Повний текст джерелаWu, Jun, Blair Moses Kamanga, Wenying Zhang, Yanhao Xu, and Le Xu. "Research progress of aldehyde oxidases in plants." PeerJ 10 (March 25, 2022): e13119. http://dx.doi.org/10.7717/peerj.13119.
Повний текст джерелаLee, Soon Goo, Kate Harline, Orchid Abar, Sakirat O. Akadri, Alexander G. Bastian, Hui-Yuan S. Chen, Michael Duan, et al. "The plant pathogen enzyme AldC is a long-chain aliphatic aldehyde dehydrogenase." Journal of Biological Chemistry 295, no. 40 (August 12, 2020): 13914–26. http://dx.doi.org/10.1074/jbc.ra120.014747.
Повний текст джерелаGilbert, Sarah, Alexander Poulev, William Chrisler, Kenneth Acosta, Galya Orr, Sarah Lebeis, and Eric Lam. "Auxin-Producing Bacteria from Duckweeds Have Different Colonization Patterns and Effects on Plant Morphology." Plants 11, no. 6 (March 8, 2022): 721. http://dx.doi.org/10.3390/plants11060721.
Повний текст джерелаWalter, Antje, Lorenzo Caputi, Sarah O’Connor, Karl-Heinz van Pée, and Jutta Ludwig-Müller. "Chlorinated Auxins—How Does Arabidopsis Thaliana Deal with Them?" International Journal of Molecular Sciences 21, no. 7 (April 7, 2020): 2567. http://dx.doi.org/10.3390/ijms21072567.
Повний текст джерелаBuneeva, O. A., O. V. Gnedenko, M. V. Medvedeva, A. S. Ivanov, and A. E. Medvedev. "Oxidative modification of glyceraldehyde-3-phosphate dehydrogenase influences its interaction with endogenous neuroprotector isatin." Biomeditsinskaya Khimiya 62, no. 2 (2016): 160–63. http://dx.doi.org/10.18097/pbmc20166202160.
Повний текст джерелаCao, Xu, Honglei Yang, Chunqiong Shang, Sang Ma, Li Liu, and Jialing Cheng. "The Roles of Auxin Biosynthesis YUCCA Gene Family in Plants." International Journal of Molecular Sciences 20, no. 24 (December 16, 2019): 6343. http://dx.doi.org/10.3390/ijms20246343.
Повний текст джерелаBakar-Ates, Filiz. "The Indole Phytoalexin Derivatives Induced a Significant Inhibition on Src Kinase Activity of Human Cancer Cells." Proceedings 22, no. 1 (August 6, 2019): 3. http://dx.doi.org/10.3390/proceedings2019022003.
Повний текст джерелаCrocetti, Letizia, Gabriella Guerrini, Maria Paola Giovannoni, Fabrizio Melani, Silvia Lamanna, Lorenzo Di Cesare Mannelli, Elena Lucarini, Carla Ghelardini, Junjie Wang, and Gerhard Dahl. "New Panx-1 Blockers: Synthesis, Biological Evaluation and Molecular Dynamic Studies." International Journal of Molecular Sciences 23, no. 9 (April 27, 2022): 4827. http://dx.doi.org/10.3390/ijms23094827.
Повний текст джерелаNegri, Stefano, Mauro Commisso, Linda Avesani, and Flavia Guzzo. "The case of tryptamine and serotonin in plants: a mysterious precursor for an illustrious metabolite." Journal of Experimental Botany 72, no. 15 (May 19, 2021): 5336–55. http://dx.doi.org/10.1093/jxb/erab220.
Повний текст джерелаShcherbakova, E. S., T. S. Sall, S. I. Sitkin, T. Ya Vakhitov, and E. V. Demyanova. "The role of bacterial metabolites derived from aromatic amino acids in non-alcoholic fatty liver disease." Almanac of Clinical Medicine 48, no. 6 (December 29, 2020): 375–86. http://dx.doi.org/10.18786/2072-0505-2020-48-066.
Повний текст джерелаPfalz, Marina, Michael Dalgaard Mikkelsen, Paweł Bednarek, Carl Erik Olsen, Barbara Ann Halkier, and Juergen Kroymann. "Metabolic Engineering in Nicotiana benthamiana Reveals Key Enzyme Functions in Arabidopsis Indole Glucosinolate Modification." Plant Cell 23, no. 2 (February 2011): 716–29. http://dx.doi.org/10.1105/tpc.110.081711.
Повний текст джерелаMano, Y., K. Nemoto, M. Suzuki, H. Seki, I. Fujii, and T. Muranaka. "The AMI1 gene family: indole-3-acetamide hydrolase functions in auxin biosynthesis in plants." Journal of Experimental Botany 61, no. 1 (November 3, 2009): 25–32. http://dx.doi.org/10.1093/jxb/erp292.
Повний текст джерелаGitis, Valeri, Alexander Derendyaev, Konstantin Petrov, Eugene Yurkov, Sergey Pirogov, Natalia Sergeeva, Boris Alekseev, and Andrey Kaprin. "Monotonic Functions Method and Its Application to Staging of Patients with Prostate Cancer According to Pretreatment Data." Applied Sciences 11, no. 9 (April 23, 2021): 3836. http://dx.doi.org/10.3390/app11093836.
Повний текст джерелаWatanabe, Shunsuke, Naoki Takahashi, Yuri Kanno, Hiromi Suzuki, Yuki Aoi, Noriko Takeda-Kamiya, Kiminori Toyooka, et al. "TheArabidopsisNRT1/PTR FAMILY protein NPF7.3/NRT1.5 is an indole-3-butyric acid transporter involved in root gravitropism." Proceedings of the National Academy of Sciences 117, no. 49 (November 20, 2020): 31500–31509. http://dx.doi.org/10.1073/pnas.2013305117.
Повний текст джерелаWang, Bing, Jinfang Chu, Tianying Yu, Qian Xu, Xiaohong Sun, Jia Yuan, Guosheng Xiong, Guodong Wang, Yonghong Wang, and Jiayang Li. "Tryptophan-independent auxin biosynthesis contributes to early embryogenesis in Arabidopsis." Proceedings of the National Academy of Sciences 112, no. 15 (March 23, 2015): 4821–26. http://dx.doi.org/10.1073/pnas.1503998112.
Повний текст джерелаReiter, Russel J., Dun Xian Tan, and Annia Galano. "Melatonin: Exceeding Expectations." Physiology 29, no. 5 (September 2014): 325–33. http://dx.doi.org/10.1152/physiol.00011.2014.
Повний текст джерелаPrudhomme, Michelle. "lndolocarbazoles as Anti-Cancer Agents." Current Pharmaceutical Design 3, no. 3 (June 1997): 265–90. http://dx.doi.org/10.2174/138161280303221007123245.
Повний текст джерелаKliebenstein, Daniel J., Jonathan Gershenzon, and Thomas Mitchell-Olds. "Comparative Quantitative Trait Loci Mapping of Aliphatic, Indolic and Benzylic Glucosinolate Production in Arabidopsis thaliana Leaves and Seeds." Genetics 159, no. 1 (September 1, 2001): 359–70. http://dx.doi.org/10.1093/genetics/159.1.359.
Повний текст джерелаLin, Hailing, Hongqiang Qiu, Yu Cheng, Maobai Liu, Maohua Chen, Youxiong Que, and Wancai Que. "Gelsemium elegans Benth: Chemical Components, Pharmacological Effects, and Toxicity Mechanisms." Molecules 26, no. 23 (November 25, 2021): 7145. http://dx.doi.org/10.3390/molecules26237145.
Повний текст джерелаLőrinczi, Bálint, Péter Simon, and István Szatmári. "Synthesis of Indole-Coupled KYNA Derivatives via C–N Bond Cleavage of Mannich Bases." International Journal of Molecular Sciences 23, no. 13 (June 28, 2022): 7152. http://dx.doi.org/10.3390/ijms23137152.
Повний текст джерелаQin, Miaomiao, Jing Wang, Tianyi Zhang, Xiangyang Hu, Rui Liu, Tian’e Gao, Shuaijing Zhao, et al. "Genome-Wide Identification and Analysis on YUCCA Gene Family in Isatis indigotica Fort. and IiYUCCA6-1 Functional Exploration." International Journal of Molecular Sciences 21, no. 6 (March 22, 2020): 2188. http://dx.doi.org/10.3390/ijms21062188.
Повний текст джерелаZhou, Cai-Jie, Bai-Ling Xie, Hai-Yang Han, Yin Wang, Yong-Hua Wang, Jing-Yi Hong, Yi-Xia Wei, et al. "Short-Chain Fatty Acids Promote Immunotherapy by Modulating Immune Regulatory Property in B Cells." Journal of Immunology Research 2021 (December 10, 2021): 1–13. http://dx.doi.org/10.1155/2021/2684361.
Повний текст джерелаGarty, Ben-Zion, Balu H. Athreya, Robert Wilmott, Nina Scarpa, Robert Doughty, and Steven D. Douglas. "Pulmonary Functions in Children With Progressive Systemic Sclerosis." Pediatrics 88, no. 6 (December 1, 1991): 1161–67. http://dx.doi.org/10.1542/peds.88.6.1161.
Повний текст джерелаStepanova, Anna N., Jeonga Yun, Linda M. Robles, Ondrej Novak, Wenrong He, Hongwei Guo, Karin Ljung, and Jose M. Alonso. "The Arabidopsis YUCCA1 Flavin Monooxygenase Functions in the Indole-3-Pyruvic Acid Branch of Auxin Biosynthesis." Plant Cell 23, no. 11 (November 2011): 3961–73. http://dx.doi.org/10.1105/tpc.111.088047.
Повний текст джерелаXia, Yan, Xiliang Zheng, Erkang Wang, Dongfeng Li, Ruibin Hou, and Jin Wang. "Synthesis of adenosine analogues with indole moiety as human adenosine A 3 receptor ligands." Royal Society Open Science 5, no. 2 (February 2018): 171596. http://dx.doi.org/10.1098/rsos.171596.
Повний текст джерелаKollath-Leiß, K., C. Bönniger, P. Sardar, and F. Kempken. "BEM46 Shows Eisosomal Localization and Association with Tryptophan-Derived Auxin Pathway in Neurospora crassa." Eukaryotic Cell 13, no. 8 (June 13, 2014): 1051–63. http://dx.doi.org/10.1128/ec.00061-14.
Повний текст джерелаOtten, Léon, and Anne Helfer. "Biological Activity of the rolB-like 5′ End of the A4-orf8 Gene from the Agrobacterium rhizogenes TL-DNA." Molecular Plant-Microbe Interactions® 14, no. 3 (March 2001): 405–11. http://dx.doi.org/10.1094/mpmi.2001.14.3.405.
Повний текст джерелаDixon, David P., Jonathan D. Sellars, and Robert Edwards. "The Arabidopsis phi class glutathione transferase AtGSTF2: binding and regulation by biologically active heterocyclic ligands." Biochemical Journal 438, no. 1 (July 27, 2011): 63–70. http://dx.doi.org/10.1042/bj20101884.
Повний текст джерелаNemoto, Keiichirou, Masamitsu Hara, Masashi Suzuki, Hikaru Seki, Toshiya Muranaka, and Yoshihiro Mano. "TheNtAMI1gene functions in cell division of tobacco BY-2 cells in the presence of indole-3-acetamide." FEBS Letters 583, no. 2 (December 31, 2008): 487–92. http://dx.doi.org/10.1016/j.febslet.2008.12.049.
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