Relevant bibliographies by topics / Phenylacetic acids

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Phenylacetic acids'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Phenylacetic acids"

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Lamas-Maceiras, Mónica, Inmaculada Vaca, Esther Rodríguez, Javier Casqueiro, and Juan F. Martín. "Amplification and disruption of the phenylacetyl-CoA ligase gene of Penicillium chrysogenum encoding an aryl-capping enzyme that supplies phenylacetic acid to the isopenicillin N-acyltransferase." Biochemical Journal 395, no. 1 (2006): 147–55. http://dx.doi.org/10.1042/bj20051599.

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A gene, phl, encoding a phenylacetyl-CoA ligase was cloned from a phage library of Penicillium chrysogenum AS-P-78. The presence of five introns in the phl gene was confirmed by reverse transcriptase-PCR. The phl gene encoded an aryl-CoA ligase closely related to Arabidopsis thaliana 4-coumaroyl-CoA ligase. The Phl protein contained most of the amino acids defining the aryl-CoA (4-coumaroyl-CoA) ligase substrate-specificity code and differed from acetyl-CoA ligase and other acyl-CoA ligases. The phl gene was not linked to the penicillin gene cluster. Amplification of phl in an autonomous repli
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Drmanic, Sasa, Bratislav Jovanovic, and Milica Misic-Vukovic. "A comparative LFER study of the reactivity of pyridineacetic, pyridineacetic acids N-oxide and substituted phenylacetic acids with diazodiphenylmethane in various alcohols." Journal of the Serbian Chemical Society 65, no. 12 (2000): 847–56. http://dx.doi.org/10.2298/jsc0012847d.

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Rate constants have been determined for the reactions of diazodiphenylmethane (DDM) with 3- and 4-pyridineacetic acid, 3- and 4-pyridineacetic acid N-oxide and some meta- and para-substituted phenylacetic acids in twelve alcohols. The determined rate constants, together with literature data, were used for calculation of Hammett ? values in a series of alcohols. Secondary ? constants have been calculated for substituents in meta and para-position of phenylacetic acids not given in literature, and also ? constants for 3N, 3N-O, 4N and 4N-O in pyridineacetic acids, in alcohols used. The transmiss
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Ribeiro da Silva, Manuel A. V., Ana I. M. C. Lobo Ferreira, Luı´s M. Spencer S. Lima, and Sandra M. M. Sousa. "Thermochemistry of phenylacetic and monochlorophenylacetic acids." Journal of Chemical Thermodynamics 40, no. 2 (2008): 137–45. http://dx.doi.org/10.1016/j.jct.2007.07.010.

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Kamat, Shrivallabh P., Asha M. D'Souza, Shashikumar K. Paknikar, and Philip S. Beauchamp. "A Convenient One-Pot Synthesis of 4-Methyl-3-Phenyl-, 3-Aryl- and 3-Aryl-4-Phenylcoumarins." Journal of Chemical Research 2002, no. 5 (2002): 242–46. http://dx.doi.org/10.3184/030823402103171834.

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Thermal condensation of 2′-hydroxyacetophenones 1a–e with phenylacetic acid 2a in refluxing diphenyl ether gives 4-methyl-3-phenylcoumarins 3a–e. Similarly, reaction of 2-hydroxybenzaldehydes 1f–m and 2-hydroxybenzo-phenones 1n–p with phenylacetic acids 2a–d gives the corresponding 3-arylcoumarins 3f–m and 3-aryl-4-phenylcoumarins 3n–p respectively. Formation of esters 4 and 5 and benzofuran 6 is also observed.
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Do, Nhan T., Khoa M. Tran, Hao T. Phan, Tuong A. To, Tung T. Nguyen, and Nam T. S. Phan. "Functionalization of activated methylene C–H bonds with nitroarenes and sulfur for the synthesis of thioamides." Organic & Biomolecular Chemistry 17, no. 40 (2019): 8987–91. http://dx.doi.org/10.1039/c9ob01751h.

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Wang, Xinchao, Hang Wang, Chunlin Zhou, Lei Yang, Lei Fu, and Gang Li. "Native carboxyl group-assisted C–H acetoxylation of hydrocinnamic and phenylacetic acids." Chemical Communications 58, no. 32 (2022): 4993–96. http://dx.doi.org/10.1039/d2cc00459c.

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Serra, Stefano, Antonio Castagna, Stefano Marzorati, and Mattia Valentino. "Biotransformation of the Proteogenic Amino Acids Phenylalanine, Tyrosine and Tryptophan by Yarrowia Species: An Application to the Preparative Synthesis of Natural Phenylacetic Acid." Catalysts 12, no. 12 (2022): 1638. http://dx.doi.org/10.3390/catal12121638.

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The biotransformation of the aromatic amino acids phenylalanine, tyrosine and tryptophan originates a number of bioactive compounds. Yeasts are the most used microorganisms for the transformation of (L)-phenylalanine into the flavour phenylethanol. Here, we reported a study on the biotransformation of the proteogenic aminoacids phenylalanine, tyrosine and tryptophan by yeast strains belonging to Yarrowia genus. We found that the latter microorganisms, in high aerobic conditions, metabolise the aromatic amino acids (L)-phenylalanine and (L)-tyrosine with the almost exclusive formation of phenyl
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Pinto, Andrea, Immacolata Serra, Diego Romano, et al. "Preparation of Sterically Demanding 2,2-Disubstituted-2-Hydroxy Acids by Enzymatic Hydrolysis." Catalysts 9, no. 2 (2019): 113. http://dx.doi.org/10.3390/catal9020113.

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Preparation of optically-pure derivatives of 2-hydroxy-2-(3-hydroxyphenyl)-2-phenylacetic acid of general structure 2 was accomplished by enzymatic hydrolysis of the correspondent esters. A screening with commercial hydrolases using the methyl ester of 2-hydroxy-2-(3-hydroxyphenyl)-2-phenylacetic acid (1a) showed that crude pig liver esterase (PLE) was the only preparation with catalytic activity. Low enantioselectivity was observed with substrates 1a–d, whereas PLE-catalysed hydrolysis of 1e proceeded with good enantioselectivity (E = 28), after optimization. Enhancement of the enantioselecti
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Grieb, Paweł, Tomasz Kryczka, Radosław Wójtowicz, Jerzy Kawiak, and Zygmunt Kazimierczuk. "5'-Esters of 2'-deoxyadenosine and 2-chloro-2'-deoxyadenosine with cell differentiation-provoking agents." Acta Biochimica Polonica 49, no. 1 (2002): 129–37. http://dx.doi.org/10.18388/abp.2002_3829.

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Phenylacetic and retinoic acids are carboxyacidic cell differentiating agents displaying anticancer activities. We report on a new class of compounds including the 5'-esters of 2'-deoxyadenosine (dA) or 2-chloro-2'-deoxyadenosine (cladribine, 2CdA) and the aforementioned acids. The rationale behind the synthesis of these esters was that if they are hydrolyzed inside the lymphoid cells, either dA will be removed from the intracellular environment by deamination, or 2CdA will be phosphorylated and accumulated. In either case targetted delivery of the differentiating agent to the lymphoid cells m
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Mohamed, Magdy, Wael Ismail, Johann Heider, and Georg Fuchs. "Aerobic metabolism of phenylacetic acids in Azoarcus evansii." Archives of Microbiology 178, no. 3 (2002): 180–92. http://dx.doi.org/10.1007/s00203-002-0438-y.

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Dissertations / Theses on the topic "Phenylacetic acids"

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Tchibouanga, Remi Rolland Ngoma. "Salts and cocrystals of substituted phenylacetic acids." Thesis, Cape Peninsula University of Technology, 2018. http://hdl.handle.net/20.500.11838/2857.

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Thesis (Master of Applied Science in Chemistry)--Cape Peninsula University of Technology, 2018.<br>The prediction of the single crystal structure that will form due to the combination of two or more compounds to form a multicomponent crystal is one of the important areas of research in crystal engineering. Since these compounds display different properties when combined as a single crystal, knowledge of synthesis and design of the resulting compound is essential. The formation of a multicomponent crystal, such as a salt or a cocrystal generally depends on the complementarity of the functional
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Tischler, Dirk, Michel Oelschlägel, Juliane Zimmerling, and Michael Schlömann. "Neue Wege in der Weißen Biotechnologie." Technische Universitaet Bergakademie Freiberg Universitaetsbibliothek "Georgius Agricola", 2016. http://nbn-resolving.de/urn:nbn:de:bsz:105-qucosa-210778.

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Mikroorganismen sind in der Lage, zahlreiche Xenobiotika abzubauen. Dazu nutzen sie unter aeroben Bedingungen oft einleitend Oxygenasen. Durch diese kann molekularer Luftsauerstoff aktiviert und auf organische Moleküle übertragen werden. Danach können die Verbindungen in den Metabolismus der Mikroorganismen eingeschleust und teils oder vollständig abgebaut werden. Am Beispiel des Styrols zeigen wir hier eine solche Abbauroute und wie wir diese biotechnologisch nutzen können, um interessante Verbindungen zu synthetisieren. Zielmoleküle der gesamten Enzymkaskade sind dabei diverse Phenylessigsäu
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Tischler, Dirk, Michel Oelschlägel, Juliane Zimmerling, and Michael Schlömann. "Neue Wege in der Weißen Biotechnologie." TU Bergakademie Freiberg, 2015. https://tubaf.qucosa.de/id/qucosa%3A23081.

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Mikroorganismen sind in der Lage, zahlreiche Xenobiotika abzubauen. Dazu nutzen sie unter aeroben Bedingungen oft einleitend Oxygenasen. Durch diese kann molekularer Luftsauerstoff aktiviert und auf organische Moleküle übertragen werden. Danach können die Verbindungen in den Metabolismus der Mikroorganismen eingeschleust und teils oder vollständig abgebaut werden. Am Beispiel des Styrols zeigen wir hier eine solche Abbauroute und wie wir diese biotechnologisch nutzen können, um interessante Verbindungen zu synthetisieren. Zielmoleküle der gesamten Enzymkaskade sind dabei diverse Phenylessigsäu
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Levandowski, Mariana Negrelli. "ESTUDO CONFORMACIONAL DE DERIVADOS DO ÁCIDO FENILACÉTICO EMPREGANDO CÁLCULOS TEÓRICOS E AS ESPECTROSCOPIAS DE RESSONÂNCIA MAGNÉTICA NUCLEAR E INFRAVERMELHO." UNIVERSIDADE ESTADUAL DE PONTA GROSSA, 2017. http://tede2.uepg.br/jspui/handle/prefix/12.

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Made available in DSpace on 2017-07-20T12:40:20Z (GMT). No. of bitstreams: 1 Mariana_N_Levandowski.pdf: 3613595 bytes, checksum: 6d13f04a1872ade8572c9eae481770c6 (MD5) Previous issue date: 2017-02-13<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>This study presents a theoretical and experimental analysis of the conformational equilibrium of phenylacetic acid and its derivatives, namely: o-fluorophenylacetic, ochlorophenylacetic, o-bromophenylacetic, o-nitrophenylacetic, hydroxyphenylacetic, m-fluorophenylacetic, p-fluorophenylacetic, p-nitrophenylacetic, p-hydroxyphenylac
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Mei-hua, Shiu, and 徐美華. "Effect of Phenylacetic Acid Analogs on Differentiation." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/33940116784148282010.

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碩士<br>中國醫藥學院<br>藥物化學研究所<br>89<br>In order to develop the novel cell differentiation agents, a series of phenylacetic acid analogs was screened for their differentiation and anti-proliferation activities of HL-60 cells. Compounds 10-1 and 11-1 were found to be the most effective to differentiate and to be the most effective to potentate the induction of differentiation by all-trans retinoic acid (ATRA). Therefore the further studies were carried out to evaluate their effects on the cell cycle and cell surface antigen expression of HL-60 cells. When treatment of compounds 10-1 and 11-
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Law, Adrienne. "Structural and functional characterization of PaaK1 & PaaK2: phenylacetate CoA ligase paralogs from Burkholderia cenocepacia J2315." Thesis, 2010. http://hdl.handle.net/1828/3613.

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Aromatic compounds comprise approximately 25% of the Earth`s biomass. Accordingly, turnover of these thermostable compounds is essential to the biogeochemical carbon cycle. Specialized microbial enzymatic pathways are largely responsible for mineralization of aromatic compounds, and are extensively studied for bioremediation purposes. The phenylacetic acid degradation pathway (PAA) is of particular interest as it is utilized for degradation of a multitude of aromatic compounds, including environmental pollutants, and appears to be widely distributed among bacteria. Intriguingly, the PAA pathwa
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Hamlin, Jason. "Regulation of phenylacetic acid degradation in Burkholderia cenocepacia K56-2." 2009. http://hdl.handle.net/1993/21488.

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Liu, Su Zhen, and 劉夙真. "Synthesis of substituted phenylacetic acid derivatives as cell differentiation inducer." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/99151209257262803502.

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Cook, SD. "A comparison of the biosynthesis of indole-3-acetic acid and phenylacetic acid." Thesis, 2018. https://eprints.utas.edu.au/28357/1/Cook_whole_thesis.pdf.

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The biosynthesis of the auxin, indole-3-acetic acid (IAA), has been well studied in recent years. It is now accepted that the indole-3-pyruvate (IPyA) pathway is the main IAA biosynthetic route and is responsible for the majority of IAA produced in plants. This pathway involves the transamination of the amino acid, tryptophan (Trp), to IPyA by the TAR (TRYPTOPHAN AMINOTRANSFERASE RELATED) enzymes, followed by the oxidative decarboxylation of IPyA to IAA by the YUCCA proteins. Recently it has been suggested that the TARs and the YUCCAs are also responsible for the biosynthesis of a less well-s
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Pribytkova, Tatiana. "The attenuated virulence of a Burkholderia cenocepacia K56-2 paaABCDE mutant is due to inhibition of quorum sensing by release of phenylacetic acid." 2014. http://hdl.handle.net/1993/23961.

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The phenylacetic acid degradation pathway of Burkholderia cenocepacia is necessary for full pathogenicity of B. cenocepacia in nematode; however, the reasons of such requirements are unknown. Unlike wild type B. cenocepacia, a deletion mutant of the phenylacetyl-CoA monooxygenase complex (ΔpaaABCDE) released phenylacetic acid extracellularly in conditions that allow infection in Caenorhabditis elegans. Addition of phenylacetic acid further decreased the pathogenicity of the ΔpaaABCDE, which cannot metabolize phenylacetic acid, but did not affect the wild type, due to phenylacetic acid consumpt
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Books on the topic "Phenylacetic acids"

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Fisher, Melvin Philip. Synthesis of Some N-Substituted Alpha-amino-alpha-phenylacetic Acid Ester Derivatives. Creative Media Partners, LLC, 2021.

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Book chapters on the topic "Phenylacetic acids"

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Schulz, Anna, and Joachim Jankowski. "Phenylacetic Acid." In Uremic Toxins. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118424032.ch7.

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Holze, Rudolf. "Ionic conductance of phenylacetic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_544.

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Madan, Sapana S., and Kailas L. Wasewar. "Removal of Phenylacetic Acid from Aqueous Streams." In Springer Proceedings in Energy. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-47257-7_19.

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Holze, Rudolf. "Ionic conductivities of Ch-Cl · phenylacetic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_24.

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Mizutani, Naoki, Mitsuo Maehara, Chiemi Hayakawa, Tomoaki Kato, Kazuyoshi Watanabe, and Sakae Suzuki. "Hyperargininemia: Treatment with Sodium Benzoate and Phenylacetic Acid." In Guanidines. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4757-0752-6_19.

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Winkelmann, Jochen. "Diffusion coefficient of phenylacetic acid in carbon dioxide." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_744.

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Luengo, José M., Sagrario Arias, Mario Arcos, and Elías R. Olivera. "The Catabolism of Phenylacetic Acid and Other Related Molecules in Pseudomonas putida U." In Pseudomonas. Springer Netherlands, 2007. http://dx.doi.org/10.1007/978-1-4020-6097-7_6.

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Deokar, Sunil, Anuja R. Jadhav, Himanshu J. Patel, Saurabh Nitin Joglekar, and Pranav Deepak Pathak. "Removal of Organic Acid From Wastewater by Adsorption: A Case Study of Acetic Acid, Propionic Acid, and Phenylacetic Acid onto a Banana Peel." In Advances in Water and Wastewater Treatment. Apple Academic Press, 2024. http://dx.doi.org/10.1201/9781003515029-12.

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Boyd, G. V. "From α-(Hydroxyamino)phenylacetic Acid and Aldehydes." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-00581.

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Taber, Douglass F. "Substituted Benzenes: The Reddy Synthesis of Isofregenedadiol." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0062.

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Jianbo Wang of Peking University (Org. Lett. 2011, 13, 4988) and Patrick Y. Toullec and Véronique Michelet of Chimie ParisTech (Org. Lett. 2011, 13, 6086) developed conditions for the electrophilic acetoxylation of a benzene derivative 1. Seung Hwan Cho and Sukbok Chang of KAIST (J. Am. Chem. Soc. 2011, 133, 16382) and Brenton DeBoef of the University of Rhode Island (J. Am. Chem. Soc. 2011, 133, 19960) devised protocols for the electrophilic imidation of a benzene derivative 3. Vladimir V. Grushin of ICIQ Tarragona devised (J. Am. Chem. Soc. 2011, 133, 10999) a simple protocol for the cyanati
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Conference papers on the topic "Phenylacetic acids"

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Singh, Himanshi, Melanie Schnell та Pablo Pinacho. "MICROSOLVATION COMPLEXES OF α-METHOXY PHENYLACETIC ACID STUDIED BY MICROWAVE SPECTROSCOPY". У 2022 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2022. http://dx.doi.org/10.15278/isms.2022.fd10.

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Ladyka, A. A., A. V. Sosnovskaya, M. V. Chernikov, and D. I. Pozdnyakov. "ANTIAPOPTOTIC EFFECT OF PHENYLACETIC ACID AMIDE DERIVATIVES. EVALUATION OF THE STRUCTURE-ACTIVITY RELATIONSHIP." In MedChem-Russia 2021. 5-я Российская конференция по медицинской химии с международным участием «МедХим-Россия 2021». Издательство Волгоградского государственного медицинского университета, 2021. http://dx.doi.org/10.19163/medchemrussia2021-2021-363.

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Castiñeiras, Alfonso, Isabel García-Santos, and Rocío Torres-Iglesias. "Multicomponent Crystalline Solid Forms of Pyridinecarboxamides and DL-2-Hydroxy-2-phenylacetic Acid." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11729.

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Singh, Himanshi, Melanie Schnell, María Quesada-Moreno, Daniel Obenchain та Pablo Pinacho. "A BROADBAND MICROWAVE STUDY OF ISOLATED α-METHOXY PHENYLACETIC ACID AND ITS MICRO-SOLVATED COMPLEX". У 2020 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.ml11.

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Singh, Himanshi, Melanie Schnell, María Quesada-Moreno, Daniel Obenchain, and Pablo Pinacho. "A BROADBAND MICROWAVE STUDY OF ISOLATED &#945;-METHOXY PHENYLACETIC ACID: STRUCTURE, INTERNAL ROTATION, AND MICRO-SOLVATION." In 2021 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2021. http://dx.doi.org/10.15278/isms.2021.rd08.

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Perez, Veronica. "(CS-27-6) The plant metabolite phenylacetaldoxime (PAOx) is a precursor for the phytohormone phenylacetic acid (PAA)." In ASPB PLANT BIOLOGY 2020. ASPB, 2020. http://dx.doi.org/10.46678/pb.20.989659.

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Reports on the topic "Phenylacetic acids"

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จันทรทิณ, เพชรรัตน์, อัจฉริยา มณีน้อย та วีระเดช สุขเอียด. การคัดเลือกต้นเปล้าน้อยที่ได้จากการเพาะเลี้ยงเนื้อเยื่อ ให้ต้านทานต่อสารพิษของเชื้อรา Glomerella cingulata : รายงานผลการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 1999. https://doi.org/10.58837/chula.res.1999.81.

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โรคใบจุดของเปล้าน้อย (Croton sublyratus Kurz.) เกิดจากเชื้อรา Glomerella cingulata โดยมี Colletotrichum gloeosporioides เป็น imperfect stage เชื้อราสามารถเจริญและสร้างสปอร์ได้ดีบนอาหาร Czapek agar (CZA) น้ำหนักแห้งของเส้นใยและปริมาณสารสกัดจากเชื้อรามีมากที่สุดเมื่อเลี้องเชื้อในอาหารเหลว Czapek dox medium เป็นเวลา 4 วัน ในการทดสอบความเป็นพิษของสารสกัดจากเชื้อราโดยวิธีการหยดสารสกัดจากเชื้อราลงบนใบเปล้าน้อยพบว่า สารสกัดจากเชื้อราความเข้มข้น 10,000 มิลลิกรัมต่อลิตร สามารถทำให้เกิดอาการใบจุดกับเปล้าน้อยได้ จากการวิเคราะห์สารสกัดจากเชื้อราด้วยวิธี HPLC พบว่า เชื้อรา Glomerella cingulata สามารถสร้างส
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Morrison, Mark, and Joshuah Miron. Molecular-Based Analysis of Cellulose Binding Proteins Involved with Adherence to Cellulose by Ruminococcus albus. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7695844.bard.

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At the beginning of this project, it was clear that R. albus adhered tightly to cellulose and its efficient degradation of this polysaccharide was dependent on micromolar concentrations of phenylacetic acid (PAA) and phenylpropionic acid (PPA). The objectives for our research were: i) to identify how many different kinds of cellulose binding proteins are produced by Ruminococcus albus; ii) to isolate and clone the genes encoding some of these proteins from the same bacterium; iii) to determine where these various proteins were located and; iv) quantify the relative importance of these proteins
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