Literatura académica sobre el tema "Functions and Indoles"
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Artículos de revistas sobre el tema "Functions and Indoles"
Moldvai, István, Eszter Gács-Baitz y Csaba Szántay. "Chemistry of indoles carrying basic functions. I. Transformation of hydroxyindolones into indoles". Recueil des Travaux Chimiques des Pays-Bas 110, n.º 11 (2 de septiembre de 2010): 437–40. http://dx.doi.org/10.1002/recl.19911101102.
Texto completoMOLDVAI, I., E. GACS-BAITZ y C. SZANTAY. "ChemInform Abstract: Chemistry of Indoles Carrying Basic Functions. Part 1. Transformation of Hydroxyindolones into Indoles." ChemInform 23, n.º 14 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199214194.
Texto completoChang, Chieh-Yu, Yu-Huan Lin y Yen-Ku Wu. "Palladium-catalyzed N1-selective allylation of indoles with allylic alcohols promoted by titanium tetraisopropoxide". Chemical Communications 55, n.º 8 (2019): 1116–19. http://dx.doi.org/10.1039/c8cc09817d.
Texto completoZhai, Yizhan, Xue Zhang y Shengming Ma. "Stereoselective rhodium-catalyzed 2-C–H 1,3-dienylation of indoles: dual functions of the directing group". Chemical Science 12, n.º 34 (2021): 11330–37. http://dx.doi.org/10.1039/d1sc02167b.
Texto completoSz�tay, Csaba, Istv� Moldval, Csaba Sz�tay Jr. y 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, n.º 2 (1992): 219. http://dx.doi.org/10.3987/com-91-5803.
Texto completoVadaq, 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 (enero de 2022): 117864692211268. http://dx.doi.org/10.1177/11786469221126888.
Texto completoMOLDVAI, I., C. JUN SZANTAY y 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, n.º 27 (21 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199227169.
Texto completoBock, Karl Walter. "Human and rodent aryl hydrocarbon receptor (AHR): from mediator of dioxin toxicity to physiologic AHR functions and therapeutic options". Biological Chemistry 398, n.º 4 (1 de abril de 2017): 455–64. http://dx.doi.org/10.1515/hsz-2016-0303.
Texto completoDuvauchelle, Valentin, David Bénimélis, Patrick Meffre y Zohra Benfodda. "Catalyst-Free Site Selective Hydroxyalkylation of 5-Phenylthiophen-2-amine with α-Trifluoromethyl Ketones through Electrophilic Aromatic Substitution". Molecules 27, n.º 3 (29 de enero de 2022): 925. http://dx.doi.org/10.3390/molecules27030925.
Texto completoBershtein, 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, n.º 2 (23 de septiembre de 2019): 53–54. http://dx.doi.org/10.14341/probl199844253-54.
Texto completoTesis sobre el tema "Functions and Indoles"
Bhasin, Jeffrey M. "Methylome Sequencing Reveals the Context-Specific Functions of DNA Methylation in Indolent Versus Aggressive Prostate Cancer". Case Western Reserve University School of Graduate Studies / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=case148120498969955.
Texto completoBrown, Asha. "Anion recognition and sensing by interlocked host structures incorporating porphyrin and indolo[2,3-a]carbazole functional groups". Thesis, University of Oxford, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543060.
Texto completoLindström, Ludvig. "How do functional riparian groups from northern Sweden respond to hydropeaking? : Short-term indoors study on germination, mortality and performance of Swedish riparian species from different species groups subjected to water treatments mimicking hydropeaking". Thesis, Umeå universitet, Institutionen för ekologi, miljö och geovetenskap, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-122394.
Texto completoMonroe-Augustus, Melanie. "Genetic approaches to elucidating the mechanisms of indole-3-acetic acid and indole-3-butyric acid function in Arabidopsis thaliana". Thesis, 2004. http://hdl.handle.net/1911/18669.
Texto completo"Structure function relationship study of Yuehchukene: a novel type non-oxygen estrogenic compound". Chinese University of Hong Kong, 1992. http://library.cuhk.edu.hk/record=b5895749.
Texto completoThesis (Ph.D.)--Chinese University of Hong Kong, 1992.
Includes bibliographical references (leaves 134-144).
Chapter Chapter One --- Introduction --- p.1
Chapter 1.1 --- Phytochemistry and Phylogeny --- p.1
Chapter 1.2 --- Biological Activity --- p.9
Chapter 1.3 --- Synthetic Estrogens and Anti-Estrogens --- p.14
Chapter 1.4 --- Estrogen Receptor and Anti-Estrogen Binding Site --- p.19
Chapter 1.5 --- Multiple and dissociated Biological Activity --- p.28
Chapter 1.6 --- A Future Role for Yuehchukene --- p.30
Chapter Chapter Two --- Materials and Methods --- p.35
Chapter 2.1 --- Chemical Synthesis --- p.35
Chapter 2.1.1 --- Synthesis of Yuehchukene --- p.35
Chapter 2.1.2 --- Substitution of Yuehchukene --- p.38
Chapter 2.1.2.1 --- Substitution at N-1' and N-5 --- p.38
Chapter 2.1.2.2 --- Substitution at C2-C5 --- p.45
Chapter 2.1.2.3 --- Saturation of C9-C10 Double Bond --- p.45
Chapter 2.1.2.4 --- Aromatic Hydroxylation --- p.45
Chapter 2.1.2.5 --- Synthesis of Benzofuran-3-HMBI --- p.47
Chapter 2.1.3 --- Stereo-selective Synthesis of R(+)- and S(-)-Camphor-yuehchukene --- p.47
Chapter 2.1.4 --- Instruments --- p.51
Chapter 2.2 --- Bioassay --- p.51
Chapter 2.2.1 --- Anti´ؤimplantation Activity --- p.52
Chapter 2.2.2 --- Uterotrophic Activity --- p.52
Chapter 2.2.3 --- Blue Test --- p.53
Chapter 2.2.4 --- Binding Assays --- p.54
Chapter 2.2.4.1 --- Uterine Cytosolic Estrogen Receptor Binding Assay --- p.54
Chapter 2.2.4.2 --- Liver Microsomal Fraction Anti-Estrogen Receptor Binding Assay --- p.55
Chapter 2.2.5 --- Enzyme Activity --- p.56
Chapter 2.2.5.1 --- Ornithine Decarboxylase Activity Assay --- p.56
Chapter 2.2.5.2 --- Glucose-6-Phosphate Dehydrogenase Activity Assay --- p.58
Chapter 2.2.6 --- Cell Culture --- p.59
Chapter 2.2.6.1 --- MCF-7 Cell Line --- p.59
Chapter 2.2.6.2 --- Growth Response Studies --- p.59
Chapter 2.3 --- Exhibit I --- p.61
Exhibit II --- p.62
Exhibit III --- p.63
Exhibit IV --- p.64
Exhibit V --- p.65
Chapter Chapter Three --- Results --- p.66
Chapter 3.1 --- Chemical Synthesis --- p.66
Chapter 3.1.1 --- Yuehchukene --- p.66
Chapter 3.1.2 --- Substitution of Yuehchukene --- p.67
Chapter 3.1.2.1 --- Substitution at N-1' and N-5 --- p.67
Chapter 3.1.2.2 --- Substitution at C2 and C5 --- p.69
Chapter 3.1.2.3 --- Saturation of C9-C10 Double Bond --- p.70
Chapter 3.1.2.4 --- Aromatic Hydroxylation --- p.71
Chapter 3.1.3 --- Stereo-selective Synthesis of R(+)- and S(-)-Camphor-yuehchukene --- p.72
Chapter 3.2 --- Bioassay --- p.72
Chapter 3.2.1 --- Anti-implantation Activity --- p.72
Chapter 3.2.2 --- Uterotrophic Activity --- p.87
Chapter 3.2.3 --- Blue Test --- p.88
Chapter 3.2.4 --- Binding Assays --- p.93
Chapter 3.2.4.1 --- Uterine Estrogen Receptor [3H]-Estradiol Binding Assay --- p.93
Chapter 3.2.4.2 --- Liver Microsomal Anti-Estrogen Binding Site [3H] -Tamoxifen Binding Assay --- p.93
Chapter 3.2.5 --- Enzyme Activity --- p.96
Chapter 3.2.5.1 --- Ornithine Decarboxylase Activity Assay --- p.96
Chapter 3.2.5.2 --- Glucose-6-Phosphate Dehydrogenase Activity Assay --- p.96
Chapter 3.2.6 --- MCF-7 Cell Growth Response --- p.99
Chapter Chapter Four --- Discussion --- p.102
Chapter 4.1 --- Species Specificity --- p.102
Chapter 4.2 --- Estrogenic Indoles --- p.104
Chapter 4.3 --- Conservative Structure --- p.108
Chapter 4.4 --- Hydroxylation Sites --- p.111
Chapter 4.5 --- Configuration and Constraints --- p.114
Chapter 4.6 --- Dissociated Responses --- p.128
Chapter 4.7 --- Summary --- p.132
References --- p.134
Weng, Yu-Ping y 翁羽平. "The proteins needed for indole induced biofilm formation and their functions in E. coli DH5α". Thesis, 2010. http://ndltd.ncl.edu.tw/handle/35091274753439763951.
Texto completo臺灣大學
生化科學研究所
98
ABSTRACT By using the two-dimensional gel method, we already discovered that when E. coli O157 was exposed to bacitracin, the expression of tryptophanase gene was induced through the EvgS/EvgA two-component system. Tryptophanase then converted tryptophan to indole,which caused biofilm formation as well as a series of related protein expression. In this study, we screened the E. coli DH5α transposon library mutants to find out which genes are crucial for indole induced biofilm formation. These results show that when yhiP, cyaA, trkA, phr, and fimE genes are disrupted by transposon, indole can not induce these mutant strains to form biofilm. By using complementary assays, we confirmed that these genes are truly necessary for Indole induced biofilm formation in E. coli DH5α. Besides, we also used the reporter gene analysis method to further confirm that indole can cause these genes expressions with the promoter activity of yhiP, cyaA increased up to 200%. Moreover, we also clarified the relationship between indole and expressions of some transcription factor genes upstream to these genes, as well as the influences of each kind of common antibiotic to the expressions of these genes. In addition, we also used other experiment material such as butanol to test if expressions of these genes also contribute to the resistence to the adverse circumstance when E. coli formed biofilm. Besides, the expression of B0363 can be induced byindole in E.coli. B0363 is an analogous protein of IcaA of staphylococcus, which is secreted to outside of cell after transcription. I also expressed and purified this protein successfully and made sure it has catalytic activity.
LeClere, Sherry. "Analysis of the function and metabolism of indole-3-acetic acid conjugates in Arabidopsis thaliana". Thesis, 2002. http://hdl.handle.net/1911/18102.
Texto completoChan, Tsung-Ta y 詹宗達. "Production of the fermentation broth of Ustilago maydis possessing anti-inflammation function using indole-3-acetic acid as marker". Thesis, 2012. http://ndltd.ncl.edu.tw/handle/25917905264842703441.
Texto completo國立臺灣大學
食品科技研究所
100
Ustilago maydis is a pathogen infecting on corn and induces tumor tissue formation. Althoug it is a pathogen, it is seen as a traditional cusine in Mexico. It can metabolize trytophan into indole-3-acetic acid (IAA) and pityriarubin with anti-inflammation bioactivity. Therefore, the goal of this research was to produce fermentation broth of Ustilago maydis possessing anti-inflammation function using indole-3-acetic acid as marker in a 5 L stirred tank fermentor. After optimization process, it was found that the fermentation process would produce 30.8±4.5 μg/ml IAA in the broth using PDB medium supplemented with 1g/L tryptophan and 20 g/L glucose with initial pH at 4. The optimal fermentation conditions in the stirred tank bioreactor are: agitation rate at 900 rpm; aeration rate at 0.5 vvm, and 24℃ for 32 h. Moreover, the broth (10%) can inhibit nitrite production up to 81.0±0.3% in RAW264.7 inflammation cell model.
PISCITELLI, FRANCESCO. "Design, synthesis and anti-HIV activity of new indolyl aryl sulfones (IASs): structure-activity relationship of substituents on the 2-carboxyamides function". Doctoral thesis, 2009. http://hdl.handle.net/11573/917534.
Texto completoLibros sobre el tema "Functions and Indoles"
service), SpringerLink (Online, ed. Functional Phthalocyanine Molecular Materials. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2010.
Buscar texto completoIndole: Synthesis, Functions and Reactions. Nova Science Publishers, Incorporated, 2019.
Buscar texto completoPratt, Bridget. Indole: Synthesis, Functions and Reactions. Nova Science Publishers, Incorporated, 2018.
Buscar texto completoMcCormick, Paul C. Intramedullary Spinal Cord Tumors. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190696696.003.0020.
Texto completoCapítulos de libros sobre el tema "Functions and Indoles"
Troxler, F. "Chemistry of Indoles Carrying Basic Functions". En Chemistry of Heterocyclic Compounds: A Series Of Monographs, 179–537. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186930.ch4.
Texto completoMaruyama, W., A. Ota, A. Takahashi, T. Nagatsu y M. Naoi. "Food-derived hetero-cyclic amines, 3-amino-1,4-dimethyl-5H-pyrido[4,3-b]indole and related amines, as inhibitors of monoamine metabolism". En Amine Oxidases: Function and Dysfunction, 327–33. Vienna: Springer Vienna, 1994. http://dx.doi.org/10.1007/978-3-7091-9324-2_43.
Texto completoOxenkrug, G. F., P. J. Requintina, R. M. Correa y A. Yuwiler. "The effect of 6-months l-deprenyl administration on pineal MAO-A and MAO-B activity and on the content of melatonin and related indoles in aged female Fisher 344N rats". En Amine Oxidases: Function and Dysfunction, 249–52. Vienna: Springer Vienna, 1994. http://dx.doi.org/10.1007/978-3-7091-9324-2_32.
Texto completoBockaert, J., L. Fagni, M. Sebben y A. Dumuis. "Pharmacological Characterization of Brain 5-HT4 Receptors: Relationship between the Effects of Indole, Benzamide and Azabicycloalkybenzimidazolone Derivatives". En Serotonin: Molecular Biology, Receptors and Functional Effects, 220–31. Basel: Birkhäuser Basel, 1991. http://dx.doi.org/10.1007/978-3-0348-7259-1_20.
Texto completoRai, Sanjay Kumar, Krishna Kumar Rai, Apoorva, Sushil Kumar y Shashi Pandey Rai. "Functional Genomics Approaches for Gene Discovery Related to Terpenoid Indole Alkaloid Biosynthetic Pathway in Catharanthus roseus". En Compendium of Plant Genomes, 155–73. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-89269-2_9.
Texto completoHarris, P. A. "10.24.4 Product Subclass 4: Pyrazino[1,2-a]indoles and Related Benzo-Fused Ring Systems". En Science of Synthesis: Knowledge Updates 2021/3. Stuttgart: Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-110-02056.
Texto completoIshchenko, Alexander A., Yurii L. Slominskii y Illia P. Sharanov. "High-efficiency polymethine dyes for passive Q-switch and mode locking of neodymium lasers". En NEW FUNCTIONAL SUBSTANCES AND MATERIALS FOR CHEMICAL ENGINEERING, 39–52. PH “Akademperiodyka”, 2021. http://dx.doi.org/10.15407/akademperiodyka.444.039.
Texto completoDe Luca, Vincenzo, Vonny Salim, Dylan Levac, Sayaka Masada Atsumi y Fang Yu. "Discovery and Functional Analysis of Monoterpenoid Indole Alkaloid Pathways in Plants". En Natural Product Biosynthesis by Microorganisms and Plants, Part A, 207–29. Elsevier, 2012. http://dx.doi.org/10.1016/b978-0-12-394290-6.00010-0.
Texto completoR. Surana, Khemchand, Ritesh B. Pawar, Ritesh A. Khairnar y Sunil K. Mahajan. "Protein Prenylation and Their Applications". En Modifications of Biomolecules [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.104700.
Texto completoTaber, Douglass F. "The Smith Synthesis of (−)-Nodulisporic Acid D". En Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0103.
Texto completoActas de conferencias sobre el tema "Functions and Indoles"
Susanti, Resti Julia, Evi Noviani y Fransiskus Fran. "Green’s function of the electric potential equation". En THE 4TH INDOMS INTERNATIONAL CONFERENCE ON MATHEMATICS AND ITS APPLICATION (IICMA 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0026050.
Texto completoТрофимов, Б., B. Trofimov, Н. Гусарова y N. Gusarova. "The development of original methodologies of directed synthesis of le-Carbs their analogs and precursors base donacetylene and its derivatives". En Topical issues of translational medicine: a collection of articles dedicated to the 5th anniversary of the day The creation of a department for biomedical research and technology of the Irkutsk Scientific Center Siberian Branch of RAS. Москва: INFRA-M Academic Publishing LLC., 2017. http://dx.doi.org/10.12737/conferencearticle_58be81ec92d17.
Texto completoYundari, Yundari, Nur'ainul Miftahul Huda, Udjianna Sekteria Pasaribu, Utriweni Mukhaiyar y Kurnia Novita Sari. "Stationary process in GSTAR(1;1) through kernel function approach". En THE 4TH INDOMS INTERNATIONAL CONFERENCE ON MATHEMATICS AND ITS APPLICATION (IICMA 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0016808.
Texto completoSultana, Sharmin, Md Sad Salabi Sawrav, Md Bokhtiar Rahma, Md Shohorab Hossain y Md Azizul Haque. "Isolation and Biochemical Characterization of Xylanase Enzyme Producing Bacteria from Goat Rumen". En International Conference on Emerging Trends in Engineering and Advanced Science. AIJR Publisher, 2022. http://dx.doi.org/10.21467/proceedings.123.1.
Texto completoWibowo, Supriyadi, V. Y. Kurniawan y Siswanto. "The relation between Fα – absolutely continuous of order α ∈ (0, 1) and function of bounded variation". En THE 4TH INDOMS INTERNATIONAL CONFERENCE ON MATHEMATICS AND ITS APPLICATION (IICMA 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0019249.
Texto completoFerraz, Marta, Paul E. Resta y Afonso O'neill. "Whole-body interaction in natural environments benefits children's cognitive function compared to sedentary interaction indoors". En AH '17: 8th Augmented Human International Conference. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3041164.3041177.
Texto completoManabe, S., H. Yanagisawa, S. Ishikawa, Y. Kitagawa, K. Tohyama, S. Abe y O. Wada. "TRYPTOPHAN PYROLYSIS PRODUCTS FOUND IN COOKED FOODS INHIBIT HUMAN PLATELET AGGREGATION BY INHIBITING CYCLOOXYGENASE". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643402.
Texto completoSopian, K., Adam M. Elradi, Shahrir Abdullah y K. V. Wong. "Heat Transfer and Pressure Drop Correlations for Double-Pass Solar Collector With and Without Porous Media". En ASME 2002 International Mechanical Engineering Congress and Exposition. ASMEDC, 2002. http://dx.doi.org/10.1115/imece2002-39542.
Texto completoD'Zmura, Michael y Geoffrey Iverson. "Color constancy: adaptation to the illumination environment". En Advances in Color Vision. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/acv.1992.fe2.
Texto completoFoust, Emine Celik. "Industry-Based Thermodynamics Case Study on Refrigeration Cycle". En ASME 2022 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/imece2022-88201.
Texto completoInformes sobre el tema "Functions and Indoles"
Chamovitz, A. Daniel y Georg Jander. Genetic and biochemical analysis of glucosinolate breakdown: The effects of indole-3-carbinol on plant physiology and development. United States Department of Agriculture, enero de 2012. http://dx.doi.org/10.32747/2012.7597917.bard.
Texto completoJander, Georg y Daniel Chamovitz. Investigation of growth regulation by maize benzoxazinoid breakdown products. United States Department of Agriculture, enero de 2015. http://dx.doi.org/10.32747/2015.7600031.bard.
Texto completoHubbard, Sarah M. y Bryan Hubbard. Investigation of Strategic Deployment Opportunities for Unmanned Aerial Systems (UAS) at INDOT. Purdue University, 2020. http://dx.doi.org/10.5703/1288284317126.
Texto completoLee, Jusang, John E. Haddock, Dario D. Batioja Alvarez y Reyhaneh Rahbar Rastegar. Quality Control and Quality Assurance of Asphalt Mixtures Using Laboratory Rutting and Cracking Tests. Purdue University, 2019. http://dx.doi.org/10.5703/1288284317087.
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