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Статті в журналах з теми "Functions and Indoles"
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 джерелаДисертації з теми "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.
Повний текст джерелаBrown, 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.
Повний текст джерелаLindström, 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.
Повний текст джерелаMonroe-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.
Повний текст джерела"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.
Повний текст джерелаThesis (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, та 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.
Повний текст джерела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.
Повний текст джерелаChan, Tsung-Ta, and 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.
Повний текст джерела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.
Повний текст джерелаКниги з теми "Functions and Indoles"
service), SpringerLink (Online, ed. Functional Phthalocyanine Molecular Materials. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2010.
Знайти повний текст джерелаIndole: Synthesis, Functions and Reactions. Nova Science Publishers, Incorporated, 2019.
Знайти повний текст джерелаPratt, Bridget. Indole: Synthesis, Functions and Reactions. Nova Science Publishers, Incorporated, 2018.
Знайти повний текст джерелаMcCormick, Paul C. Intramedullary Spinal Cord Tumors. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190696696.003.0020.
Повний текст джерелаЧастини книг з теми "Functions and Indoles"
Troxler, F. "Chemistry of Indoles Carrying Basic Functions." In 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.
Повний текст джерелаMaruyama, W., A. Ota, A. Takahashi, T. Nagatsu, and 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." In Amine Oxidases: Function and Dysfunction, 327–33. Vienna: Springer Vienna, 1994. http://dx.doi.org/10.1007/978-3-7091-9324-2_43.
Повний текст джерелаOxenkrug, G. F., P. J. Requintina, R. M. Correa, and 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." In Amine Oxidases: Function and Dysfunction, 249–52. Vienna: Springer Vienna, 1994. http://dx.doi.org/10.1007/978-3-7091-9324-2_32.
Повний текст джерелаBockaert, J., L. Fagni, M. Sebben, and A. Dumuis. "Pharmacological Characterization of Brain 5-HT4 Receptors: Relationship between the Effects of Indole, Benzamide and Azabicycloalkybenzimidazolone Derivatives." In 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.
Повний текст джерелаRai, Sanjay Kumar, Krishna Kumar Rai, Apoorva, Sushil Kumar, and Shashi Pandey Rai. "Functional Genomics Approaches for Gene Discovery Related to Terpenoid Indole Alkaloid Biosynthetic Pathway in Catharanthus roseus." In Compendium of Plant Genomes, 155–73. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-89269-2_9.
Повний текст джерелаHarris, P. A. "10.24.4 Product Subclass 4: Pyrazino[1,2-a]indoles and Related Benzo-Fused Ring Systems." In Science of Synthesis: Knowledge Updates 2021/3. Stuttgart: Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-110-02056.
Повний текст джерелаIshchenko, Alexander A., Yurii L. Slominskii, and Illia P. Sharanov. "High-efficiency polymethine dyes for passive Q-switch and mode locking of neodymium lasers." In NEW FUNCTIONAL SUBSTANCES AND MATERIALS FOR CHEMICAL ENGINEERING, 39–52. PH “Akademperiodyka”, 2021. http://dx.doi.org/10.15407/akademperiodyka.444.039.
Повний текст джерелаDe Luca, Vincenzo, Vonny Salim, Dylan Levac, Sayaka Masada Atsumi, and Fang Yu. "Discovery and Functional Analysis of Monoterpenoid Indole Alkaloid Pathways in Plants." In 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.
Повний текст джерелаR. Surana, Khemchand, Ritesh B. Pawar, Ritesh A. Khairnar, and Sunil K. Mahajan. "Protein Prenylation and Their Applications." In Modifications of Biomolecules [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.104700.
Повний текст джерелаTaber, Douglass F. "The Smith Synthesis of (−)-Nodulisporic Acid D." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0103.
Повний текст джерелаТези доповідей конференцій з теми "Functions and Indoles"
Susanti, Resti Julia, Evi Noviani, and Fransiskus Fran. "Green’s function of the electric potential equation." In THE 4TH INDOMS INTERNATIONAL CONFERENCE ON MATHEMATICS AND ITS APPLICATION (IICMA 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0026050.
Повний текст джерелаТрофимов, Б., B. Trofimov, Н. Гусарова, and N. Gusarova. "The development of original methodologies of directed synthesis of le-Carbs their analogs and precursors base donacetylene and its derivatives." In 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.
Повний текст джерелаYundari, Yundari, Nur'ainul Miftahul Huda, Udjianna Sekteria Pasaribu, Utriweni Mukhaiyar, and Kurnia Novita Sari. "Stationary process in GSTAR(1;1) through kernel function approach." In THE 4TH INDOMS INTERNATIONAL CONFERENCE ON MATHEMATICS AND ITS APPLICATION (IICMA 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0016808.
Повний текст джерелаSultana, Sharmin, Md Sad Salabi Sawrav, Md Bokhtiar Rahma, Md Shohorab Hossain, and Md Azizul Haque. "Isolation and Biochemical Characterization of Xylanase Enzyme Producing Bacteria from Goat Rumen." In International Conference on Emerging Trends in Engineering and Advanced Science. AIJR Publisher, 2022. http://dx.doi.org/10.21467/proceedings.123.1.
Повний текст джерелаWibowo, Supriyadi, V. Y. Kurniawan та Siswanto. "The relation between Fα – absolutely continuous of order α ∈ (0, 1) and function of bounded variation". У THE 4TH INDOMS INTERNATIONAL CONFERENCE ON MATHEMATICS AND ITS APPLICATION (IICMA 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0019249.
Повний текст джерелаFerraz, Marta, Paul E. Resta, and Afonso O'neill. "Whole-body interaction in natural environments benefits children's cognitive function compared to sedentary interaction indoors." In AH '17: 8th Augmented Human International Conference. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3041164.3041177.
Повний текст джерелаManabe, S., H. Yanagisawa, S. Ishikawa, Y. Kitagawa, K. Tohyama, S. Abe, and O. Wada. "TRYPTOPHAN PYROLYSIS PRODUCTS FOUND IN COOKED FOODS INHIBIT HUMAN PLATELET AGGREGATION BY INHIBITING CYCLOOXYGENASE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643402.
Повний текст джерелаSopian, K., Adam M. Elradi, Shahrir Abdullah, and K. V. Wong. "Heat Transfer and Pressure Drop Correlations for Double-Pass Solar Collector With and Without Porous Media." In ASME 2002 International Mechanical Engineering Congress and Exposition. ASMEDC, 2002. http://dx.doi.org/10.1115/imece2002-39542.
Повний текст джерелаD'Zmura, Michael, and Geoffrey Iverson. "Color constancy: adaptation to the illumination environment." In Advances in Color Vision. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/acv.1992.fe2.
Повний текст джерелаFoust, Emine Celik. "Industry-Based Thermodynamics Case Study on Refrigeration Cycle." In ASME 2022 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/imece2022-88201.
Повний текст джерелаЗвіти організацій з теми "Functions and Indoles"
Chamovitz, A. Daniel, and 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, January 2012. http://dx.doi.org/10.32747/2012.7597917.bard.
Повний текст джерелаJander, Georg, and Daniel Chamovitz. Investigation of growth regulation by maize benzoxazinoid breakdown products. United States Department of Agriculture, January 2015. http://dx.doi.org/10.32747/2015.7600031.bard.
Повний текст джерелаHubbard, Sarah M., and Bryan Hubbard. Investigation of Strategic Deployment Opportunities for Unmanned Aerial Systems (UAS) at INDOT. Purdue University, 2020. http://dx.doi.org/10.5703/1288284317126.
Повний текст джерелаLee, Jusang, John E. Haddock, Dario D. Batioja Alvarez, and 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.
Повний текст джерела