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Relevant bibliographies by topics / Acetyl

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Academic literature on the topic 'Acetyl'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 April 2022

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Journal articles on the topic "Acetyl"

1

Sastre, Juan A. López, José Molina Molina, Dolores Portal Olea, and Cristina Romero-Avila. "A new synthesis of 2,5-anhydro-D-mannose derivatives." Canadian Journal of Chemistry 66, no. 12 (December 1, 1988): 2975–80. http://dx.doi.org/10.1139/v88-462.

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Penta-O-acetyl-D-glucose diethyl dithioacetal monoxide 3 was obtained by oxidation of penta-O-acetyl-D-glucose diethyl dithioacetal 2 with 3-chloroperbenzoic acid. By reaction of 3 with sodium methoxide in methanol and further acetylation, 3,4,6-tri-O-acetyl-2,5-anhydro-D-mannose-diethyl dithioacetal monoxide 8 and the reduction product 3,4,6-tri-O-acetyl-2,5-anhydro-1,1-bis(ethylthio)-1-deoxy-D-arabino-hex-1-enitol 4 were obtained. Reduction of 8 yielded the corresponding dithioacetal derivative 9, which was converted to 3,4,6-tri-O-acetyl-2,5-anhydro-D-mannose diethyl acetal 11.

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2

Pan, Xuejun, Neil Gilkes, and Jack N. Saddler. "Effect of acetyl groups on enzymatic hydrolysis of cellulosic substrates." Holzforschung 60, no. 4 (July 1, 2006): 398–401. http://dx.doi.org/10.1515/hf.2006.062.

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Abstract Evidence showed that acetyl groups introduced during acetic acid delignification was a primary cause of the poor enzymatic digestibility of acetic acid pulp. The inhibition by acetyl groups could be removed by saponification. Acetyl groups might inhibit the enzymes by interfering with the productive binding (hydrogen bonds) between cellulose and the catalytic domain of cellulases, by affecting the binding of CBD to cellulose, or by increasing the diameter of the cellulose chain.

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3

Hadzic, Pavle, Nada Vukojevic, Mirjana Popsavin, and Janos Canadi. "Nucleophilic opening of the 3,5-anhydro ring in 1,2-O-cyclohexylidene- -D-xylofuranose." Journal of the Serbian Chemical Society 66, no. 1 (2001): 1–8. http://dx.doi.org/10.2298/jsc0101001h.

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The reactivity of the oxetane ring in 3,5-anhydro-1,2-O-cyclohexylidene- -D-xylofuranose (1) was exemplified by its regiospecific nucleophilic opening. The action of concentrated hydrobromic or hydroiodic acid on 1 resulted in the exclusive formation of the 5-deoxy-5-halo derivatives, while the action of acetyl chloride or acetyl bromide yielded the corresponding 3-O-acetyl-5-deoxy-5-halo derivatives in 70 - 90 % yield. Under strongly acidic reaction conditions, the protection of the cyclohexylidene acetal function remained intact.

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4

Hanaya, Tadashi, Kiyoshi Torigoe, Kazuyuki Soranaka, Horoshi Yamamoto, Yao Qizhengt, and Wolfgang Pfleiderer. "Pteridines CV." Pteridines 6, no. 1 (February 1995): 1–7. http://dx.doi.org/10.1515/pteridines.1995.6.1.1.

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Summary Treatment of L-biopterin (I) with N,N-dimethyformamide dimethyl- (or diethyl)acetal and then with acetic anhydride in pyridine gave 1',2'-di-O-acetyl-N'-(N,N-dimethylaminomethylene)-L-biopterin (4), which was converted by the Mitsunobu reaction into 3-methyl (5) and 3-p-nitrophenetyl derivatives (7). The protective groups on the side chain diols and N2 of these compounds were selectively cleaved to furnish products 6, 8-10, among which 9 is naturally occurring 3-methyl-L-biopterin and 8 is N',N(3)-protected biopterin, a versatile intermediate for various reactions on the side-chain diol. In contrast, the same Mitsunobu reactions of tri-N2:I',2'-0-acetyl-L-biopterin (II) afforded 04-methyl (12) and 04-NPE derivatives (13), both of which yielded 0 4-methyl-L-biopterin (14) and subsequently led to 4-amino-L-biopterin (18).

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5

Kantlehner, Willi, Birgit Heckel, and Jochen Mezger. "Orthoamide und Iminiumsalze, CI. Umsetzungen von N,N,N′,N′-Tetramethylharnstoffdiethylacetal mit CH2-aciden Verbindungen." Zeitschrift für Naturforschung B 75, no. 9-10 (November 26, 2020): 865–80. http://dx.doi.org/10.1515/znb-2020-0072.

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AbstractN,N,N′,N′-Tetramethylurea diethylacetal reacts with CH2-acidic compounds as benzylcyanide, cyanoacetic acid derivatives malonodinitrile and nitromethane to give ketene aminals or ketene-O,N-acetales. Low polar solvents favour mostly the formation of ketenaminals. The yields of ketenaminals and ketene-O,N-acetals can be improved in some cases by addition of trimethylsilyldimethylamine. The reactions of the urea acetal with diethylmalonate, ore acetyl acetone, stops at the stage of the N,N′,N″-permethylated guanidinium salts with carbanionic counterions. The formation of bis(dimethylamino)methylene-diethylmalonate from the urea acetal and diethylmalonate can be initiated by addition of trimethylsilyldimethylamine/trimethylsilylcyanide. N,N,N′,N′,N″,N″-Hexamethylguanidinium cyanide is formed in the analogous reactions of the urea acetal with N,N-dimethylcyanacetamide or diethylsuccinate. The N,N′,N″-Hexamethyl-guanidinium nitrite can be obtained from the urea acetal and nitropropane.

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6

Phalke, Pallavi L. "Synthesis of different α, β- unsaturated oxazolone derivatives." Journal of Drug Delivery and Therapeutics 9, no. 1 (January 15, 2019): 124–27. http://dx.doi.org/10.22270/jddt.v9i1.2189.

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Acetyl glycine were prepared from glycine acetic anhydride and then 2, 4-disubstituted Oxazol-5-one were prepared from acetyl glycine, substituted aldehydes, acetic anhydride, and sodium acetate as a catalyst. The formed product is evaluated and characterized by thin layer chromatography, infrared spectroscopy and melting point. The, β- unsaturated shows ability to react with various nucleophilic reagents for synthesis of new fused oxazole compounds. Keywords: glycine, acetic anhydride, aldehyde Sodium acetate, Oxazolone, E. coli, Antibacterial Activity.

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7

Rosenqvist, Marie. "Acetyl Group Distribution in Acetylated Wood Investigated by Microautoradiography." Holzforschung 55, no. 3 (April 25, 2001): 270–75. http://dx.doi.org/10.1515/hf.2001.045.

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Summary Sapwood of Scots pine (Pinus silvestris L.) was acetylated with 14C- and 3H-labelled acetic anhydride. The distribution of acetyl groups was investigated with microautoradiography and microautoradiographs were evaluated with ESEM, Environmental Scanning Electron Microscopy. The investigation showed that the impregnation of wood with radioisotope-labelled substances provides a good opportunity to investigate the location of substances covalently bonded to the wood material. Introduced 14C-labelled acetyl groups show an even distribution in the wood cell wall, with no discernible concentration gradients at acetylation levels of about 5, 15 and 20% weight gain. 3H-labelled acetyl groups show an even distribution in the wood cell wall at 15 and 20% weight gain, with no discernible concentration gradients. At the 5% weight gain level, however, an uneven distribution of 3H-labelled acetyl groups over the cell wall is observed. Nevertheless, the unevenness is random and no concentration gradient is discernible at this level. 3H with a relatively high resolution, 0.5–1 μm, compared to 14C with a resolution of 2–5 μm, gives more accurate information about where exactly the acetyl groups are situated in the wood cell wall. Acetic anhydride was evenly distributed when a full impregnation procedure was used. The chemical and physical properties of acetic anhydride allow a uniform penetration into the pine cell wall and a complete acetylation takes place when the specimens are heated.

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Sekar, M., S. Vanitha, and K. J. Rajendra Prasad. "Synthesis of Novel 3-Acetyl-2-hydroxy-1-N,N-diacetylaminocarbazole Derivatives." Zeitschrift für Naturforschung B 49, no. 5 (May 1, 1994): 687–90. http://dx.doi.org/10.1515/znb-1994-0521.

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Abstract The synthesis of hitherto unknown 3-acetyl-2-hydroxy-1-N,N-diacetylaminocarbazole (3a-f), is reported. The hydroxyiminocarbazoles (2a-f), prepared from 1-oxo-1,2,3,4-tetra-hydrocarbazoles (1a -f) on treatment with acetyl chloride in acetic anhydride yielded the title compounds (3a-f).

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9

Chênevert, Robert, Michel Desjardins, and René Gagnon. "Enzyme Catalyzed Asymmetric Hydrolysis of Chloral Acetyl Methyl Acetal." Chemistry Letters 19, no. 1 (January 1990): 33–34. http://dx.doi.org/10.1246/cl.1990.33.

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10

Patil, Ravikant, Joseph Genco, Hemant Pendse, and Adriaan Van Heiningen. "Process for producing acetic acid in hardwood kraft pulp mills." May 2017 16, no. 05 (2017): 287–300. http://dx.doi.org/10.32964/tj16.5.287.

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To determine the economic feasibility of producing acetic acid from commercial hardwood chips in kraft pulp mills, laboratory experiments were conducted to obtain sufficient data to perform a preliminary economic analysis for a proposed acetic acid recovery process. The acetyl groups in northeast hardwood were hydrolyzed from the xylan polymers in the wood to obtain sodium acetate. The extraction experiments were performed by using 4%–6% sodium hydroxide at low temperature (50°C–80°C). Sodium acetate from the extract was concentrated and then converted into acetic acid and sodium hydroxide by salt splitting using bipolar membrane electrodialysis (BPMED). Flow diagrams were prepared and cost estimates made for the capital and operating costs for the proposed acetic acid recovery process. The discounted cash flow rate of return on investment was estimated for pulp mills in the range of 1000–2000 tons/day. A preliminary economic analysis showed that the discounted cash flow rate of return on investment is primarily a function of (1) the plant size, (2) the selling price of acetic acid, and (3) the content of acetyl groups present in wood species. The income for the process and thus the rate of return on investment increases with increasing acetyl content in the wood and selling price of the acetic acid. When food grade acetic acid is produced, for example, the rate of return varies between 9% and 16% depending upon the size of the pulp mill, assuming the wood contains 3.5% acetyl groups on a dry basis and the selling price of acetic acid is US$900/ton.

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Dissertations / Theses on the topic "Acetyl"

1

Grünig, Andreas Paul. "Acetyl-CoA: L-Glutamat N-Acetyl-Transferase /." [S.l : s.n.], 1985. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.

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Babka, Heather Leigh. "Acetyl-CoA in plant biology." [Ames, Iowa : Iowa State University], 2009. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3389084.

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Atalay, Aycin. "N-acetyl Transferase (nat1&amp." Master's thesis, METU, 2007. http://etd.lib.metu.edu.tr/upload/2/12607767/index.pdf.

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Breast cancer is the most frequent malignancy among women, especially in Western societies. Highly penetrant genes such as BRCA1 and BRCA2, together with the reproductive history can constitute only 30% of the cause, so there should be other common genes, which may play a role in breast carcinogenesis according to one'
s lifestyle. In our case, the effect of N-acetyl transferases (NAT1, NAT2) and glutathione-S transferases (GSTM1&
GSTT1) were investigated, since variations in these genes may alter their enzymatic activity and therefore their capacity to biotransform xenobiotic compounds. To evaluate the potential association between NAT1, NAT2, GSTM1 and GSTT1 genotypes and development of breast cancer, a hospital based case-control study was conducted in a Turkish study population consisting of 37 histologically confirmed incident breast cancer cases and 34 control subjects with no present or previous history of cancer. The only recognizable difference between case and control groups is the percentage of GSTM1 deletion, 67.6% and 44.1% respectively (p=0.047). The frequency of rapid NAT2 acetylator genotype is 44.4% in cases and 23.5% in controls. Especially, women with NAT2 rapid acetylator and GSTM1 null genotypes were at the elevated risk (OR, 3.8
CI, 0.9-15.4). NAT1 rapid acetylator genotype showed no association with breast cancer. These results suggest that GSTM1 null genotype is a susceptibility factor for breast cancer, particularly in the presence of NAT2 rapid acetylator genotype.

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4

Sheridan, Rose Mary. "Acetyl CoA metabolism in Candida albicans." Thesis, University of Hull, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241601.

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5

Anconi, Glasiela Lemos. "Aplicação de peptídeos em cosméticos: desenvolvimento de formulações, estabilidade e eficácia." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/60/60137/tde-31032009-144332/.

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O objetivo desta pesquisa foi o desenvolvimento, avaliação da estabilidade e da eficácia de formulações cosméticas contendo acetil hexapeptídeo-3 (AHP) ou acetil tetrapeptídeo-5 (ATP) ou mistura de di e tripeptídeos (DTP). Para tal, foram desenvolvidas 6 formulações à base hidroxietilcelulose (HEC), metilfenil polissiloxano (MFP) e álcool batílico e lecitina de soja (ABL) (F1), ou de HEC, MFP, ésteres de polietilenoglicol com cadeia alquílica com 12 a 20 carbonos (EP) (F2), ou de polímero de acrilatos (PA), MFP e ABL (F3) ou de PA, MFP e EP (F4), ou de HEC e MFP (F5) ou de PA e MFP (F6), contendo ou não (veículo) 10% de AHP, ou 10% de ATP ou 4% de DTP, as quais foram submetidas a um estudo de estabilidade física por determinação da reologia e a uma avaliação sensorial. Para o estudo de eficácia dos peptídeos objeto de estudo as formulações foram aplicadas nos antebraços, na face, na região dos olhos e da boca de 60 voluntárias, sendo realizadas medidas do conteúdo aquoso do estrato córneo, da perda de água transepidérmica (TEWL), do micro-relevo cutâneo e das propriedades mecânicas da pele (anisotropia), antes (basal), após 2 horas da aplicação única (efeitos imediatos) e após 15 e 30 dias de uso contínuo (efeitos a longo prazo) das formulações. Os dados foram analisados estatisticamente pelo teste paramétrico análise de variância. Nos testes de estabilidade física, as formulações de nos 1, 2 e 5 foram consideradas as mais estáveis e as formulações de nº 5 e 6 foram as que apresentaram melhor sensorial, sendo, portanto, selecionada a formulação de nº 5 como veículo para os estudos de eficácia. Na avaliação dos efeitos imediatos na pele, observou-se que as formulações estudadas proporcionaram um aumento significativo no conteúdo aquoso do estrato córneo dos antebraços, enquanto que, somente as formulações acrescidas dos peptídeos provocaram um aumento significativo neste conteúdo na face. Em relação ao micro-relevo cutâneo, as formulações contendo ou não os peptídeos provocaram uma redução do parâmetro Ser (aspereza da pele) e Rt (rugosidade) nos antebraços e a formulação contendo DTP provocou um efeito imediato significativo no parâmetro Sesm (textura da pele). Na avaliação dos efeitos a longo prazo, as formulações ocasionaram uma diminuição significativa na TEWL e as acrescidas dos peptídeos objetos de estudo proporcionaram um aumento significativo no conteúdo aquoso do estrato córneo na região dos olhos, enquanto que nos antebraços e na região da boca todas as formulações acrescidas ou não dos peptídeos ocasionaram um aumento nesse parâmetro. Em relação ao micro-relevo cutâneo, a aplicação das formulações contendo os peptídeos, na região da boca, provocou um aumento significativo nos valores de Sesm. A aplicação das formulações contendo os peptídeos objeto de estudo, nos antebraços ocasionou uma diminuição significativa da anisotropia da pele. A formulação nº 5 contendo os peptídeos objeto de estudo, apresentou efeitos imediatos na hidratação, aspereza, rugosidade e textura da pele e, efeitos a longo prazo, na hidratação, textura e anisotropia da pele, mostrando a importância do emprego destes peptídeos em produtos cosméticos com finalidades hidratantes e antienvelhecimento.
The aim of this study was the development, evaluation of the stability and the efficacy of cosmetic formulations containing acetyl hexapeptide-3 (AHP), or acetyl tetrapeptide-5 (ATP) or mixture of di- and peptides (DTP). For this purpose the 6 following formulations (F) were developed: F1- containing hydroxyethyl cellulose (HEC), methylphenyl polysiloxane (MPPS), batyl alcohol, and lecithin (BAL); F2- HEC, MPPS and C12-C20 PEG-8 alkyl ester (AE); F3- acrylate copolymer (AC), MPPS and BAL; F4- AC, MPPS and AE; F5- HEC and MPPS and F6- AC and MPPS, which were supplemented or not (vehicle) with 10% of AHP or 10% of ATP or 4% of DTP and submitted to the evaluation of physical stability by the determination of the rheologic behavior and also to the sensorial analysis. For clinical efficacy studies, formulations were applied to the volar forearm and to the face skin (eye corner and cheek region), of 60 female volunteers. Skin conditions in terms of skin moisture, transepidermal water loss (TEWL), skin mechanical properties (anisotropy) and skin microrelief, before and after 2 hours (immediate effects) and after 15 and 30-day period of daily application (long term effects). Results obtained were statistically analyzed using the ANOVA parametric test. In the rheological study, the formulations number 1, 2, and 5 were considered more stable than the others. Moreover, the formulations number 5 and 6 showed the best sensorial attributes, and for this reason the formulation number 5 was selected for the efficacy study. The evaluation of immediate effects of formulations showed that the application of the formulations studied in the volar forearm increased the water content of the stratum corneum, while only the formulations containing the peptides provoked an increased in this content, when face skin was analyzed. When the volar forearm skin microrelief was analyzed, the application of all the formulations studied provoked a significant decrease in skin roughness (Ser) and depth of roughness (Rt), furthermore only the formulation supplemented with the DTP showed a significant increase in the skin smoothness (Sesm). In the evaluation of long term effects, all formulations provoked a significant reduction in TEWL values and the formulations containing the peptides studied provoked a significant increase in the water content of the stratum corneum of eye corner; when the volar forearms and the cheek region were analyzed, all the formulations containing or not the peptides studied, provoked an increase in this parameter. When the skin microrelief was analyzed, only the formulation supplemented with AHP or ATP or DTP, provoked a significant increase in the skin smoothness (Sesm), when applied in the cheek region. The application of formulations containing the peptides studied in the volar forearms provoked a significant decrease in the skin anisotropy. The formulation nº 5 (F5) containing the peptides studied, showed immediate effects on skin hydration, roughness and smoothness, and also long-term effects on skin hydration, smoothness and mechanical properties, which demonstrated the importance of the use of these peptides in cosmetic formulations with hydration and anti-aging purposes.

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Khew-Goodall, Yee Sim. "Pyruvate carboxylase: its interactions with acetyl CoA /." Title page, table of contents and summary only, 1985. http://web4.library.adelaide.edu.au/theses/09PH/09phk454.pdf.

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Evans, Michael R. "Labeled mimics of N-Acetyl-D-Fucosamine /." Connect to resource online, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1210527108.

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Watkins, Richard William. "Assimilation of acetyl-CoA by methylotrophic bacteria." Thesis, Cranfield University, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278721.

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Evans, Michael Ryan. "Labeled Mimics of N-Acetyl-D-Fucosamine." Youngstown State University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1210527108.

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Quayle, Katherine Amanda. "Regulation of rat liver acetyl CoA carboxylase." Thesis, University of British Columbia, 1986. http://hdl.handle.net/2429/26028.

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Acetyl-CoA carboxylase was purified 750-fold from rat liver cytosol using a modified purification procedure involving high speed ultracentrifugation, sucrose density step gradients, ion-exchange chromatography and avidin-sepharose affinity chromatography. The purified preparation had a specific activity of about 2 U/mg protein and a Km of 80uM for acetyl-CoA. Silver stain of the sample separated by denaturing polyacrylamide gel electrophoresis indicated 95% of the protein migrates as a single protein band with subunit Mr approximately 230Kd. There is approximately 2% contamination of low molecular mass material and 3-5% of the protein runs as a minor band of 240Kd. As the major protein band co-migrates on SDS-po1yacry1 amide gels with immunoprecipitated acetyl-CoA carboxylase from a fresh rat epididymal fat pad tissue extract, it appears that the 240Kd band in the rat liver sample may be a pre-form of the enzyme which undergoes post-translational modification to the mature form of the enzyme. Despite appearing almost homogeneous after silver-stain, the purified enzyme preparation still contains both cyclic AMP-independent and cyclic AMP-dependent protein kinase activity, the former causing incorporation of 0.1mol Pi/mol acetyl-CoA carboxylase subunit/hr, and the latter causing incorporation of 0.5mol Pi/mol subunit/hr. Addition of specific inhibitor to cyclic AMP-dependent protein kinase effectively blocks all cyclic AMP-dependent protein kinase activity. The cyclic AMP-independent protein kinase activity co-purifying with acetyl-CoA carboxylase phosphorylates the "control sites" as demonstrated by 2 -dimensional peptide analysis of radioactively labelled ACC. This phosphorylation has no apparent effect on enzyme activity. Phosphorylation by cyclic AMP-dependent protein kinase increases phosphorylation of the control sites and also results in incorporation of [32p] into the two A peptides and one of the B group of phosphopeptides. Neither of these endogenous protein kinase activities cause incorporation of the label into the insulin responsive site of acetyl-CoA carboxylase. At least 90% of the cyclic AMP-independent protein kinase activity (assayed using ACC as substrate) in the rat liver cytosol co-purifies with acetyl-CoA carboxylase upon sucrose density gradient centrifugation. Under the conditions described, approximately 90% of this protein kinase activity is separated from ACC by DEAE-ce11ulose chromatography, eluting with the other unbound protein from this column. 2-dimensiona1 tryptic peptide analysis of acetyl-CoA carboxylase phosphorylated by this protein kinase fraction increases incorporation of [32p] mainly into the control sites. Further fractionation of this sample however does not reveal increased I site phosphorylation. Protein kinase activity eluted together with ACC (at high salt) from DEAE-cellulose appeared to lead mainly to phosphorylation of the B group of peptides. However, in this case further fractionation of the DEAE-HS fraction on casein-sepharose produces a protein kinase fraction (eluted at 0.5M KC1) which brings about phosphorylation of the insulin-directed site of acetyl-CoA carboxylase. Thus a cyclic AMP-independent protein kinase activity which phosphorylates acetyl-CoA carboxylase at an insulin responsive site, has been partially purified from rat liver cytosol. We are therefore in a position to explore the effects of insulin-directed phosphorylation on the activity of acetyl-CoA carboxylase.
Medicine, Faculty of
Biochemistry and Molecular Biology, Department of
Graduate

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Books on the topic "Acetyl"

1

Broaders, Marie. Acetylcholine receptor binding and enzymic activities of the duvernoys' secretions from the colubrid snakes Boiga blandingi (Hallowell, 1857) and Boiga dendrophila (Boie, 1827)(Squamata: Colubridae). Dublin: University College Dublin, 1998.

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Gibbs, Roslyn Victoria. Recognition of N-acetyl [gamma]-D-galactosamine by the seed lectin from Dolichos biflorus. Portsmouth: Portsmouth Polytechnic, School of Pharmacy and Biomedical Sciences, 1992.

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Hitt, Mark Edward. Hepatocellular cytoprotection against the pathobiologic effects of thiacetarsamine in vitro and in vivo using N-acetyl-L-cysteine. Charlottetown: University of Prince Edward Island, 1992.

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Hitt, Mark Edward. Hepatocellular cytoprotection against the pathobiologic effects of thiacetarsamine in vitro and in vivo using N-acetyl-L-cysteine. Ottawa: National Library of Canada, 1992.

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Denyer, Kay. The source of plastidial acetyl coenzyme A for fatty acid synthesis in plastids of developing pea cotyledons. Norwich: University of East Anglia, 1987.

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Johnson, Ann-Christin. The ototoxic effect of toluene and the influence of noise, acetyl salicylic acid, or genotype: A study inrats and mice. Oslo: Scandinavian University Press, 1993.

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Bjorkman, Camilla. Methodological and biochemical aspects of acetylcholinesterase and acetate in blood from cattle , and acetyl-CoA synthesizing enzymes in spinal cord from ruminants and monogastric animals. Uppsala: Sveriges Lantbruksuniversitet, 1989.

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Basic Health Publications user's guide to L-carnitine and acetyl-L-carnitine: Learn how to use these supplements to boost your energy and mental focus. Laguna Beach, CA: Basic Health Publications, 2006.

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Hood, Rosemary Anne. Measurement of the enzyme N-acetyl-b-D-glucosaminidase for detection of subclinical mastitis in a random sample of bulk tank milk in Prince Edward Island. Charlottetown: University of Prince Edward Island, 1992.

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Hood, Rosemary Anne. Measurement of the enzyme N-acetyl-b-D-glucosaminidase for detection of subclinical mastitis in a random sample of bulk tank milk in Prince Edward Island. Ottawa: National Library of Canadad, 1992.

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Book chapters on the topic "Acetyl"

1

Gooch, Jan W. "Acetyl." In Encyclopedic Dictionary of Polymers, 10. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_121.

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Lipmann, Fritz. "Acetyl Phosphate." In Advances in Enzymology - and Related Areas of Molecular Biology, 231–67. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/9780470122518.ch6.

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Bährle-Rapp, Marina. "Acetyl Glutamine." In Springer Lexikon Kosmetik und Körperpflege, 5. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_85.

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Bährle-Rapp, Marina. "Acetyl Tyrosine." In Springer Lexikon Kosmetik und Körperpflege, 6. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_97.

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Bährle-Rapp, Marina. "Acetyl Methionine." In Springer Lexikon Kosmetik und Körperpflege, 6. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_91.

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Gooch, Jan W. "Acetyl Chloride." In Encyclopedic Dictionary of Polymers, 10–11. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_126.

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Gooch, Jan W. "Acetyl Value." In Encyclopedic Dictionary of Polymers, 12. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_139.

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Gooch, Jan W. "Acetyl Peroxide." In Encyclopedic Dictionary of Polymers, 11. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_133.

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Gooch, Jan W. "Acetyl Ricinoleates." In Encyclopedic Dictionary of Polymers, 11. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_135.

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Bährle-Rapp, Marina. "Acetyl Cysteine." In Springer Lexikon Kosmetik und Körperpflege, 5. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_82.

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Conference papers on the topic "Acetyl"

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Šadžius, R., J. Šulskus, and R. J. Rakauskas. "Conformational effects in acetyl methoxyphenols." In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47702.

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Hojilla-Evangelista, Mila. "Production of Protein Isolate and Mucilage from Camelina Engineered to Produce Acetyl-triacylglycerols (Camelina Acetyl-TAG)." In Virtual 2020 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2020. http://dx.doi.org/10.21748/am20.233.

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Margulès, L., V. Ilyushin, Isabelle Kleiner, Atef Jabri, Jose Cernicharo, Belén Tercero, J. C. Guillemin, and R. Motiyenko. "SUBMILLIMETER WAVE SPECTROSCOPY OF ACETYL ISOCYANATE : CH3C(O)NCO." In 69th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.wf10.

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Cin, Gunseli Turgut, Seda Demirel Topel, Neslihan Nohut Maslakci, Esin Eren, and Aysegul Uygun Oksuz. "Plasma modified chitosan/N-acetyl-2-pyrazoline derivative nanofibers." In 2015 IEEE International Conference on Plasma Sciences (ICOPS). IEEE, 2015. http://dx.doi.org/10.1109/plasma.2015.7179648.

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Cai, Xiaoyu, Marcio de Queiroz, Glen Meades, and Grover Waldrop. "Modeling the Negative Feedback Mechanism in the Enzyme Carboxyltransferase." In ASME 2011 Dynamic Systems and Control Conference and Bath/ASME Symposium on Fluid Power and Motion Control. ASMEDC, 2011. http://dx.doi.org/10.1115/dscc2011-6171.

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Abstract:

The enzyme acetyl-CoA carboxylase catalyzes the first committed step in fatty acid synthesis in all organisms. The E. coli form of the carboxyltransferase subunit was recently found to regulate its own activity and expression by binding its own mRNA. By binding acetyl-CoA or the mRNA encoding its own subunits, Carboxyltransferase is able to sense the metabolic state of the cell and attenuate its own translation and enzymatic activity using a negative feedback mechanism. In this paper, this network of interactions is modeled mathematically using mass action kinetics. Numerical simulations of the model show agreement with experimental results.

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Wellen, Kathryn E. "Abstract IA24: Acetyl-CoA metabolism, gene regulation, and stress management." In Abstracts: AACR Special Conference: Metabolism and Cancer; June 7-10, 2015; Bellevue, WA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1557-3125.metca15-ia24.

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Deshmukh, Shirish, Dattatraya Mangte, and Anvita S. Dandale. "Per–O–acetyl Lactosyl Isothiourea Derivatives: Synthesis and Antimicrobial Activities." In The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00423.

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Nguyen, Thanh Dinh, and Giang Kim Thi Nguyen. "ISATIN (PER-O-ACETYL-b-D-GALACTOPYRANOSYL)THIOSEMICARBAZONES." In The 15th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00776.

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Sutrisno, Husni Wahyu Wijaya, Rini Retnosari, and Daratu Eviana Eka Putri. "Effectiveness of menthyl acetate synthesis with different acetyl groups equivalent." In INTERNATIONAL CONFERENCE ON ENERGY AND ENVIRONMENT (ICEE 2021). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0059481.

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Levene, C., T. J. Dines, S. Ostavour pour, Nighat Kausar, B. Z. Chowdhry, E. W. Blanch, P. M. Champion, and L. D. Ziegler. "An Experimental And Theoretical Raman and ROA Study Of Di-amino Acid Peptides (DAAPs): α- and β-N-acetyl-L-Asp-L-Glu And Their Derivatives: N-acetyl-L-Asp, N-acetyl-L-Glu and L-Asp-L-Glu." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482842.

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Reports on the topic "Acetyl"

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GRAHAM, DAVID A. ACETYL-COA CLEAVAGE AND SYNTHESIS IN METHANOGENS; CHARACTERIZATION OF SUBOMPONENT INTERACTIONS IN THE ACETYL-COA DECARBONYLASE/SYNTHASE MULTIENZYME COMPLEX. Office of Scientific and Technical Information (OSTI), October 2013. http://dx.doi.org/10.2172/1097089.

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Kent, Michael S., Kenneth L. Sale, James Bryce Ricken, Daniella Victoria Martinez, Miranda Juarros, and Walrdop-Grover. Screening for Dimerization Inhibitors for Bacterial Acetyl CoA Carboxylase. Office of Scientific and Technical Information (OSTI), November 2019. http://dx.doi.org/10.2172/1573932.

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Shibata, Yoshimi. Oral Administration of N-acetyl-D Glucosamine Polymer Particles Down-Regulates Airway Allergic Responses. Fort Belvoir, VA: Defense Technical Information Center, May 2008. http://dx.doi.org/10.21236/ada484241.

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Shibata, Yoshimi. Oral Administration of N-Acetyl-D Glucosamine Polymer Particles Down-Regulates Airway Allergic Responses. Fort Belvoir, VA: Defense Technical Information Center, March 2005. http://dx.doi.org/10.21236/ada442684.

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Shibata, Yoshimi. Oral Administration of N-Acetyl-D Glucosamine Polymer Particles Down-Regulates Airway Allergic Responses. Fort Belvoir, VA: Defense Technical Information Center, March 2006. http://dx.doi.org/10.21236/ada454070.

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Shibata, Yoshimi. Oral Administration of N-Acetyl-D-Glucosamine Polymer Particles Down-Regulates Airway Allergic Responses. Fort Belvoir, VA: Defense Technical Information Center, March 2007. http://dx.doi.org/10.21236/ada469207.

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Pereboom, D. P. K. H., R. C. J. Dam, T. C. van Rijk, M. de Nijs, and J. G. J. Mol. Proficiency test for deoxynivalenol (DON), acetyl-DONs and DON-3G in cereals : EURL-PT_MP01 (2018). Wageningen: RIKILT Wageningen University & Research, 2019. http://dx.doi.org/10.18174/476812.

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Shibata, Yoshimi. Oral Administration of a N-Acetyl-D-Glucosamine Polymer Particles Down-Regulates Airway Allergic Responses. Fort Belvoir, VA: Defense Technical Information Center, March 2004. http://dx.doi.org/10.21236/ada424227.

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Poston, Shelly L., and Arnold Reisman. The Relative Stabilities of Tungsten Hexacarbonyl, Silver Neodecanoate, Some Metal Acetyl- and Hexafluoroacetyl-Acetonates and the Thermal Properties of the Pallidium (2) Acetonates. Fort Belvoir, VA: Defense Technical Information Center, February 1989. http://dx.doi.org/10.21236/ada204790.

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O'Day, Stephen C., and John W. McMaster. The ACETEF HLA Interface. Fort Belvoir, VA: Defense Technical Information Center, September 1999. http://dx.doi.org/10.21236/ada375781.

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