Статті в журналах з теми "Side chain linked"
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Zhang, Yan-Ni, Yuwei Zhang, Shan Su, Han-Ying Zhu, Wei Xu, Lu Wang, Meng Wu, et al. "Neutralizing SARS-CoV-2 by dimeric side chain-to-side chain cross-linked ACE2 peptide mimetics." Chemical Communications 58, no. 11 (2022): 1804–7. http://dx.doi.org/10.1039/d1cc06301d.
Повний текст джерелаUllah, Raja Summe, Li Wang, Haojie Yu, Nasir M. Abbasi, Muhammad Akram, Zain -ul-Abdin, Muhammad Saleem, Muhammad Haroon, and Rizwan Ullah Khan. "Synthesis of polyphosphazenes with different side groups and various tactics for drug delivery." RSC Advances 7, no. 38 (2017): 23363–91. http://dx.doi.org/10.1039/c6ra27103k.
Повний текст джерелаSchiller, Peter W., Thi M. D. Nguyen, Carole Lemieux, and Louise A. Maziak. "A novel side-chain-linked antiparallel cyclic dimer of enkephalin." FEBS Letters 191, no. 2 (October 28, 1985): 231–34. http://dx.doi.org/10.1016/0014-5793(85)80014-4.
Повний текст джерелаByrne, CJ, and AD Ward. "The Preparation of Analogs of the Ether-Linked Dimer and Oligomer Components of Hematoporphyrin Derivative." Australian Journal of Chemistry 44, no. 3 (1991): 411. http://dx.doi.org/10.1071/ch9910411.
Повний текст джерелаByrne, CJ, IK Morris, and AD Ward. "The Synthesis of the Dimer and Trimer Ether-Linked Components of Hematoporphyrin Derivative." Australian Journal of Chemistry 43, no. 11 (1990): 1889. http://dx.doi.org/10.1071/ch9901889.
Повний текст джерелаDu, Xinming, Minghui Li, Zhe Wang, and Jingmei Xu. "The ordered side chain imidazole functionalized cross-linked anion exchange membrane." Chinese Science Bulletin 64, no. 2 (October 31, 2018): 180–86. http://dx.doi.org/10.1360/n972018-00679.
Повний текст джерелаAngiolini, Luigi, Tiziana Benelli, Valentina Cocchi, Massimiliano Lanzi, and Elisabetta Salatelli. "Side chain porphyrin moiety linked to polymer-fullerene composite solar cell." Reactive and Functional Polymers 73, no. 9 (September 2013): 1198–206. http://dx.doi.org/10.1016/j.reactfunctpolym.2013.05.007.
Повний текст джерелаVerjans, Jente, Alexis André, Evelyne Van Ruymbeke, and Richard Hoogenboom. "Physically Cross-Linked Polybutadiene by Quadruple Hydrogen Bonding through Side-Chain Incorporation of Ureidopyrimidinone with Branched Alkyl Side Chains." Macromolecules 55, no. 3 (January 19, 2022): 928–41. http://dx.doi.org/10.1021/acs.macromol.1c01908.
Повний текст джерелаWang, Xiaoxuan, Zhaoxia Li, Haiying Zhao, and Shufeng Chen. "New azobenzene liquid crystal with dihydropyrazole heterocycle and photoisomerization studies." Royal Society Open Science 7, no. 7 (July 2020): 200474. http://dx.doi.org/10.1098/rsos.200474.
Повний текст джерелаMoehle, C. M., C. K. Dixon, and E. W. Jones. "Processing pathway for protease B of Saccharomyces cerevisiae." Journal of Cell Biology 108, no. 2 (February 1, 1989): 309–25. http://dx.doi.org/10.1083/jcb.108.2.309.
Повний текст джерелаYousuf, Sammer, Shafqat Hussain, Khalid Mohammed Khan, Muhammad Shabeer, and Shahnaz Perveen. "Crystal structure of methyl 2-(7-hydroxy-2-oxo-2H-chromen-4-yl)acetate." Acta Crystallographica Section E Crystallographic Communications 71, no. 9 (August 22, 2015): o677—o678. http://dx.doi.org/10.1107/s2056989015014061.
Повний текст джерелаKhripach, Vladimir, Vladimir Zhabinskii, Alexey Antonchick, Raissa Litvinovskaya, Svetlana Drach, Oleg Sviridov, Andrey Pryadko, Tatyana Novik, Vitaliy Matveentsev, and Bernd Schneider. "A New Type of Modified Brassinosteroids for Enzyme-linked Immunosorbent Assay." Natural Product Communications 3, no. 5 (May 2008): 1934578X0800300. http://dx.doi.org/10.1177/1934578x0800300513.
Повний текст джерелаDiwakara, Shashini D., Gregory T. McCandless, Sampath B. Alahakoon, and Ronald A. Smaldone. "Synthesis of Side-Chain-Free Hydrazone-Linked Covalent Organic Frameworks through Supercritical Carbon Dioxide Activation." Organic Materials 03, no. 02 (April 2021): 277–82. http://dx.doi.org/10.1055/a-1477-5123.
Повний текст джерелаMountaki, Stella Afroditi, Maria Kaliva, Konstantinos Loukelis, Maria Chatzinikolaidou, and Maria Vamvakaki. "Responsive Polyesters with Alkene and Carboxylic Acid Side-Groups for Tissue Engineering Applications." Polymers 13, no. 10 (May 18, 2021): 1636. http://dx.doi.org/10.3390/polym13101636.
Повний текст джерелаMarshall, Jonathan, Jake Hooton, Yang Han, Adam Creamer, Raja Shahid Ashraf, Yoann Porte, Thomas D. Anthopoulos, et al. "Polythiophenes with vinylene linked ortho, meta and para-carborane sidechains." Polym. Chem. 5, no. 21 (2014): 6190–99. http://dx.doi.org/10.1039/c4py00767k.
Повний текст джерелаChatani, Eri, Keisuke Yuzu, Yumiko Ohhashi, and Yuji Goto. "Current Understanding of the Structure, Stability and Dynamic Properties of Amyloid Fibrils." International Journal of Molecular Sciences 22, no. 9 (April 21, 2021): 4349. http://dx.doi.org/10.3390/ijms22094349.
Повний текст джерелаPrasad, N. L., M. S. Krishnamurthy, H. Nagarajaiah, and Noor Shahina Begum. "Crystal structure of ethyl 5-acetyl-2-{[(dimethylamino)methylidene]amino}-4-methylthiophene-3-carboxylate." Acta Crystallographica Section E Crystallographic Communications 71, no. 10 (September 17, 2015): o762—o763. http://dx.doi.org/10.1107/s2056989015016217.
Повний текст джерелаItano, Misaki, Yuichiro Kobayashi, Yoshinori Takashima, Akira Harada, and Hiroyasu Yamaguchi. "Mechanical properties of supramolecular polymeric materials cross-linked by donor–acceptor interactions." Chemical Communications 55, no. 26 (2019): 3809–12. http://dx.doi.org/10.1039/c9cc01472a.
Повний текст джерелаTegge, Werner, Carlos F. S. Bonafe, Aileen Teichmann та Christian Erck. "Synthesis of Peptides from α- and β-Tubulin Containing Glutamic Acid Side-Chain Linked Oligo-Glu with Defined Length". International Journal of Peptides 2010 (15 грудня 2010): 1–4. http://dx.doi.org/10.1155/2010/189396.
Повний текст джерелаAngiolini, Luigi, Daniele Caretti, Stefano Rossetti, Elisabetta Salatelli, and Marco Scoponi. "Radical polymeric photoinitiators bearing side-chain camphorquinone moieties linked to the main chain through a flexible spacer." Journal of Polymer Science Part A: Polymer Chemistry 43, no. 23 (2005): 5879–88. http://dx.doi.org/10.1002/pola.21055.
Повний текст джерелаWang, Qiang, Zhuan Ni Yu, and Liang Min Yu. "Anti-Biofouling of a Novel Cross-Linked Copolymer Containing a HMBA Side Chain." Journal of Biomimetics, Biomaterials and Tissue Engineering 10 (May 2011): 1–5. http://dx.doi.org/10.4028/www.scientific.net/jbbte.10.1.
Повний текст джерелаMATSUMOTO, Shunsuke, and Daisuke KOHDA. "Structural Basis of the Asparagine Side Chain Activation in N-Linked Protein Glycosylation." Seibutsu Butsuri 54, no. 3 (2014): 158–59. http://dx.doi.org/10.2142/biophys.54.158.
Повний текст джерелаSkaff, Ojia, Katrina A. Jolliffe, and Craig A. Hutton. "Synthesis of the Side Chain Cross-Linked Tyrosine Oligomers Dityrosine, Trityrosine, and Pulcherosine." Journal of Organic Chemistry 70, no. 18 (September 2005): 7353–63. http://dx.doi.org/10.1021/jo051076m.
Повний текст джерелаWelsch, Nicole, Ashley C. Brown, Thomas H. Barker, and L. Andrew Lyon. "Enhancing clot properties through fibrin-specific self-cross-linked PEG side-chain microgels." Colloids and Surfaces B: Biointerfaces 166 (June 2018): 89–97. http://dx.doi.org/10.1016/j.colsurfb.2018.03.003.
Повний текст джерелаKishimoto, Tadashi, Mayumi Watanabe, Toshiaki Mitsui, and Hidetaka Hori. "Glutelin Basic Subunits Have a Mammalian Mucin-Type O-Linked Disaccharide Side Chain." Archives of Biochemistry and Biophysics 370, no. 2 (October 1999): 271–77. http://dx.doi.org/10.1006/abbi.1999.1406.
Повний текст джерелаBrown, DJ, and K. Mori. "Heterocyclic Amplifiers of Phleomycin. VI. Some Phenylpurines, Phenylpteridines, Phenylquinazolines and Related Compounds." Australian Journal of Chemistry 38, no. 3 (1985): 467. http://dx.doi.org/10.1071/ch9850467.
Повний текст джерелаOtake, Shinya, Norihiro Ogawa, Yoshikazu Kitano, Keiji Hasumi, and Eriko Suzuki. "Isoprene Side-chain of SMTP is Essential for Soluble Epoxide Hydrolase Inhibition and Cellular Localization." Natural Product Communications 11, no. 2 (February 2016): 1934578X1601100. http://dx.doi.org/10.1177/1934578x1601100223.
Повний текст джерелаIssa, Mohamady A. "Structural investigation of water-hyacinth (Eichhornia crassipes) polysaccharides. Part I. Water-soluble polysaccharides." Canadian Journal of Chemistry 66, no. 11 (November 1, 1988): 2777–81. http://dx.doi.org/10.1139/v88-428.
Повний текст джерелаAirinei, Anton, Elena Rusu, and Virgil Barboiu. "Responsive behavior of 4-(N-maleimido)azobenzene in polymers with aromatic main chain and side chain linked units." Journal of the Brazilian Chemical Society 21, no. 3 (2010): 489–95. http://dx.doi.org/10.1590/s0103-50532010000300014.
Повний текст джерелаSharma, Gangavaram V. M., Gonuguntla Anjaiah, Marumudi Kanakaraju, Bommeda Sudhakar, Deepak Chatterjee та Ajit C. Kunwar. "Synthesis of a new β-amino acid with a 3-deoxy-l-ara furnaoside side chain: the influence of the side chain on the conformation of α/β-peptides". Organic & Biomolecular Chemistry 14, № 2 (2016): 503–15. http://dx.doi.org/10.1039/c5ob01753j.
Повний текст джерелаYapo, Beda M. "Pectin Rhamnogalacturonan II: On the “Small Stem with Four Branches” in the Primary Cell Walls of Plants." International Journal of Carbohydrate Chemistry 2011 (December 29, 2011): 1–11. http://dx.doi.org/10.1155/2011/964521.
Повний текст джерелаYu, Kaijin, Shuai Bi, Wenyong Ming, Weiwei Wei, Yinghang Zhang, Junsong Xu, Peirong Qiang, Feng Qiu, Dongqing Wu та Fan Zhang. "Side-chain-tuned π-extended porous polymers for visible light-activated hydrogen evolution". Polymer Chemistry 10, № 27 (2019): 3758–63. http://dx.doi.org/10.1039/c9py00512a.
Повний текст джерелаKISHIMOTO, Tadashi, Hidetaka HORI, Mayumi WATANABE, and Toshiaki MITSUI. "Basic Subunit of Glutelin, Rice Major Storage Protein, has N-Linked Sugar Side Chain." Plant Biotechnology 17, no. 3 (2000): 217–24. http://dx.doi.org/10.5511/plantbiotechnology.17.217.
Повний текст джерелаSala-Rabanal, Monica, Larryn W. Peterson, Michaela Serpi, Ivan S. Krylov, Boris A. Kashemirov, Jae Seung Kim, Stefanie Mitchell, John M. Hilfinger, and Charles E. McKenna. "Interactions Between the Human Oligopeptide Transporter, hPepT1 and Serine Side-chain-linked Cidofovir Prodrugs." Antiviral Research 82, no. 2 (May 2009): A53—A54. http://dx.doi.org/10.1016/j.antiviral.2009.02.124.
Повний текст джерелаFawzi, Nicolas L., Mark R. Fleissner, Nicholas J. Anthis, Tamás Kálai, Kálmán Hideg, Wayne L. Hubbell, and G. Marius Clore. "A rigid disulfide-linked nitroxide side chain simplifies the quantitative analysis of PRE data." Journal of Biomolecular NMR 51, no. 1-2 (September 2011): 105–14. http://dx.doi.org/10.1007/s10858-011-9545-x.
Повний текст джерелаPiekielna, Justyna, Luca Gentilucci, Rossella De Marco, Renata Perlikowska, Anna Adamska, Jacek Olczak, Marzena Mazur, et al. "Cyclic side-chain-linked opioid analogs utilizing cis - and trans -4-aminocyclohexyl- d -alanine." Bioorganic & Medicinal Chemistry 22, no. 23 (December 2014): 6545–51. http://dx.doi.org/10.1016/j.bmc.2014.10.022.
Повний текст джерелаBreed, Peter G., James A. Ramsden, and John M. Brown. "Scope and limitations of ruthenium-catalyzed metathesis of simple polymer-bound alkenes." Canadian Journal of Chemistry 79, no. 5-6 (May 1, 2001): 1049–57. http://dx.doi.org/10.1139/v01-045.
Повний текст джерелаSreenivasa, S., M. S. Nanjundaswamy, K. E. Manojkumar, S. Madankumar, N. K. Lokanath, and P. A. Suchetan. "1-Fluoro-4-[(E)-2-nitrovinyl]benzene." Acta Crystallographica Section E Structure Reports Online 70, no. 2 (January 11, 2014): o124. http://dx.doi.org/10.1107/s1600536814000348.
Повний текст джерелаParkinson, J. F., C. J. Vlahos, S. C. B. Yan, and N. U. Bang. "Recombinant human thrombomodulin. Regulation of cofactor activity and anticoagulant function by a glycosaminoglycan side chain." Biochemical Journal 283, no. 1 (April 1, 1992): 151–57. http://dx.doi.org/10.1042/bj2830151.
Повний текст джерелаZhao, Zhe-Han, Xian-Yan Ju, Kui-Wu Wang, Xin-Juan Chen, Hong-Xiang Sun, and Ke-Jun Cheng. "Structure Characterization, Antioxidant and Immunomodulatory Activities of Polysaccharide from Pteridium aquilinum (L.) Kuhn." Foods 11, no. 13 (June 22, 2022): 1834. http://dx.doi.org/10.3390/foods11131834.
Повний текст джерелаArtheswari, G., V. Maheshwaran, and N. Gautham. "Crystal structure and Hirshfeld surface analysis of 3-(cyclopropylmethoxy)-4-(difluoromethoxy)-N-(pyridin-2-ylmethyl)benzamide." Acta Crystallographica Section E Crystallographic Communications 75, no. 10 (September 20, 2019): 1515–18. http://dx.doi.org/10.1107/s2056989019012866.
Повний текст джерелаWang, Yajian, Huifang Liu, Pengpeng Li, and Linbing Wang. "The Effect of Cross-Linking Type on EPDM Elastomer Dynamics and Mechanical Properties: A Molecular Dynamics Simulation Study." Polymers 14, no. 7 (March 24, 2022): 1308. http://dx.doi.org/10.3390/polym14071308.
Повний текст джерелаSoo Choi, Moon, Hyung Jun Kim, Taek Seung Lee, and Won Seok Lyoo. "Newly Synthesized Branch-type Aromatic Oxadiazole Polymer and Binary Fluorescence Patterning on its Film." High Performance Polymers 19, no. 5-6 (October 2007): 531–40. http://dx.doi.org/10.1177/0954008306081195.
Повний текст джерелаKuroki, Aki, Yasuhiro Kuroda, Shuichi Kikuchi, Frédéric Lajaunias, Thierry Fulpius, Yves Pastore, Liliane Fossati-Jimack, et al. "Level of galactosylation determines cryoglobulin activity of murine IgG3 monoclonal rheumatoid factor." Blood 99, no. 8 (April 15, 2002): 2922–28. http://dx.doi.org/10.1182/blood.v99.8.2922.
Повний текст джерелаHoang, Huy N., Timothy A. Hill, Gloria Ruiz-Gómez, Frederik Diness, Jody M. Mason, Chongyang Wu, Giovanni Abbenante, Nicholas E. Shepherd, and David P. Fairlie. "Twists or turns: stabilising alpha vs. beta turns in tetrapeptides." Chemical Science 10, no. 45 (2019): 10595–600. http://dx.doi.org/10.1039/c9sc04153b.
Повний текст джерелаSwain, Jonathan A., Stephen R. Walker, Matthew B. Calvert, and Margaret A. Brimble. "The tryptophan connection: cyclic peptide natural products linked via the tryptophan side chain." Natural Product Reports 39, no. 2 (2022): 410–43. http://dx.doi.org/10.1039/d1np00043h.
Повний текст джерелаAshry, El Sayed H. El, Nagwa Rashed, Laila F. Awad, Adel A. H. Abdel-Rahman, and Hanna A. Rasheed. "Synthesis of New 7-Alkylated Theophyllines by Chemical Modification of Dyphylline." Journal of Chemical Research 2001, no. 4 (April 2001): 129–30. http://dx.doi.org/10.3184/030823401103169405.
Повний текст джерелаDong, Shengli, Sylvia A. McPherson, Yun Wang, Mei Li, Pengfei Wang, Charles L. Turnbough, and David G. Pritchard. "Characterization of the Enzymes Encoded by the Anthrose Biosynthetic Operon of Bacillus anthracis." Journal of Bacteriology 192, no. 19 (July 30, 2010): 5053–62. http://dx.doi.org/10.1128/jb.00568-10.
Повний текст джерелаZhang, Hui, Yan Shang, Hong Zhao, Xuan Wang, Baozhong Han, and Zesheng Li. "Theoretical study on the tailored side-chain architecture of benzil-like voltage stabilizers for enhanced dielectric strength of cross-linked polyethylene." RSC Advances 6, no. 14 (2016): 11618–30. http://dx.doi.org/10.1039/c5ra23718a.
Повний текст джерелаGyarmati, Benjámin, Aysel Mammadova, Gergely Stankovits, Dóra Barczikai, and András Szilágyi. "Effect of Side Groups on the Hydrolytic Stability of Thiolated and Disulfide Cross-linked Polyaspartamides." Periodica Polytechnica Chemical Engineering 65, no. 2 (January 25, 2021): 183–91. http://dx.doi.org/10.3311/ppch.16869.
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