Artykuły w czasopismach na temat „Lipophilic Groups”
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Gaddale Devanna, Kishore K., Justyna M. Gawel, Tracy A. Prime, Filip Cvetko, Cristiane Benincá, Stuart T. Caldwell, Alexander Negoda i in. "Tetra-arylborate lipophilic anions as targeting groups". Chemical Communications 57, nr 25 (2021): 3147–50. http://dx.doi.org/10.1039/d0cc07924c.
Pełny tekst źródłaMadak, Joseph, i Nouri Neamati. "Membrane Permeable Lipophilic Cations as Mitochondrial Directing Groups". Current Topics in Medicinal Chemistry 15, nr 8 (13.03.2015): 745–66. http://dx.doi.org/10.2174/1568026615666150302105622.
Pełny tekst źródłaKoval'ov, N., I. Kuznetsova, E. Burakova, V. Sil'nikov, M. Zenkova i V. Vlassov. "Ribonuclease Activity of Cationic Structures Conjugated to Lipophilic Groups". Nucleosides, Nucleotides and Nucleic Acids 23, nr 6-7 (31.12.2004): 977–81. http://dx.doi.org/10.1081/ncn-200026050.
Pełny tekst źródłaVillanueva, María Emilia, Ana Salinas, Joaquín Antonio González, Sergio Teves i Guillermo Javier Copello. "Dual antibacterial effect of immobilized quaternary ammonium and aliphatic groups on PVC". New Journal of Chemistry 39, nr 12 (2015): 9200–9206. http://dx.doi.org/10.1039/c5nj01766a.
Pełny tekst źródłaGasiorowski, J., N. Pootrakulchote, C. Reanprayoon, K. Jaisabuy, P. Vanalabhpatana, N. S. Sariciftci i P. Thamyongkit. "Porphyrin containing lipophilic amide groups as a photosensitizer for dye-sensitized solar cells". RSC Advances 5, nr 89 (2015): 72900–72906. http://dx.doi.org/10.1039/c5ra10538b.
Pełny tekst źródłaZhao, Changming, Yulian Jiang, Mengwei Li, Tiexin Cheng, Wensheng Yang i Guangdong Zhou. "The effect of NaOH on lowering interfacial tension of oil/alkylbenzene sulfonates solution". RSC Advances 8, nr 11 (2018): 6169–77. http://dx.doi.org/10.1039/c7ra11287d.
Pełny tekst źródłaCzech, Bronislaw P., Anna Czech, Byungki Son, Han Koo Lee i Richard A. Bartsch. "Synthesis of lipophilic crown ethers with pendant carboxylic acid groups". Journal of Heterocyclic Chemistry 23, nr 2 (marzec 1986): 465–71. http://dx.doi.org/10.1002/jhet.5570230231.
Pełny tekst źródłaKong, Xiangjun, Junhe Zhao, Lijun Zhang, Zupei Liang i Jinlan Wang. "Design, synthesis and characterization of bitumen emulsifiers based on molecular simulation". Kemija u industriji 68, nr 1-2 (2019): 1–6. http://dx.doi.org/10.15255/kui.2018.013.
Pełny tekst źródłaDegtyareva, Ekaterina Aleksandrovna, Liliya Ivanovna Vyshnevska, Svetlana Vasil'yevna Garnaya i Ekaterina Aleksandrovna Kalko. "THE STUDY OF PHYSICO-TECHNOLOGICAL FACTORS’ INFLUENCE ON THE OUTPUT OF LIPOPHILIC SUB-STANCES FROM MEDICINAL PLANT MATERIALS". chemistry of plant raw material, nr 3 (7.04.2019): 299–305. http://dx.doi.org/10.14258/jcprm.2019035098.
Pełny tekst źródłaReichardt, Christian, Stefan Löbbecke, Abdol Mohammed Mehranpour i Gerhard Schäfer. "Pyridinium N-phenoxide betaines and their application to the determination of solvent polarities, XXIV. Syntheses and UV-vis spectroscopic properties of new lipophilic tert-butyl- and 1-adamantyl substituted, negatively solvatochromic pyridinium N-phenolate betaine dyes". Canadian Journal of Chemistry 76, nr 6 (1.06.1998): 686–94. http://dx.doi.org/10.1139/v98-019.
Pełny tekst źródłaHu, Hui, i Richard A. Bartsch. "Synthesis of lipophilic lariat ethers with pendantN-(X)sulfonyl carboxamide groups". Journal of Heterocyclic Chemistry 41, nr 4 (lipiec 2004): 557–62. http://dx.doi.org/10.1002/jhet.5570410412.
Pełny tekst źródłaÖzdemir, Mücahit, Begümhan Karapınar, Bahattin Yalçın, Ümit Salan, Mahmut Durmuş i Mustafa Bulut. "Synthesis and characterization of novel 7-oxy-3-ethyl-6-hexyl-4-methylcoumarin substituted metallo phthalocyanines and investigation of their photophysical and photochemical properties". Dalton Transactions 48, nr 34 (2019): 13046–56. http://dx.doi.org/10.1039/c9dt02687h.
Pełny tekst źródłaSilverio, Flaviano O., Luiz C. A. Barbosa, Celia R. A. Maltha, Armando J. D. Silvestre, Dorila Pilo-Veloso i Jose L. Gomide. "Characterization of lipophilic wood extractives from clones of Eucalyptus urograndis cultivate in Brazil". BioResources 2, nr 2 (27.02.2007): 157–68. http://dx.doi.org/10.15376/biores.2.2.157-168.
Pełny tekst źródłaEspaña Orozco, Sebastian, Philipp Zeitlinger, Karin Fackler, Robert H. Bischof i Antje Potthast. "A solid-phase extraction method that eliminates matrix effects of complex pulp mill effluents for the analysis of lipophilic wood extractives". Nordic Pulp & Paper Research Journal 35, nr 4 (18.11.2020): 577–88. http://dx.doi.org/10.1515/npprj-2020-0039.
Pełny tekst źródłaMacKellar, Calum, Duncan Graham, David W. Will, Stephen Burgess i Tom Brown. "Synthesis and physical properties ofanti-HIV antisense oligonucleotides bearing terminal lipophilic groups". Nucleic Acids Research 20, nr 13 (1992): 3411–17. http://dx.doi.org/10.1093/nar/20.13.3411.
Pełny tekst źródłaKim, Jong Seung, Jin Hyun Pang, Il Hwan Suh, Dae Whang Kim i Dong Won Kim. "Novel Calix[4]arene Dibenzocrown Ethers Bearing Lipophilic Alkyl Groups Symmetrically Branched". Synthetic Communications 28, nr 4 (luty 1998): 677–85. http://dx.doi.org/10.1080/00397919808005940.
Pełny tekst źródłaMelnyk, Inna, Nadiya Kovalska, Uliana Karpiuk i Nadiya Skripchenko. "The study of biological active compounds of lipophilic fraction of Schisandra chinensis (Turcz.) Baill seeds". Ukrainian Scientific Medical Youth Journal 131, nr 2 (23.06.2022): 78–84. http://dx.doi.org/10.32345/usmyj.2(131).2022.78-84.
Pełny tekst źródłaBrown, Charles R., David Culley, Meredith Bonierbale i Walter Amorós. "Anthocyanin, Carotenoid Content, and Antioxidant Values in Native South American Potato Cultivars". HortScience 42, nr 7 (grudzień 2007): 1733–36. http://dx.doi.org/10.21273/hortsci.42.7.1733.
Pełny tekst źródłaReguera, Beatriz, i Juan Blanco. "Dinophysis Toxins: Distribution, Fate in Shellfish and Impacts". Toxins 11, nr 7 (16.07.2019): 413. http://dx.doi.org/10.3390/toxins11070413.
Pełny tekst źródłaUeno, Yoshihito, Koshi Kawada, Tomoharu Naito, Aya Shibata, Kayo Yoshikawa, Hye-Sook Kim, Yusuke Wataya i Yukio Kitade. "Synthesis and silencing properties of siRNAs possessing lipophilic groups at their 3′-termini". Bioorganic & Medicinal Chemistry 16, nr 16 (sierpień 2008): 7698–704. http://dx.doi.org/10.1016/j.bmc.2008.07.010.
Pełny tekst źródłaUeno, Y., K. Kawada, A. Shibata, K. Yoshikawa, Y. Wataya i Y. Kitade. "Synthesis and silencing properties of siRNAs possessing lipophilic groups at their 3'-termini". Nucleic Acids Symposium Series 52, nr 1 (1.09.2008): 503–4. http://dx.doi.org/10.1093/nass/nrn255.
Pełny tekst źródłaBerlepsch, H. v., B. N. S. Thota, M. Wyszogrodzka, S. de Carlo, R. Haag i C. Böttcher. "Controlled self-assembly of stomatosomes by use of single-component fluorinated dendritic amphiphiles". Soft Matter 14, nr 25 (2018): 5256–69. http://dx.doi.org/10.1039/c8sm00243f.
Pełny tekst źródłaKobylańska, A., E. Pluskota, M. Swiatkowska, M. Wójcik, A. Cierniewska-Cieślak, A. Krakowiak, M. Boczkowska i in. "Inhibition of plasminogen activator inhibitor release in endothelial cell cultures by antisense oligodeoxyribonucleotides with a 5'-end lipophilic modification." Acta Biochimica Polonica 46, nr 3 (30.09.1999): 679–91. http://dx.doi.org/10.18388/abp.1999_4140.
Pełny tekst źródłaCaldwell, Stuart T., Donald B. McPhail, Garry G. Duthie i Richard C. Hartley. "Synthesis of polyhydroxylated flavonoids bearing a lipophilic decyl tail as potential therapeutic antioxidants". Canadian Journal of Chemistry 90, nr 1 (styczeń 2012): 23–33. http://dx.doi.org/10.1139/v11-087.
Pełny tekst źródłaSłota, Rudolf, Gabriela Dyrda, Maria Hofer, Giuseppe Mele, Ermelinda Bloise i Roberta del Sole. "Novel Lipophilic Lanthanide Bis-Phthalocyanines Functionalized by Pentadecylphenoxy Groups: Synthesis, Characterization and UV-Photostability". Molecules 17, nr 9 (7.09.2012): 10738–53. http://dx.doi.org/10.3390/molecules170910738.
Pełny tekst źródłaSeung Kim, J. "Metal ion complexation by acyclic polyethers with lipophilic amide, thioamide, and amine end groups". Talanta 51, nr 1 (24.01.2000): 99–105. http://dx.doi.org/10.1016/s0039-9140(99)00253-2.
Pełny tekst źródłaPozsgay, Vince. "A new strategy in oligosaccharide synthesis using lipophilic protecting groups: synthesis of a tetracosasaccharide". Tetrahedron: Asymmetry 11, nr 1 (styczeń 2000): 151–72. http://dx.doi.org/10.1016/s0957-4166(99)00553-4.
Pełny tekst źródłaHe, Ning, Kevin S. Warner, Doungdaw Chantasart, Dalia S. Shaker, William I. Higuchi i S. Kevin Li. "Mechanistic study of chemical skin permeation enhancers with different polar and lipophilic functional groups". Journal of Pharmaceutical Sciences 93, nr 6 (czerwiec 2004): 1415–30. http://dx.doi.org/10.1002/jps.20030.
Pełny tekst źródłaSmirnova, Alla L., Serguey S. Levitchev, Valentina L. Khitrova, Aleksandr L. Grekovich, Yurii G. Vlasov, Andree Schwake i Karl Cammann. "Effect of Simultaneous Existence of Two Ion-Exchangers with Opposite Charges of Lipophilic Groups". Electroanalysis 11, nr 10-11 (lipiec 1999): 763–69. http://dx.doi.org/10.1002/(sici)1521-4109(199907)11:10/11<763::aid-elan763>3.0.co;2-w.
Pełny tekst źródłaKIM, J. S., J. H. PANG, I. H. SUH, D. W. KIM i D. W. KIM. "ChemInform Abstract: Novel Calix[4]arene Dibenzocrown Ethers Bearing Lipophilic Alkyl Groups Symmetrically Branched." ChemInform 29, nr 26 (21.06.2010): no. http://dx.doi.org/10.1002/chin.199826203.
Pełny tekst źródłaWu, Ming Hua, Jian Peng Dong, Dong Ming Qi, Chong Qian i Xin Jiang. "Influence of the Hydrophile-Lipophile Property of Cross-Linker on the Properties of Acrylate Latex and its Film". Advanced Materials Research 441 (styczeń 2012): 466–72. http://dx.doi.org/10.4028/www.scientific.net/amr.441.466.
Pełny tekst źródłaLeyva-Valencia, Ignacio, Jesús Hernández-Castro, Christine Band-Schmidt, Andrew Turner, Alison O’Neill, Erick Núñez-Vázquez, David López-Cortés, José Bustillos-Guzmán i Francisco Hernández-Sandoval. "Lipophilic Toxins in Wild Bivalves from the Southern Gulf of California, Mexico". Marine Drugs 19, nr 2 (9.02.2021): 99. http://dx.doi.org/10.3390/md19020099.
Pełny tekst źródłaMarchesi, Elena, Rita Cortesi, Lorenzo Preti, Paola Rimessi, Maddalena Sguizzato, Matteo Bovolenta i Daniela Perrone. "Antisense Oligonucleotides Conjugated with Lipophilic Compounds: Synthesis and In Vitro Evaluation of Exon Skipping in Duchenne Muscular Dystrophy". International Journal of Molecular Sciences 23, nr 8 (12.04.2022): 4270. http://dx.doi.org/10.3390/ijms23084270.
Pełny tekst źródłaGagnon, M. Karen J., Timothy R. St. Germain, Christopher M. Vogels, Robert A. McNamara, Nicholas J. Taylor i Stephen A. Westcott. "Synthesis and hydroboration of lipophilic hydroxy-pyridinones and their complexes with molybdenum(VI)". Australian Journal of Chemistry 53, nr 8 (2000): 693. http://dx.doi.org/10.1071/ch00094.
Pełny tekst źródłaSpohr, Ulrike, Naohiko Morishima, Ole Hindsgaul i Raymond U. Lemieux. "Molecular recognition. IV. The binding of the Lewis b human blood group determinant by a hybridoma monoclonal antibody". Canadian Journal of Chemistry 63, nr 10 (1.10.1985): 2659–63. http://dx.doi.org/10.1139/v85-441.
Pełny tekst źródłaGrijalvo, Santiago, Montserrat Terrazas, Anna Aviñó i Ramón Eritja. "Stepwise synthesis of oligonucleotide–peptide conjugates containing guanidinium and lipophilic groups in their 3′-termini". Bioorganic & Medicinal Chemistry Letters 20, nr 7 (kwiecień 2010): 2144–47. http://dx.doi.org/10.1016/j.bmcl.2010.02.049.
Pełny tekst źródłaSVINARCHUK, F., D. KONEVETZ, O. PLIASUNOVA, A. POKROVSKY i V. VLASSOV. "Inhibition of HIV proliferation in MT-4 cells by antisense oligonucleotide conjugated to lipophilic groups". Biochimie 75, nr 1-2 (1993): 49–54. http://dx.doi.org/10.1016/0300-9084(93)90024-m.
Pełny tekst źródłaBratton, Larry D., Hwang Huh i Richard A. Bartsch. "New lipophilic crown ethers with intraannular carboxylic acid groups: Synthesis and alkali metal cation extraction". Journal of Heterocyclic Chemistry 37, nr 4 (lipiec 2000): 815–19. http://dx.doi.org/10.1002/jhet.5570370424.
Pełny tekst źródłaServinis, Linden, Kathleen M. Beggs, Christina Scheffler, Enrico Wölfel, James D. Randall, Thomas R. Gengenbach, Baris Demir i in. "Electrochemical surface modification of carbon fibres by grafting of amine, carboxylic and lipophilic amide groups". Carbon 118 (lipiec 2017): 393–403. http://dx.doi.org/10.1016/j.carbon.2017.03.064.
Pełny tekst źródłaCzech, Bronislaw P., Dhimant H. Desai, Jacek Koszuk, Anna Czech, David A. Babb, Thomas W. Robison i Richard A. Bartsch. "Synthesis of lipophilic crown ethers with pendant phosphonic acid or phosphonic acid monoethyl ester groups". Journal of Heterocyclic Chemistry 29, nr 4 (lipiec 1992): 867–75. http://dx.doi.org/10.1002/jhet.5570290433.
Pełny tekst źródłaXu, Bao Cai, Gui Ju Zhang, Yun Xia Li i Lu Cui. "Preparation and Properties of Amide Surfactants". Advanced Materials Research 550-553 (lipiec 2012): 99–102. http://dx.doi.org/10.4028/www.scientific.net/amr.550-553.99.
Pełny tekst źródłaPuchkov, Pavel A., i Michael A. Maslov. "Lipophilic Polyamines as Promising Components of Liposomal Gene Delivery Systems". Pharmaceutics 13, nr 6 (21.06.2021): 920. http://dx.doi.org/10.3390/pharmaceutics13060920.
Pełny tekst źródłaEblinger, Frank, i Hans-Jörg Schneider. "A Stereoselective Peptide-Based Artificial Receptor for Sugar Derivatives". Collection of Czechoslovak Chemical Communications 65, nr 5 (2000): 667–72. http://dx.doi.org/10.1135/cccc20000667.
Pełny tekst źródłaGao, Li Ming, Ramón Hernández, Jaime Matta i Enrique Meléndez. "Synthesis, Structure, Electrochemistry, and Cytotoxic Properties of Ferrocenyl Ester Derivatives". Metal-Based Drugs 2009 (24.03.2009): 1–8. http://dx.doi.org/10.1155/2009/420784.
Pełny tekst źródłaBurilov, Vladimir, Egor Makarov, Diana Mironova, Elza Sultanova, Islamiya Bilyukova, Kevser Akyol, Vladimir Evtugyn i in. "Calix[4]arene Polyamine Triazoles: Synthesis, Aggregation and DNA Binding". International Journal of Molecular Sciences 23, nr 23 (28.11.2022): 14889. http://dx.doi.org/10.3390/ijms232314889.
Pełny tekst źródłaGreen, Jerry M., i Theresa Hale. "Increasing and Decreasing pH to Enhance the Biological Activity of Nicosulfuron". Weed Technology 19, nr 2 (czerwiec 2005): 468–75. http://dx.doi.org/10.1614/wt-04-001r5.
Pełny tekst źródłaNeis, Christian, Günter J. Merten i Kaspar Hegetschweiler. "Tris(cis-2-hydroxycyclohexane-1,3,5-triaminium) hydrogen sulfate octachloride dihydrate". Acta Crystallographica Section E Structure Reports Online 68, nr 6 (26.05.2012): o1899—o1900. http://dx.doi.org/10.1107/s1600536812022374.
Pełny tekst źródłaLavoie, Jean-Michel, i Tatjana Stevanovic. "Yield and composition of lipophylic extracts of yellow birch (Betula alleghaniensis Britton) as a function of wood age and aging under industrial conditions". Holzforschung 60, nr 2 (1.03.2006): 184–89. http://dx.doi.org/10.1515/hf.2006.030.
Pełny tekst źródłaSteiner, Andreas J., Arnold E. Stütz, Chris A. Tarling, Stephen G. Withers i Tanja M. Wrodnigg. "Synthesis and Biological Evaluation of 1,5-Dideoxy-1,5-iminoxylitol–Amino Acid Hybrids as Xylosidase Inhibitors". Australian Journal of Chemistry 62, nr 6 (2009): 553. http://dx.doi.org/10.1071/ch09040.
Pełny tekst źródłaHaverkate, Natalie A., Euphemia Leung, Lisa I. Pilkington i David Barker. "Tethered Aryl Groups Increase the Activity of Anti-Proliferative Thieno[2,3-b]Pyridines by Targeting a Lipophilic Region in the Active Site of PI-PLC". Pharmaceutics 13, nr 12 (26.11.2021): 2020. http://dx.doi.org/10.3390/pharmaceutics13122020.
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