Статті в журналах з теми "Cocrystallization studies"
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Ren, Zhongqi, Xinjian Chen, Guojia Yu, Yinglei Wang, Bin Chen, and Zhiyong Zhou. "Molecular simulation studies on the design of energetic ammonium dinitramide co-crystals for tuning hygroscopicity." CrystEngComm 22, no. 31 (2020): 5237–44. http://dx.doi.org/10.1039/d0ce00602e.
Повний текст джерелаTimofeeva, Tatiana, Sofia Antal, Sergiu Draguta, Karla Ordonez, Raul Castaneda, and Evgeniya Leonova. "Cocrystallization of acetaminophen and glutaric acid with different coformers." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1028. http://dx.doi.org/10.1107/s2053273314089712.
Повний текст джерелаManoj, K., Rui Tamura, Hiroki Takahashi, and Hirohito Tsue. "Crystal engineering of homochiral molecular organization of naproxen in cocrystals and their thermal phase transformation studies." CrystEngComm 16, no. 26 (2014): 5811–19. http://dx.doi.org/10.1039/c3ce42415d.
Повний текст джерелаDuan, Binghui, Yuanjie Shu, Ning Liu, Yingying Lu, Bozhou Wang, Xianming Lu, and Jiaoqiang Zhang. "Comparative studies on structure, sensitivity and mechanical properties of CL-20/DNDAP cocrystal and composite by molecular dynamics simulation." RSC Advances 8, no. 60 (2018): 34690–98. http://dx.doi.org/10.1039/c8ra07387b.
Повний текст джерелаAsojo, Oluwatoyin Ajibola, Oluyomi Adebola Asojo, Michelle N. Ngamelue, Kohei Homma, and Oksana Lockridge. "Cocrystallization studies of full-length recombinant butyrylcholinesterase (BChE) with cocaine." Acta Crystallographica Section F Structural Biology and Crystallization Communications 67, no. 4 (March 24, 2011): 434–37. http://dx.doi.org/10.1107/s1744309111004805.
Повний текст джерелаXu, Jia, Qin Shi, Yanan Wang, Yong Wang, Junbo Xin, Jin Cheng, and Fang Li. "Recent Advances in Pharmaceutical Cocrystals: A Focused Review of Flavonoid Cocrystals." Molecules 28, no. 2 (January 6, 2023): 613. http://dx.doi.org/10.3390/molecules28020613.
Повний текст джерелаHiendrawan, Stevanus, Bambang Veriansyah, and Raymond R. Tjandrawinata. "SOLID-STATE PROPERTIES AND SOLUBILITY STUDIES OF NOVEL PHARMACEUTICAL COCRYSTAL OF ITRACONAZOLE." International Journal of Applied Pharmaceutics 10, no. 5 (September 8, 2018): 97. http://dx.doi.org/10.22159/ijap.2018v10i5.26663.
Повний текст джерелаMikheev, N. B., I. V. Melikhov, and S. A. Kulyukhin. "Cocrystallization processes in physicochemical studies of radioactive elements in various media." Radiochemistry 49, no. 6 (December 2007): 549–60. http://dx.doi.org/10.1134/s106636220706001x.
Повний текст джерелаShahbaz, Muhammad, Umair Ahmed Khan, M. Iqbal Chaudhary, and Sammer Yousuf. "A new bioactive cocrystal of coumarin-3-carboxylic acid and thiourea: detailed structural features and biological activity studies." Acta Crystallographica Section C Structural Chemistry 78, no. 3 (February 16, 2022): 192–200. http://dx.doi.org/10.1107/s205322962200081x.
Повний текст джерелаCarlucci, Lucia, and Angelo Gavezzotti. "A quantitative measure of halogen bond activation in cocrystallization." Physical Chemistry Chemical Physics 19, no. 28 (2017): 18383–88. http://dx.doi.org/10.1039/c7cp03322b.
Повний текст джерелаSalgado-Moran, Guillermo, Rodrigo Ramirez-Tagle, Daniel Glossman-Mitnik, Samuel Ruiz-Nieto, Pran Kishore-Deb, Marta Bunster, and Francisco Lobos-Gonzalez. "Docking Studies of Binding of Ethambutol to the C-Terminal Domain of the Arabinosyltransferase fromMycobacterium tuberculosis." Journal of Chemistry 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/601270.
Повний текст джерелаCHAMPAGNE, Claude P., Yves RAYMOND, Francine MONDOU, and Jean-Paul JULIEN. "Studies on the Encapsulation of Bifidobacterium longum Cultures by Spray-Coating or Cocrystallization." Bifidobacteria and Microflora 14, no. 1 (1995): 7–14. http://dx.doi.org/10.12938/bifidus1982.14.1_7.
Повний текст джерелаMashhadi, Syed Muddassir Ali, Andrei S. Batsanov, Syed Arslan Sajjad, Yasir Nazir, Moazzam Hussain Bhatti, and Uzma Yunus. "Isoniazid-Gentisic acid cocrystallization: Solubility, Stability, Dissolution rate, Antioxidant and Flowability Properties Studies." Journal of Molecular Structure 1226 (February 2021): 129388. http://dx.doi.org/10.1016/j.molstruc.2020.129388.
Повний текст джерелаGołdyn, Mateusz, Anna Komasa, Mateusz Pawlaczyk, Aneta Lewandowska, and Elżbieta Bartoszak-Adamska. "Salts of purine alkaloids caffeine and theobromine with 2,6-dihydroxybenzoic acid as coformer: structural, theoretical, thermal and spectroscopic studies." Acta Crystallographica Section C Structural Chemistry 77, no. 11 (October 27, 2021): 713–24. http://dx.doi.org/10.1107/s2053229621010883.
Повний текст джерелаKyu, Thein, and Parimal Vadhar. "Cocrystallization and miscibility studies of blends of ultrahigh molecular weight polyethylene with conventional polyethylenes." Journal of Applied Polymer Science 32, no. 6 (November 5, 1986): 5575–84. http://dx.doi.org/10.1002/app.1986.070320625.
Повний текст джерелаGao, Lei, and Xianrui Zhang. "Cocrystallization of Febuxostat with Pyridine Coformers: Crystal Structural and Physicochemical Properties Analysis." Journal of Chemistry 2021 (December 16, 2021): 1–8. http://dx.doi.org/10.1155/2021/3834368.
Повний текст джерелаBrandt, Ali K., Derek J. Boyle, Jacob P. Butler, Abigail R. Gillingham, Scott E. Penner, Jacqueline M. Spaniol, Alaina K. Stockdill, et al. "Molecular Recognition and Shape Studies of 3- and 4-Substituted Diarylamide Quasiracemates." Crystals 11, no. 12 (December 20, 2021): 1596. http://dx.doi.org/10.3390/cryst11121596.
Повний текст джерелаDalgarno, Scott J., Daniel B. Bassil, Sheryl A. Tucker, and Jerry L. Atwood. "Cocrystallization and Encapsulation of a Fluorophore with Hexameric Pyrogallol[4]arene Nanocapsules: Structural and Fluorescence Studies." Angewandte Chemie 118, no. 42 (October 27, 2006): 7177–80. http://dx.doi.org/10.1002/ange.200601961.
Повний текст джерелаDalgarno, Scott J., Daniel B. Bassil, Sheryl A. Tucker, and Jerry L. Atwood. "Cocrystallization and Encapsulation of a Fluorophore with Hexameric Pyrogallol[4]arene Nanocapsules: Structural and Fluorescence Studies." Angewandte Chemie International Edition 45, no. 42 (October 27, 2006): 7019–22. http://dx.doi.org/10.1002/anie.200601961.
Повний текст джерелаEmami, Shahram, Mohammadreza Siahi-Shadbad, Khosro Adibkia, and Mohammad Barzegar-Jalali. "Recent advances in improving oral drug bioavailability by cocrystals." BioImpacts 8, no. 4 (May 31, 2018): 305–20. http://dx.doi.org/10.15171/bi.2018.33.
Повний текст джерелаHoffmann, Sven, Bert Vanhaecht, Jan Devroede, Wim Bras, Cor E. Koning, and Sanjay Rastogi. "Cocrystallization in Piperazine-Based Polyamide Copolymers: Small- and Wide-Angle X-ray Diffraction Studies at 30 °C." Macromolecules 38, no. 5 (March 2005): 1797–803. http://dx.doi.org/10.1021/ma048456e.
Повний текст джерелаFaizan, Mohd, Vítor Hugo Nunes Rodrigues, and Shabbir Ahmad. "Cocrystallization of 2,3-dimethylquinoxaline with 3,5-dinitrobenzoic acid: Crystal structure, Hirshfeld surface, spectroscopic features and DFT studies." Journal of Molecular Structure 1198 (December 2019): 126894. http://dx.doi.org/10.1016/j.molstruc.2019.126894.
Повний текст джерелаSaikia, Prakash J., Narendra N. Dass, and Shashi D. Baruah. "Cocrystallization behavior of poly(n-docosyl acrylate) withn-docosanoic acid by X-ray and differential scanning calorimetry studies." Journal of Applied Polymer Science 97, no. 5 (2005): 2140–46. http://dx.doi.org/10.1002/app.21951.
Повний текст джерелаWróblewska, Aneta, Justyna Śniechowska, Sławomir Kaźmierski, Ewelina Wielgus, Grzegorz D. Bujacz, Grzegorz Mlostoń, Arkadiusz Chworos, Justyna Suwara, and Marek J. Potrzebowski. "Application of 1-Hydroxy-4,5-Dimethyl-Imidazole 3-Oxide as Coformer in Formation of Pharmaceutical Cocrystals." Pharmaceutics 12, no. 4 (April 15, 2020): 359. http://dx.doi.org/10.3390/pharmaceutics12040359.
Повний текст джерелаTilborg, Anaelle, Andrea Carletta, and Johan Wouters. "Structural and energy insights on solid-state complexes with trimethoprim: a combined theoretical and experimental investigation." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 71, no. 4 (July 14, 2015): 406–15. http://dx.doi.org/10.1107/s2052520615008422.
Повний текст джерелаMohana, Marimuthu, Packianathan Thomas Muthiah, and Colin D. McMillen. "Supramolecular architectures in two 1:1 cocrystals of 5-fluorouracil with 5-bromothiophene-2-carboxylic acid and thiophene-2-carboxylic acid." Acta Crystallographica Section C Structural Chemistry 73, no. 6 (May 25, 2017): 481–85. http://dx.doi.org/10.1107/s2053229617007550.
Повний текст джерелаP. Ahirrao, Sapana, Mayur P. Sonawane, Deepak S. Bhambere, Pavan B. Udavant, Eknath D. Ahire, Rupali Kanade, and Dinesh kuber. "Cocrystal Formulation: A Novel Approach to Enhance Solubility and Dissolution of Etodolac." Biosciences Biotechnology Research Asia 19, no. 1 (March 31, 2022): 111–19. http://dx.doi.org/10.13005/bbra/2971.
Повний текст джерелаKaplan, Nachum, Monique Albert, Donald Awrey, Elias Bardouniotis, Judd Berman, Teresa Clarke, Mandy Dorsey, et al. "Mode of Action,In VitroActivity, andIn VivoEfficacy of AFN-1252, a Selective Antistaphylococcal FabI Inhibitor." Antimicrobial Agents and Chemotherapy 56, no. 11 (September 4, 2012): 5865–74. http://dx.doi.org/10.1128/aac.01411-12.
Повний текст джерелаTemel, Ersin, Can Alaşalvar, Hande Eserci, and Erbil Ağar. "Experimental (X-ray, IR and UV–vis.) and DFT studies on cocrystallization of two tautomers of a novel Schiff base compound." Journal of Molecular Structure 1128 (January 2017): 5–12. http://dx.doi.org/10.1016/j.molstruc.2016.08.038.
Повний текст джерелаRodríguez-Ruiz, Christian, Pedro Montes-Tolentino, Jorge Guillermo Domínguez-Chávez, Hugo Morales-Rojas, Herbert Höpfl, and Dea Herrera-Ruiz. "Tailoring Chlorthalidone Aqueous Solubility by Cocrystallization: Stability and Dissolution Behavior of a Novel Chlorthalidone-Caffeine Cocrystal." Pharmaceutics 14, no. 2 (January 30, 2022): 334. http://dx.doi.org/10.3390/pharmaceutics14020334.
Повний текст джерелаGuan, Danyingzi, Bianfei Xuan, Chengguang Wang, Ruitao Long, Yaqin Jiang, Lina Mao, Jinbing Kang, Ziwen Wang, Shing Fung Chow, and Qun Zhou. "Improving the Physicochemical and Biopharmaceutical Properties of Active Pharmaceutical Ingredients Derived from Traditional Chinese Medicine through Cocrystal Engineering." Pharmaceutics 13, no. 12 (December 15, 2021): 2160. http://dx.doi.org/10.3390/pharmaceutics13122160.
Повний текст джерелаSpeetzen, Erin D., Chideraa I. Nwachukwu, Nathan P. Bowling та Eric Bosch. "Complementary, Cooperative Ditopic Halogen Bonding and Electron Donor-Acceptor π-π Complexation in the Formation of Cocrystals". Molecules 27, № 5 (24 лютого 2022): 1527. http://dx.doi.org/10.3390/molecules27051527.
Повний текст джерелаAsha, R. Nandini, V. Vel Murugan, P. Pon Matheswari, S. Kumaresan, N. Bhuvanesh та B. Ravindran Durai Nayagam. "Cocrystallization of 2,4-Diamino-6-phenyl-1,3,5-triazine with β-(phenylthio)propionic acid: Crystal structure, Hirshfeld surface, DFT studies and molecular docking". Chemical Data Collections 29 (жовтень 2020): 100520. http://dx.doi.org/10.1016/j.cdc.2020.100520.
Повний текст джерелаRavaud, Stephanie, Patrice Gouet, Richard Haser, and Nushin Aghajari. "Probing the Role of Divalent Metal Ions in a Bacterial Psychrophilic Metalloprotease: Binding Studies of an Enzyme in the Crystalline State by X-Ray Crystallography." Journal of Bacteriology 185, no. 14 (July 15, 2003): 4195–203. http://dx.doi.org/10.1128/jb.185.14.4195-4203.2003.
Повний текст джерелаWasim, Muhammad, Abdul Mannan, Muhammad Hassham Hassan Bin Asad, Muhammad Imran Amirzada, Muhammad Shafique, and Izhar Hussain. "Fabrication of Carbamazepine Cocrystals: Characterization, In Vitro and Comparative In Vivo Evaluation." BioMed Research International 2021 (March 15, 2021): 1–9. http://dx.doi.org/10.1155/2021/6685806.
Повний текст джерелаReddy, B. K. Kishore, Sudhir Landge, Sudha Ravishankar, Vikas Patil, Vikas Shinde, Subramanyam Tantry, Manoj Kale, et al. "Assessment of Mycobacterium tuberculosis Pantothenate Kinase Vulnerability through Target Knockdown and Mechanistically Diverse Inhibitors." Antimicrobial Agents and Chemotherapy 58, no. 6 (March 31, 2014): 3312–26. http://dx.doi.org/10.1128/aac.00140-14.
Повний текст джерелаBuysschaert, Geraldine, Kenneth Verstraete, Savvas N. Savvides, and Bjorn Vergauwen. "Crystallization of an atypical short-chain dehydrogenase fromVibrio vulnificuslacking the conserved catalytic tetrad." Acta Crystallographica Section F Structural Biology and Crystallization Communications 68, no. 7 (June 27, 2012): 771–74. http://dx.doi.org/10.1107/s1744309112018672.
Повний текст джерелаBala, Madhu, Manoj Kumar Gautam, and Renu Chadha. "What if Cocrystallization Fails for Neutral Molecules? Screening Offered Eutectics as Alternate Pharmaceutical Materials: Leflunomide-a Case Study." Pharmaceutical Sciences 25, no. 3 (September 30, 2019): 235–43. http://dx.doi.org/10.15171/ps.2019.46.
Повний текст джерелаSrivastava, Dipti, Zeeshan Fatima, Chanchal D. Kaur, Sachin L. Tulsankar, Sanap S. Nashik, and Dilshad A. Rizvi. "Pharmaceutical Cocrystal: A Novel Approach to Tailor the Biopharmaceutical Properties of a Poorly Water Soluble Drug." Recent Patents on Drug Delivery & Formulation 13, no. 1 (July 8, 2019): 62–69. http://dx.doi.org/10.2174/1872211313666190306160116.
Повний текст джерелаLi, Congwei, Pengfei Du, Meilin Zhou, Liuxin Yang, Haoyue Zhang, Jing Wang та Caiqin Yang. "Spectroscopic Methodology and Molecular Docking Studies on Changes in Binding Interaction of Felodipine with Bovine Serum Albumin Induced by Cocrystallization with β-Resorcylic Acid". Chemical and Pharmaceutical Bulletin 68, № 10 (1 жовтня 2020): 946–53. http://dx.doi.org/10.1248/cpb.c20-00212.
Повний текст джерелаPramanik, Titas, Mysore S. Pavan, and Tayur N. Guru Row. "Do halogen bonds dictate the packing preferences in solid solutions?" Faraday Discussions 203 (2017): 201–12. http://dx.doi.org/10.1039/c7fd00084g.
Повний текст джерелаGonzález-González, Juan Saulo, Raquel Jiménez-López, David Ortegón-Reyna, Gabino Gonzalez-Carrillo, and Francisco Javier Martínez-Martínez. "Mechanochemical Synthesis of the Catechol-Theophylline Cocrystal: Spectroscopic Characterization and Molecular Structure." Applied Sciences 11, no. 9 (April 23, 2021): 3810. http://dx.doi.org/10.3390/app11093810.
Повний текст джерелаBiscaia, Isabela Fanelli Barreto, Samantha Nascimento Gomes, Larissa Sakis Bernardi, and Paulo Renato Oliveira. "Obtaining Cocrystals by Reaction Crystallization Method: Pharmaceutical Applications." Pharmaceutics 13, no. 6 (June 17, 2021): 898. http://dx.doi.org/10.3390/pharmaceutics13060898.
Повний текст джерелаDoores, Katie J., and Dennis R. Burton. "Variable Loop Glycan Dependency of the Broad and Potent HIV-1-Neutralizing Antibodies PG9 and PG16." Journal of Virology 84, no. 20 (August 4, 2010): 10510–21. http://dx.doi.org/10.1128/jvi.00552-10.
Повний текст джерелаVandebroek, Laurens, Luc Van Meervelt, and Tatjana N. Parac-Vogt. "Direct observation of the ZrIV interaction with the carboxamide bond in a noncovalent complex between Hen Egg White Lysozyme and a Zr-substituted Keggin polyoxometalate." Acta Crystallographica Section C Structural Chemistry 74, no. 11 (October 19, 2018): 1348–54. http://dx.doi.org/10.1107/s2053229618010690.
Повний текст джерелаDhibar, Manami, Santanu Chakraborty, Souvik Basak, Paramita Pattanayak, Tanmay Chatterjee, Balaram Ghosh, Mohamed Raafat, and Mohammed A. S. Abourehab. "Critical Analysis and Optimization of Stoichiometric Ratio of Drug-Coformer on Cocrystal Design: Molecular Docking, In Vitro and In Vivo Assessment." Pharmaceuticals 16, no. 2 (February 13, 2023): 284. http://dx.doi.org/10.3390/ph16020284.
Повний текст джерелаSgourakis, Nikolaos, Kannan Natarajan, David Margulies, and Ad Bax. "A structural approach to the study of viral immune evasion mechanisms (TECH1P.850)." Journal of Immunology 192, no. 1_Supplement (May 1, 2014): 69.18. http://dx.doi.org/10.4049/jimmunol.192.supp.69.18.
Повний текст джерелаGuzei, Ilia A., and Kelsey C. Miles. "Ab initioX-ray structural characterization of an inclusion compound with a compositionally disordered chiral guest: no prior knowledge of the crystal composition." Acta Crystallographica Section C Structural Chemistry 72, no. 3 (February 10, 2016): 179–83. http://dx.doi.org/10.1107/s2053229616001972.
Повний текст джерелаSjuts, Hanno, Attilio V. Vargiu, Steven M. Kwasny, Son T. Nguyen, Hong-Suk Kim, Xiaoyuan Ding, Alina R. Ornik, et al. "Molecular basis for inhibition of AcrB multidrug efflux pump by novel and powerful pyranopyridine derivatives." Proceedings of the National Academy of Sciences 113, no. 13 (March 14, 2016): 3509–14. http://dx.doi.org/10.1073/pnas.1602472113.
Повний текст джерелаXiang, Yong, Khanita Karaveg та Kelley W. Moremen. "Substrate recognition and catalysis by GH47 α-mannosidases involved in Asn-linked glycan maturation in the mammalian secretory pathway". Proceedings of the National Academy of Sciences 113, № 49 (17 листопада 2016): E7890—E7899. http://dx.doi.org/10.1073/pnas.1611213113.
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