Статті в журналах з теми "Molecular cocrystals"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Molecular cocrystals".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Yang, Shiying, Qiwen Liu, Weiwen Ji, Qi An, Junke Song, Cheng Xing, Dezhi Yang, Li Zhang, Yang Lu, and Guanhua Du. "Cocrystals of Praziquantel with Phenolic Acids: Discovery, Characterization, and Evaluation." Molecules 27, no. 6 (March 21, 2022): 2022. http://dx.doi.org/10.3390/molecules27062022.
Повний текст джерелаWan, Mei, Jiyuan Fang, Jiadan Xue, Jianjun Liu, Jianyuan Qin, Zhi Hong, Jiusheng Li, and Yong Du. "Pharmaceutical Cocrystals of Ethenzamide: Molecular Structure Analysis Based on Vibrational Spectra and DFT Calculations." International Journal of Molecular Sciences 23, no. 15 (August 1, 2022): 8550. http://dx.doi.org/10.3390/ijms23158550.
Повний текст джерелаGonzález-González, Juan Saulo, Ana María Monserrat Martínez-Santiago, Francisco Javier Martínez-Martínez, María José Emparán-Legaspi, Armando Pineda-Contreras, Marcos Flores-Alamo, and Héctor García-Ortega. "Cocrystals of Isoniazid with Polyphenols: Mechanochemical Synthesis and Molecular Structure." Crystals 10, no. 7 (July 2, 2020): 569. http://dx.doi.org/10.3390/cryst10070569.
Повний текст джерелаManin, Alex N., Denis E. Boycov, Olga R. Simonova, Tatyana V. Volkova, Andrei V. Churakov, and German L. Perlovich. "Formation Thermodynamics of Carbamazepine with Benzamide, Para-Hydroxybenzamide and Isonicotinamide Cocrystals: Experimental and Theoretical Study." Pharmaceutics 14, no. 9 (September 6, 2022): 1881. http://dx.doi.org/10.3390/pharmaceutics14091881.
Повний текст джерелаMir, Niyaz A., Ritesh Dubey, and Gautam R. Desiraju. "Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence." IUCrJ 3, no. 2 (January 5, 2016): 96–101. http://dx.doi.org/10.1107/s2052252515023945.
Повний текст джерелаPatel, Diksha J., and Prashant K. Puranik. "Pharmaceutical Co-crystal : An Emerging Technique to enhance Physicochemical properties of drugs." International Journal of ChemTech Research 13, no. 3 (2020): 283–90. http://dx.doi.org/10.20902/ijctr.2019.130326.
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 джерелаDubey, Ritesh, Niyaz A. Mir, and Gautam R. Desiraju. "Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)." IUCrJ 3, no. 2 (January 5, 2016): 102–7. http://dx.doi.org/10.1107/s2052252515023957.
Повний текст джерелаTutughamiarso, Maya, and Ernst Egert. "Cocrystals of 5-fluorocytosine. II. Coformers with variable hydrogen-bonding sites." Acta Crystallographica Section B Structural Science 68, no. 4 (July 17, 2012): 444–52. http://dx.doi.org/10.1107/s0108768112029977.
Повний текст джерелаRajkumar, Madhu, and Gautam R. Desiraju. "Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol." IUCrJ 8, no. 2 (January 11, 2021): 178–85. http://dx.doi.org/10.1107/s2052252520016589.
Повний текст джерелаTopić, Filip, Katarina Lisac, Mihails Arhangelskis, Kari Rissanen, Dominik Cinčić, and Tomislav Friščić. "Cocrystal trimorphism as a consequence of the orthogonality of halogen- and hydrogen-bonds synthons." Chemical Communications 55, no. 93 (2019): 14066–69. http://dx.doi.org/10.1039/c9cc06735c.
Повний текст джерелаSun, Shanhu, Haobin Zhang, Jinjiang Xu, Hongfan Wang, Shumin Wang, Zhihui Yu, Chunhua Zhu, and Jie Sun. "Design, preparation, characterization and formation mechanism of a novel kinetic CL-20-based cocrystal." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 75, no. 3 (May 9, 2019): 310–17. http://dx.doi.org/10.1107/s2052520619002816.
Повний текст джерелаDudek, Marta K., Ewelina Wielgus, Piotr Paluch, Justyna Śniechowska, Maciej Kostrzewa, Graeme M. Day, Grzegorz D. Bujacz, and Marek J. Potrzebowski. "Understanding the formation of apremilast cocrystals." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 75, no. 5 (September 7, 2019): 803–14. http://dx.doi.org/10.1107/s205252061900917x.
Повний текст джерелаSathisaran, Indumathi, and Sameer Dalvi. "Engineering Cocrystals of Poorly Water-Soluble Drugs to Enhance Dissolution in Aqueous Medium." Pharmaceutics 10, no. 3 (July 31, 2018): 108. http://dx.doi.org/10.3390/pharmaceutics10030108.
Повний текст джерелаMacGillivray, L. R., A. N. Sokolov, D. K. Bucar, and P. Kaushik. "Functional molecular cocrystals." Acta Crystallographica Section A Foundations of Crystallography 63, a1 (August 22, 2007): s41. http://dx.doi.org/10.1107/s0108767307099084.
Повний текст джерелаSun, Shanhu, Haobin Zhang, Jinjiang Xu, Shumin Wang, Hongfan Wang, Zhihui Yu, Lang Zhao, Chunhua Zhu, and Jie Sun. "The competition between cocrystallization and separated crystallization based on crystallization from solution." Journal of Applied Crystallography 52, no. 4 (July 8, 2019): 769–76. http://dx.doi.org/10.1107/s1600576719008094.
Повний текст джерелаÁlvarez-Vidaurre, Raquel, Alfonso Castiñeiras, Isabel García-Santos та Rocío Torres-Iglesias. "Interactions between Isoniazid and α-Hydroxycarboxylic Acids". Chemistry Proceedings 3, № 1 (14 листопада 2020): 73. http://dx.doi.org/10.3390/ecsoc-24-08355.
Повний текст джерелаJones, William, W. D. Samuel Motherwell, and Andrew V. Trask. "Pharmaceutical Cocrystals: An Emerging Approach to Physical Property Enhancement." MRS Bulletin 31, no. 11 (November 2006): 875–79. http://dx.doi.org/10.1557/mrs2006.206.
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 джерелаKloda, Matouš, Irena Matulková, Ivana Císařová, Petra Becker, Ladislav Bohatý, Petr Němec, Róbert Gyepes, and Ivan Němec. "Cocrystals of 2-Aminopyrimidine with Boric Acid—Crystal Engineering of a Novel Nonlinear Optically (NLO) Active Crystal." Crystals 9, no. 8 (August 3, 2019): 403. http://dx.doi.org/10.3390/cryst9080403.
Повний текст джерелаLiu, Yan, Chongwei An, Jin Luo, and Jingyu Wang. "High-density HNIW/TNT cocrystal synthesized using a green chemical method." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 74, no. 4 (July 23, 2018): 385–93. http://dx.doi.org/10.1107/s2052520618008442.
Повний текст джерелаXie, Yifei, Penghui Yuan, Tianyu Heng, Lida Du, Qi An, Baoxi Zhang, Li Zhang, Dezhi Yang, Guanhua Du, and Yang Lu. "Insight into the Formation of Cocrystal and Salt of Tenoxicam from the Isomer and Conformation." Pharmaceutics 14, no. 9 (September 19, 2022): 1968. http://dx.doi.org/10.3390/pharmaceutics14091968.
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 джерелаRoy, Monalisa, Keyao Li, Madiha Nisar, Lawrence W. Y. Wong, Herman H. Y. Sung, Richard K. Haynes, and Ian D. Williams. "Varying degrees of homostructurality in a series of cocrystals of antimalarial drug 11-azaartemisinin with salicylic acids." Acta Crystallographica Section C Structural Chemistry 77, no. 6 (May 6, 2021): 262–70. http://dx.doi.org/10.1107/s2053229621004460.
Повний текст джерелаBolla, Geetha, Vladimir Chernyshev, and Ashwini Nangia. "Acemetacin cocrystal structures by powder X-ray diffraction." IUCrJ 4, no. 3 (March 8, 2017): 206–14. http://dx.doi.org/10.1107/s2052252517002305.
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 джерелаEvtushenko, Diana N., Sergey G. Arkhipov, Alexander V. Fateev, Tatyana I. Izaak, Lidia A. Egorova, Nina A. Skorik, Olga V. Vodyankina, and Elena V. Boldyreva. "A cocrystal of L-ascorbic acid with picolinic acid: the role of O—H...O, N—H...O and C—H...O hydrogen bonds and L-ascorbic acid conformation in structure stabilization." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 76, no. 6 (November 3, 2020): 967–78. http://dx.doi.org/10.1107/s2052520620012421.
Повний текст джерелаDevogelaer, Jan-Joris, Hugo Meekes, Elias Vlieg, and René de Gelder. "Cocrystals in the Cambridge Structural Database: a network approach." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 75, no. 3 (May 18, 2019): 371–83. http://dx.doi.org/10.1107/s2052520619004694.
Повний текст джерелаBalakrishnan, C., M. Manonmani, S. Rafi Ahamed, G. Vinitha, S. P. Meenakshisundaram, and R. M. Sockalingam. "Supramolecular cocrystals of O—H...O hydrogen-bonded 18-crown-6 with isophthalic acid derivatives: Hirshfeld surface analysis and third-order nonlinear optical properties." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 76, no. 2 (March 19, 2020): 241–51. http://dx.doi.org/10.1107/s2052520620001821.
Повний текст джерелаXue, Na, Yutao Jia, Congwei Li, Binnan He, Caiqin Yang та Jing Wang. "Characterizations and Assays of α-Glucosidase Inhibition Activity on Gallic Acid Cocrystals: Can the Cocrystals be Defined as a New Chemical Entity During Binding with the α-Glucosidase?" Molecules 25, № 5 (5 березня 2020): 1163. http://dx.doi.org/10.3390/molecules25051163.
Повний текст джерелаKarothu, Durga Prasad, Ilma Jahović, Gligor Jovanovski, Branko Kaitner, and Panče Naumov. "Ionic cocrystals of molecular saccharin." CrystEngComm 19, no. 30 (2017): 4338–44. http://dx.doi.org/10.1039/c7ce00627f.
Повний текст джерелаWang, Na, Xin Huang, Lihang Chen, Jinyue Yang, Xin Li, Jiayuan Ma, Ying Bao, Fei Li, Qiuxiang Yin, and Hongxun Hao. "Consistency and variability of cocrystals containing positional isomers: the self-assembly evolution mechanism of supramolecular synthons of cresol–piperazine." IUCrJ 6, no. 6 (October 9, 2019): 1064–73. http://dx.doi.org/10.1107/s2052252519012363.
Повний текст джерелаRahmani, Maryam, Vijith Kumar, Julia Bruno-Colmenarez, and Michael J. Zaworotko. "Crystal Engineering of Ionic Cocrystals Sustained by Azolium···Azole Heterosynthons." Pharmaceutics 14, no. 11 (October 28, 2022): 2321. http://dx.doi.org/10.3390/pharmaceutics14112321.
Повний текст джерелаJavoor, Manjunath, Pradip Mondal, and Deepak Chopra. "Cocrystals: A Review of Recent Trends in Pharmaceutical and Material Science Applications." Material Science Research India 14, no. 1 (June 17, 2017): 09–18. http://dx.doi.org/10.13005/msri/140103.
Повний текст джерелаGawade, Ashwini, Ashwin Kuchekar, Sanjay Boldhane, and Akshay Baheti. "Improvement of Physicochemical and Solubility of Dipyridamole by Cocrystallization Technology." Journal of Drug Delivery and Therapeutics 11, no. 1-s (February 15, 2021): 43–48. http://dx.doi.org/10.22270/jddt.v11i1-s.4696.
Повний текст джерелаMcArdle, Patrick, and Andrea Erxleben. "Sublimation – a green route to new solid-state forms." CrystEngComm 23, no. 35 (2021): 5965–75. http://dx.doi.org/10.1039/d1ce00715g.
Повний текст джерелаAakeröy, C. B. "Constructing, deconstructing, and reconstructing molecular cocrystals." Acta Crystallographica Section A Foundations of Crystallography 63, a1 (August 22, 2007): s39. http://dx.doi.org/10.1107/s0108767307099138.
Повний текст джерелаTojiboev, A., R. Okmanov, K. Turgunov, B. Tashkhodjaev, N. Mukarramov, and K. Shakhidoyatov. "Molecular cocrystals of peganole with peganine." Acta Crystallographica Section A Foundations of Crystallography 64, a1 (August 23, 2008): C477. http://dx.doi.org/10.1107/s0108767308084675.
Повний текст джерелаRodríguez-Hornedo, Naír. "Cocrystals: Molecular Design of Pharmaceutical Materials." Molecular Pharmaceutics 4, no. 3 (June 2007): 299–300. http://dx.doi.org/10.1021/mp070042v.
Повний текст джерелаBrittain, Harry G. "Vibrational Spectroscopic Study of the Cocrystal Products Formed by Cinchona Alkaloids with 5-Nitrobarbituric Acid." Journal of Spectroscopy 2015 (2015): 1–13. http://dx.doi.org/10.1155/2015/340460.
Повний текст джерелаMswahili, Medard Edmund, Min-Jeong Lee, Gati Lother Martin, Junghyun Kim, Paul Kim, Guang J. Choi, and Young-Seob Jeong. "Cocrystal Prediction Using Machine Learning Models and Descriptors." Applied Sciences 11, no. 3 (February 1, 2021): 1323. http://dx.doi.org/10.3390/app11031323.
Повний текст джерелаSun, Lingjie, Weigang Zhu, Fangxu Yang, Baili Li, Xiaochen Ren, Xiaotao Zhang, and Wenping Hu. "Molecular cocrystals: design, charge-transfer and optoelectronic functionality." Physical Chemistry Chemical Physics 20, no. 9 (2018): 6009–23. http://dx.doi.org/10.1039/c7cp07167a.
Повний текст джерелаRajendrakumar, Satyasree, Anuja Surampudi Venkata Sai Durga, and Sridhar Balasubramanian. "Strategic synthon approach in obtaining cocrystals and cocrystal polymorphs of a high-Z′ system deferiprone – an anti-thalassemia drug." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 77, no. 6 (November 12, 2021): 946–64. http://dx.doi.org/10.1107/s205252062100980x.
Повний текст джерелаLee, Min-Jeong, Srinivasulu Aitipamula, Guang J. Choi, and Pui Shan Chow. "Agomelatine–hydroquinone (1:1) cocrystal: novel polymorphs and their thermodynamic relationship." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 75, no. 6 (November 6, 2019): 969–77. http://dx.doi.org/10.1107/s2052520619011739.
Повний текст джерелаMohamed, Sharmarke, Ahmad A. Alwan, Tomislav Friščić, Andrew J. Morris, and Mihails Arhangelskis. "Towards the systematic crystallisation of molecular ionic cocrystals: insights from computed crystal form landscapes." Faraday Discussions 211 (2018): 401–24. http://dx.doi.org/10.1039/c8fd00036k.
Повний текст джерелаTutughamiarso, Maya, Guido Wagner, and Ernst Egert. "Cocrystals of 5-fluorocytosine. I. Coformers with fixed hydrogen-bonding sites." Acta Crystallographica Section B Structural Science 68, no. 4 (July 17, 2012): 431–43. http://dx.doi.org/10.1107/s010876811202561x.
Повний текст джерелаLynch, Daniel E., Manpreet Singh, and Simon Parsons. "Molecular cocrystals of 2-amino-5-chlorobenzooxazole." Crystal Engineering 3, no. 1 (March 2000): 71–79. http://dx.doi.org/10.1016/s1463-0184(00)00029-0.
Повний текст джерелаLiu, Wenwen, Ru Ma, Feifei Liang, Chenxin Duan, Guisen Zhang, Yin Chen, and Chao Hao. "New Cocrystals of Antipsychotic Drug Aripiprazole: Decreasing the Dissolution through Cocrystallization." Molecules 26, no. 9 (April 21, 2021): 2414. http://dx.doi.org/10.3390/molecules26092414.
Повний текст джерелаKamis, Mohamad Nor Amirul Azhar, Hamizah Mohd Zaki, Nornizar Anuar, and Mohammad Noor Jalil. "Synthesis, Characterization and Morphological Study of Nicotinamide and p-Coumaric Acid Cocrystal." Indonesian Journal of Chemistry 20, no. 3 (May 9, 2020): 661. http://dx.doi.org/10.22146/ijc.45530.
Повний текст джерелаSarmah, Kashyap Kumar, Trishna Rajbongshi, Sourav Bhowmick, and Ranjit Thakuria. "First-line antituberculosis drug, pyrazinamide, its pharmaceutically relevant cocrystals and a salt." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 73, no. 5 (September 29, 2017): 1007–16. http://dx.doi.org/10.1107/s2052520617011477.
Повний текст джерела