Artículos de revistas sobre el tema "Stoichiometric cocrystal"
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Mir, Niyaz A., Ritesh Dubey y Gautam R. Desiraju. "Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence". IUCrJ 3, n.º 2 (5 de enero de 2016): 96–101. http://dx.doi.org/10.1107/s2052252515023945.
Texto completoTopić, Filip y Tomislav Friščić. "No regioselectivity for the steroid α-face in cocrystallization of exemestane with aromatic cocrystal formers based on phenanthrene and pyrene". Canadian Journal of Chemistry 98, n.º 7 (julio de 2020): 386–93. http://dx.doi.org/10.1139/cjc-2020-0073.
Texto completoDhibar, Manami, Santanu Chakraborty, Souvik Basak, Paramita Pattanayak, Tanmay Chatterjee, Balaram Ghosh, Mohamed Raafat y 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, n.º 2 (13 de febrero de 2023): 284. http://dx.doi.org/10.3390/ph16020284.
Texto completoRajkumar, Madhu y Gautam R. Desiraju. "Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol". IUCrJ 8, n.º 2 (11 de enero de 2021): 178–85. http://dx.doi.org/10.1107/s2052252520016589.
Texto completoPanzade, Prabhakar, Priyanka Somani y Pavan Rathi. "Nevirapine Pharmaceutical Cocrystal: Design, Development and Formulation". Drug Delivery Letters 9, n.º 3 (20 de agosto de 2019): 240–47. http://dx.doi.org/10.2174/2210303109666190411125857.
Texto completoTupe, Suraj Ankush, Shital Prabhakar Khandagale y Amrapali B. Jadhav. "Pharmaceutical Cocrystals: An Emerging Approach to Modulate Physicochemical Properties of Active Pharmaceutical Ingredients". Journal of Drug Delivery and Therapeutics 13, n.º 4 (15 de abril de 2023): 101–12. http://dx.doi.org/10.22270/jddt.v13i4.6016.
Texto completoKimoto, Kouya, Mitsuo Yamamoto, Masatoshi Karashima, Miyuki Hohokabe, Junpei Takeda, Katsuhiko Yamamoto y Yukihiro Ikeda. "Pharmaceutical Cocrystal Development of TAK-020 with Enhanced Oral Absorption". Crystals 10, n.º 3 (18 de marzo de 2020): 211. http://dx.doi.org/10.3390/cryst10030211.
Texto completoBiscaia, Isabela Fanelli Barreto, Samantha Nascimento Gomes, Larissa Sakis Bernardi y Paulo Renato Oliveira. "Obtaining Cocrystals by Reaction Crystallization Method: Pharmaceutical Applications". Pharmaceutics 13, n.º 6 (17 de junio de 2021): 898. http://dx.doi.org/10.3390/pharmaceutics13060898.
Texto completoNajih, Yuli Ainun, Farizah Izazi, Siswandono Siswandono y Bella Anggraini Putri. "STUDI IN SILICO PEMBENTUKAN KOKRISTAL MELOXICAM DENGAN BERBAGAI KOFORMER PERBANDINGAN (1 : 1)". Jurnal Ilmiah Ibnu Sina (JIIS): Ilmu Farmasi dan Kesehatan 8, n.º 1 (31 de marzo de 2023): 31–38. http://dx.doi.org/10.36387/jiis.v8i1.1086.
Texto completoRodríguez-Ruiz, Christian, Pedro Montes-Tolentino, Jorge Guillermo Domínguez-Chávez, Hugo Morales-Rojas, Herbert Höpfl y Dea Herrera-Ruiz. "Tailoring Chlorthalidone Aqueous Solubility by Cocrystallization: Stability and Dissolution Behavior of a Novel Chlorthalidone-Caffeine Cocrystal". Pharmaceutics 14, n.º 2 (30 de enero de 2022): 334. http://dx.doi.org/10.3390/pharmaceutics14020334.
Texto completoPatel, Diksha J. y Prashant K. Puranik. "Pharmaceutical Co-crystal : An Emerging Technique to enhance Physicochemical properties of drugs". International Journal of ChemTech Research 13, n.º 3 (2020): 283–90. http://dx.doi.org/10.20902/ijctr.2019.130326.
Texto completoWicaksono, Yudi, Dwi Setyawan y Siswandono Siswandono. "Formation of Ketoprofen-Malonic Acid Cocrystal by Solvent Evaporation Method". Indonesian Journal of Chemistry 17, n.º 2 (31 de julio de 2017): 161. http://dx.doi.org/10.22146/ijc.24884.
Texto completoRajendrakumar, Satyasree, Anuja Surampudi Venkata Sai Durga y 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, n.º 6 (12 de noviembre de 2021): 946–64. http://dx.doi.org/10.1107/s205252062100980x.
Texto completoWang, Hui y Wei Jun Jin. "Cocrystal assembled by 1,4-diiodotetrafluorobenzene and phenothiazine based on C—I...π/N/S halogen bond and other assisting interactions". Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 73, n.º 2 (29 de marzo de 2017): 210–16. http://dx.doi.org/10.1107/s2052520617002918.
Texto completoLi, Zi y Adam J. Matzger. "Influence of Coformer Stoichiometric Ratio on Pharmaceutical Cocrystal Dissolution: Three Cocrystals of Carbamazepine/4-Aminobenzoic Acid". Molecular Pharmaceutics 13, n.º 3 (3 de febrero de 2016): 990–95. http://dx.doi.org/10.1021/acs.molpharmaceut.5b00843.
Texto completoAvdeef, Alex. "Cocrystal solubility-pH and drug solubilization capacity of sodium dodecyl sulfate – mass action model for data analysis and simulation to improve design of experiments". ADMET and DMPK 6, n.º 2 (16 de junio de 2018): 105–39. http://dx.doi.org/10.5599/admet.505.
Texto completoSouza, Fayene Zeferino Ribeiro de, Amanda Cosmo de Almeida, Patr�cia Osorio Ferreira, Richard Perosa Fernandes y Fl�vio Junior Caires. "Screening of coformers for quercetin cocrystals through mechanochemical methods". Ecl�tica Qu�mica Journal 47, n.º 1 (1 de enero de 2022): 64–75. http://dx.doi.org/10.26850/1678-4618eqj.v47.1.2022.p64-75.
Texto completoLiu, Xiaojiao, Adam A. L. Michalchuk, Colin R. Pulham y Elena V. Boldyreva. "An acetonitrile-solvated cocrystal of piroxicam and succinic acid with co-existing zwitterionic and non-ionized piroxicam molecules". Acta Crystallographica Section C Structural Chemistry 75, n.º 1 (1 de enero de 2019): 29–37. http://dx.doi.org/10.1107/s2053229618016911.
Texto completoHong, Chao, Yan Xie, Yashu Yao, Guowen Li, Xiurong Yuan y Hongyi Shen. "A Novel Strategy for Pharmaceutical Cocrystal Generation Without Knowledge of Stoichiometric Ratio: Myricetin Cocrystals and a Ternary Phase Diagram". Pharmaceutical Research 32, n.º 1 (18 de junio de 2014): 47–60. http://dx.doi.org/10.1007/s11095-014-1443-y.
Texto completoZhou, Zhengzheng, Hok Man Chan, Herman H. Y. Sung, Henry H. Y. Tong y Ying Zheng. "Identification of New Cocrystal Systems with Stoichiometric Diversity of Salicylic Acid Using Thermal Methods". Pharmaceutical Research 33, n.º 4 (7 de enero de 2016): 1030–39. http://dx.doi.org/10.1007/s11095-015-1849-1.
Texto completoZotova, Julija, Zaneta Wojnarowska, Brendan Twamley y Lidia Tajber. "Formation of stoichiometric and non-stoichiometric ionic liquid and cocrystal multicomponent phases of lidocaine with azelaic acid by changing counterion ratios". Journal of Molecular Liquids 344 (diciembre de 2021): 117737. http://dx.doi.org/10.1016/j.molliq.2021.117737.
Texto completoZotova, Julija, Zaneta Wojnarowska, Brendan Twamley y Lidia Tajber. "Formation of stoichiometric and non-stoichiometric ionic liquid and cocrystal multicomponent phases of lidocaine with azelaic acid by changing counterion ratios". Journal of Molecular Liquids 344 (diciembre de 2021): 117737. http://dx.doi.org/10.1016/j.molliq.2021.117737.
Texto completoHajjar, Christelle, Tamali Nag, Hashim Al Sayed, Jeffrey S. Ovens y David L. Bryce. "Stoichiomorphic halogen-bonded cocrystals: a case study of 1,4-diiodotetrafluorobenzene and 3-nitropyridine". Canadian Journal of Chemistry 100, n.º 4 (abril de 2022): 245–51. http://dx.doi.org/10.1139/cjc-2021-0245.
Texto completoOh, Se Ye, Christopher W. Nickels, Felipe Garcia, William Jones y Tomislav Friščić. "Switching between halogen- and hydrogen-bonding in stoichiometric variations of a cocrystal of a phosphine oxide". CrystEngComm 14, n.º 19 (2012): 6110. http://dx.doi.org/10.1039/c2ce25653c.
Texto completoDurán-Palma, Melissa Hidekel, Sonia Sanet Mendoza-Barraza, Nancy Evelyn Magaña-Vergara, Francisco Javier Martínez-Martínez y Juan Saulo González-González. "Crystal structure of pharmaceutical cocrystals of 2,6-diaminopyridine with piracetam and theophylline". Acta Crystallographica Section C Structural Chemistry 73, n.º 10 (20 de septiembre de 2017): 767–72. http://dx.doi.org/10.1107/s205322961701230x.
Texto completoMachado Cruz, Ricardo, Tereza Boleslavská, Josef Beránek, Eszter Tieger, Brendan Twamley, Maria Jose Santos-Martinez, Ondřej Dammer y Lidia Tajber. "Identification and Pharmaceutical Characterization of a New Itraconazole Terephthalic Acid Cocrystal". Pharmaceutics 12, n.º 8 (6 de agosto de 2020): 741. http://dx.doi.org/10.3390/pharmaceutics12080741.
Texto completoT, Mamatha, Sama M y Husna K. Qureshi. "Development and Evaluation of Mesalamine—Glutamine Cocrystal Tablets for Colon Specific Delivery". International Journal of Pharmaceutical Sciences and Nanotechnology 10, n.º 5 (30 de septiembre de 2017): 3866–74. http://dx.doi.org/10.37285/ijpsn.2017.10.5.8.
Texto completoClark, Nathaniel E., Adam Katolik, Kenneth M. Roberts, Alexander B. Taylor, Stephen P. Holloway, Jonathan P. Schuermann, Eric J. Montemayor et al. "Metal dependence and branched RNA cocrystal structures of the RNA lariat debranching enzyme Dbr1". Proceedings of the National Academy of Sciences 113, n.º 51 (6 de diciembre de 2016): 14727–32. http://dx.doi.org/10.1073/pnas.1612729114.
Texto completoTrask, Andrew V., Jacco van de Streek, W. D. Samuel Motherwell y William Jones. "Achieving Polymorphic and Stoichiometric Diversity in Cocrystal Formation: Importance of Solid-State Grinding, Powder X-ray Structure Determination, and Seeding". Crystal Growth & Design 5, n.º 6 (noviembre de 2005): 2233–41. http://dx.doi.org/10.1021/cg0501682.
Texto completoMartinez, Valentina, Nikola Bedeković, Vladimir Stilinović y Dominik Cinčić. "Tautomeric Equilibrium of an Asymmetric β-Diketone in Halogen-Bonded Cocrystals with Perfluorinated Iodobenzenes". Crystals 11, n.º 6 (18 de junio de 2021): 699. http://dx.doi.org/10.3390/cryst11060699.
Texto completoMarquez, Jason, Egor Novikov, Sergei Rigin, Marina S. Fonari, Raúl Castañeda, Tatiana Kornilova y Tatiana V. Timofeeva. "Exploiting Supramolecular Synthons in Cocrystals of Two Racetams with 4-Hydroxybenzoic Acid and 4-Hydroxybenzamide Coformers". Chemistry 5, n.º 2 (8 de mayo de 2023): 1089–100. http://dx.doi.org/10.3390/chemistry5020074.
Texto completoNisar, Madiha, Lawrence W. Y. Wong, Herman H. Y. Sung, Richard K. Haynes y Ian D. Williams. "Cocrystals of the antimalarial drug 11-azaartemisinin with three alkenoic acids of 1:1 or 2:1 stoichiometry". Acta Crystallographica Section C Structural Chemistry 74, n.º 6 (24 de mayo de 2018): 742–51. http://dx.doi.org/10.1107/s2053229618006320.
Texto completoEshtiagh-Hosseini, H., H. Aghabozorg, M. Mirzaei, S. A. Beyramabadi, H. Eshghi, A. Morsali, A. Shokrollahi y R. Aghaei. "Hydrothermal synthesis, experimental and theoretical characterization of a novel cocrystal compound in the 2:1 stoichiometric ratio containing 6-methyluracil and dipicolinic acid". Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 78, n.º 5 (mayo de 2011): 1392–96. http://dx.doi.org/10.1016/j.saa.2011.01.016.
Texto completoGao, Jiaoyang, Huifei Zhai, Peng Hu y Hui Jiang. "The Stoichiometry of TCNQ-Based Organic Charge-Transfer Cocrystals". Crystals 10, n.º 11 (2 de noviembre de 2020): 993. http://dx.doi.org/10.3390/cryst10110993.
Texto completoRanjan, Subham, Ramesh Devarapalli, Sudeshna Kundu, Subhankar Saha, Shubham Deolka, Venu R. Vangala y C. Malla Reddy. "Isomorphism: `molecular similarity to crystal structure similarity' in multicomponent forms of analgesic drugs tolfenamic and mefenamic acid". IUCrJ 7, n.º 2 (7 de enero de 2020): 173–83. http://dx.doi.org/10.1107/s205225251901604x.
Texto completoHamilton, Darren G., Daniel E. Lynch, Karl A. Byriel y Colin H. L. Kennard. "A Neutral Donor-Acceptor p-Stack: Solid-State Structures of 1 : 1 Pyromellitic Diimide-Dialkoxynaphthalene Cocrystals". Australian Journal of Chemistry 50, n.º 5 (1997): 439. http://dx.doi.org/10.1071/c97033.
Texto completoKhurshid, Asma, Aamer Saeed, Tuncer Hökelek, Umama Taslim, Madiha Irfan, Saba Urooge Khan, Aneela Iqbal y Hesham R. El-Seedi. "Experimental and Hirshfeld Surface Investigations for Unexpected Aminophenazone Cocrystal Formation under Thiourea Reaction Conditions via Possible Enamine Assisted Rearrangement". Crystals 12, n.º 5 (25 de abril de 2022): 608. http://dx.doi.org/10.3390/cryst12050608.
Texto completoKhurshid, Asma, Aamer Saeed, Tuncer Hökelek, Umama Taslim, Madiha Irfan, Saba Urooge Khan, Aneela Iqbal y Hesham R. El-Seedi. "Experimental and Hirshfeld Surface Investigations for Unexpected Aminophenazone Cocrystal Formation under Thiourea Reaction Conditions via Possible Enamine Assisted Rearrangement". Crystals 12, n.º 5 (25 de abril de 2022): 608. http://dx.doi.org/10.3390/cryst12050608.
Texto completoKhurshid, Asma, Aamer Saeed, Tuncer Hökelek, Umama Taslim, Madiha Irfan, Saba Urooge Khan, Aneela Iqbal y Hesham R. El-Seedi. "Experimental and Hirshfeld Surface Investigations for Unexpected Aminophenazone Cocrystal Formation under Thiourea Reaction Conditions via Possible Enamine Assisted Rearrangement". Crystals 12, n.º 5 (25 de abril de 2022): 608. http://dx.doi.org/10.3390/cryst12050608.
Texto completoPeloquin, Andrew J., Srikar Alapati, Colin D. McMillen, Timothy W. Hanks y William T. Pennington. "Polymorphism, Halogen Bonding, and Chalcogen Bonding in the Diiodine Adducts of 1,3- and 1,4-Dithiane". Molecules 26, n.º 16 (17 de agosto de 2021): 4985. http://dx.doi.org/10.3390/molecules26164985.
Texto completoSaikia, Basanta, Debabrat Pathak y Bipul Sarma. "Variable stoichiometry cocrystals: occurrence and significance". CrystEngComm 23, n.º 26 (2021): 4583–606. http://dx.doi.org/10.1039/d1ce00451d.
Texto completoJayasankar, Adivaraha, L. Sreenivas Reddy, Sarah J. Bethune y Naír Rodríguez-Hornedo. "Role of Cocrystal and Solution Chemistry on the Formation and Stability of Cocrystals with Different Stoichiometry". Crystal Growth & Design 9, n.º 2 (4 de febrero de 2009): 889–97. http://dx.doi.org/10.1021/cg800632r.
Texto completoČejka, Jan y Martin Lenz. "Growing cocrystals by stoichiometric cosublimation". Acta Crystallographica Section A Foundations and Advances 71, a1 (23 de agosto de 2015): s457. http://dx.doi.org/10.1107/s2053273315093274.
Texto completoBorodi, Gheorghe, Alexandru Turza, Oana Onija y Attila Bende. "Succinic, fumaric, adipic and oxalic acid cocrystals of promethazine hydrochloride". Acta Crystallographica Section C Structural Chemistry 75, n.º 2 (16 de enero de 2019): 107–19. http://dx.doi.org/10.1107/s2053229618017904.
Texto completoTumanova, Natalia, Nikolay Tumanov, Franziska Fischer, Fabrice Morelle, Voraksmy Ban, Koen Robeyns, Yaroslav Filinchuk, Johan Wouters, Franziska Emmerling y Tom Leyssens. "Exploring polymorphism and stoichiometric diversity in naproxen/proline cocrystals". CrystEngComm 20, n.º 45 (2018): 7308–21. http://dx.doi.org/10.1039/c8ce01338a.
Texto completoSetyawan, Dwi, Firdaus Rendra Adyaksa, Hanny Lystia Sari, Diajeng Putri Paramita y Retno Sari. "Cocrystal formation of loratadine-succinic acid and its improved solubility". Journal of Basic and Clinical Physiology and Pharmacology 32, n.º 4 (25 de junio de 2021): 623–30. http://dx.doi.org/10.1515/jbcpp-2020-0456.
Texto completoMavračić, Juraj, Dominik Cinčić y Branko Kaitner. "Halogen bonding ofN-bromosuccinimide by grinding". CrystEngComm 18, n.º 19 (2016): 3343–46. http://dx.doi.org/10.1039/c6ce00638h.
Texto completoCruz, Silvia, Jairo Quiroga, José M. de la Torre, Justo Cobo, John N. Low y Christopher Glidewell. "3-[5-(4-Bromophenyl)-1H-pyrazol-3-ylamino]-5,5-dimethylcyclohex-2-en-1-one–(Z)-3-(4-bromophenyl)-3-chloroacrylonitrile (2/1): a stoichiometric cocrystal of a reaction product with one of its early precursors". Acta Crystallographica Section C Crystal Structure Communications 62, n.º 10 (12 de septiembre de 2006): o608—o611. http://dx.doi.org/10.1107/s0108270106033968.
Texto completoFael, Hanan, Rafael Barbas, Rafel Prohens, Clara Ràfols y Elisabet Fuguet. "Synthesis and Characterization of a New Norfloxacin/Resorcinol Cocrystal with Enhanced Solubility and Dissolution Profile". Pharmaceutics 14, n.º 1 (27 de diciembre de 2021): 49. http://dx.doi.org/10.3390/pharmaceutics14010049.
Texto completoArhangelskis, Mihails, Filip Topić, Poppy Hindle, Ricky Tran, Andrew J. Morris, Dominik Cinčić y Tomislav Friščić. "Mechanochemical reactions of cocrystals: comparing theory with experiment in the making and breaking of halogen bonds in the solid state". Chemical Communications 56, n.º 59 (2020): 8293–96. http://dx.doi.org/10.1039/d0cc02935a.
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