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For: Surov AO, Manin AN, Churakov AV, Perlovich GL. New Solid Forms of the Antiviral Drug Arbidol: Crystal Structures, Thermodynamic Stability, and Solubility. Mol Pharmaceutics 2015;12:4154-65. [DOI: 10.1021/acs.molpharmaceut.5b00629] [Cited by in Crossref: 21] [Cited by in F6Publishing: 18] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Zhang R, Jin S, Wan Y, Lin S, Yan Z. HBr/H 2 O 2 -mediated formation of C–S bond with thiosulfates. Tetrahedron Letters 2018;59:841-7. [DOI: 10.1016/j.tetlet.2018.01.055] [Cited by in Crossref: 9] [Cited by in F6Publishing: 2] [Article Influence: 2.3] [Reference Citation Analysis]
2 Li Y, Lin Z, Gong G, Guo M, Xu T, Wang C, Zhao M, Xia Y, Tang Y, Zhong J, Chen Y, Hua L, Huang Y, Zeng F, Zhu B. Inhibition of H1N1 influenza virus-induced apoptosis by selenium nanoparticles functionalized with arbidol through ROS-mediated signaling pathways. J Mater Chem B 2019;7:4252-62. [DOI: 10.1039/c9tb00531e] [Cited by in Crossref: 29] [Article Influence: 9.7] [Reference Citation Analysis]
3 Surov AO, Vasilev NA, Churakov AV, Stroh J, Emmerling F, Perlovich GL. Solid Forms of Ciprofloxacin Salicylate: Polymorphism, Formation Pathways, and Thermodynamic Stability. Crystal Growth & Design 2019;19:2979-90. [DOI: 10.1021/acs.cgd.9b00185] [Cited by in Crossref: 12] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
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5 Drozd KV, Manin AN, Perlovich GL. Comparative analysis of experimental methods for determining thermodynamic parameters of formation of multi-component molecular crystals: Benefits and limitations. Journal of Molecular Liquids 2019;295:111644. [DOI: 10.1016/j.molliq.2019.111644] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
6 Perlovich GL. Two-component molecular crystals: evaluation of the formation thermodynamics based on melting points and sublimation data. CrystEngComm 2017;19:2870-83. [DOI: 10.1039/c7ce00554g] [Cited by in Crossref: 30] [Article Influence: 6.0] [Reference Citation Analysis]
7 Anwer MK, Iqbal M, Ahmed MM, Aldawsari MF, Ansari MN, Ezzeldin E, Khalil NY, Ali R. Improving the Solubilization and Bioavailability of Arbidol Hydrochloride by the Preparation of Binary and Ternary β-Cyclodextrin Complexes with Poloxamer 188. Pharmaceuticals (Basel) 2021;14:411. [PMID: 33926020 DOI: 10.3390/ph14050411] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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9 Manin A, Surov A, Churakov A, Perlovich G. Crystal Structures, Thermal Analysis, and Dissolution Behavior of New Solid Forms of the Antiviral Drug Arbidol with Dicarboxylic Acids. Crystals 2015;5:650-69. [DOI: 10.3390/cryst5040650] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 1.1] [Reference Citation Analysis]
10 Perlovich GL. Formation Thermodynamics of Two-Component Molecular Crystals: Polymorphism, Stoichiometry, and Impact of Enantiomers. Crystal Growth & Design 2020;20:5526-37. [DOI: 10.1021/acs.cgd.0c00695] [Cited by in Crossref: 13] [Cited by in F6Publishing: 3] [Article Influence: 6.5] [Reference Citation Analysis]
11 Zeng LY, Yang J, Liu S. Investigational hemagglutinin-targeted influenza virus inhibitors. Expert Opin Investig Drugs 2017;26:63-73. [PMID: 27918208 DOI: 10.1080/13543784.2017.1269170] [Cited by in Crossref: 34] [Cited by in F6Publishing: 31] [Article Influence: 5.7] [Reference Citation Analysis]
12 Fischer F, Lubjuhn D, Greiser S, Rademann K, Emmerling F. Supply and Demand in the Ball Mill: Competitive Cocrystal Reactions. Crystal Growth & Design 2016;16:5843-51. [DOI: 10.1021/acs.cgd.6b00928] [Cited by in Crossref: 36] [Cited by in F6Publishing: 19] [Article Influence: 6.0] [Reference Citation Analysis]
13 Évora AOL, Bernardes CES, Piedade MFM, Conceição ACL, Minas da Piedade ME. Energetics of Glycine Cocrystal or Salt Formation with Two Regioisomers: Fumaric Acid and Maleic Acid. Crystal Growth & Design 2019;19:5054-64. [DOI: 10.1021/acs.cgd.9b00379] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.7] [Reference Citation Analysis]
14 Zhu B, Fang X, Zhang Q, Mei X, Ren G. Study of Crystal Structures, Properties, and Form Transformations among a Polymorph, Hydrates, and Solvates of Apatinib. Crystal Growth & Design 2019;19:3060-9. [DOI: 10.1021/acs.cgd.9b00397] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 2.3] [Reference Citation Analysis]
15 Li X, Wang X, Jiang Q, Chi F, Liu Q, Zhang T. The delivery of arbidol by salt engineering: synthesis, physicochemical properties and pharmacokinetics. Drug Dev Ind Pharm 2017;43:151-9. [PMID: 27533023 DOI: 10.1080/03639045.2016.1225755] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
16 Zeng X, Xiong X, Yang H, Tang B, Du Q, Hou Q, Suo Z, Li H. Quantitative Monitoring the Anti-Solvent Crystallization and Storage Process for Nandrolone by Near-Infrared Spectroscopy. J Pharm Sci 2018;107:1928-36. [PMID: 29339135 DOI: 10.1016/j.xphs.2018.01.011] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
17 Jankovic S, Tsakiridou G, Ditzinger F, Koehl NJ, Price DJ, Ilie A, Kalantzi L, Kimpe K, Holm R, Nair A, Griffin B, Saal C, Kuentz M. Application of the solubility parameter concept to assist with oral delivery of poorly water-soluble drugs – a PEARRL review. Journal of Pharmacy and Pharmacology 2019;71:441-63. [DOI: 10.1111/jphp.12948] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
18 Wen T, Wang H, Li C, Xu J, Zhang C. Insight into the role of hydrochloric acid in the thermodynamics and nucleation kinetics behavior of Arbidol hydrochloride monohydrate from metastable zone widths. CrystEngComm 2022;24:389-403. [DOI: 10.1039/d1ce01426a] [Reference Citation Analysis]
19 Surov AO, Solanko KA, Bond AD, Bauer-brandl A, Perlovich GL. Cocrystals of the antiandrogenic drug bicalutamide: screening, crystal structures, formation thermodynamics and lattice energies. CrystEngComm 2016;18:4818-29. [DOI: 10.1039/c6ce00931j] [Cited by in Crossref: 30] [Article Influence: 5.0] [Reference Citation Analysis]
20 Vertzoni M, Alsenz J, Augustijns P, Bauer-Brandl A, Bergström C, Brouwers J, Müllerz A, Perlovich G, Saal C, Sugano K, Reppas C. UNGAP best practice for improving solubility data quality of orally administered drugs. Eur J Pharm Sci 2021;168:106043. [PMID: 34662708 DOI: 10.1016/j.ejps.2021.106043] [Reference Citation Analysis]