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Cited by in F6Publishing
For: Zhang Z, Li D, Luo C, Huang C, Qiu R, Deng Z, Zhang H. Cocrystals of Natural Products: Improving the Dissolution Performance of Flavonoids Using Betaine. Crystal Growth & Design 2019;19:3851-9. [DOI: 10.1021/acs.cgd.9b00294] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Meng S, Yu Y, Bu F, Yan C, Wu Z, Li Y. Directional Self-Assembly of Ofloxacin and Syringic Acid: The First Salt Cocrystal of Ofloxacin with Phenolic Acid Displays Superior In V itro/Vivo Biopharmaceutical Property and Enhanced Antibacterial Activity. Crystal Growth & Design. [DOI: 10.1021/acs.cgd.2c00896] [Reference Citation Analysis]
2 Li Z, Zhou J, Zhang K, Zhang Y, Wu S, Gong J. Playing with Isostructurality from Binary Cocrystals to Ternary Cocrystal Solvates of Quercetin: Tuning Colors of Pigment. Crystal Growth & Design. [DOI: 10.1021/acs.cgd.2c00424] [Reference Citation Analysis]
3 de Paula V, Guedes M, van Tilburg M, Vieira I, Silva J, dos Santos R, Echeverry J, Costa G, Silva B, Maia F, Caetano E, Freire V. Optical absorption measurements and optoelectronic DFT calculations for ethanol solvated quercetin and anhydrous/hydrated quercetin crystals. Journal of Solid State Chemistry 2022;312:123242. [DOI: 10.1016/j.jssc.2022.123242] [Reference Citation Analysis]
4 Uchiyama H, Kadota K, Tozuka Y. A review of transglycosylated compounds as food additives to enhance the solubility and oral absorption of hydrophobic compounds in nutraceuticals and pharmaceuticals. Crit Rev Food Sci Nutr 2022;:1-18. [PMID: 35757865 DOI: 10.1080/10408398.2022.2092056] [Reference Citation Analysis]
5 Jin S, Sanii R, Song B, Zaworotko MJ. Crystal Engineering of Ionic Cocrystals Sustained by the Phenol–Phenolate Supramolecular Heterosynthon. Crystal Growth & Design. [DOI: 10.1021/acs.cgd.2c00471] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
6 Liu L, Liu M, Zhang Y, Feng Y, Wu L, Zhang L, Zhang Y, Liu Y, Zou D, Su X. The role of hydroxyl group of ethanol in the self-assembly of pharmaceutical cocrystal of myricetin with 4,4′-bipyridine. Journal of Molecular Structure 2022;1250:131848. [DOI: 10.1016/j.molstruc.2021.131848] [Reference Citation Analysis]
7 Wang W, Liu F, Li J, Xue J, Li Y, Liu R. A cocrystal for effectively reducing the hepatotoxicity of ethionamide. Journal of Molecular Structure 2021;1243:130729. [DOI: 10.1016/j.molstruc.2021.130729] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Mondal PK, Mirmehrabi M, Rohani S. Insight into the Formation of Heteromolecular Hydrogen Bonds between Dasatinib and GRAS Molecules. Org Process Res Dev 2021;25:1579-88. [DOI: 10.1021/acs.oprd.0c00549] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
9 Dias JL, Lanza M, Ferreira SR. Cocrystallization: A tool to modulate physicochemical and biological properties of food-relevant polyphenols. Trends in Food Science & Technology 2021;110:13-27. [DOI: 10.1016/j.tifs.2021.01.035] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
10 Li C, Wu D, Li J, Ji X, Qi L, Sun Q, Wang A, Xie C, Gong J, Chen W. Multicomponent crystals of clotrimazole: a combined theoretical and experimental study. CrystEngComm 2021;23:6977-93. [DOI: 10.1039/d1ce00934f] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
11 Yin H, Wu N, Zhou B, Hong M, Zhu B, Qi M, Ren G. Slow-Release Drug–Drug Cocrystals of Oxaliplatin with Flavonoids: Delaying Hydrolysis and Reducing Toxicity. Crystal Growth & Design 2021;21:75-85. [DOI: 10.1021/acs.cgd.0c00622] [Cited by in Crossref: 14] [Cited by in F6Publishing: 16] [Article Influence: 4.7] [Reference Citation Analysis]
12 Ming H, Wang Q, Wu Y, Liu H, Zheng L, Zhang G. Transcriptome analysis reveals the mechanism of anthocyanidins biosynthesis during grains development in purple corn (Zea mays L.). J Plant Physiol 2021;257:153328. [PMID: 33373828 DOI: 10.1016/j.jplph.2020.153328] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Wang X, Gao D, Li D, Xie Q, Deng Z, Zhang H. Collecting the Molecular and Ionization States of Irbesartan in the Solid State. Crystal Growth & Design 2020;20:5664-9. [DOI: 10.1021/acs.cgd.0c00891] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
14 Baenziger M, Baierl M, Devanathan K, Eswaran S, Fu P, Gschwend B, Haller M, Kasinathan G, Kovacic N, Langlois A, Li Y, Schuerch F, Shen X, Wan Y, Wickendick R, Xie S, Zhang K. Synthesis Development of the Selective Estrogen Receptor Degrader (SERD) LSZ102 from a Suzuki Coupling to a C–H Activation Strategy. Org Process Res Dev 2020;24:1405-19. [DOI: 10.1021/acs.oprd.0c00076] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
15 Alshehri S, Imam SS, Altamimi MA, Hussain A, Shakeel F, Elzayat E, Mohsin K, Ibrahim M, Alanazi F. Enhanced Dissolution of Luteolin by Solid Dispersion Prepared by Different Methods: Physicochemical Characterization and Antioxidant Activity. ACS Omega 2020;5:6461-71. [PMID: 32258881 DOI: 10.1021/acsomega.9b04075] [Cited by in Crossref: 33] [Cited by in F6Publishing: 36] [Article Influence: 11.0] [Reference Citation Analysis]
16 Huang S, Xu J, Peng Y, Guo M, Cai T. Facile Tuning of the Photoluminescence and Dissolution Properties of Phloretin through Cocrystallization. Crystal Growth & Design 2019;19:6837-44. [DOI: 10.1021/acs.cgd.9b01111] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 1.3] [Reference Citation Analysis]