Unveiling the gemcitabine drug complexation with cucurbit[n]urils (n = 6–8): a computational analysis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics
Link
https://link.springer.com/content/pdf/10.1007/s11224-023-02133-z.pdf
Reference65 articles.
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3. Kim J, Jung IS, Kim SY, Lee E, Kang JK, Sakamoto S, Yamaguchi K, Kim K (2000) New cucurbituril homologues: syntheses, isolation, characterization, and X-ray crystal structures of cucurbit [n] uril (n = 5, 7, and 8). J Am Chem Soc 122:540–541
4. Shetty D, Khedkar JK, Park KM, Kim K (2015) Can we beat the biotin–avidin pair?: Cucurbit[7]uril-based ultrahigh affinity host–guest complexes and their applications. Chem Soc Rev 44:8747–8761
5. Jansen K, Buschmann HJ, Wego A, Döpp D, Mayer C, Drexler HJ, Holdt HJ (2001) Schollmeyer, E.: Cucurbit[5]uril, decamethylcucurbit[5]uril and cucurbit[6]uril. Synthesis, solubility and amine complex formation. J Incl Phenom Macrocyclic Chem 39:357–363
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