http://www.cnr.it/ontology/cnr/individuo/prodotto/ID166996
Towards the design of highly selective recognition sites into molecular imprinting polymers: A computational approach (Articolo in rivista)
- Type
- Label
- Towards the design of highly selective recognition sites into molecular imprinting polymers: A computational approach (Articolo in rivista) (literal)
- Anno
- 2006-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.bios.2006.05.017 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Monti S.; Cappelli C.; Bronco S.; Giusti P.; Ciardelli G. (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
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- Pubme (literal)
- Scopu (literal)
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Politecn Turin, Dipartimento Meccan, I-10129 Turin, Italy;
Ist Proc Chim Fis, CNR, I-156124 Pisa, Italy;
Univ Pisa, Dipartimento Chim & Chim Ind,
PolyLab CNR, I-56126 Pisa, Italy;
Univ Pisa, Dipartimento Ingn Chim Chim Ind Sci Mat, I-56126 Pisa, Italy (literal)
- Titolo
- Towards the design of highly selective recognition sites into molecular imprinting polymers: A computational approach (literal)
- Abstract
- A computational approach to simulate the formation of possible imprinted polymers in acetonitrile solution for theophylline (THO) is proposed, using combined molecular dynamics (MD), molecular mechanics (MM), docking and site mapping computational techniques. Methacrylic acid (MAA) and methylmethacrylate (MMA) monomers are used to simulate possible homo and copolymer structures. The model is able predict binding affinity and selectivity when considering THO analogues, such as caffeine, theobromine, xanthine and 3-methylxanthine. Comparison with available experimental data is proposed. (c) 2006 Elsevier B.V All rights reserved. (literal)
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