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Multisite Binding of Drugs and Natural Products in an Entropically Favorable, Heteroleptic Receptor.
Rizzuto, Felix J; Carpenter, John P; Nitschke, Jonathan R.
Afiliación
  • Rizzuto FJ; Department of Chemistry , University of Cambridge , Cambridge CB2 1EW , United Kingdom.
  • Carpenter JP; Department of Chemistry , University of Cambridge , Cambridge CB2 1EW , United Kingdom.
  • Nitschke JR; Department of Chemistry , University of Cambridge , Cambridge CB2 1EW , United Kingdom.
J Am Chem Soc ; 141(22): 9087-9095, 2019 06 05.
Article en En | MEDLINE | ID: mdl-31079455
The cavities of artificial receptors are defined by how their components fit together. The encapsulation of specific molecules can thus be engineered by considering geometric principles; however, intermolecular interactions and steric fit scale with receptor size, such that the ability to bind multiple guests from a specific class of compounds remains a current challenge. By employing metal-organic self-assembly, we have prepared a triangular prism from two different ligands that is capable of binding more than 20 different natural products, drugs, and steroid derivatives within its prolate cavity. Encapsulation inflates the host, enhancing its ability to bind other guests in peripheral pockets and thus enabling our system to bind combinations of different drug and natural product cargoes in different locations simultaneously. This new mode of entropically favorable self-assembly thus enables central encapsulation to amplify guest-binding events around the periphery of an artificial receptor.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Esteroides / Alcaloides Indólicos / Receptores Artificiales / Metaloporfirinas / Derivados de la Morfina Idioma: En Revista: J Am Chem Soc Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Esteroides / Alcaloides Indólicos / Receptores Artificiales / Metaloporfirinas / Derivados de la Morfina Idioma: En Revista: J Am Chem Soc Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido