{"title":"避免耐药的替代方法:多面体无机和金属大环3d形状客体与变构位点和/或大分子界面强结合。","authors":"Yan Z Voloshin","doi":"10.1002/asia.202401842","DOIUrl":null,"url":null,"abstract":"<p><p>The emergence of drug resistance is one of the global problems. Prospective approach for its solution is based on the development of new and improved pharmacological principles, including the use of allosteric inhibitors of biomacromolecules and the generation of those unfolded or misfolded. Allosteric sites as hosts can be sterically blocked by rigid 3D-shaped effectors as guests. Because host bioreceptors recognize only their external surface, the nature of abiotic and artificial 3D-molecular platforms plays no important role in the supramolecular host-guest binding. Another of their modus operandi is based on blocking a surface of supramolecular interactions between biomacromolecules to cause the appearance of misfolded macromolecular assemblies or their disaggregation. 3D-shaped polyhedral inorganic and metallocomplex molecules, the periphery of which is decorated with terminal biorelevant or vector group(s), seem to be promising antitumor and antiviral drug candidates, in the case of which the emergence of drug resistance is not observed.</p>","PeriodicalId":145,"journal":{"name":"Chemistry - An Asian Journal","volume":" ","pages":"e01842"},"PeriodicalIF":3.3000,"publicationDate":"2025-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Alternative Approach to Avoid Drug Resistance: Polyhedral Inorganic and Metallomacrobicyclic 3D-Shaped Guests Strongly Binding to Allosteric Sites and/or Macromolecular Interfaces.\",\"authors\":\"Yan Z Voloshin\",\"doi\":\"10.1002/asia.202401842\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The emergence of drug resistance is one of the global problems. Prospective approach for its solution is based on the development of new and improved pharmacological principles, including the use of allosteric inhibitors of biomacromolecules and the generation of those unfolded or misfolded. Allosteric sites as hosts can be sterically blocked by rigid 3D-shaped effectors as guests. Because host bioreceptors recognize only their external surface, the nature of abiotic and artificial 3D-molecular platforms plays no important role in the supramolecular host-guest binding. Another of their modus operandi is based on blocking a surface of supramolecular interactions between biomacromolecules to cause the appearance of misfolded macromolecular assemblies or their disaggregation. 3D-shaped polyhedral inorganic and metallocomplex molecules, the periphery of which is decorated with terminal biorelevant or vector group(s), seem to be promising antitumor and antiviral drug candidates, in the case of which the emergence of drug resistance is not observed.</p>\",\"PeriodicalId\":145,\"journal\":{\"name\":\"Chemistry - An Asian Journal\",\"volume\":\" \",\"pages\":\"e01842\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-06-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry - An Asian Journal\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://doi.org/10.1002/asia.202401842\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry - An Asian Journal","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1002/asia.202401842","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Alternative Approach to Avoid Drug Resistance: Polyhedral Inorganic and Metallomacrobicyclic 3D-Shaped Guests Strongly Binding to Allosteric Sites and/or Macromolecular Interfaces.
The emergence of drug resistance is one of the global problems. Prospective approach for its solution is based on the development of new and improved pharmacological principles, including the use of allosteric inhibitors of biomacromolecules and the generation of those unfolded or misfolded. Allosteric sites as hosts can be sterically blocked by rigid 3D-shaped effectors as guests. Because host bioreceptors recognize only their external surface, the nature of abiotic and artificial 3D-molecular platforms plays no important role in the supramolecular host-guest binding. Another of their modus operandi is based on blocking a surface of supramolecular interactions between biomacromolecules to cause the appearance of misfolded macromolecular assemblies or their disaggregation. 3D-shaped polyhedral inorganic and metallocomplex molecules, the periphery of which is decorated with terminal biorelevant or vector group(s), seem to be promising antitumor and antiviral drug candidates, in the case of which the emergence of drug resistance is not observed.
期刊介绍:
Chemistry—An Asian Journal is an international high-impact journal for chemistry in its broadest sense. The journal covers all aspects of chemistry from biochemistry through organic and inorganic chemistry to physical chemistry, including interdisciplinary topics.
Chemistry—An Asian Journal publishes Full Papers, Communications, and Focus Reviews.
A professional editorial team headed by Dr. Theresa Kueckmann and an Editorial Board (headed by Professor Susumu Kitagawa) ensure the highest quality of the peer-review process, the contents and the production of the journal.
Chemistry—An Asian Journal is published on behalf of the Asian Chemical Editorial Society (ACES), an association of numerous Asian chemical societies, and supported by the Gesellschaft Deutscher Chemiker (GDCh, German Chemical Society), ChemPubSoc Europe, and the Federation of Asian Chemical Societies (FACS).