The Application of Bicyclo[1.1.1]pentane as a Bioisostere of the Phenyl Ring in Pharmaceutical Chemistry
Abstract Bicyclo[1.1.1]pentane (BCP) is a bridging ring skeleton with three-dimensional structure. BCP is a bioisostere of the phenyl ring, tert-butyl group, and alkynes; it has excellent physical and chemical properties compared with phenyl ring, so it has been widely considered by the pharmaceutical chemistry. This short review examines related reports of BCP as a bioisostere of the phenyl ring, and the changes in physicochemical properties and biological activity after substitution. The solubility, clogP, and metabolic toxicity of the drug are improved by BCP bioisosteres, but the biological activity of BCP is lower than the phenyl ring. The application of BCP in drug research and development will be further expanded to provide more possibilities for future drug innovation and development. 1 Introduction 2 Replacement of Phenyl Rings by BCP 3 Conclusion
Authors
- Nian‐Feng Wan (ORCID: https://orcid.org/0000-0001-9486-9150)
- Wu‐Lin Yang (ORCID: https://orcid.org/0000-0001-7985-5017)
- Xuhong Qian (ORCID: https://orcid.org/0000-0003-0394-1968)
- Xuehe Lu
- Zhaoyang Fang
Institutions
- East China University of Science and Technology (CN)
- Shanghai Jiao Tong University (CN)
Publication Details
- Journal
- Synthesis
- Published
- 2024-09-20
- DOI
- https://doi.org/10.1055/s-0043-1775395
- Citations
- 16
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 3.33
Funders
- National Natural Science Foundation of China