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2000
Volume 9, Issue 5
  • ISSN: 1389-5575
  • E-ISSN: 1875-5607

Abstract

As an example of a multi-template approach, we focused on the 3,3-diphenylpentane (DPP) skeleton, which has been demonstrated to act as a steroid skeleton substitute. Various ligands for nuclear receptors (NRs), including vitamin D receptor (VDR), androgen receptor (AR) and farnesoid X receptor (FXR), and inhibitors of steroid metabolismrelated enzymes, including 5α-reductase and HMG-CoA reductase (HMGR), have been efficiently created by introducing various substituents onto the DPP skeleton.

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/content/journals/mrmc/10.2174/138955709788167574
2009-05-01
2025-10-03
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