1. Academic Validation
  2. Optimization of a urea-containing series of nicotinamide phosphoribosyltransferase (NAMPT) activators

Optimization of a urea-containing series of nicotinamide phosphoribosyltransferase (NAMPT) activators

  • Bioorg Med Chem Lett. 2021 Jun 1;41:128007. doi: 10.1016/j.bmcl.2021.128007.
Anthony B Pinkerton 1 E Hampton Sessions 2 Paul Hershberger 2 Patrick R Maloney 2 Satyamaheshwar Peddibhotla 2 Meghan Hopf 3 Eduard Sergienko 2 Chen-Ting Ma 2 Layton H Smith 2 Michael R Jackson 2 Jun Tanaka 4 Takashi Tsuji 4 Mayuko Akiu 4 Steven E Cohen 5 Tsuyoshi Nakamura 4 Stephen J Gardell 3
Affiliations

Affiliations

  • 1 Conrad Prebys Center for Chemical Genomics, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA. Electronic address: [email protected].
  • 2 Conrad Prebys Center for Chemical Genomics, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.
  • 3 Translational Research Institute. AdventHealth, Orlando, FL 32804, USA.
  • 4 R&D Division, Daiichi Sankyo Co., Ltd., 1-2-58 Hiromachi, Shinagawa-ku, Tokyo 140-8710, Japan.
  • 5 Daiichi Sankyo, Inc., Global Business Development, Basking Ridge, NJ 07920, USA.
Abstract

NAD+ is a crucial cellular factor that plays multifaceted roles in wide ranging biological processes. Low levels of NAD+ have been linked to numerous diseases including metabolic disorders, Cardiovascular Disease, neurodegeneration, and muscle wasting disorders. A novel strategy to boost NAD+ is to activate nicotinamide phosphoribosyltransferase (NAMPT), the putative rate-limiting step in the NAD+ salvage pathway. We previously showed that NAMPT activators increase NAD+ levels in vitro and in vivo. Herein we describe the optimization of our NAMPT activator prototype (SBI-0797812) leading to the identification of 1-(4-((4-chlorophenyl)sulfonyl)phenyl)-3-(oxazol-5-ylmethyl)urea (34) that showed far more potent NAMPT activation and improved oral bioavailability.

Keywords

NAD(+) booster; NAMPT; NAMPT activators; Ureas.

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