Medicinal Chemistry of the Noncanonical Cyclic Nucleotides cCMP and cUMP

Handb Exp Pharmacol. 2017:238:307-337. doi: 10.1007/164_2015_41.

Abstract

After decades of intensive research on adenosine-3',5'-cyclic monophosphate (cAMP)- and guanosine-3',5'-cyclic monophosphate (cGMP)-related second messenger systems, also the noncanonical congeners cyclic cytidine-3',5'-monophosphate (cCMP) and cyclic uridine-3',5'-monophosphate (cUMP) gained more and more interest. Until the late 1980s, only a small number of cCMP and cUMP analogs with sometimes undefined purities had been described. Moreover, most of these compounds had been rather synthesized as precursors of antitumor and antiviral nucleoside-5'-monophosphates and hence had not been tested for any second messenger activity. Along with the recurring interest in cCMP- and cUMP-related signaling in the early 2000s, it became evident that well-characterized small molecule analogs with reliable purities would serve as highly valuable tools for the evaluation of a putative second messenger role of cyclic pyrimidine nucleotides. Meanwhile, for this purpose new cCMP and cUMP derivatives have been developed, and already known analogs have been resynthesized and highly purified. This chapter summarizes early medicinal chemistry work on cCMP and cUMP and analogs thereof, followed by a description of recent synthetic developments and an outlook on potential future directions.

Keywords: DB-cCMP; Lipophilicity; Prodrugs; cCMP; cCMP agarose; cCMP analogs; cUMP; cUMP agarose; cUMP analogs.

Publication types

  • Review

MeSH terms

  • Animals
  • Crystallization
  • Cyclic CMP / analogs & derivatives
  • Cyclic CMP / chemical synthesis*
  • Cyclic CMP / metabolism
  • Cyclic CMP / pharmacology
  • Humans
  • Molecular Structure
  • Nucleotides, Cyclic / chemical synthesis*
  • Nucleotides, Cyclic / metabolism
  • Nucleotides, Cyclic / pharmacology
  • Permeability
  • Prodrugs / chemical synthesis*
  • Prodrugs / metabolism
  • Prodrugs / pharmacology
  • Uridine Monophosphate / chemical synthesis*
  • Uridine Monophosphate / metabolism
  • Uridine Monophosphate / pharmacology

Substances

  • Nucleotides, Cyclic
  • Prodrugs
  • Cyclic CMP
  • cyclic 3',5'-uridine monophosphate
  • Uridine Monophosphate