The Effect of Nitroxyalkyl Succinimides on Activity of Cyclic Guanosine Monophosphate Phosphodiesterase

Bull Exp Biol Med. 2020 Jan;168(3):330-333. doi: 10.1007/s10517-020-04702-2. Epub 2020 Jan 15.

Abstract

The effect of N-nitroxymethyl succinimide (1), N-(2-nitroxyethyl) succinimide (2) and N-(3-nitroxypropyl) succinimide (3) on enzymatic activity of cyclic guanosine monophosphate (cGMP) phosphodiesterase was studied and crystal structure of compound (2) was determined. It was shown that all studied N-nitroxy succinimides inhibited cGMP phosphodiesterase in a concentration range of 0.1-0.001 mM. Compound (2) noncompetitively and reversibly inhibited hydrolytic function of enzyme with Ki=1.7×10-5 М. Inhibition constant for the reference compound N-(2-nitroethyl) nicotinamide (nicorandil) was 3×10-5 М.

Keywords: N-nitroxyalkyl succinimides; X-ray analysis; cGMP phosphodiesterase; inhibition.

MeSH terms

  • Animals
  • Cyclic GMP / metabolism*
  • Enzyme Activation / drug effects
  • Guanosine Monophosphate / metabolism*
  • Kinetics
  • Phosphoric Diester Hydrolases / metabolism*
  • Rats
  • Rats, Wistar
  • Succinimides / pharmacology*

Substances

  • Succinimides
  • Guanosine Monophosphate
  • Phosphoric Diester Hydrolases
  • Cyclic GMP