A series of homochiral sterically hindered mono- and bicyclic amidines was
prepared as hypoglycaemic agents by lethargic reaction of O-methylcaprolact
im and 3-ethoxy-2-azabicyclo[2.2.2]oct-2-ene, respectively, with homochiral
cis-2-substituted cyclopentane amines provided by asymmetrical reductive a
mination of racemic 2-substituted cyclopentanones. All compounds, except th
e cyclohexylmethylisoqoinuclidone derivative which inhibited secretion at 1
00 mu M, significantly stimulated insulin secretion 2-8-fold at 10 mu M and
100 mu M in INS-1 cells. The most potent activator was the 2-cyclopentyl-s
ubstituted caprolactam derivative 5e. The stimulatory effects on secretion
increased with rising steric hindrance of both the amidine alpha-carbon and
the bicyclic amidine moiety itself. Enantiomeric discrimination was observ
ed for the 2-[(cis-2-bulkysubstituted cyclopentyl)imino]hexahydroazepine ha
lides 5e and 5f and for the 3-[(cis-2-substituted cyclopentyl)imino]-2-azab
icyclo[2.2.2]octane halides 6a and 6c. The amidines depolarized INS-1 cells
and generated action potentials, accompanied by a decrease of membrane con
ductance. Simultaneously [Ca2+](i) increased, probably due to Ca2+-entry th
rough voltage-dependent Ca2+-channels. At high concentrations, where inhibi
tion of secretion was observed, [Ca2+](i) still rose upon application of th
e amidines, indicating an additional inhibitory pathway downstream to the e
levation of [Ca2+](i). Even at high concentrations (100 mu M), the amidines
had no toxic effects on insulin secreting INS-1 cells. (C) 2000 Editions s
cientifiques et medicales Elsevier SAS.