Natural and synthetic cyclopropanes bearing simple functionalities are endo
wed with a large spectrum of biological properties ranging from enzyme inhi
bitions to insecticidal, antifungal, herbicidal, antimicrobial, antibiotic,
antibacterial, antitumor and antiviral activities.
The simple 2-substituted 1-aminocyclopropanecarboxylic acids (ACCs) are cur
rently attracting special attention because of their potential use in confo
rmationally restricted peptides, providing biosynthetic and mechanistic pro
bes. As the immediate biosynthetic precursor of ethylene, the phytohormone
that initiates and regulates many aspects of plant growth (germination, inh
ibition, senescence, fruit ripening, etc.), the parent ACC, structurally re
lated to glycine, is a potent and selective ligand of the glycine modulatio
n site coupled to the N-methyl-D-aspartate (NMDA) receptor, one of the four
different receptors that mediate the action of the excitatory amino acids
(EAA) in the brain transmitter systems; thus, such amino acids have also be
en proven to be useful in neurochemical studies. The mechanisms responsible
for the diverse specific biological activities of compounds containing thr
ee-membered carbocyclic moieties are also being discussed.