Lanthionine ketimine (LK), cystathionine ketimine (CK) and thialisine ketimine (AECK) represent a new class of cyclic sulfur-containing iminoacids recently identified in the CNS and humane urine. These natural compounds have been synthesized and chemically characterized in our laboratories. In order to define the role of these iminoacids as putative neuromodulators we made ready the synthesis and the purification of [35S]LK. Binding experiments performed on bovine cerebral membranes indicate the presence of a ligand site for LK, exhibiting the basic criteria of saturability and reversibility typical of a receptor-ligand system. Scatchard analysis indicates the presence of a single population of sites with an affinity constant of about 30 nM...
Neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and Parkinson’s disease (PD) ...
Human peripheral blood polymorphonuclear leukocytes were preincubated with lanthionine, S-(2-aminoet...
The heterogeneous binding behavior exhibited by classical quaternary muscarinic antagonists was furt...
2H-1,4-Thiazine-5,6-dihydro-3,5-dicarboxylic acid (trivial name: lanthionine ketimine) is a cyclic s...
Lanthionine ketimine (LK) binding sites were solubilized from bovine brain membranes using 3-[(3-cho...
Aminoethylcysteine, lanthionine, cystathionine and cystine are mono-deaminated either by l-amino-aci...
Lanthionine (Lan), the thioether analog of cystine, is a natural but nonproteogenic amino acid thoug...
AbstractGas-liquid chromatography of enriched bovine brain extract revealed the occurrence of severa...
Abstract: The reaction of opioid peptides with mushroom tyrosinase in the presence of an excess of a...
A binding site for [3H]cimetidine was obtained from rat brain membranes solubilized with digitonin. ...
The binding sites for [3H]leukotriene C4 were studied in membrane preparations of mouse brain and li...
The σ-receptor, a distinct binding site in brain tissue that may mediate some of the psychotomimetic...
[[abstract]]The majority of L-glutamate binding sites in the synaptic membranes isolated from porcin...
The binding sites for [3H]leukotriene C4 were studied in membrane preparations of mouse brain and li...
In this study two novel series of rigid dopamine analogues were tested for dopamine-like activity us...
Neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and Parkinson’s disease (PD) ...
Human peripheral blood polymorphonuclear leukocytes were preincubated with lanthionine, S-(2-aminoet...
The heterogeneous binding behavior exhibited by classical quaternary muscarinic antagonists was furt...
2H-1,4-Thiazine-5,6-dihydro-3,5-dicarboxylic acid (trivial name: lanthionine ketimine) is a cyclic s...
Lanthionine ketimine (LK) binding sites were solubilized from bovine brain membranes using 3-[(3-cho...
Aminoethylcysteine, lanthionine, cystathionine and cystine are mono-deaminated either by l-amino-aci...
Lanthionine (Lan), the thioether analog of cystine, is a natural but nonproteogenic amino acid thoug...
AbstractGas-liquid chromatography of enriched bovine brain extract revealed the occurrence of severa...
Abstract: The reaction of opioid peptides with mushroom tyrosinase in the presence of an excess of a...
A binding site for [3H]cimetidine was obtained from rat brain membranes solubilized with digitonin. ...
The binding sites for [3H]leukotriene C4 were studied in membrane preparations of mouse brain and li...
The σ-receptor, a distinct binding site in brain tissue that may mediate some of the psychotomimetic...
[[abstract]]The majority of L-glutamate binding sites in the synaptic membranes isolated from porcin...
The binding sites for [3H]leukotriene C4 were studied in membrane preparations of mouse brain and li...
In this study two novel series of rigid dopamine analogues were tested for dopamine-like activity us...
Neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and Parkinson’s disease (PD) ...
Human peripheral blood polymorphonuclear leukocytes were preincubated with lanthionine, S-(2-aminoet...
The heterogeneous binding behavior exhibited by classical quaternary muscarinic antagonists was furt...