Zobrazeno 1 - 10
of 95
pro vyhledávání: '"E, Toja"'
Autor:
E Toja, O Agostini
Publikováno v:
Journal of Chromatography B: Biomedical Sciences and Applications. 661:313-318
7-[(2,2-Dimethyl)propyl)]-1-methylxanthine (I, Lab code MX2/120) is a new potent antibronchospastic agent. A rapid and simple HPLC assay for I in guinea pig plasma has been developed. Compound I was extracted from plasma with dichloromethane by a sol
Autor:
E Toja, P. Hunt, M. L. Formento, Michel Fortin, Alina Butti, F. Barzaghi, A. Maggioni, A. Nencioni, C. Bonetti, Giulio Galliani
Publikováno v:
ChemInform. 23
On the basis of the knowledge acquired from basic studies of several known arecoline derivatives about the structural requirements for potent agonistic activity and oral efficacy, a series of 1-alkyl-1,2,5,6-tetrahydropyridine-3-carboxaldehyde- O -al
Publikováno v:
ChemInform. 22
A series of 5-alkoxy-1-arylcarbonyl-2-pyrrolidinones ( 1–27 ) were prepared by condensation of arylcarbonyl chlorides with 5-alkoxy-2 pyrrolidinones in the presence of butyl lithium in tetrahydrofuran. Alkylation of these intermediates with substit
Autor:
F. Barzaghi, Alina Butti, A. Nencioni, C. Bonetti, M. L. Formento, A. Maggioni, P. Hunt, Giulio Galliani, E Toja, Michel Fortin
Publikováno v:
ChemInform. 24
Our previous attempts to design muscarinic agonists related to arecoline with the prerequisites for clinical use were successful with the discovery of 1,2,5,6-tetrahydropyridine-3-carboxaldehyde-O-methyloxime hydrochloride, RU 35963, and structurally
Autor:
O. Agostini, E. Toja, Stefano Evangelista, A Castellucci, Lido Ballati, G. Bonacchi, G. Di Marco, M. Borgianni, Boni P
Publikováno v:
ChemInform. 26
A series of 7-(2,2-dimethyl)propyl substituted xanthines were synthesized and tested for their antibronchospastic activity in comparison with theophylline. In vitro, the inhibition of carbachol-induced increase in bronchial tone was determined. In vi
Autor:
Michel Fortin, Giulio Galliani, F. Barzaghi, P. Hunt, Alina Butti, A. Maggioni, E Toja, M. L. Formento, A. Nencioni, C. Bonetti
Publikováno v:
European Journal of Medicinal Chemistry. 27:519-526
Our previous attempts to design muscarinic agonists related to arecoline with the prerequisites for clinical use were successful with the discovery of 1,2,5,6-tetrahydropyridine-3-carboxaldehyde-O-methyloxime hydrochloride, RU 35963, and structurally
Autor:
Michel Fortin, Giulio Galliani, Alina Butti, E Toja, M. L. Formento, F. Barzaghi, A. Maggioni, A. Nencioni, C. Bonetti, P. Hunt
Publikováno v:
European Journal of Medicinal Chemistry. 26:853-868
On the basis of the knowledge acquired from basic studies of several known arecoline derivatives about the structural requirements for potent agonistic activity and oral efficacy, a series of 1-alkyl-1,2,5,6-tetrahydropyridine-3-carboxaldehyde- O -al
Publikováno v:
European Journal of Medicinal Chemistry. 26:415-422
A series of 5-alkoxy-1-arylcarbonyl-2-pyrrolidinones ( 1–27 ) were prepared by condensation of arylcarbonyl chlorides with 5-alkoxy-2 pyrrolidinones in the presence of butyl lithium in tetrahydrofuran. Alkylation of these intermediates with substit
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Publikováno v:
Arzneimittel-Forschung. 45(6)
7-[(2,2-Dimethyl)propyl]-1-methyl xanthine (CAS 155006-67-0, MX2/120) is a new potent antibronchospastic agent with negligible side effects. The synthesis involves the alkylation of 3-benzyl-1-methyl xanthine with neopentyl bromide followed by remova