Results 161 to 170 of about 1,668 (193)
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ChemInform Abstract: SYNTHESIS AND ADRENERGIC β‐BLOCKING ACTIVITY OF SOME PROPANOLAMINE DERIVATIVES
Chemischer Informationsdienst, 1978AbstractEs werden einige Propanolamin‐Derivate wie z.B. (I) und (II) dargestellt, von denen erstere bessere β‐Blocker als Sotalol sind.
H. OBASE +7 more
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Synthesis of carbon‐14 labeled (±)‐2‐methyl‐3,3‐diphenyl‐3‐propanolamine (2‐MDP)
Journal of Labelled Compounds and Radiopharmaceuticals, 1988AbstractThe preparation of 14C labeled (±)‐2‐methyl‐3,3‐diphenyl‐3‐propanolamine (3) from [14C]‐carbonyl‐benzophenone is described.
Brian De Costa +3 more
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Pharmacokinetic Studies on Some Novel (2-Nitro-1-Imidazolyl) Propanolamine Radiosensitizers
1982One area of current interest in radiosensitizer development is in the use of nitroimidazoles of a more polar nature than misonida-zole, combining the benefits of a shorter half-life, and thus reduced tissue exposure, which has been correlated with the neuropathy observed with misonidazole (1), while also minimising brain penetration through the blood ...
M. R. L. Stratford +3 more
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ChemInform Abstract: β‐ADRENERGIC BLOCKING AGENTS. α‐ AND Γ‐METHYL(ARYLOXY)PROPANOLAMINES
Chemischer Informationsdienst, 1982Abstractα‐Naphthol und Phenole (I) reagieren mit dem Epoxid (II) und Aminen zu den Aminoethern (III) und (IV), die durch Säulenchromatographie an Kieselgel voneinander getrennt werden können.
T. L. LEMKE +4 more
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Drug design and discovery, 1992
A novel class of 1-(1-[4-phenyl(n-butyl or methyl)-3-(4,4-dimethyloxazolin-2-yl)-1,4- dihydropyridyl])-3-tert-butyl(or isopropyl)amino-2-propanols (7-12) were synthesized for evaluation as beta-adrenergic antagonists. Replacement of the naphthyloxy moiety of propranolol by a 1-[1-(4-n-butyl)-3-(4,4-dimethyloxazolin-2-yl)-1,4-dihydropyrid yl] group ...
D, Vo, M W, Wolowyk, E E, Knaus
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A novel class of 1-(1-[4-phenyl(n-butyl or methyl)-3-(4,4-dimethyloxazolin-2-yl)-1,4- dihydropyridyl])-3-tert-butyl(or isopropyl)amino-2-propanols (7-12) were synthesized for evaluation as beta-adrenergic antagonists. Replacement of the naphthyloxy moiety of propranolol by a 1-[1-(4-n-butyl)-3-(4,4-dimethyloxazolin-2-yl)-1,4-dihydropyrid yl] group ...
D, Vo, M W, Wolowyk, E E, Knaus
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2-methyl-3,3-diphenyl-3-propanolamine (2-MDP) selectively antagonises N-methyl-aspartate (NMA)
Pharmacology Biochemistry and Behavior, 1986Using electrophoretic application to rat central neurones in vivo, and bath application to frog spinal cord in vitro, 2-methyl-3,3-diphenyl-3-propanolamine was found to be a selective antagonist of N-methyl-DL-aspartate, but not of quisqualate or kainate.
J C, Blake +4 more
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The molecular structure of tri-n-propanolamine borate
Inorganic and Nuclear Chemistry Letters, 1973Zenei Taira, Kenji Osaki
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Farmaco (Societa chimica italiana : 1989), 1995
In an attempt to change the beta-adrenergic properties of completely aliphatic 3-(methyleneaminoxy)propanolamine derivatives, from antagonist to agonist, while still retaining the beta 2-selectivity, we described, in a previous paper, the synthesis of a series of such derivatives possessing a hydroxy or methoxy group linked to the aliphatic substituent
GENTILI D +8 more
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In an attempt to change the beta-adrenergic properties of completely aliphatic 3-(methyleneaminoxy)propanolamine derivatives, from antagonist to agonist, while still retaining the beta 2-selectivity, we described, in a previous paper, the synthesis of a series of such derivatives possessing a hydroxy or methoxy group linked to the aliphatic substituent
GENTILI D +8 more
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1995
The N-isopropyl- and N-t-butyl-substituted 1-[o-(3-amino-2-hydroxypropoxy)benzylideneaminoxy]-3-amino-2-propa nols (7a,b) and their meta (8a,b) and para (9a,b) isomers, in which a single aromatic ring is substituted both by the oxypropanolaminic chain of (aryloxy)propanolaminic beta-adrenergic antagonists (AOPAs) and the [(methyleneamino)oxy ...
BALSAMO A +7 more
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The N-isopropyl- and N-t-butyl-substituted 1-[o-(3-amino-2-hydroxypropoxy)benzylideneaminoxy]-3-amino-2-propa nols (7a,b) and their meta (8a,b) and para (9a,b) isomers, in which a single aromatic ring is substituted both by the oxypropanolaminic chain of (aryloxy)propanolaminic beta-adrenergic antagonists (AOPAs) and the [(methyleneamino)oxy ...
BALSAMO A +7 more
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o-Allyloxy-phenoxy-propanolamine, eine neue Gruppe adrenergischer β-Rezeptoren-Blocker
Experientia, 1967M. Wilhelm, P. Hedwall, M. Meier
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