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2D QSAR of heteroaryl-substituted propanolamines as antihypertensive agents

Medicinal Chemistry Research, 2013
Propanolamines are well known for their ability to reduce blood pressure. A number of propanolamines have been approved as antihypertensive agents. A series of propanolamines was selected and different models based on multiple linear regression (MLR) were generated to find out correlation between the physicochemical parameters and the biological ...
Prasanna A Datar
exaly   +2 more sources

o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as .beta.-blocking/diuretic agents

Journal of Medicinal Chemistry, 1993
A series of compounds 1b-f, 2b-f, and 3b-f having an o-chlorobenzenesulfonamidic diuretic moiety variously linked to the nitrogen side chain of the beta-blocking (aryloxy)propanolamine pharmacophore were prepared and tested for their beta 1-adrenoceptor affinity.
Violetta Cecchetti   +2 more
exaly   +4 more sources

Enzyme catalyzed stereoselective synthesis of (S)-propanolamines

Tetrahedron: Asymmetry, 1994
Abstract Stereoselective synthesis of (S)-propanolamines has been carried out by the ring opening of racemic epoxides with 2-propylamine in presence of lipases and subtilisin. The effect of solvent towards selectivity has also been studied.
Ahmed Kamal, Maddamsetty V Rao
exaly   +2 more sources

Choline cannot be replaced by propanolamine in mice

Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, 2007
Choline is an important nutrient for humans and animals. Animals obtain choline from the diet and from the catabolism of phosphatidylcholine made by phosphatidylethanolamine N-methyltransferase (PEMT). The unique model of complete choline deprivation is Pemt(-/-) mice that are fed a choline-deficient diet.
Zhaoyu, Li, Dennis E, Vance
openaire   +2 more sources

.beta.-Adrenergic blocking agents. .alpha.- and .gamma.-Methyl(aryloxy)propanolamines

Journal of Medicinal Chemistry, 1981
A series of gamma-methyl- (5) and alpha-methyl(aryloxy)propanolamines (6) were synthesized and evaluated for beta-adrenergic blocking action. The binding constant (KD) was determined for compounds 5a-j on cultured C6-2B astrocytoma cells. Compounds 5a-j and 6a-e were evaluated for beta 1-antagonist action on guinea pig atria and beta 2-antagonist ...
T L, Lemke   +4 more
openaire   +2 more sources

THE REACTION OF PHOSPHORUS TRICHLORIDE WITH PROPANOLAMINE-1.3

Phosphorus, Sulfur, and Silicon and the Related Elements, 1994
Abstract The reaction of PCl3 with propanolamine-1.3 in the presence of Net3 was studied and found to form two heterocyclic compounds, the 2-chloro-3-dichlorophosphanyl-1.3.2-oxazaphosphorinane and the 2-aminopropoxy-1.3.2-oxazaphosphorinane, which could be isolated and characterized.
Cornelia Mundt, Lothar Riesel
openaire   +1 more source

ChemInform Abstract: Enzyme‐Catalyzed Stereoselective Synthesis of (S)‐Propanolamines.

ChemInform, 1995
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
A. KAMAL, M. V. RAO
openaire   +1 more source

3-(Acyloxy)propanolamines: agents with β-adrenergic blocking activity

European Journal of Medicinal Chemistry, 1994
Abstract A series of totally aliphatic 3-(acyloxy)propanolamine derivatives were prepared and their pA2-values were determined employing the guinea-pig atrium. Compounds with an acetyl or methyl succinoyl half ester moiety showed a pronounced β1-adrenergic blocking activity.
J Leuschner, H Schäfer, F Leuschner
exaly   +2 more sources

Substituted propanolamines and alkylamines derived from fluoxetine as potent appetite suppressants

Bioorganic & Medicinal Chemistry, 2005
A series of propanolamine and alkylamine analogues of fluoxetine (7-26, 28-31) were synthesized and assessed for their anorexigenic and antidepressant activities. Effect of various substituents at C-4 aryl position of fluoxetine has also been studied.
Kalpana, Bhandari   +3 more
openaire   +2 more sources

b-Adrenergic blocking agents. Nitrogen heteroaryl-substituted 2-propanolamines and ethanolamines

Journal of Medicinal Chemistry, 1973
Eine Reihe von Methylheterocyclen (I) wird in Form ihrer Lithiumderivate (II) mit den Aminoacetonitrilen (III) zu den Enaminen (IV) umgesetzt, die durch Hydrolyse, Reduktion mit Natriumborhydrid und hydrierende Debenzylierung in Propanolamine (VII) umgewandelt werden.
R F, Meyer   +3 more
exaly   +3 more sources

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