Results 151 to 160 of about 1,962 (207)

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.
Dennis E. Vance, Zhaoyu Li
openaire   +3 more sources

beta 1-selective adrenoceptor antagonists. 1. Synthesis and beta-adrenergic blocking activity of a series of binary (aryloxy)propanolamines.

Journal of Medicinal Chemistry, 1983
A series of binary (aryloxy)propanolamines has been prepared and examined in vitro and in vivo for beta-adrenoreceptor blocking activity. These symmetrical compounds consist of two (S)-(phenyloxy)propanolamine pharmacophores coupled through alkylenedioxy
R. W. Kierstead, A. Faraone, F. Mennona, Mullin John Guilfoyle, R. Guthrie, H. Crowley, B. Simko, L. Blaber   +7 more
semanticscholar   +1 more source

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   +2 more sources

Binding of arylpiperazines, (aryloxy)propanolamines, and tetrahydropyridylindoles to the 5-HT1A receptor: contribution of the molecular lipophilicity potential to three-dimensional quantitative structure-affinity relationship models.

Journal of Medicinal Chemistry, 1996
A set of 280 5-HT1A receptor ligands were selected from available literature data according to predefined criteria and subjected to three-dimensional quantitative structure-affinity relationship analysis using comparative molecular field analysis.
P. Gaillard, P. Carrupt, Bernard Testa, Philippe Schambel   +3 more
semanticscholar   +1 more source

Ultra-short-acting beta-adrenergic receptor blocking agents. 1. (Aryloxy)propanolamines containing esters in the nitrogen substituent.

Journal of Medicinal Chemistry, 1982
In an attempt to produce short-acting beta-adrenergic receptor blocking agents, we prepared several (aryloxy)propanolamines with ester functions incorporated into the nitrogen substituent.
P. Erhardt, C. Woo, R. Gorczynski, W. G. Anderson   +3 more
semanticscholar   +1 more source

ChemInform Abstract: Synthesis of Propanolamine Derivatives and Study of Their Antiviral Activity.

ChemInform, 1987
AbstractThe propanolamine derivatives (III), (VI), and (IX) are prepared from the epoxides (I) or the amines (IV) and (VII) as shown in the reaction scheme.
Kh. S. Azhami, A. P. Stankyavichyus, S. P. Riselis, G. V. Vladyko, L. V. Korobchenko, E. I. Boreko, L. M. M. Stankyavichene, P. B. Terent'ev, M. S. Sapragonene   +8 more
openaire   +2 more sources

Ethanolamines and Propanolamines

, 2001
The article contains sections titled: 1. Introduction 2. Ethanolamines 2.1. Properties 2.1.1. Physical Properties 2.1.2. Chemical Properties 2.2. Production 2.3. Quality Specifications 2.4. Uses 2.5. Economic Aspects 3.
M. Frauenkron, Johann‐Peter Melder, Günther Dr. Ruider, R. Rossbacher, H. Höke   +4 more
semanticscholar   +1 more source

Ultra-short-acting beta-adrenergic receptor blocking agents. 2. (Aryloxy)propanolamines containing esters on the aryl function.

Journal of Medicinal Chemistry, 1982
Several short-acting beta-adrenergic receptor blocking agents have been prepared by incorporating ester functions into the aryl portion of certain (aryloxy)propanolamine systems.
P. Erhardt, C. Woo, W. G. Anderson, R. Gorczynski   +3 more
semanticscholar   +1 more source

Ultra-short-acting beta-adrenergic receptor blocking agents. 3. Ethylenediamine derivatives of (aryloxy)propanolamines having esters on the aryl function.

Journal of Medicinal Chemistry, 1983
Various ethylenediamine derivatives have been incorporated into the nitrogen substituent of certain short-acting (aryloxy)propanolamine systems that contain esters on their aryl functions.
P. Erhardt, C. Woo, W. Matier, R. Gorczynski, W. G. Anderson   +4 more
semanticscholar   +2 more sources

Substituted alpha-dialkylaminoalkyl-l-naphthalenemethanols; some Mannich ketones and derived propanolamines.

The Journal of Organic Chemistry, 1946
S. WINSTEIN, THOMAS L. JACOBS, DEXTER SEYMOUR, GUSTAVE B. LINDEN   +3 more
semanticscholar   +4 more sources