Results 1 to 10 of about 1,668 (193)

Synthesis and Adrenolytic Activity of New Propanolamines [PDF]

open access: goldMolecules, 2010
The synthesis of (2R,S)-1-(6-methoxy-4-(methoxymethyl)-1H-indol-5-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)propan-2-ol and (2R,S)-1-(4-methoxy-6-(methoxymethyl)-1H-indol-5-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)propan-2-ol is described.
Grażyna Groszek   +6 more
doaj   +5 more sources

Synthesis and adrenergic .BETA.-blocking activity of some propanolamine derivatives.

open access: bronzeChemical and Pharmaceutical Bulletin, 1978
Some propanolamine derivatives were synthesized and their β-adrenergic blocking activities were determined. Among the compounds tested, all compounds with benzothiazole nucleus were found to have potent β-adrenergic blocking activity, and those with other nuclei failed to produce substantial β-blocking activity with one exception.
H. OBASE   +7 more
openalex   +4 more sources

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

open access: greenJournal 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   +5 more
openalex   +4 more sources

Enantiomeric Propanolamines as selectiveN-Methyl-d-aspartate 2B Receptor Antagonists [PDF]

open access: greenJournal of Medicinal Chemistry, 2008
Enantiomeric propanolamines have been identified as a new class of NR2B-selective NMDA receptor antagonists. The most effective agents are biaryl structures, synthesized in six steps with overall yields ranging from 11-64%. The compounds are potent and selective inhibitors of NR2B-containing recombinant NMDA receptors with IC 50 values between 30-100 ...
Yesim A. Tahirovic   +17 more
openalex   +3 more sources

Antibiotic activities of propanolamine containing 1,4-benzoxazin-3-ones against phytopathogenic bacteria

open access: goldRSC Advances, 2020
Various 1,4-benzoxazin-3-one derivatives containing propanolamine groups have been shown to exhibit good antibacterial activity againstPseudomonas syringaepvactinidiae(Psa),X. axonopodispvcitri(Xac) andXanthomonas oryzaepvoryzae(Xoo).
Jia‐Rui Rao   +5 more
openalex   +4 more sources

ANTIMICROBIAL PROPERTIES OF BUTANOLAMINES AND PROPANOLAMINES IN METAL WORKING FLUIDS

open access: bronzeThe Journal of General and Applied Microbiology, 1979
Seventeen propanolamines, six diisopropanolamines, and two butanolamines were studied for their antimicrobial properties against a mixed flora of fungi and bacteria in cutting fluids. All of the propanolamines showed inhibitory properties in the lubricants.
E. O. Bennett, M.C. Adams, G. Tavana
openalex   +3 more sources

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

open access: greenJournal 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 ...
Thomas Lemke   +4 more
openalex   +3 more sources

New chiral and isomeric cyclopropyl ketoxime propanolamine derivatives with potent .beta.-adrenergic blocking properties

open access: greenJournal of Medicinal Chemistry, 1985
The synthesis of R-(+) and S-(-) isomers of O-[3-tert-butylamino)-2-hydroxypropyl] cyclopropyl methyl ketone oxime (falintolol) is described. The syn and anti isomers of falintolol were obtained in two different ways from cyclopropyl methyl ketoxime or from falintolol.
Mohamed Bouzoubaa   +3 more
openalex   +3 more sources

Flavones. 1. Synthesis and antihypertensive activity of (3-phenylflavonoxy)propanolamines without .beta.-adrenoceptor antagonism

open access: greenJournal of Medicinal Chemistry, 1987
The synthesis of a series of (3-phenylflavonoxy)propanolamines is described. These compounds were evaluated for potential antihypertensive activity in spontaneously hypertensive rats, as well as for in vivo and in vitro evidence of beta-adrenoceptor antagonism. Some of the compounds of this series exhibited effective antihypertensive properties but did
E. S. C. WU   +7 more
openalex   +3 more sources

Home - About - Disclaimer - Privacy