Results 1 to 10 of about 1,956 (206)

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   +7 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%.
Yesim A. Tahirovic   +17 more
semanticscholar   +5 more sources

SOME PHARMACOLOGICAL PROPERTIES OF 3:3‐DIPHENYL‐PROPANOLAMINES, ‐ALLYLAMINES, AND ‐PROPYLAMINES [PDF]

open access: bronzeBritish Journal of Pharmacology and Chemotherapy, 1951
This programme was undertaken with the knowledge that some compounds containing this structure exhibit pharmacological activity. This is exemplified by Hochst 10116 (Ph2CH.CH2CH2NCH2), which is a component of the anti-asthmatic mixture "Aspasan," in ...
A. C. White, A. F. GREEN, A.G. Hudson
semanticscholar   +6 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.
E. O. Bennett, M.C. Adams, G. Tavana
semanticscholar   +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   +5 more sources

CATECHOL‐SUBSTITUTED PHENOXY‐PROPANOLAMINES: ADRENOCEPTOR ACTIVITY IN THE ANAESTHETIZED CAT [PDF]

open access: greenBritish Journal of Pharmacology, 1977
1 The pharmacological actions of racemic noradrenaline, adrenaline, isoprenaline and N‐t‐butylnoradrenaline have been compared with those of their corresponding derivatives containing an oxymethylene (OXY) link between the ring and ethanolamine side ...
H. Dowd, G. S. Keh, C. Raper
openalex   +2 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   +5 more sources

Vanillylamide-Based Propanolamine Derivative Displays α/β-Adrenoceptor Blocking and Vasodilating Properties

open access: bronzeJournal of Cardiovascular Pharmacology, 2002
A propanolamine derivative with vanillylamide base, KMUP 880602, was first investigated under in vivo and in vitro conditions. IV KMUP 880602 (0.1, 0.5, 1.0, and 2.0 mg/kg) produced dose-dependent hypotensive and bradycardia responses in pentobarbital-anesthetized Wistar rats. KMUP 880602 also markedly inhibited both the tachycardia effects induced by (
Jwu‐Lai Yeh   +7 more
openalex   +4 more sources

Aryl propanolamines: comparison of activity at human β3 receptors, rat β3 receptors and rat atrial receptors mediating tachycardia [PDF]

open access: greenBritish Journal of Pharmacology, 1999
Marlene L. Cohen   +4 more
openalex   +2 more sources

(11)Preparation of Propanolamine Oleate

open access: bronzeThe Journal of the Society of Chemical Industry, Japan, 1952
Masumi Saito, Minoru Imoto
openalex   +4 more sources

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