Search references for PROPANOLAMINES. Phrases containing PROPANOLAMINES
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Class of chemical compounds
Phenylpropanolamine Pindolol Practolol Propranolol Ritodrine Timolol Propanolamine Phenoxyethylamine Propanolamines at the U.S. National Library of Medicine Medical Subject
Propanolamines
Multiple organic compounds with the parent structure C3H9NO
propylene oxide. The propanolamines include many derivatives where the amine is secondary or tertiary. The parent propanolamines are colorless liquids
Propanolamine
Chemical compound
Melder; Franz Ingo Berger; Christian Koch (2022). "Ethanolamines and Propanolamines". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH
Tyrosinol
Chemical compound
Ruider; Roland Rossbacher; Hartmut Höke (2002). "Ethanolamines and Propanolamines". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH
Choline_chloride
Chemical compound
Günther; Rossbacher, Roland; Höke, Hartmut (2001). "Ethanolamines and Propanolamines". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH
3-Amino-1-propanol
Chemical compound
Ruider; Roland Rossbacher; Hartmut Höke (2002). "Ethanolamines and Propanolamines". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH
Dimethylethanolamine
Beta blocker drug
100 times the binding affinity for beta adrenergic receptors. It is a propanolamine, a secondary amine and functionally related to 1-naphthol.[citation
Propranolol
Chemical compound
"Phencyclidine-like behavioral effects of 2-methyl-3,3-diphenyl-3-propanolamine (2-MDP)". Pharmacology, Biochemistry, and Behavior. 20 (2): 209–213
2-MDP
Chemical compound
Melder; Franz Ingo Berger; Christian Koch (2022). "Ethanolamines and Propanolamines". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH
Ethanolamine
Chemical compound
Melder; Franz Ingo Berger; Christian Koch (2022). "Ethanolamines and Propanolamines". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH
Alaninol
Chemical compound
Ruider, Günther; Rossbacher, Roland; Höke, Hartmut. "Ethanolamines and Propanolamines". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH
Triethanolamine
Chemical compound
Günther Ruider, Roland Rossbacher, Hartmut Höke “Ethanolamines and Propanolamines” in Ullmann's Encyclopedia of Industrial Chemistry 2002 by Wiley-VCH
Diethanolamine
Chemical compound
Günther Ruider, Roland Rossbacher, Hartmut Höke "Ethanolamines and Propanolamines" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH,
Methyldiethanolamine
Organic compounds with hydroxyl and amino groups on an alkane backbone
of longer aminoalcohols include Heptaminol, a cardiac stimulant, and propanolamines. 1,3-Aminoalcohols are present in several bioactive molecules, such
Alkanolamine
Chemical compound
1-[Bis(2-hydroxypropyl)amino]propan-2-ol Tris(2-hydroxypropyl)amine Tri-2-propanolamine Tri-iso-propanolamine Tris(2-propanol)amine Identifiers CAS Number 122-20-3 Y 3D
Triisopropanolamine
Chemical compound
pathway is the most important catabolic pathway of threonine in mammals. Propanolamines Aminoaldehydes and aminoketones Nomenclature of Organic Chemistry :
Aminoacetone
Chemical compound
demethylation and hydroxylation pathways) in a way similar to proadifen. Propanolamines Brimblecombe RW, Pinder RM (1975). "Indolealkylamines and Related Compounds"
Phenoxyethylamine
Chemical compound
Günther Ruider, Roland Rossbacher, Hartmut Höke "Ethanolamines and Propanolamines" in Ullmann's Encyclopedia of Industrial Chemistry, 2002, Wiley-VCH
N-Methylethanolamine
Chemical compound
B.; Sullivan, Mark E. (October 1990). "Synthesis of novel (aryloxy)propanolamines and related compounds possessing both class II and class III antiarrhythmic
Methanesulfonic_anhydride
Index of chemical compounds with the same molecular formula
C3H9NO (molar mass: 75.11 g/mol, exact mass: 75.0684 u) may refer to: Propanolamine Alaninol 1-Amino-2-propanol 3-Amino-1-propanol N-Methylethanolamine
C3H9NO
Chemical compound
F.; Sum, Check Y.; Anderson, William G. (1984). "[(Arylcarbonyl)oxy]propanolamines. 1. Novel .beta.-blockers with ultrashort duration of action". Journal
Flestolol
Drug discovery
moiety, scientists synthesized a group of para-acylphenoxyethanol and propanolamines, and selected practolol for clinical trials. Practolol had one property
Discovery and development of beta-blockers
Discovery_and_development_of_beta-blockers
Chemical compound
(1988). "Early phase-II semi double-blind study of the new alkaline propanolamine derivative enciprazine (short communication)". Arzneimittelforschung
Enciprazine
Chemical compound
Joachim; Cox, David Alexander & Ham, Allan Leslie, "Propanolaminderivate [Propanolamine derivates]", published 1973-02-22, assigned to Pfizer Corp. v t e
Primidolol
heptaminol MeSH D02.033.100.400 – isoetharine MeSH D02.033.100.624 – propanolamines MeSH D02.033.100.624.151 – carvedilol MeSH D02.033.100.624.302 – ephedrine
List_of_MeSH_codes_(D02)
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