Results 41 to 50 of about 1,467 (158)

Mixed-model QSAR at the glucocorticoid and liver X receptors [PDF]

, 2009
The presence of hormonally active compounds in the biosphere has become a worldwide environmental concern, and measures such as policy acts and regulations try to address the problem, both in Europe and in the United States.
Spreafico, Morena
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Кардиопротекторные средства с биароматической структурой. Часть 2. Блокаторы HCN-каналов

, 2022
Hyperpolarization-activated cyclic nucleotide–gated (HCN) channels, primarily their HCN4 subtype, are one of the promising targets for the development of cardioprotective agents.
G. V. Mokrov, Г. В. Мокров
core   +1 more source

Studies of Some beta-Propanolamines, Imidazo [2,1-b] Thiazoles and Ylides, by X-Ray Analysis [PDF]

, 1975
In this thesis, single crystal X-ray diffraction techniques have been used to determine the crystal and molecular structures of ten compounds. The contents are presented in four Parts, the first of which is a brief discussion on some theoretical aspects ...
Cameron, Ian R
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Benzisothiazoles and β-adrenoceptors: Synthesis and pharmacological investigation of novel propanolamine and oxypropanolamine derivatives in isolated rat tissues

, 2005
In an attempt to examine the ability of benzisothiazole-based drugs to interact with beta-adrenoceptors, a series of 1,2-benzisothiazole derivatives, which were substituted with various propanolamine or oxypropanolamine side chains in the 2 or 3 position,
POZZOLI, Cristina, MENOZZI, Alessandro, POLI, Enzo, COMINI M., MORINI G.   +4 more
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Ethanolamines and Propanolamines

, 2022
Franz Ingo Berger, Christian Koch, Johann‐Peter Melder, Martin Ernst   +3 more
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Synthesis and adrenergic beta-blocking activity of ortho-, meta- and para-oxypropanolamino-substituted [(benzylideneamino)oxy]propanolamines.

, 1995
The N-isopropyl- and N-t-butyl-substituted 1-[o-(3-amino-2-hydroxypropoxy)benzylideneaminoxy]-3-amino-2-propa nols (7a,b) and their meta (8a,b) and para (9a,b) isomers, in which a single aromatic ring is substituted both by the oxypropanolaminic chain of
M. PINZA, B. MACCHIA, ROSSELLO, ARMANDO, ORLANDINI, ELISABETTA, A. BALSAMO, G. FERNI, LAPUCCI, ANNALINA, MACCHIA, MARCO   +7 more
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SOME PHARMACOLOGICAL PROPERTIES OF 3:3‐DIPHENYL‐PROPANOLAMINES, ‐ALLYLAMINES, AND ‐PROPYLAMINES [PDF]

British Journal of Pharmacology and Chemotherapy, 1951
A C, WHITE, A F, GREEN, A, HUDSON
openaire   +2 more sources

Reversing multidrug resistance (MDR) in cancer cells by targeting p-glycoprotein (P-gp) : insights into the mechanism of MDR reversal from in silico P-gp modeling

, 2017
Tese de doutoramento, Farmácia (Química Farmacêutica e Terapêutica), Universidade de Lisboa, Faculdade de Farmácia, 2017Multidrug resistance (MDR) in cancer is one of the major impairments in the success of chemotherapy.
Ferreira, Ricardo J
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Synthesis and adrenergic ß-blocking activity of (oxypropanolamino)-substituted [(benzylideneamino)oxy]propanolamines

, 1995
The N-isopropyl- and N-t-butyl-substituted 1-[o-(3-amino-2-hydroxypropoxy)benzylideneaminoxy]-3-amino-2-propa nols (7a,b) and their meta (8a,b) and para (9a,b) isomers, in which a single aromatic ring is substituted both by the oxypropanolaminic chain of
ROSSELLO, ARMANDO, MACCHIA BRUNO, ORLANDINI, ELISABETTA, PINZA MARIO, BALSAMO A, FERNI GIOVANNI, LAPUCCI, ANNALINA, MACCHIA, MARCO   +7 more
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(11)Preparation of Propanolamine Oleate

The Journal of the Society of Chemical Industry, Japan, 1952
Masumi Saito, Minoru Imoto
openaire   +2 more sources