Search Results - "Malo, P E"
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1
Symmetrical Bis(heteroarylmethoxyphenyl)alkylcarboxylic Acids as Inhibitors of Leukotriene Biosynthesis
Published in Journal of medicinal chemistry (24-08-2000)“…Symmetrical bis(quinolylmethoxyphenyl)alkylcarboxylic acids were investigated as inhibitors of leukotriene biosynthesis and…”
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2
Heteroarylmethoxyphenylalkoxyiminoalkylcarboxylic Acids as Leukotriene Biosynthesis Inhibitors
Published in Journal of medicinal chemistry (24-02-2000)“…A novel series of heteroarylmethoxyphenylalkoxyiminoalkylcarboxylic acids was studied as leukotriene biosynthesis inhibitors. A hypothesis of…”
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3
Optimization of the potency and duration of action of N-hydroxyurea 5-lipoxygenase inhibitors
Published in The Journal of pharmacology and experimental therapeutics (01-02-1995)“…As in vitro glucuronidation assay and several biochemical assays were utilized to discover potent new N-hydroxyurea-containing 5-lipoxygenase inhibitors with…”
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4
Chronological relationships between mediator release and changes in airway dynamics during an ascaris response in sensitive cynomolgus monkeys
Published in Prostaglandins, leukotrienes and essential fatty acids (01-02-1989)“…Recently identified Ascaris suum sensitive cynomolgus monkeys were further characterized to determine if a chronologic relationship existed between mediator…”
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5
Specific enhancement of LTD4-induced contractions of isolated guinea pig trachea by 5-hydroxyeicosatetraenoic acid (5-HETE)
Published in Prostaglandins (01-05-1989)“…In view of the likely production of monohydroxyeicosatetraenoic acids (HETEs) in bronchial asthma, the role of these lipoxygenase products in the development…”
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6
Design of inhibitors of leukotriene biosynthesis and their therapeutic potential
Published in Pure and applied chemistry (28-02-1998)“…Abstract…”
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7
Preclinical and clinical activity of zileuton and A-78773
Published in Annals of the New York Academy of Sciences (01-11-1993)“…The importance of leukotrienes as mediators of inflammation and bronchoconstriction was examined with two recently described 5-lipoxygenase inhibitors,…”
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8
Leukotriene D4 (LTD4) induces mucus secretion from goblet cells in the guinea pig respiratory epithelium
Published in Experimental lung research (01-01-1990)“…To study the potential role of leukotriene (LTD4) as a mucus secretagogue, anesthetized and spontaneously breathing guinea pigs were intubated and challenged…”
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9
Characterization of substance P-induced contractions of guinea-pig trachea
Published in The Journal of pharmacology and experimental therapeutics (01-06-1986)“…In light of current interest in substance P as a bronchoconstrictor, several pharmacologic antagonists of known mediators of anaphylaxis were tested for…”
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10
Characterization of A-93178, an iminoxy-quinoline inhibitor of leukotriene biosynthesis
Published in Advances in experimental medicine and biology (1997)Get more information
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11
Effects of intravenous and aerosol nifedipine on prostaglandin F2 alpha and histamine-induced bronchoconstriction in anesthetized dogs
Published in The Journal of pharmacology and experimental therapeutics (01-05-1982)“…The effect of nifedipine, a calcium slow channel blocking drug, was investigated by varying routes of administration in a canine model of pharmacologically…”
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12
The effect of calcium antagonists on histamine and leukotriene-induced tracheal microvascular permeability in the guinea pig
Published in Prostaglandins (01-08-1986)“…The effects of several calcium antagonists, i.e., nifedipine, verapamil and 8-[N,N-diethylamino]-octyl 3,4,5-trimethoxybenzoate hydrochloride (TMB-8), were…”
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13
Enhancement of leukotriene D4-induced contraction of guinea-pig isolated trachea by platelet activating factor
Published in Prostaglandins (01-02-1987)“…The effect of platelet activating factor (PAF), a potent lipid mediator of inflammation, was examined in the induction of airway hyperreactivity to known…”
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14
The properties of A-69412: a small hydrophilic 5-lipoxygenase inhibitor
Published in Agents and Actions (01-03-1993)“…A compound which inhibits leukotriene biosynthesis could be clinically useful in treating several allergic and inflammatory diseases. One site for such…”
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15
The effects of nifedipine and verapamil on antigen-induced bronchoconstriction in dogs
Published in European journal of pharmacology (19-08-1983)“…The effects of calcium channel blockers, nifedipine and verapamil (i.v. and aerosol), were investigated in beagle dogs natively allergic to Ascaris suum…”
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16
(R)-(+)-N-[3-[5-[4-fluorophenylmethyl]-2-thienyl]-1-methyl-2-propynyl]-N-hydroxyurea (ABT-761), a second-generation 5-lipoxygenase inhibitor
Published in Journal of medicinal chemistry (24-11-1995)“…Structure-activity optimization of inhibitory potency and duration of action of N-hydroxyurea containing 5-lipoxygenase inhibitors was conducted. The…”
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17
The role of platelet-activating factor (PAF) and the efficacy of ABT-491, a highly potent and selective PAF antagonist, in experimental allergic rhinitis
Published in The Journal of pharmacology and experimental therapeutics (01-01-1998)“…Platelet-activating factor (PAF) may be an important mediator of allergic rhinitis. In the present study we evaluated the effectiveness of a recently described…”
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18
ABT-761 attenuates bronchoconstriction and pulmonary inflammation in rodents
Published in The Journal of pharmacology and experimental therapeutics (01-03-1997)“…Our primary goal has been to discover leukotriene biosynthesis inhibitors with characteristics that are appropriate for use as clinical agents. The success of…”
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19
The 5-lipoxygenase inhibitory activity of zileuton in in vitro and in vivo models of antigen-induced airway anaphylaxis
Published in Pulmonary pharmacology (Edinburgh) (01-04-1994)“…Leukotrienes are biologically active lipid mediators capable of producing airway inflammation, hyperresponsiveness and bronchoconstriction. The first enzyme in…”
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20
A-78773: a selective, potent 5-lipoxygenase inhibitor
Published in Journal of lipid mediators (01-03-1993)“…The potency and selectivity of A-78773, a newly discovered 5-lipoxygenase inhibitor, were examined. The compound was significantly more potent than zileuton in…”
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