Search Results - "Yanni, J M"
-
1
Characterization of the ocular antiallergic and antihistaminic effects of olopatadine (AL-4943A), a novel drug for treating ocular allergic diseases
Published in The Journal of pharmacology and experimental therapeutics (01-09-1996)“…Olopatadine (AL-4943A; KW-4679) [(Z)-11-[3-(dimethylamino)propylidene]-6, 11-dihydrodibenz[b,e]oxepine-2-acetic acid hydrochloride] is an…”
Get more information
Journal Article -
2
Histamine-stimulated cytokine secretion from human conjunctival epithelial cells: inhibition by the histamine H1 antagonist emedastine
Published in International archives of allergy and immunology (01-04-1998)“…The present studies demonstrate that histamine induces the secretion of IL-6, IL-8 and GM-CSF from human conjunctival epithelial cells in a dose- and…”
Get more information
Journal Article -
3
The in vitro and in vivo ocular pharmacology of olopatadine (AL-4943A), an effective anti-allergic/antihistaminic agent
Published in Journal of ocular pharmacology and therapeutics (1996)“…Olopatadine (AL-4943A; KW-4679) [(z)-11-[3-(dimethylamino)propylidene]-6, 11-dihydrodibenz[b,e]oxepine-2 acetic acid hydrochloride] is an anti-allergic agent…”
Get more information
Journal Article -
4
Comparative effects of topical ocular anti-allergy drugs on human conjunctival mast cells
Published in Annals of allergy, asthma, & immunology (01-12-1997)“…The concept of mast cell heterogeneity is well established. Recent data indicate that human conjunctival tissue mast cells and human connective tissue mast…”
Get more information
Journal Article -
5
Olopatadine (AL-4943A): ligand binding and functional studies on a novel, long acting H1-selective histamine antagonist and anti-allergic agent for use in allergic conjunctivitis
Published in Journal of ocular pharmacology and therapeutics (1996)“…AL-4943A (Olopatadine) is a new antihistaminic and anti-allergic drug. It was tested for its ability to compete for [3H]pyrilamine, [3H]tiotidine and…”
Get more information
Journal Article -
6
Emedastine: a potent, high affinity histamine H1-receptor-selective antagonist for ocular use: receptor binding and second messenger studies
Published in Journal of ocular pharmacology (1994)“…The antihistaminic agent, emedastine, was tested for its ability to compete for [3H]pyrilamine, [3H]tiotidine and [3H]N-methyl histamine binding to rodent…”
Get more information
Journal Article -
7
Preclinical efficacy of emedastine, a potent, selective histamine H1 antagonist for topical ocular use
Published in Journal of ocular pharmacology (1994)“…Emedastine [1-(2-ethoxyethyl)-2-(4-methyl-1-homopiperazinyl)- benzimidazole difumarate] was evaluated for topical ocular anti-histaminic activity in histamine…”
Get more information
Journal Article -
8
Inhibition of histamine-induced human conjunctival epithelial cell responses by ocular allergy drugs
Published in Archives of ophthalmology (1960) (01-05-1999)“…To evaluate the effects of topical ocular drugs with histamine H1-antagonist activity on histamine-stimulated phosphatidylinositol turnover and interleukin…”
Get more information
Journal Article -
9
Nepafenac, a unique nonsteroidal prodrug with potential utility in the treatment of trauma-induced ocular inflammation: II. In vitro bioactivation and permeation of external ocular barriers
Published in Inflammation (01-08-2000)“…Nepafenac, the amide analog of the NSAID amfenac, was examined in vitro for its bioactivation by ocular tissue components and its ability to permeate external…”
Get full text
Journal Article -
10
Secretory response of mast cells contained in monodispersed human choroidal preparations
Published in International archives of allergy and immunology (01-01-1997)“…Mast cells have been identified in the choroid of numerous species including man. However, functional studies involving these human mast cells have not been…”
Get more information
Journal Article -
11
Nepafenac, a unique nonsteroidal prodrug with potential utility in the treatment of trauma-induced ocular inflammation: I. Assessment of anti-inflammatory efficacy
Published in Inflammation (01-08-2000)“…Nepafenac, the amide analog of 2-amino-3-benzoylbenzeneacetic acid (amfenac), was examined in preclinical models for its potential utility as a topical ocular…”
Get full text
Journal Article -
12
Synthesis and antiallergy activity of 4-(diarylhydroxymethyl)-1-[3-(aryloxy)propyl]piperidines and structurally related compounds
Published in Journal of medicinal chemistry (1989)“…A series of 4-(diarylhydroxymethyl)-1-[3-(aryloxy)propyl]piperidines was synthesized and evaluated for antiallergy activity. Several analogues had potent…”
Get full text
Journal Article -
13
Inflammation-mediated retinal edema in the rabbit is inhibited by topical nepafenac
Published in Inflammation (01-10-2003)“…The purpose of this study was to evaluate the ability of the nonsteroidal anti-inflammatory drug nepafenac to prevent development of mitogen-induced…”
Get full text
Journal Article -
14
Interactions of olopatadine and selected antihistamines with model and natural membranes
Published in Ocular immunology and inflammation (01-12-2003)“…Objective: Olopatadine, an effective topical ocular human conjunctival mast cell stabilizer/antihistaminic antiallergic drug, was evaluated and compared to…”
Get full text
Journal Article -
15
AHR-14310C: a potent, long-acting, nonsedating H1-antihistamine that prevents antigen-induced mucus formation in sensitive rats
Published in The Journal of pharmacology and experimental therapeutics (01-06-1990)“…AHR-14310C(5-[2-[4-[bis(4-fluorophenyl)hydroxymethyl- 1-piperidinyl]ethyl]-3-methyl]-2-oxazolidinone ethanedioate, hydrochloride salt) displays potent and…”
Get more information
Journal Article -
16
Synthesis and substance P antagonist activity of naphthimidazolium derivatives
Published in Journal of medicinal chemistry (01-04-1992)“…The synthesis of unsymmetrical naphth[2,3-d]imidazolium and bridged naphth[2,3-d]imidazolium derivatives and their substance P (SP) antagonist activity are…”
Get full text
Journal Article -
17
Effects of AHR-5333, a new potential antiallergy compound, in in vivo models of immediate hypersensitivity
Published in International archives of allergy and applied immunology (1988)“…AHR-5333 [1-[4-[3-[4-[bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl] propoxy]-3-methoxyphenyl]ethanone] possessed potent, long-acting activity in rat and…”
Get more information
Journal Article -
18
Imidazo[4,5-b]quinoxaline cyanines as neurokinin antagonists
Published in Journal of medicinal chemistry (01-05-1991)“…Substance P (SP) is an undecapeptide neuromodulator that belongs to the neurokinin (NK) family, which includes the structurally related neurokinin A (NKA) and…”
Get full text
Journal Article -
19
Effect of antihistamines on antigen-induced increase of rat tracheal mucous gel layer thickness
Published in International archives of allergy and applied immunology (1988)“…The effect of orally administered H1 and H2 antihistamines on antigen-induced changes in tracheal mucous gel layer thickness of actively sensitized rats was…”
Get more information
Journal Article -
20
Preparation and characterization of monoclonal antibodies to substance P
Published in Hybridoma (01-12-1991)“…A series of mouse hybridomas that produced monoclonal antibodies reactive with Substance P was prepared in an attempt to find a surrogate NK-1 receptor. When…”
Get more information
Journal Article