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Dive into the research topics where Martin Winn is active.

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Featured researches published by Martin Winn.


Journal of Pharmacy and Pharmacology | 1987

A new nasal decongestant, A-57219: a comparison with oxymetazoline

John F. DeBernardis; Martin Winn; Daniel J. Kerkman; John J. Kyncl; Steven A. Buckner; Bruce Horrom

2‐(4‐Amino‐3,5‐dichlorobenzyl)imidazolin hydrochloride (A‐57219), has α1‐agonist/α2‐antagonist activity and was more effective and long‐acting than oxymetazoline on canine nasal mucosa, in‐vitro and in‐vivo. Upon intranasal administration to dogs, the compound was devoid of systemic effects up to a concentration 1000 times that needed for local decongestant effect (1ṁ65 μg, atomized from a 1 μg mL‐1 solution) suggesting limited mucosal absorption. After nasal administration to rats for 15 days at a concentration 1000 times greater than that required for nasal decongestion, no mucosal tissue toxicity or systemic effects were seen.


Journal of Medicinal Chemistry | 1985

Conformationally defined adrenergic agents. 1. Design and synthesis of novel .alpha.2-selective adrenergic agents: electrostatic repulsion based conformational prototypes

John F. DeBernardis; Daniel J. Kerkman; Martin Winn; Eugene N. Bush; David L. Arendsen; William J. McClellan; John J. Kyncl; Fatima Z. Basha


Journal of Medicinal Chemistry | 1976

Drugs derived from cannabinoids. 5. delta6a,10a-Tetrahydrocannabinol and heterocyclic analogs containing aromatic side chains.

Martin Winn; Arendsen D; Dodge P; Anthony T. Dren; Dunnigan D; Hallas R; Hwang K; Kyncl J; Lee Yh; N. P. Plotnikoff; Young P; Zaugg H


Journal of Medicinal Chemistry | 1986

Conformationally defined adrenergic agents. 3. Modifications to the carbocyclic ring of 5,6-dihydroxy-1-(2-imidazolinyl)tetralin: improved separation of .alpha.1 and .alpha.2 adrenergic activities

John F. DeBernardis; Martin Winn; David L. Arendsen; Daniel J. Kerkman; John J. Kyncl


Journal of Medicinal Chemistry | 1986

Conformationally defined adrenergic agents. 2. Catechol imidazoline derivatives: biological effects at alpha 1 and alpha 2 adrenergic receptors.

John F. DeBernardis; John J. Kyncl; Fatima Z. Basha; David L. Arendsen; Yvonne C. Martin; Martin Winn; Daniel J. Kerkman


Journal of Medicinal Chemistry | 1976

Drugs derived from cannabinoids. 4. Effect of alkyl substitution in sulfur and carbocyclic analogs

Raj K. Razdan; G. R. Handrick; Haldean C. Dalzell; John F. Howes; Martin Winn; N. P. Plotnikoff; Patrick W. Dodge; Anthony T. Dren


Journal of Medicinal Chemistry | 1975

N-Cyclopropyltryptamines, potent monoamine oxidase inhibitors

Martin Winn; Horrom Bw; Rasmussen Rr; Chappell Eb; N. P. Plotnikoff


Journal of Medicinal Chemistry | 1975

Homologs of dopa, alpha-methyldopa, and dopamine as potential cardiovascular drugs.

Martin Winn; Rasmussen Rr; Minard F; Kyncl J; N. P. Plotnikoff


Archive | 1974

2,4,7-substituted 5-hydroxy benzopyrans and esters

David L. Arendsen; Martin Winn


Archive | 1977

Alkyl substituted-4-oxo-cyclopenta benzopyrans

Martin Winn; Raj K. Razdan; Haldean C. Dalzell; Joyce Ruth Krei

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David L. Arendsen

Howard Hughes Medical Institute

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John F. DeBernardis

Massachusetts Institute of Technology

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Fatima Z. Basha

Massachusetts Institute of Technology

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John F. Howes

University of North Carolina at Chapel Hill

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