Substituted N-phenylcarbamates as histamine H3 receptor antagonists with improved in vivo potency

Pharmazie

Volumn 55, Issue 2, 2000, Pages 83-86

  Reidemeister, S ^a   Stark, Holger ^c   Ligneau, X ^a   Ganellin, C R ^a   Schwartz, J C ^b   Schunack, W ^a  

^a Department of Chemistry ^*

^b U Neurobiologie Pharmacologie M   (France)

^c Institut fur Pharmazie   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CARBAMIC ACID DERIVATIVE; HISTAMINE H3 RECEPTOR; HISTAMINE H3 RECEPTOR ANTAGONIST;

ANIMAL CELL; ARTICLE; DRUG MECHANISM; DRUG METABOLISM; DRUG POTENCY; DRUG STRUCTURE; NONHUMAN; RAT; RECEPTOR BINDING;

ANIMALS; CARBAMATES; CEREBRAL CORTEX; GUINEA PIGS; HISTAMINE ANTAGONISTS; HISTAMINE H1 ANTAGONISTS; HISTAMINE H2 ANTAGONISTS; HISTAMINE RELEASE; ILEUM; METHYLHISTAMINES; MICE; MUSCARINIC ANTAGONISTS; MUSCLE CONTRACTION; RATS; RECEPTOR, MUSCARINIC M3; RECEPTORS, HISTAMINE H3; RECEPTORS, MUSCARINIC; SYNAPTOSOMES;

EID: 0034095290     PISSN: 00317144     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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