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Volumn 41, Issue 21, 1998, Pages 4171-4176
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4-Alkynylphenyl imidazolylpropyl ethers as selective histamine H3- receptor antagonists with high oral central nervous system activity
a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
4 ALKYNYLPHENYL IMIDAZOLYLPROPYL ETHER DERIVATIVE;
4 ETHYNYLPHENYL 3 (1H IMIDAZOL 4 YL) PROPYL ETHER;
CLOBENPROPIT;
HISTAMINE H1 RECEPTOR;
HISTAMINE H2 RECEPTOR;
HISTAMINE H3 RECEPTOR;
HISTAMINE H3 RECEPTOR ANTAGONIST;
THIOPERAMIDE;
UNCLASSIFIED DRUG;
ANIMAL EXPERIMENT;
ANIMAL TISSUE;
ARTICLE;
BRAIN SYNAPTOSOME;
CENTRAL NERVOUS SYSTEM;
CONTROLLED STUDY;
DRUG ACTIVITY;
DRUG PENETRATION;
DRUG POTENCY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
IN VITRO STUDY;
IN VIVO STUDY;
MOUSE;
NONHUMAN;
ORAL DRUG ADMINISTRATION;
RAT;
ADMINISTRATION, ORAL;
ANIMALS;
CEREBRAL CORTEX;
ETHERS;
GUINEA PIGS;
HISTAMINE ANTAGONISTS;
HISTAMINE RELEASE;
ILEUM;
IMIDAZOLES;
MICE;
MYOCARDIUM;
RATS;
RECEPTORS, HISTAMINE H1;
RECEPTORS, HISTAMINE H2;
RECEPTORS, HISTAMINE H3;
SYNAPTOSOMES;
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EID: 0032497594
PISSN: 00222623
EISSN: None
Source Type: Journal
DOI: 10.1021/jm9802970 Document Type: Article |
Times cited : (26)
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References (27)
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