Hydroxyl-Substituted sulfonylureas as potent inhibitors of specific [3H]Glyburide binding to rat brain synaptosomes

Bioorganic and Medicinal Chemistry

Volumn 11, Issue 9, 2003, Pages 2099-2113

  Hill, Ronald A ^a   Rudra, Sonali ^a   Peng, Bo ^a,c   Roane, David S ^a   Bounds, Jeffrey K ^a,d   Zhang, Yang ^a   Adloo, Ahmad ^a   Lu, Tiansheng ^b,e  

^a UNIVERSITY OF LOUISIANA AT MONROE   (United States)

^b LOUISIANA STATE UNIVERSITY   (United States)

^c BIOGEN   (United States)

^d ENVIRON INTERNATIONAL CORPORATION   (United States)

^e Ricerca Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

(2 CARBOXY 5 METHOXYPHENYL)ACETIC ACID; 1 [4 [2 (5 CHLORO 2 METHOXYBENZAMIDO)ETHYL]PHENYL]SULFONYL] 3 (3 HYDROXYCYCLOHEXYL)UREA; 1 [4 [2 (5 CHLORO 2 METHOXYBENZAMIDO)ETHYL]PHENYL]SULFONYL] 3 (4 HYDROXYCYCLOHEXYL)UREA; ACETIC ACID DERIVATIVE; ADENOSINE TRIPHOSPHATE; GLIBENCLAMIDE; GLIQUIDONE; HYDROXYL GROUP; POTASSIUM CHANNEL BLOCKING AGENT; SULFONYLUREA DERIVATIVE; TRITIUM; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BRAIN SYNAPTOSOME; BRAIN TISSUE; CONTROLLED STUDY; DRUG ACTIVITY; DRUG BINDING; DRUG INHIBITION; DRUG POTENCY; MALE; NONHUMAN; RAT; SUBSTITUTION REACTION; SYNAPTOSOME;

EID: 0037401962     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(02)00606-5     Document Type: Article

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