Amiloride derivatives are potent blockers of KATP channels

Naunyn-Schmiedeberg's Archives of Pharmacology

Volumn 364, Issue 4, 2001, Pages 351-358

  Bollensdorff, C ^a   Zimmer, T ^a   Benndorf, K ^a  

^a FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

Author keywords

ATP; Ischemia; K+ currents; Na+ Ca2+ exchange; Na+ H+ exchange

Indexed keywords

5 (N ETHYL N ISOPROPYL)AMILORIDE; ADENOSINE TRIPHOSPHATE; AMILORIDE DERIVATIVE; DICHLOROBENZAMIL; POTASSIUM CHANNEL; POTASSIUM ION; PROTEIN SUBUNIT; SULFONYLUREA RECEPTOR;

ANIMAL TISSUE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; DELETION MUTANT; DIURESIS; DRUG POTENCY; FEMALE; HEART MUSCLE ISCHEMIA; IC 50; MONOCYTE; MOUSE; NONHUMAN; PROTON SODIUM EXCHANGE; SODIUM CALCIUM EXCHANGE;

AMILORIDE; ANIMALS; ATP-BINDING CASSETTE TRANSPORTERS; CARBONYL CYANIDE P-TRIFLUOROMETHOXYPHENYLHYDRAZONE; ELECTROPHYSIOLOGY; HEART; MEMBRANE POTENTIALS; MICE; MYOCARDIUM; OOCYTES; PLASMIDS; POTASSIUM CHANNEL BLOCKERS; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RNA, COMPLEMENTARY; SODIUM-HYDROGEN ANTIPORTER; UNCOUPLING AGENTS; XENOPUS;

EID: 0034794894     PISSN: 00281298     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002100100466     Document Type: Article

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