Real-time intracellular Ca2+ mobilization by travoprost acid, bimatoprost, unoprostone, and other analogs via endogenous mouse, rat, and cloned human FP prostaglandin receptors

Journal of Pharmacology and Experimental Therapeutics

Volumn 304, Issue 1, 2003, Pages 238-245

  Kelly, Curtis R ^a   Williams, Gary W ^a   Sharif, Najam A ^a  

^a ALCON RESEARCH LTD   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

11 FLUORO 9,15 DIHYDROXY 15 (2 INDANYL) 16,17,18,19,20 PENTANORPROSTA 5,13 DIENOIC ACID; 11BETA FLUORO 15 EPI 15 INDANYL TETRANOR PROSTAGLANDIN F2 ALPHA; BIMATOPROST; CALCIUM ION; PROSTAGLANDIN F2 ALPHA; PROSTAGLANDIN F2 ALPHA DERIVATIVE; PROSTAGLANDIN RECEPTOR; TRAVOPROST; UNCLASSIFIED DRUG; UNOPROSTONE ISOPROPYL ESTER;

ANIMAL CELL; ARTICLE; CALCIUM MOBILIZATION; CELL STRAIN 3T3; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG POTENCY; DRUG RECEPTOR BINDING; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; RAT; RECEPTOR AFFINITY; SIGNAL TRANSDUCTION;

3T3 CELLS; AMIDES; ANIMALS; CALCIUM; CLONING, MOLECULAR; CLOPROSTENOL; DINOPROST; FIBROBLASTS; HUMANS; KIDNEY; LIPIDS; MICE; MUSCLE, SMOOTH, VASCULAR; PROSTAGLANDINS, SYNTHETIC; RATS; RECEPTORS, PROSTAGLANDIN;

EID: 0037214424     PISSN: 00223565     EISSN: None     Source Type: Journal    
DOI: 10.1124/jpet.102.042556     Document Type: Article

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