Pharmacological characterization of chloride channels belonging to the ClC family by the use of chiral clofibric acid derivatives

Molecular Pharmacology

Volumn 58, Issue 3, 2000, Pages 498-507

  Pusch, Michael ^a   Liantonio, Antonella ^a,b   Bertorello, Lara ^a   Accardi, Alessio ^a   De Luca, Annamaria ^b   Pierno, Sabata ^b   Tortorella, Vincenzo ^b   Camerino, Diana Conte ^b  

^a CNR   (Italy)

^b UNIVERSITY OF BARI   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE CHANNEL; CLOFIBRIC ACID DERIVATIVE;

ANIMAL CELL; ARTICLE; CHANNEL GATING; CHIRALITY; CONCENTRATION RESPONSE; CONTROLLED STUDY; NONHUMAN; OOCYTE; PH; PRIORITY JOURNAL; RAT; SKELETAL MUSCLE; STEREOCHEMISTRY; TISSUE SPECIFICITY; TORPEDO MARMORATA; TRANSPORT KINETICS; XENOPUS LAEVIS;

EID: 0033851904     PISSN: 0026895X     EISSN: None     Source Type: Journal    
DOI: 10.1124/mol.58.3.498     Document Type: Article

References (29)

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4. Phosphorylation and IGF-1 mediated dephosphorylation pathways control the activity and the pharmacological properties of skeletal muscle chloride channels
5. Chloride channels of skeletal muscle from developing, adult and aged rats are differently affected by enantiomers of 2-(p-chlorophenoxy) propionic acid
6. Opposite effect of enantiomers of clofibric acid derivative on rat skeletal muscle chloride conductance: Antagonism studies and theoretical modeling of two different receptor site interactions
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14. The skeletal muscle chloride channel in dominant and recessive human myotonia
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16. Mutations in the chloride channel ClC-5 are associated with X-linked hypercalciuric nephrolithiasis
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18. Two physically distinct pores in the dimeric ClC-0 chloride channel
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22. Low single-channel conductance of the major skeletal muscle chloride channel ClC-1
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29. A chloride channel widely expressed in epithelial and non-epithelial cells