Name | 2-(2-chlorophenyl)-2,2-diphenylacetonitrile |
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Synonyms |
(2-chlorophenyl)-diphenylacetonitrile
TRAM-39 TRAM 39 |
Description | TRAM-39 is a selective blocker of intermediate conductance Ca2+-activated K+ (IKCa) channels. TRAM-39 inhibits KCa3.1 channel with an IC50 value of 60 nM. TRAM-39 can be used for the research of ataxia, epilepsy, memory disorders, schizophrenia and Parkinson’s disease[1][2][3][4]. |
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Related Catalog | |
Target |
IC50: 60 nM (KCa3.1 channel)[4] |
In Vitro | TRAM-39 (1 μM) reduces the peak amplitude of gKCa2 in sympathetic LAH neurons (mean percentage change 56%) in BAE cells[2]. TRAM-39 (200 nM) diminishes lipopolysaccharide (LPS)-induced cryptdin release from paneth cells[3]. |
In Vivo | TRAM-39 (1 μM; adds to the perfusate) fully blocks all IKCa channels in multicellular preparations[1]. |
Molecular Formula | C20H14ClN |
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Molecular Weight | 303.78500 |
Exact Mass | 303.08100 |
PSA | 23.79000 |
LogP | 5.19798 |
Storage condition | -20°C |