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1 y of cocaine in brain and plasma relative to cocaethylene.
4 A similar rate is observed for hydrolysis of cocaethylene, a more potent cocaine metabolite that has
5 e-dependent decrements in CAP amplitude, but cocaethylene and isopropylcocaine at medium to high conc
6 erve impulse blockade by lidocaine, cocaine, cocaethylene and isopropylcocaine using rat sciatic nerv
7 he active cocaine metabolites norcocaine and cocaethylene and its inability to hydrolyze benzoylecgon
9 aine and potent cocaine derivatives, such as cocaethylene, and for additional humanization of the ant
10 Cocaine, ecgonine methyl ester, norcocaine, cocaethylene, and mephedrone were mainly transformed by
11 estigated the local anesthetic properties of cocaethylene as well as isopropylcocaine, another potent
12 t additional mechanisms, such as more stable cocaethylene binding, may be a more important determinan
16 ivation slow the recovery and potentiate the cocaethylene inhibition of the Nav1.5 channel by distinc
18 iminated rapid inactivation and weakened the cocaethylene inhibition, consistent with an important ro
21 n, and ability to hydrolyze both cocaine and cocaethylene make cocE an attractive candidate for rapid
23 candidates, and suggest a mechanism whereby cocaethylene produces a decreased euphoria in humans com
25 The present study assessed the ability of cocaethylene to induce sensitization to the behavioral a
26 the behavioral and neurochemical effects of cocaethylene treatment in Long-Evans (LE) and Sprague-Da
27 Serotonin synthesis was also suppressed by cocaethylene treatment, however this phenomenon was less
28 l, suggesting that this mutation facilitates cocaethylene untrapping, which seems to be the rate-limi
30 t the aptamer binds cocaine, norcocaine, and cocaethylene with similar affinities and aminoglycosides
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