Site- and species-specific hydrolysis rates of cocaine

被引:1
|
作者
Szocs, Levente [1 ]
Volgyi, Gergely [1 ]
Urai, Akos [1 ]
Hosztafi, Sandor [1 ]
Toth, Gergo [1 ]
Gergo, Lajos [2 ]
Noszal, Bela [1 ]
机构
[1] Semmelweis Univ, Hungarian Acad Sci, Dept Pharmaceut Chem, Res Grp Drugs Abuse & Doping Agents, Hogyes E U 9, H-1092 Budapest, Hungary
[2] Eotvos Lorand Univ, Fac Informat, Dept Numer Anal, Budapest, Hungary
关键词
Cocaine; Ester hydrolysis; Protonation; Rate constant; Microconstant; LIQUID-CHROMATOGRAPHY; DOPAMINE; BINDING; BUTYRYLCHOLINESTERASE; PHARMACOKINETICS; METABOLITES; STABILITY; HUMANS; URINE;
D O I
10.1016/j.jpba.2017.07.005
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The hydroxide-catalyzed non-enzymatic hydrolysis of cocaine is quantified in terms of ten site- and species-specific rate constants in connection with also ten site- and species-specific acid-base equilibrium constants, comprising all the twelve coexisting species in solution. This characterization involves the major and minor decomposition pathways via benzoylecgonine and ecgonine methyl ester, respectively, leading to ecgonine, the final product Hydrolysis has been found to be 10-330 times faster at site 2 than at site 3, depending on the ionization status of the amino moiety and the rest of the molecule. Nitrogen protonation accelerates the hydrolyses approximately ten times both at site 2 and site 3. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:372 / 378
页数:7
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