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Di Zhang

School of Chemistry and Chemical Engineering, Guangxi University, 100 Daxue Dong Road, Nanning, Guangxi 530004, China.

2 papers in the library · 6 citations · publishing 2022-2023

Papers

Structure identification and analysis of the suspected chemical precursor of 2-fluorodeschloroketamine and its decomposition products.

Drug testing and analysis June 1, 2022 Xuan Luo, Di Zhang, Qiulian Luo et al. 4 citations

A suspected chemical precursor of the drug 2-fluorodeschloroketamine (2-FDCK), called 2-fluorodeschlorohydroxylimine, was identified using gas chromatography-mass spectrometry and gas chromatography-quadrupole/time-of-flight mass spectrometry, with comparisons to ketamine and its precursor hydroxylimine. The fragmentation pathway under electron ionization was theorized, and decomposition mechanisms in protic solvents were elucidated. In such solvents, the imine group protonates, then traces of water hydrolyze it, yielding a carbon cation that either forms the major product (2'-fluorophenyl)(1″-hydroxycyclopentyl)methanone via classical imine decomposition or undergoes loop expansion to 2-(2'-fluorophenyl)-2-hydroxycyclohexan-1-one. Structures were confirmed by theoretical calculation, GC-MS, NMR, ACDLabs-Structure Elucidator Suite, and diffusion-ordered spectroscopy. Methods for qualitative analysis of the precursor were established.

Comparative Analysis and Structure Identification of Oxidative Metabolites and Hydrogenation Metabolite Enantiomers for 2-Fluorodeschloroketamine.

Journal of analytical toxicology May 19, 2023 Xuan Luo, Di Zhang, Fang Zhang et al. 2 citations

Using mass spectrometry and theoretical calculations, 17 oxidative metabolites of the drug 2-fluorodeschloroketamine (2-FDCK) were identified in human urine and grouped into four categories. The study clarified how the site of oxidative metabolism relates to the electron cloud density in the molecule. Two mirror-image forms of a related compound, dihydro-2-FDCK, were distinguished using a lab-made reference standard and computational predictions. The work also revealed which enzymes favor particular molecular shapes during hydrogenation in the body. These findings provide a foundation for identifying metabolites of similar ketamine-type drugs.