E. A. Mukhutdinov scite author profile

Data of IR, UV, and NMR ( 31 P, 1 H, 13 C) spectroscopy, X-ray crystallography, and quantum chemical calculations are presented for phosenazid and CAPAH molecules possessing psychotropic properties. In comparison to phosenazid, CAPAH exhibits a broader spectrum of neurotropic activity, which can be related to the presence of the P1 -O3 polar ester bond and, therefore, a higher reactivity of this molecule in metabolic processes. 690091-150X/07/4102-0069

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E. A. Mukhutdinov

Quantum-chemical predictions of the formation of H-bonds between the N-phenyl-N’-isopropyl-p-phenylenediamine and N,N’-diphenyl-p-phenylenediamine molecules

Crystal structure of N-phenyl-N′-isopropylp-phenylenediamine

Quantum-Chemical Modelling of the Migration of Inhibitors of Tyre Rubbers

Comparative study of the structure and biological activity of potential psychotropic drugs phosenazid and CAPAH

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