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In vitro and in vivo Reactivation of Cholinesterases Inhibited by Highly Toxic Organophosphorus Compounds

M. Maksimović ; High Military Technical School, Zagreb, Yugoslavia
B. Bošković ; High Military Technical School, Zagreb, Yugoslavia
Z . Binenfeld ; High Military Technical School, Zagreb, Yugoslavia

Puni tekst: engleski, pdf (5 MB) str. 195-199 preuzimanja: 42* citiraj
APA 6th Edition
Maksimović, M., Bošković, B. i Binenfeld, Z. (1968). In vitro and in vivo Reactivation of Cholinesterases Inhibited by Highly Toxic Organophosphorus Compounds. Croatica Chemica Acta, 40 (3), 195-199. Preuzeto s https://hrcak.srce.hr/208048
MLA 8th Edition
Maksimović, M., et al. "In vitro and in vivo Reactivation of Cholinesterases Inhibited by Highly Toxic Organophosphorus Compounds." Croatica Chemica Acta, vol. 40, br. 3, 1968, str. 195-199. https://hrcak.srce.hr/208048. Citirano 04.03.2021.
Chicago 17th Edition
Maksimović, M., B. Bošković i Z . Binenfeld. "In vitro and in vivo Reactivation of Cholinesterases Inhibited by Highly Toxic Organophosphorus Compounds." Croatica Chemica Acta 40, br. 3 (1968): 195-199. https://hrcak.srce.hr/208048
Harvard
Maksimović, M., Bošković, B., i Binenfeld, Z. (1968). 'In vitro and in vivo Reactivation of Cholinesterases Inhibited by Highly Toxic Organophosphorus Compounds', Croatica Chemica Acta, 40(3), str. 195-199. Preuzeto s: https://hrcak.srce.hr/208048 (Datum pristupa: 04.03.2021.)
Vancouver
Maksimović M, Bošković B, Binenfeld Z. In vitro and in vivo Reactivation of Cholinesterases Inhibited by Highly Toxic Organophosphorus Compounds. Croatica Chemica Acta [Internet]. 1968 [pristupljeno 04.03.2021.];40(3):195-199. Dostupno na: https://hrcak.srce.hr/208048
IEEE
M. Maksimović, B. Bošković i Z. Binenfeld, "In vitro and in vivo Reactivation of Cholinesterases Inhibited by Highly Toxic Organophosphorus Compounds", Croatica Chemica Acta, vol.40, br. 3, str. 195-199, 1968. [Online]. Dostupno na: https://hrcak.srce.hr/208048. [Citirano: 04.03.2021.]

Sažetak
The in vitro and in vivo reactivating power of 1,3-acetone-
bis-(4-hydroxyiminoformyl pyridinium) dibromide (MBM-3) was
compared with that of 1,3-trjmethylene~bis-(4-hydroxyjminoformyl
pynidinium) dibromide (TMB-4) and 1,3-dimethylether-bis-(4-hydroxyiminoformyl pyridinium) dibromide (Toxogonin). As a source of
choli'nesterase rat's whole blood, plasma, erythrocytes, and brain ho~
mogenate, were u sed. The cholinesterase inhibition was performed
by ethyl N-dimethylaminophosphorocyanidate (Taibun); ethyl 4-
-nitrophenyl phosphonate (Armin), 0,0-diethyl-S-(2-diethylaminoethyl)
phosphorothioate (Amitone-3); pinacolyl-methyl-phosphorofluoridate
(Soman); and O-ethyl-S-(2-diethylamino ethyl phosphorothioate
(Edemo-3).

Hrčak ID: 208048

URI
https://hrcak.srce.hr/208048

Posjeta: 86 *