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
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).