Brachialactone isomers and derivatives of Brachiaria humidicola reveal contrasting nitrification inhibiting activity

2020 ◽  
Vol 154 ◽  
pp. 491-497
Author(s):  
Konrad Egenolf ◽  
Jürgen Conrad ◽  
Jochen Schöne ◽  
Christina Braunberger ◽  
Uwe Beifuß ◽  
...  
1979 ◽  
Vol 44 (3) ◽  
pp. 946-951 ◽  
Author(s):  
Antonín Černý ◽  
Jiří Křepelka ◽  
Miroslav Semonský

Compounds III-XX exhibiting antilactation and antinidation effects in tests on rats were prepared on N(6)-alkylation of D-8-cyanomethylergoline-I (I) or D-8-methylergoline-I (II) with corresponding bromo (chloro) derivatives in dimethylformamide. The most distinct prolactin-inhibiting activity was found in compound III.


1973 ◽  
Vol 46 (2) ◽  
pp. 517-523
Author(s):  
L. K. Zolotarevskaya ◽  
A. M. Lipkin ◽  
A. E. Grinberg ◽  
L. G. Angert

Abstract In the nature of non-staining antiozonants, a new class of compounds, 1,1,4-derivatives of thiosemicarbazide, are proposed. The mechanism of reaction of thiosemicarbazide derivatives with ozone is analogous to the mechanism of this reaction with thiourea derivatives. Within this, the rate constant of the initial reaction of the thiosemicarbazide derivatives with ozone is somewhat higher than that of the thiourea derivatives. 1,1,4-Trialkyl-substituted thiosemicarbazides appear to be the most effective antiozonants, not changing the color of light vulcanizates. Of the investigated compounds, 1,1,4-tributylthiosemicarbazide, being distinguished by a large protective effect against ozone, inhibiting activity in the process of heat aging of the vulcanizates, and lesser ability for leaching out of the vulcanizates by water than tributylthiourea, presents the greatest practical interest.


Author(s):  
V. V. Ershov ◽  
K. B. Piotrovskii ◽  
N. A. Tupikina ◽  
G. A. Nikiforov ◽  
A. A. Volod'kin ◽  
...  

Author(s):  
Mohamed Rbaa ◽  
Loubna Lakhrissi ◽  
Younes Lakhrissi ◽  
Parul Dohare ◽  
Brahim Lakhrissi

In this chapter, the authors present a synthesis of some works carried out within the framework of the study of the corrosion inhibiting activity of a set of monosaccharide derivatives as new biodegradable, nontoxic corrosion inhibitors, and respectful of the environment. The comparative study that they present reveals the existence of more than 20 compounds derivatives of monosaccharide used as corrosion inhibitors in neutral and acidic mediums, and which have given rise to very good corrosion inhibiting efficiencies. These studies of the corrosion inhibiting effect were studied using potentiodynamic polarization curves and electrochemical impedance spectroscopy methods.


2018 ◽  
Vol 352 (2) ◽  
pp. 1800225 ◽  
Author(s):  
Anastasia V. Galochkina ◽  
Rakesh K. Bollikanda ◽  
Vladimir V. Zarubaev ◽  
Dmitry G. Tentler ◽  
Irina N. Lavrenteva ◽  
...  

1979 ◽  
Vol 44 (11) ◽  
pp. 3385-3390 ◽  
Author(s):  
Miloš Beran ◽  
Jiří Křepelka ◽  
Miroslav Semonský

D-6-Alkyl-8-cyanomethylergolines-I were converted either by known procedures via the corresponding methyl esters I-III and hydrazides IV-VI to amides VII-IX, or by hydration of the nitrile group under the conditions of ionic pair extraction to amides VIII and X-XIII. In the same system D-6-methyl-8-ergolin-I-ylacetamide (DeprenonR) was prepared from D-6-methyl-8-cyanomethylergoline-I. Amides VII, VIII and XI had a considerably higher prolactin inhibiting activity than Deprenon.


1976 ◽  
Vol 7 (38) ◽  
pp. no-no
Author(s):  
V. V. ERSHOV ◽  
K. B. PIOTROVSKII ◽  
N. A. TUPIKINA ◽  
G. A. NIKIFOROV ◽  
A. A. VOLOD'KIN ◽  
...  

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