Zobrazeno 1 - 10
of 59
pro vyhledávání: '"GODOVIKOV NN"'
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 109:381-384
Syntheses of S-alkynyl derivatives of phosphorus monothioacids with the triple bonds in the α, β, and γ positions are described. Compounds of the type R2P(O)SC≡CR′ show unusually high anticholinesterase ability (“acetylenic effect”).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55ad9f9195cb9249e2e0f521e3f83b16
https://doi.org/10.1080/10426509608545170
https://doi.org/10.1080/10426509608545170
Autor:
V I Rosengart, Godovikov Nn, Yu G Zhukovskii, A. P. Brestkin, L. A. Vikhreva, M. I. Kabachnik, S.N. Moralev, Sherstobitov Oe
Publikováno v:
Russian Chemical Reviews. 60:885-902
Data are given in the review on the anticholinesterase activity of 58 specially synthesised esters of phosphorus thioacids containing an acetylenic bond in the thioester group. It was established that compounds containing an acetylenic group in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c7acedf777a5593b759ce2cc015ee63
https://doi.org/10.1070/rc1991v060n08abeh001117
https://doi.org/10.1070/rc1991v060n08abeh001117
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 111:87-87
We have shown that thioesters of phosphoric acids of general formula (RO)2P(X)C[tbnd]CR1, were X=O or S, containing an acetylenic bond in α-position of the S-ester group has unugually high destructive effect on some isoforms of cytochrome P 450 of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfad74765fd4695e19c185170f03454f
https://doi.org/10.1080/10426509608054716
https://doi.org/10.1080/10426509608054716
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 111:115-115
The first examples of B-substituted carboranyl thio- and selenoesters of trivalent phosphorus acids were synthesized. On the basis of these samples, a series of new corresponding pentavalent phosphorus acids derivatives, potentialy bioactive compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62fcfbbfa1ba2722a29a35bee45f23b0
https://doi.org/10.1080/10426509608054744
https://doi.org/10.1080/10426509608054744
Akademický článek
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Akademický článek
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Akademický článek
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Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 51:208-208
New methods for synthesis of carboranylthio- and carbor-anylselenoesters of pentavalent phosphorus acids, where the carboranyl group is connected through the carbon or boron atom, have been developed. Through interaction between bis (alkoxythiophosph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f4e9497d7088b8217721dce2b3342c5
https://doi.org/10.1080/10426509008040742
https://doi.org/10.1080/10426509008040742
Publikováno v:
Russian Chemical Reviews. 52:918-930
The review deals with the synthesis and anticholinesterase activities of phosphorylated derivatives of certain alkaloids and nitrogen-containing heterocycles. It is shown that the conformational properties of the alkaloid and nitrogen-containing hete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2e87ebb056934c0f7f314476a2d9962
https://doi.org/10.1070/rc1983v052n10abeh002895
https://doi.org/10.1070/rc1983v052n10abeh002895
Autor:
B.A Khaskin, A.E. Khovanskikh, Abduvakhabov Aa, Tatyana A. Mastryukova, E.B. Maizel, Godovikov Nn, A.P. Brestkin, I.N. Sazonova, A. E. Shipov, K.V. Novozhilov, S.N. Moralev, M. I. Kabachnik
Publikováno v:
Insect Biochemistry. 16:701-707
Anticholinesterase potency and toxicity for spring grain aphids of 52 organophosphorous inhibitors (OPI) of different structures were investigated. As regards sensitivity to OPI, the acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f44f6c81e2ddd5ef9751488a7bc33441
https://doi.org/10.1016/0020-1790(86)90014-4
https://doi.org/10.1016/0020-1790(86)90014-4