Search Results - "Tilyabaev, Z."

Phosphorus-Containing Esters of Anabasine and Piperidine by Tilyabaev, Z., Dalimov, D. N., Babaev, B. N., Kuvshinova, N. D., Khashimova, M. Kh, Oimatov, M.

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Crystal Structures of the Solvates of Di-ethylaminogossypol with Ethyl Acetate and Pyridine by Tilyabaev, Kamil Z, Talipov, Samat A, Ibragimov, Bakhtiyar T, Dowd, Michael K, Yuldashev, Abdurasul M

“…The crystal structures of di-ethylaminogossypol with ethyl acetate (DEAG-EA) and pyridine (DEAG-P) were studied by room-temperature X-ray diffraction. The…”
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Synthesis, structures, and acute toxicity of gossypol nonsymmetrical aldehyde derivatives by Tilyabaev, K. Z, Kamaev, F. G, Vypova, N. L, Yuldashev, A. M, Ibragimov, B. T, Talipov, S. A

“…Nonsymmetrical aldehyde derivatives of gossypol, a yellow polyphenolic pigment of cottonseed, were synthesized by reactions with ammonia, aniline,…”
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Membrane-active properties and antiradical activity of gossypol and its derivatives by Tukfatullina, I. I, Tilyabaev, K. Z, Mamadrakhimov, A, Salakhutdinov, B. A, Kamaev, F. G, Yuldashev, A. M, Dowd, M. K, Talipov, S. A, Ibragimov, B. T, Aripov, T. F

“…A novel asymmetric gossypol derivative was synthesized. The antioxidant activity of gossypol and certain of its derivatives at the aldehyde groups and the…”
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Alkaloids ofAnabasis aphylla and their cholinergic activities by Tilyabaev, Z., Abduvakhabov, A. A.

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1H NMR study on the solvent effect on imine-enamine tautomerism of the condensation product of gossypol with 4-aminoantipyrine by Tilyabaev, K. Z., Kamaev, F. G., Yuldashev, A. M., Ibragimov, B. T.

“…According to the 1 H NMR data, the condensation product of gossypol with 4-aminoantipyrine in chloroform- d exists in the imine form, while in DMSO- d 6 , as…”
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An investigation of the venom of the spiderSegestria florentina as a blocker of the catalytic activities of esterases by Tilyabaev, Z., Sadykov, A. A., Abduvakhabov, A. A.

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Methylphosphonothionates of N-(?-hydroxypropyl)anabasine ? Synthesis, structure, and sensitivity of cholinesterases to them by Dalimov, D. N., Gafurov, M. B., Tilyabaev, Z., Kamaev, F. G., Abdugakhabov, A. A.

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Biochemical characteristics of the cholinesterase of the turnip mothAgrotis segetum by Kushiev, Kh. Kh, Tilyabaev, Z., Dalimov, D. N., Turakhanov, U. A.

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Relationship between the structure and cholinergic efficiency of various derivatives of the alkaloid anabasine by Tilyabaev, Z., Dalimov, D. N., Kushiev, Kh. Kh, Gafurov, M. B., Abduvakhabov, A. A.

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New phosphorylated derivatives of anabasine and of lupinine, and their anticholinesterase properties by Tilyabaev, Z., Baimirzaev, S. S., Kushiev, Kh. Kh, Dalimov, D. N., Gafurov, M. B.

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Effect of a hydrophobic interaction in the reaction of S-(β-alkylthioethyl) O-propyl methylphosphonothionates and their methyl methosulfates with cholinesterases of warm-blooded animals by Gulyamov, M., Tilyabaev, Z., Dalimov, D. N., Abduvakhabov, A. A.

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Anabasine and cytisine derivatives as reversible cholinesterase inhibitors by Dobren'kov, A. G., Tilyabaev, Z., Dalimov, D. N., Abduvakhabov, A. A.

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Interaction with cholinesterases and conformational analysis of analogs of acetylcholine containing the alkaloids ephedrine and pseudoephedrine by Dobren'kov, A. G., Leont'ev, V. B., Tilyabaev, Z., Dalimov, D. N., Abduvakhabov, A. A.

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Synthesis of organophosphorus derivatives of anabasine and investigation of their cholinergic activity by Gazaliev, A. M., Zhurinov, M. Zh, Tilyabaev, Z., Dalimov, D. N., Mukanova, K. D., Dyusembaev, S. A.

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Synthesis of some bis(2-morpholino-1-methylethyl) esters of carboxylic acids and study of their interaction with the cholinesterases of warm-blooded animals by Gulyamov, M., Dalimov, D. N., Tilyabaev, Z., Kamaev, F. G., Abduvakhabov, A. A.

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Synthesis, reaction with esterases, and toxicity of O-alkyl S-(carbalkoxymethylmercapto)methyl methylthiophosphonates by Mastryukova, T. A., Shipov, A. ., Emkuzheva, Z. K., Brestkin, A. P., Brik, I. L., Mandel'shtam, Yu. E., Fedin, A. N., Nozhko, T. I., Tilyabaev, Z., Roslavtseva, S. A., Kagan, Yu. S., Ershova, E. A., Kabachnik, M. I.

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