Zobrazeno 1 - 10
of 19
pro vyhledávání: '"G I, Miagkova"'
Publikováno v:
Тонкие химические технологии, Vol 7, Iss 5, Pp 23-27 (2012)
Externí odkaz:
https://doaj.org/article/a284de16588949f9b4d0ba7dfbeb86ca
Publikováno v:
Тонкие химические технологии, Vol 4, Iss 5, Pp 3-19 (2009)
Studying of a physiological role of natural polyunsaturated fatty acids (PUFAs) at a new step of development of scientific and technical progress is actual. The present review is devoted questions of biosynthesis PUFAs, their regulatory functions, di
Externí odkaz:
https://doaj.org/article/04443a16ee364239badc26aa1be43039
Publikováno v:
Тонкие химические технологии, Vol 3, Iss 6, Pp 26-33 (2008)
Lipid peroxidation is common to all biological systems, both appearing in developmentally and environmentally regulated processes of plants. The hydroperoxy polyunsaturated fatty acids, synthesized by the action of various highly specialized forms of
Externí odkaz:
https://doaj.org/article/6d2a973804c840c49f5130a760e65938
Publikováno v:
Bioorganicheskaia khimiia. 24(2)
Approaches to the chemical synthesis of cytochrome P-450-dependent metabolites of arachidonic acid and the biological role of novel metabolites in the arachidonic acid cascade are discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2accfccb38a47fb299317933a1d9fe5d
https://pubmed.ncbi.nlm.nih.gov/10335404
https://pubmed.ncbi.nlm.nih.gov/10335404
Publikováno v:
Biulleten' eksperimental'noi biologii i meditsiny. 116(10)
The effects of two acyclic derivatives of arachidonic acid which are formed under the action of 5- and 12-lipoxygenases 5(S)-hydroxy-(6,8Z,11Z,14Z)-eicosatetraenoic acid (5-HETE) and (8R/S)-hydroxy-(11S,12S)-epoxy-5Z,9E,14Z-eicosatrienoi c acid (hepo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eb59c094b1d653aa9a18ab63c9355b36
https://pubmed.ncbi.nlm.nih.gov/8117956
https://pubmed.ncbi.nlm.nih.gov/8117956
Publikováno v:
Bioorganicheskaia khimiia. 19(6)
The review covers the aspects of classification, specificity and structure--biological activity relations in leukotriene receptor antagonists which blockade the action of the acyclic arachidonate metabolites. Prospects of designing new medicines base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a40ecd1b4d4036ad85e2b859b2916f1
https://pubmed.ncbi.nlm.nih.gov/8395845
https://pubmed.ncbi.nlm.nih.gov/8395845
Publikováno v:
Zhurnal vysshei nervnoi deiatelnosti imeni I P Pavlova. 41(6)
On identified Helix neurones RPa3 and LPa3 with the use of the double-electrode voltage clamp technique on the membrane the influence was studied of three polyacetilenic analogues of natural polyenoic acids which were the inhibitors of their lipoxyge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7879515f504b519a7d9f01635b4d02d6
https://pubmed.ncbi.nlm.nih.gov/1369571
https://pubmed.ncbi.nlm.nih.gov/1369571
Publikováno v:
Biulleten' eksperimental'noi biologii i meditsiny. 112(7)
The impact of a non-cyclized arachidonic acid derivative 15S-hydroxy-5Z, 8Z, 11Z, 13E-eicosatetraenoic acid (15-HETE) upon the dynamics of the inward current extinction, caused by repeated ion-tophoretic acetylcholine applications on the soma, was st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::902cd2ef4cc48050c81f7f149457357e
https://pubmed.ncbi.nlm.nih.gov/1793843
https://pubmed.ncbi.nlm.nih.gov/1793843
Publikováno v:
Patologicheskaia fiziologiia i eksperimental'naia terapiia. (6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3fb3864282b63e3802ee794923f8fad8
https://pubmed.ncbi.nlm.nih.gov/2832811
https://pubmed.ncbi.nlm.nih.gov/2832811
Publikováno v:
Bioorganicheskaia khimiia. 12(12)
Rac-leukotriene A4 methyl ester has been synthesized from propargylic alcohol and 1-heptyne. The synthetic strategy involves the assembly of carbon chain by acetylenide anion condensations and the introduction of (Z)-double bonds by the triple bond h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a50ed3e782feafbd91b2822edb9b019e
https://pubmed.ncbi.nlm.nih.gov/3028431
https://pubmed.ncbi.nlm.nih.gov/3028431