Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Evstigneeva, Rima P."'
Autor:
Larkina, Ekaterina A., Balashova, Tamara A., Luzgina, Valentina N., Konovalova, Nadezhda V., Evstigneeva, Rima P.
Publikováno v:
In Mendeleev Communications 2005 15(6):234-236
Publikováno v:
Journal of Porphyrins and Phthalocyanines. :691-702
As part of an investigation aimed at developing artificial models for mimicking haemoprotein activity, four C-aminoacyl protohaemin IX derivatives with one or two -L-Leu-L- HisOMe (complexes 3 and 1) or -β-Ala-L- HisOMe (complexes 4 and 2) peptide f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05ec5e79b1a1b1fbbbc249a0430a811e
https://doi.org/10.1002/(sici)1099-1409(199912)3:8<691::aid-jpp142>3.0.co
https://doi.org/10.1002/(sici)1099-1409(199912)3:8<691::aid-jpp142>3.0.co
Autor:
Evstigneeva Rima P, Zheltukhina Galina A, Elena A. Rozhkova, Natalya L. Sakina, Valentina N. Yermakova, Mark A. Babizhayev
Publikováno v:
Clinica Chimica Acta. 254:1-21
The naturally occurring compound N alpha-acetylcarnosine (NAC) is proposed as the prodrug of L-carnosine (C) resistant to enzymatic hydrolysis by human serum carnosinase. Rabbit eyes were treated with 1% NAC, C or placebo and extracts of the aqueous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::670202d4ef9cf442a8903a651b203a48
https://doi.org/10.1016/0009-8981(96)06356-5
https://doi.org/10.1016/0009-8981(96)06356-5
Publikováno v:
Russian Chemical Reviews. 59:482-500
In this reivew lipoxygenase inhibitors are classified and their inhibitory activity, mode of action, specificity, and chemical synthesis are examined. The future prospects for using them to study enzymatic conversions and the development of antialler
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5522ef831a052981ee0fbc06ac660ff
https://doi.org/10.1070/rc1990v059n05abeh003538
https://doi.org/10.1070/rc1990v059n05abeh003538
Autor:
Ol'shevskaya, Valentina A., Evstigneeva, Rima P., Luzgina, Valentina N., Gyul’malieva, Maya A., Petrovskii, Pavel V., Morris, John H., Zakharkin, Leonid I.
Publikováno v:
In Mendeleev Communications 2001 11(1):14-15
Publikováno v:
Drug Design Reviews-Online; August 2005, Vol. 2 Issue: 5 p349-359, 11p
Autor:
Evstigneeva, Rima P., Zaitsev, Andrei V., Luzgina, Valentina N., Ol'shevskaya, Valentina A., Shtil, Alexander A.
Publikováno v:
Current Medicinal Chemistry - Anti-Cancer Agents; November 01, 2003, Vol. 3 Issue: 6 p383-392, 10p
Publikováno v:
Russian Chemical Reviews. 49:784-798
Methods for the synthesis of bisbenzylisoquinoline alkaloids and also 1-benzylisoquinoline bases, which are biogenetic precursors of the dimeric alkaloids, are surveyed in the biogenetic sequence of the alkaloids. Not only total but also partial and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4a287d69a22db841125bce683473958
https://doi.org/10.1070/rc1980v049n08abeh002505
https://doi.org/10.1070/rc1980v049n08abeh002505
Publikováno v:
Chemistry of Natural Compounds. 13:382-405
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fca91127505f7632bdc6870d5b2996d1
https://doi.org/10.1007/bf00565820
https://doi.org/10.1007/bf00565820
Publikováno v:
Chemistry of Natural Compounds. 17:337-340
A new synthesis of O-methyldauricine has been effected through an intermediate bisthioamide obtained by means of the Wilgerodt-Kindler reaction from 2-acetyl-5-methoxyphenyl 4′-acetylphenyl ether and homoveratrylamine. Subsequent Bischler-Napierals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::015dab8ede1a831a80785759c10d34c4
https://doi.org/10.1007/bf01185261
https://doi.org/10.1007/bf01185261