Zobrazeno 1 - 10
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pro vyhledávání: '"Glutathione transferase, (GST)"'
Publikováno v:
Malaysian Applied Biology. Oct2022, Vol. 51 Issue 4, p177-184. 8p.
Akademický článek
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Publikováno v:
Malaysian Applied Biology. 51:177-184
The study aimed at identifying and purifying cytosolic glutathione transferase isoforms expressed in Pseudomonas sp. UW4. Search at UniProt (https://www.uniprot.org/uniprot/), has indicated that there were 20 genes encoding putative glutathione trans
Autor:
LaCourse, E. James, Hernandez-Viadel, Mariluz, Jefferies, James R., Svendsen, Claus, Spurgeon, David J., Barrett, John, John Morgan, A., Kille, Peter, Brophy, Peter M.
Publikováno v:
In Environmental Pollution 2009 157(8):2459-2469
Autor:
Griesbeck, Axel G.1 griesbeck@uni‐koeln.de, Maaßen, Andreas1, Bräutigam, Maria1,2, Pietsch, Markus2
Publikováno v:
European Journal of Organic Chemistry. Jul2015, Vol. 2015 Issue 20, p4349-4352. 4p.
Autor:
Andrea Calderan, Paolo Ruzza
Publikováno v:
Pharmaceutics, Vol 5, Iss 2, Pp 220-231 (2013)
Glutathione transferase (formerly GST) catalyzes the inactivation of various electrophile-producing anticancer agents via conjugation to the tripeptide glutathione. Moreover, several data link the overexpression of some GSTs, in particular GSTP1-1, t
Externí odkaz:
https://doaj.org/article/adfbc4a29de44b058983907eb7d0d971
Autor:
Higgins, Larry G.1 (AUTHOR), Hayes, John D.1 (AUTHOR) j.d.hayes@dundee.ac.uk
Publikováno v:
Drug Metabolism Reviews. May2011, Vol. 43 Issue 2, p92-137. 46p. 2 Black and White Photographs, 8 Diagrams, 5 Charts.
Autor:
Ruzza, Paolo1 paolo.ruzza@unipd.it, Calderan, Andrea1 andrea.calderan@unipd.it
Publikováno v:
Pharmaceutics. Jun2013, Vol. 5 Issue 2, p220-231. 12p. 6 Diagrams.
Disorder-to-Order Transition of the Active Site of Human Class Pi Glutathione Transferase, GST P1-1.
Publikováno v:
Biochemistry; 10/2/2001, Vol. 40 Issue 39, p11660, 10p, 2 Diagrams, 10 Graphs
Publikováno v:
European Journal of Organic Chemistry. 2015:4349-4352
The 1,2-hydroxy hydroperoxide 7 was obtained with high threo diastereoselectivity from the ester-conjugated allylic alcohol 6 through a porphyrin-sensitized singlet oxygen ene reaction. Compound 7 was used as substrate for peroxy(trans)acetalization