Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kastis Krikštopaitis"'
Autor:
Evelina Polmickaitė-Smirnova, Jonas Šarlauskas, Kastis Krikštopaitis, Živilė Lukšienė, Zita Staniulytė, Žilvinas Anusevičius
Publikováno v:
Applied Sciences, Vol 10, Iss 12, p 4062 (2020)
The antitumor drug 3-amino-1,2,4-benzotriazine-1,4-dioxide (tirapazamine, TPZ (1)) along with a number of newly synthesized tirapazamine derivatives (TPZs) bearing substitutions at the 3-amine position of TPZ (1) were estimated for their antibacteria
Externí odkaz:
https://doaj.org/article/00b6d7faf6014048b796cdbce74ee316
Publikováno v:
Chemija. 33
We compared the redox properties of recombinant cytosolic (TrxR1) and mitochondrial (TrxR2) isoforms of human flavosulfoselenoenzyme NADPH:thioredoxin reductase. The standard redox potentials of isoenzymes (E0 7), determined according to the redox eq
Autor:
Jonas Šarlauskas, Evelina Polmickaitė-Smirnova, Živilė Lukšienė, Žilvinas Anusevičius, Zita Staniulytė, Kastis Krikštopaitis
Publikováno v:
Applied sciences, Basel : MDPI, 2020, vol. 10, iss. 12, art. no. 4062, p. [1-15]
Applied Sciences, Vol 10, Iss 4062, p 4062 (2020)
Applied Sciences
Volume 10
Issue 12
Applied Sciences, Vol 10, Iss 4062, p 4062 (2020)
Applied Sciences
Volume 10
Issue 12
The antitumor drug 3-amino-1,2,4-benzotriazine-1,4-dioxide (tirapazamine, TPZ (1)) along with a number of newly synthesized tirapazamine derivatives (TPZs) bearing substitutions at the 3-amine position of TPZ (1) were estimated for their antibacteria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::744a66fa628c51d8a5c846bdc27467ad
https://repository.vu.lt/VU:ELABAPDB80577691&prefLang=en_US
https://repository.vu.lt/VU:ELABAPDB80577691&prefLang=en_US
Autor:
Žilvinas Anusevičius, Narimantas Čėnas, Evelina Polmickaitė-Smirnova, Jonas Šarlauskas, Kastis Krikštopaitis
Publikováno v:
Chemija. 30
The antibacterial activity of a series of structurally diverse nitroaromatic compounds (NACs) (nitrobenzene and nitroheterocyclic derivatives) was estimated in terms of the minimum inhibitory concentrations (MICs) against Gram-positive Staphylococcus
Autor:
Lina Misevičienė, Narimantas Čėnas, Aleksey Yantsevich, Audrius Laurynėnas, Laimonas Karvelis, Kastis Krikštopaitis, Audronė Marozienė, Jonas Šarlauskas, Žilvinas Anusevičius, Jonita Stankevičiūtė
Publikováno v:
International Journal of Molecular Sciences
Volume 15
Issue 12
Pages 23307-23331
International journal of molecular sciences, Basel : MDPI AG, 2014, Vol. 15, iss. 12, p. 23307-23331
International Journal of Molecular Sciences, Vol 15, Iss 12, Pp 23307-23331 (2014)
Volume 15
Issue 12
Pages 23307-23331
International journal of molecular sciences, Basel : MDPI AG, 2014, Vol. 15, iss. 12, p. 23307-23331
International Journal of Molecular Sciences, Vol 15, Iss 12, Pp 23307-23331 (2014)
The enzymatic reactivity of a series of benzo[1,2-c]1,2,5-oxadiazole N-oxides (benzofuroxans
BFXs) towards mammalian single-electron transferring NADPH:cytochrome P-450 reductase (P-450R) and two-electron (hydride) transferring NAD(P)H:quinone o
BFXs) towards mammalian single-electron transferring NADPH:cytochrome P-450 reductase (P-450R) and two-electron (hydride) transferring NAD(P)H:quinone o