Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Dijana Saftić"'
Autor:
Nataša Župančić, Željka Ban, Josipa Matić, Dijana Saftić, Ljubica Glavaš-Obrovac, Biserka Žinić
Publikováno v:
Croatica Chemica Acta, Vol 88, Iss 1, Pp 43-52 (2015)
An efficient approach to reversed nucleosides which enables their synthesis in gram quantities is described. N-1′-Pyrimidine reversed nucleosides were prepared by treating of the sodium salt of pyrimidine bases with protected 5-tosyl ribose. Addi
Externí odkaz:
https://doaj.org/article/57398a9642294f2b9352730c6fd8eb8d
Autor:
Ljubica Glavaš-Obrovac, Dijana Saftić, Robert Vianello, Teuta Opačak-Bernardi, Tana Tandarić, Biserka Žinić, Marijana Jukić, Hamit Ismaili, Željka Ban, Josipa Matić
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids
The synthesis of novel 6- chloro/morpholino/amino/-9-sulfonylpurine derivatives was accomplished in two ways, either (i) involving the condensation reaction of 6- chloropurine with commercially available arylsulfonyl chlorides in acetone and the pres
Publikováno v:
Current Medicinal Chemistry
Among the most intensively studied classes of small molecules (molecular weight < 650) in biomedical research are small molecules that non-covalently bind to DNA/RNA, and another intensively studied class is nucleobase derivatives. Both classes have
Autor:
Josipa Matić, Ljubica Glavaš-Obrovac, Dijana Saftić, Željka Ban, Marijana Jukić, Katarina Mišković, Biserka Žinić, Ivana Marković
Publikováno v:
Journal of Trace Elements in Medicine and Biology
In an attempt to enhance the previously observed antiproliferative capacity of 1-( p -toluenesulfonyl)cytosine ( N -1-tosylcytosine, ligand 1 ), its copper(II) complex (Cu(1-TsC- N 3) 2 Cl 2 , complex 2 ) was prepared and tested in vitro on various c
Autor:
Ivo Piantanida, Goran Baranović, Edyta Paradowska, Zbigniew J. Leśnikowski, Mirosława Studzińska, Magdalena Białek-Pietras, Dijana Saftić
Publikováno v:
Bioorganic Chemistry
In this study, a series of uridine (U) and 2′-deoxyuridine (dU) conjugates containing an isomeric ortho-, meta- or para-carborane cluster (C2B10H12) attached at C-5 through an ethynyl linker were synthesized. The effect of carborane cluster isomeri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aeaf77b1fd28e6d4ba0f9694135bdcd
https://www.bib.irb.hr/1035462
https://www.bib.irb.hr/1035462
Autor:
Konrad Głąbała, Kamil Karolczak, Katarzyna Bednarska-Szczepaniak, Tomasz Przygodzki, Kenneth A. Jacobson, Dijana Saftić, Cezary Watala, Lidia Stanczyk, Harsha Rao, Adam Mieczkowski, Zbigniew J. Leśnikowski, Aleksandra Kierozalska, Zhan-Guo Gao
Publikováno v:
Eur J Med Chem
A series of adenosine and 2′-deoxyadenosine pairs modified with a 1,12-dicarba-closo-dodecaborane cluster or alternatively with a phenyl group at the same position was synthesized, and their affinity was determined at A(1), A(2A), A(2B) and A(3) ad
Autor:
Ivo Piantanida, Lidija-Marija Tumir, Ljubica Glavaš-Obrovac, Dijana Saftić, Marijana Jukić, Biserka Žinić, Marijana Radić Stojković
Publikováno v:
New Journal of Chemistry
A new group of multifunctional ligands for DNA and RNA were prepared, comprising phenanthridinium and triazolyluracil connected by various aliphatic or peptide linkers. The peptide linker conjugates showed at least one order of magnitude higher affin
Autor:
Dijana, Saftić, Mirosława, Studzińska, Edyta, Paradowska, Ivo, Piantanida, Goran, Baranović, Magdalena, Białek-Pietras, Zbigniew J, Leśnikowski
Publikováno v:
Bioorganic chemistry. 94
In this study, a series of uridine (U) and 2'-deoxyuridine (dU) conjugates containing an isomeric ortho-, meta- or para-carborane cluster (C
Autor:
Josipa Matić, Dijana Saftić, Ljubica Glavaš-Obrovac, Marijana Jukić, Željka Ban, Hamit Ismaili, Biserka Žinić
Publikováno v:
Croatica Chemica Acta
Volume 92
Issue 2
Volume 92
Issue 2
Efficient synthesis of 5-aminosulfonyl uracil derivatives 2-9 and results of their antiproliferative activity are provided. Sulfonylation of the amino group in 5-aminouracil 1 with selected arylsulfonyl chlorides occurs regioselectively when the reac
Autor:
Dijana Saftić, Mirosława Studzińska, Ljubica Glavaš-Obrovac, Zbigniew J. Leśnikowski, Edyta Paradowska, Biserka Žinić
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids
As a part of the research aimed on identification of new nucleobase derivatives with improved biological properties, a series of novel 8-substituted acyclovir derivatives were synthesized. The 8-azidoguanosine 4 and novel 8-azidoacyclovir 9 were synt