|1.||Urbańczyk-Lipkowska, Zofia: 1 article (01/2015)|
|2.||Bielawska, Anna: 1 article (01/2015)|
|3.||Bielawski, Krzysztof: 1 article (01/2015)|
|4.||Wysocki, Waldemar: 1 article (01/2015)|
|5.||Ławecka, Justyna: 1 article (01/2015)|
|6.||Karczmarzyk, Zbigniew: 1 article (01/2015)|
|7.||Kalicki, Przemysław: 1 article (01/2015)|
|8.||Yurttaş, Leyla: 1 article (11/2014)|
|9.||Atlı, Özlem: 1 article (11/2014)|
|10.||Ilgın, Sinem: 1 article (11/2014)|
01/01/2001 - "The role of uncondensed 1,2,4-triazine compounds and related heterobicyclic systems in AIDS and Cancer is reviewed. "
01/01/2015 - "Synthetic approaches for sulfur derivatives containing 1,2,4-triazine moiety: their activity for in vitro screening towards two human cancer cell lines."
09/01/1999 - "Synthesis of some new heterobicyclic nitrogen systems bearing the 1,2,4-triazine moiety as anti-HIV and anti-cancer drugs, Part II."
11/01/2004 - "Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating 1,2,4-triazine moieties."
|3.||Breast Neoplasms (Breast Cancer)
01/01/2015 - "A series of sulfur 1,2,4-triazine derivatives were prepared and evaluated as anticancer compounds for two human breast cancer cell lines (MCF-7, MDA-MB-231) with some of them acting as low micromolar inhibitors. "
11/15/2014 - "In vitro antitumor activity evaluation of some 1,2,4-triazine derivatives bearing piperazine amide moiety against breast cancer cells."
|4.||Dehydration (Water Stress)
04/01/2014 - "The reaction take place in four steps, namely: (1) formation of a guanylhydrazone-acetylcarbinol adduct by condensation of AG and MG; (2) dehydration of the adduct; (3) formation of an 1,2,4-triazine derivative by ring closure; and (4) dehydration with the formation of 5-methyl 3-amino-1,2,4-triazine as the final product. "
|5.||Acquired Immunodeficiency Syndrome (AIDS)
|5.||Carbonic Anhydrase Inhibitors
|6.||Carbonic Anhydrases (Carbonic Anhydrase)