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Usled stalne potrebe za novim antitumorskim lekovima, počevši od androstanskog bis(semikarbazona), sintetisan je novi bis(karbazatni) estar (bisKBZ) za koji je određena antimikrobna aktivnost, citotoksična aktivnost na tri maligne ćelijske linije, i urađen je brine shrimp test toksičnosti. Novo jedinjenje se nije pokazalo kao dobar antimikrobni agens, ispoljilo je umerenu citotoksičnost prema testiranim ćelijskim linijama i pokazalo se kao pet puta manje toksično od cisplatina za račiće Artemia salina što je u dobroj korelaciji sa citotoksičnošću prema HeLa ćelijskoj liniji. Due to the constant need for new antitumor drugs, starting from androstane bis(semicarbazone), a new bis(carbazate) ester (bis-KBZ) was synthesized; antimicrobial activity and cytotoxicity against three malignant cell lines were determined, and the brine shrimp toxicity test was performed. The new compound did not prove to be a good antimicrobial agent, it showed moderate cytotoxicity to the tested cell lines, and proved to be five times less toxic than cisplatin to Artemia salina, which correlates well with the cytotoxicity to HeLa cell line.

U potrazi za biološki aktivnim jedinjenjima, počev od progesterona i 3-okso- α,β-nezasićenih androstenskih steroida, u okviru ove disertacije sintetisano je i potpuno okarakterisano pedeset novih derivata steroidnih hidrazona, od kojih po jedanaest tiosemikarbazona, tijadiazolina i semikarbazona, dvanaest tiazolidin-4-ona i pet karbazatnih estara. Po prvi put je urađena detaljna analiza stereohemije steroidnih hidrazona u položajima C-3/17 androstenskih, odnosno C-3/20 progesteronskih derivata. Struktura i stereohemija potvrđene su rezultatima rendgenske strukturne analize za tijadiazolin 7a, prvo okarakterisano steroidno jedinjenje koje sadrži šestočlani ugljenični prsten kondenzovan sa spiro-tijadiazolinskim prstenom, i tiazolidinon 9b-E, prvi steroidni derivat sa poznatom konfiguracijom dvostruke veze u položaju C-3 hidrazonotiazolidin- 4-onskog fragmenta. Sintetisana jedinjenja su ispoljila najjaču citotoksičnost prema HeLa ćelijama adenokarcinoma cerviksa i prema K562 ćelijama hronične mijeloidne leukemije, a po svojoj aktivnosti istakli su se tiosemikarbazoni 2a, 2b, 2c i 2f, tijadiazolini 8a i 8e i tiazolidin-4-oni 9a i 10a. Pritom su koeficijenti selektivnosti u antikancerskom dejstvu prema malignim ćelijama u odnosu na normalne humane PBMC, kako na nestimulisane tako i na mitogenom stimulisane, bili daleko veći od vrednosti 2,5 što ova jedinjenja svrstava u potencijalne kandidate za in vivo ispitivanja. Sumporni derivati bili su daleko aktivniji od kiseoničnih. Najaktivniji derivati indukovali su apoptozu posredstvom kaspaza-3, -8 i -9 i inhibirali angiogezu in vitro zbog čega se smatra da poseduju značajan antikancerski potencijal. Searching for biologically active compounds, within this doctoral dissertation fifty new steroidal hydrazone derivatives, of which 11 thiosemicarbazones, 11 thiadiazolines, 12 thiazolidin-4-ones, 11 semicarbazones and 5 carbazate esters, were synthesized starting with progesterone and 3-oxo-α,β-unsaturated androstene steroids, and fully characterized. For the first time, detailed stereochemistry analyses of steroidal hydrazones in the C- 3/17 positions of androstene derivatives, or C-3/20 positions of progesterone derivatives was done. Structure and stereochemistry were confirmed by the results of X-ray analyses for thiadiazoline 7a, the first characterized steroid compound that contains sixmembered carbon ring condensed with the spiro-thiadiazoline ring, and thiazolidinone 9b-E, the first steroidal derivative with known configuration of double bond in C-3 position of the hydrazono-thiazolidin-4-one fragment. Synthesised compounds manifested the best cytotoxicity towards HeLa cervix adenocarcinoma cells, and K562 cells of chronic myeloide leukemia, the best activity being showed by thiosemicarbazones 2a, 2b, 2c and 2f, thiadiazolines 8a and 8e, and thiazolidin-4-ones 9a and 10a. All of these compounds exhibited considerably higher intensities of cytotoxic action against malignant cells when compared with normal human PBMC, both resting and mitogen-stimulated, with coefficient of selectivity higher than 2.5, which makes these compounds potential candidates for in vivo experiments. Sulfur derivatives were much more active than oxygen derivatives. The most active derivatives induced apoptosis mediated by caspase-3, -8 and -9, and they inhibited angiogenesis in vitro, because of what they are considered to have significant anticancer potential.