Synthesis and activity studies on some novel 1,4-disubstitutedpiperazine derivatives
Is this your thesis?
This record came from a bulk archive import. If it’s yours, link it to your profile.
Abstract (EN)
ABSTRACTGürdal, E. E., Synthesis and Activity Studies On Some Novel 1,4-Disubstitutedpiperazines. Yeditepe University Institute of Health Sciences, Ph. D. Thesis of Pharmaceutical Chemistry Programme, Istanbul, 2012.In this study, fifty one compounds with structures of N-substituted-4-[((4-substituted)diphenyl)methyl]piperazine-1-thioamide/-carbothioamide and N-[substitutedbenzoyl/phenylsulfonyl]-4-[((4-substituted)diphenyl)methyl]piperazine were prepared. Seventy four compounds are original. In vitro cytotoxic activities were screened in comparison with the reference drugs camptothecin (positive control) and 5-fluorouracil (reference).Benzhydrylpiperazine, 4-chlorobenzhydrylpiperazine and 4,4?-difluoro-benzhydrylpiperazine were synthesized by reflux of piperazine and suitable benzhydryl chlorides in alkali medium. Compounds were synthesized with reactions of benzhydrylpiperazine derivatives with suitable isocyanates, isothiocyanates, benzoyl chlorides and sulfonyl chlorides in room temperature with triethylamine.Structures of compounds were clarified with IR, 1H-NMR, 13C-NMR, mass spectroscopies, X-Ray crystallography and elemental analyses, also their physical characteristics and Rf values on thin layer chromatography were determined. In vitro cytotoxic activity screening of compounds were performed with sulphorodamine B method against breast cancer (MCF-7), hepatocellular carcinoma (HUH-7) and colorectal carcinoma (HCT-116) cell lines.Against HUH-7 cell line, in general, 4-chlorobenzhydrylpiperazine derivatives were more potent than other derivatives. The most potent compound against this cell line was N-(4-cyanophenyl)-4-[(4-chlorophenyl)(phenyl)methyl]piperazine-1-carboxamide (compound 25; IC50 = 1.29 micromolar).The most potent compound against MCF-7 cell line was 1-(4-bromobenzoyl)-4-[bis(4-fluorophenyl)methyl]piperazine HCl (compound 36; IC50 = 2.21 micromolar).The most potent compounds against HCT-116 cell line were N-tert-butyl-4-(diphenylmethyl)piperazine-1-carboxamide (compound 2; IC50 = 1.01 micromolar) and N-(4-cyanophenyl)-4-[(4-chlorophenyl)(phenyl)methyl]piperazine-1-carboxamide (compound 25; IC50 = 1.81 micromolar).Keywords: Piperazine, 1-benzhydrylpiperazine derivatives, isocyanate, isothiocyanate, benzoyl chloride, sulfonyl chloride, cytotoxic activity
Author
Enise Ece Gürdal
How to Cite
Enise Ece Gürdal (Doctorate thesis). Synthesis and activity studies on some novel 1,4-disubstitutedpiperazine derivatives, 2012, Yeditepe University.
License
Tüm Hakları Saklıdır
This work is shared under the specified license terms.
More theses from Yeditepe University
- Washington ambassadors in Turkish-US relations (1927-1960)(2023)
- Metamorphosis of female voices: A study of the violation of women in Greek and Roman mythology and feminist rewritings reclaiming the narrative(2022)
- The relationship between machiavelism, grandiose and vulnerable narcissism, and loneliness among white collar workers(2023)
- Evaluation of drug-drug interaction checkers along clinically relevant adverse drug events in oncology and hematology pediatric patients(2023)
- Declaration obligation of the insurant during the conclusion of the contract(2021)
- Investigation on the transformation of Hochbunkers built in Germany in the 20th century(2021)