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Pregled bibliografske jedinice broj: 832192

Novel urea and bis-urea primaquine derivatives with hydroxyphenyl and halogenphenyl substituents: synthesis and biological evaluation


Perković, Ivana; Antunović, Maja; Marijanović, Inga; Pavić, Kristina; Ester, Katja; Kralj, Marijeta; Vlainić, Josipa; Kosalec, Ivan; Schols, Dominique; Hadjipavlou-Litina, Dimitra et al.
Novel urea and bis-urea primaquine derivatives with hydroxyphenyl and halogenphenyl substituents: synthesis and biological evaluation // European journal of medicinal chemistry, 124 (2016), 622-636 doi:10.1016/j.ejmech.2016.08.021 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 832192 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Novel urea and bis-urea primaquine derivatives with hydroxyphenyl and halogenphenyl substituents: synthesis and biological evaluation

Autori
Perković, Ivana ; Antunović, Maja ; Marijanović, Inga ; Pavić, Kristina ; Ester, Katja ; Kralj, Marijeta ; Vlainić, Josipa ; Kosalec, Ivan ; Schols, Dominique ; Hadjipavlou-Litina, Dimitra ; Pontiki, Eleni ; Zorc, Branka

Izvornik
European journal of medicinal chemistry (0223-5234) 124 (2016); 622-636

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Primaquine ; Urea ; Bis-urea ; Antiproliferative activity ; Antioxidative activity ; Antimicrobial activity
(Primaquine ; Urea ; Bis-urea ; Antiproliferative activity ; Antioxidative activity ; Antimicrobial activit)

Sažetak
A series of novel compounds 3a-j and 6a-j with primaquine and hydroxyl or halogen substituted benzene moieties bridged by urea or bis-urea functionalities were designed, synthesized and evaluated for biological activity. The title compounds were prepared using benzotriazole as the synthon, through several synthetic steps. 3-[3, 5-Bis(trifluoromethyl)phenyl]-1-{; ; ; ; ; 4-[(6-methoxyquinolin-8-yl)amino]pentyl}; ; ; ; ; urea (3j) was the most active urea and 1-[({; ; ; ; ; 4-[(6-methoxyquinolin-8-yl)amino]pentyl}; ; ; ; ; carbamoyl)amino]-3-[3-(trifluoromethyl)phenyl]urea (6h) the most active bis-urea derivative in antiproliferative screening in vitro against eight tested cancer cell lines. Urea derivatives 3a-g with hydroxy group or one halogen atom showed moderate antiproliferative effects against all the tested cell lines, but stronger activity against breast carcinoma MCF-7 cell line, while trifluoromethyl derivatives 3h-j showed antiproliferative effects against all the tested cell lines in low micromolar range. Finally, bis-ureas with hydroxy and fluoro substituents 6a-d showed extreme selectivity and chloro or bromo derivatives 6e-g high selectivity against MCF-7 cells (IC50 0.1-2.6 µM). p-Fluoro derivative 6d, namely 3-(4-fluorophenyl)-1-[({; ; ; ; ; 4-[(6-methoxyquinolin-8-yl)amino]pentyl}; ; ; ; ; carbamoyl)amino]urea, is the most promising compound. Further biological experiments showed that 6d affected cell cycle and induced cell death of MCF-7 cell line. Due to its high activity against MCF-7 cell line (IC50 0.31 µM), extreme selectivity and full agreement with the Lipinski’s and Gelovani’s rules for prospective small molecular drugs, 6d may be considered as a lead compound in development of breast carcinoma drugs. Urea 3b and almost all bis-ureas showed high antioxidant activity in DPPH assay, but urea derivatives were more active in lipid peroxidation test. Only few compounds exhibited weak inhibition of soybean lipoxygenase. Compound 3j exhibited the strongest antimicrobial activity in susceptibility assay in vitro (MIC = 1.6–12.5 μg ml–1).

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Biologija, Temeljne medicinske znanosti



POVEZANOST RADA


Projekti:
006-0000000-3216 - Sinteza, karakterizacija i djelovanje potencijalnih i poznatih ljekovitih tvari (Zorc, Branka, MZOS ) ( POIROT)
HRZZ-IP-2014-09-1501 - Dizajniranje, sinteza i evaluacija derivata primakina, vorinostata i sorafeniba kao potencijalnih citostatika (PVSderivatives) (HRZZ - 2014-09) ( POIROT)
098-0982464-2514 - Uloga različitih mehanizama odgovora stanica na terapiju oštećenjem DNA (Kralj, Marijeta, MZOS ) ( POIROT)

Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb

Citiraj ovu publikaciju

Perković, Ivana; Antunović, Maja; Marijanović, Inga; Pavić, Kristina; Ester, Katja; Kralj, Marijeta; Vlainić, Josipa; Kosalec, Ivan; Schols, Dominique; Hadjipavlou-Litina, Dimitra et al.
Novel urea and bis-urea primaquine derivatives with hydroxyphenyl and halogenphenyl substituents: synthesis and biological evaluation // European journal of medicinal chemistry, 124 (2016), 622-636 doi:10.1016/j.ejmech.2016.08.021 (međunarodna recenzija, članak, znanstveni)
Perković, I., Antunović, M., Marijanović, I., Pavić, K., Ester, K., Kralj, M., Vlainić, J., Kosalec, I., Schols, D. & Hadjipavlou-Litina, D. (2016) Novel urea and bis-urea primaquine derivatives with hydroxyphenyl and halogenphenyl substituents: synthesis and biological evaluation. European journal of medicinal chemistry, 124, 622-636 doi:10.1016/j.ejmech.2016.08.021.
@article{article, year = {2016}, pages = {622-636}, DOI = {10.1016/j.ejmech.2016.08.021}, keywords = {Primaquine, Urea, Bis-urea, Antiproliferative activity, Antioxidative activity, Antimicrobial activity}, journal = {European journal of medicinal chemistry}, doi = {10.1016/j.ejmech.2016.08.021}, volume = {124}, issn = {0223-5234}, title = {Novel urea and bis-urea primaquine derivatives with hydroxyphenyl and halogenphenyl substituents: synthesis and biological evaluation}, keyword = {Primaquine, Urea, Bis-urea, Antiproliferative activity, Antioxidative activity, Antimicrobial activity} }
@article{article, year = {2016}, pages = {622-636}, DOI = {10.1016/j.ejmech.2016.08.021}, keywords = {Primaquine, Urea, Bis-urea, Antiproliferative activity, Antioxidative activity, Antimicrobial activit}, journal = {European journal of medicinal chemistry}, doi = {10.1016/j.ejmech.2016.08.021}, volume = {124}, issn = {0223-5234}, title = {Novel urea and bis-urea primaquine derivatives with hydroxyphenyl and halogenphenyl substituents: synthesis and biological evaluation}, keyword = {Primaquine, Urea, Bis-urea, Antiproliferative activity, Antioxidative activity, Antimicrobial activit} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • Arts & Humanities Citation Index (A&HCI)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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