نتایج جستجو برای: 4 thiazolidinone

تعداد نتایج: 1303703  

2015
Yan Mu Yin Liu Liwen Li Cong Tian Hongyu Zhou Qiu Zhang Bing Yan

The dose-limiting toxicity caused by standard chemotherapy has become a major roadblock to successful rhabdomyosarcoma chemotherapy. By screening a thiazolidinone library including 372 compounds, a novel synthetic compound, 2-((4-hydroxyphenyl)imino)-5-(3-methoxybenzylidene)thiazolidin-4-one (MHPT), was identified as a potent and selective anti-rhabdomyosarcoma agent. MHPT inhibited 50% of the ...

Journal: :Journal of pharmacological sciences 2013
Qiu Zhang Xiaojun Liu Xiue Li Changlong Li Hongyu Zhou Bing Yan

Glioblastoma is the most lethal brain cancer. In spite of intensive therapy, the prognosis of patients with glioblastoma is very poor. To discover novel therapeutic agents, we screened a combinatorial compound library containing 372 thiazolidinone compounds using U87MG human glioblastoma cells. (2E,5Z)-5-(2-hydroxybenzylidene)-2-((4-phenoxyphenyl)imino) thiazolidin-4-one (HBPT) was identified a...

Journal: :iranian chemical communication 0
rahimeh hajinasiri department of chemistry, islamic azad university, qaemshahr branch, p.o. box 163, qaemshahr, iran sanaz baravardeh department of chemistry, qaemshahr branch, islamic azad university, p.o. box 163, qaemshahr, iran sobhan rezayati department of chemistry, payame noor university, po box 19395-4697, tehran, iran

derivatives of thiazolidinone ring systems are known to act as anti-hiv infections , analgesic, anti-bacterial, anti-convulsant, anti parasitic, potential anti-inflammatory and herbicidal agents. due biological activities of thiazolidinones ring, several methods for their synthesis have been illustrated in literature. imidazolidine-2-thiones were synthesized by the oxidative cyclization of 1-be...

Journal: :Acta poloniae pharmaceutica 2016
Dareen A Jaiash Amany Belal Mohamed A Abdelgawad Khaled R A Abdellatif

2-Chloroacetylamino-pyrrolo[1,2-a]azepine-3-ethyl ester 3 was synthesized, condensed with ammonium thiocyanate to obtain a hybrid molecule of pyrrolo [1,2-a]azepine and thiazolidinone moiety 4. Coupling of the obtained hybrid molecule with the appropriate aldehydes or diazonium salt afforded novel substituted hybrids 5a,b and 6. Chemical structures were confirmed by spectral and elemental analy...

Journal: :Bioorganic & medicinal chemistry 2014
Katalin Czifrák András Páhi Szabina Deák Attila Kiss-Szikszai Katalin E Kövér Tibor Docsa Pál Gergely Kyra-Melinda Alexacou Maria Papakonstantinou Demetres D Leonidas Spyros E Zographos Evangelia D Chrysina László Somsák

The reaction of thiourea with O-perbenzoylated C-(1-bromo-1-deoxy-β-D-glucopyranosyl)formamide gave the new anomeric spirocycle 1R-1,5-anhydro-D-glucitol-spiro-[1,5]-2-imino-1,3-thiazolidin-4-one. Acylation and sulfonylation with the corresponding acyl chlorides (RCOCl or RSO₂Cl where R=tBu, Ph, 4-Me-C₆H₄, 1- and 2-naphthyl) produced the corresponding 2-acylimino- and 2-sulfonylimino-thiazolidi...

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2010
C S Carvalho E J T de Melo R P Tenório A J S Góes

Toxoplasma, which infects all eukaryotic cells, is considered to be a good system for the study of drug action and of the behavior of infected host cells. In the present study, we asked if thiosemicarbazone derivatives can be effective against tachyzoites and which morphological and ultrastructural features of host cells and parasites are associated with the destruction of Toxoplasma. The compo...

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