Academic Journal

Design, synthesis and Cytotoxic Evaluation of a New Series of 3-Substituted-spiro[(dihydropirazin-2,5-dione)-6,3’-(2’,3’-dihydrothieno[2,3-b]naphtho-4’,9’-dione)] Derivatives

التفاصيل البيبلوغرافية
العنوان: Design, synthesis and Cytotoxic Evaluation of a New Series of 3-Substituted-spiro[(dihydropirazin-2,5-dione)-6,3’-(2’,3’-dihydrothieno[2,3-b]naphtho-4’,9’-dione)] Derivatives
المؤلفون: GOMEZ MONTERREY, ISABEL MARIA, CAROTENUTO, ALFONSO, GRIECO, PAOLO, NOVELLINO, ETTORE, P. CAMPIGLIA, D. CALIFANO, C. PISANO, L. VESCI, T. LAMA, A. BERTAMINO, M. SALA, A. MAZZELLA di BOSCO
المساهمون: GOMEZ MONTERREY, ISABEL MARIA, P., Campiglia, Carotenuto, Alfonso, D., Califano, C., Pisano, L., Vesci, T., Lama, A., Bertamino, M., Sala, A., MAZZELLA di BOSCO, Grieco, Paolo, Novellino, Ettore
سنة النشر: 2007
المجموعة: IRIS Università degli Studi di Napoli Federico II
الوصف: A series of 3-substituted spiro[(dihydropyrazine-2,5-dione)-6,3¢-(2¢,3¢-dihydrothieno[2,3-b]naphtho-4¢,9¢- dione)] derivatives were prepared using an easy synthetic route via condensation of the 3-amino-3- (ethoxycarbonyl)-2,3-dihydrothieno[2,3-b]naphtho-4,9-dione system and amino acids followed by intramolecular lactamization. Amino acids containing alkyl and aryl, linear and cyclic, polar and apolar, and basic and acid residues were incorporated. Evaluation of these analogues against the MCF-7 human breast carcinoma and SW 620 human colon carcinoma cell lines revealed, for the 3S,3¢R isomers derived from Pro , Cys , and Met and the 3R,3¢S isomer derived from D-Pro , a cytotoxic potency comparable to or greater than that of doxorubicin. Some of these selected analogues were potent cytotoxic agents in several other sensible and resistant human solid tumor cell lines and may be able to circumvent the multiple-drugresistance mechanism. In particular, only a partial cross-resistance to these compounds was observed in selected tumor cell sublines known to be resistant to doxorubicin (MCF-7/Dx and A2780/Dx), whereas a very low level of cross-resistance to compounds containing the Pro and Met residues was found in a tumor cell subline selected for resistance to cisplatin (A2780/DDP).
نوع الوثيقة: article in journal/newspaper
وصف الملف: STAMPA
اللغة: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/17375902; info:eu-repo/semantics/altIdentifier/wos/WOS:000245634500009; volume:50; issue:8; firstpage:1787; lastpage:1798; numberofpages:10; journal:JOURNAL OF MEDICINAL CHEMISTRY; http://hdl.handle.net/11588/336435; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-34247204851
DOI: 10.1021/jm0612158
الاتاحة: http://hdl.handle.net/11588/336435
https://doi.org/10.1021/jm0612158
Rights: info:eu-repo/semantics/closedAccess
رقم الانضمام: edsbas.B09936A2
قاعدة البيانات: BASE