Synthetic chalcones, flavanones, and flavones as antitumoral agents:: Biological evaluation and structure-activity relationships

被引:287
作者
Cabrera, Mauricio
Simoens, Macarena
Falchi, Gabriela
Lavaggi, M. Laura
Piro, Oscar E.
Castellano, Eduardo E.
Vidal, Anabel
Azqueta, Amaia
Monge, Antonio
de Cerain, Adela Lopez
Sagrera, Gabriel
Scoane, Gustavo
Cerecetto, Hugo
Gonzalez, Mercedes [1 ]
机构
[1] Univ Republica, Fac Quim, Dept Quim Organ, Montevideo 11400, Uruguay
[2] Univ Republica, Fac Ciencias, Montevideo 11400, Uruguay
[3] Natl Univ La Plata, CONICET, IFLP, Dept Fis,Fac Ciencias Exactas, RA-1900 La Plata, Argentina
[4] Univ Sao Paulo, Inst Fis Sao Carlos, BR-13560 Sao Carlos, SP, Brazil
[5] Univ Navarra, CIFa, Pamplona, Spain
基金
巴西圣保罗研究基金会;
关键词
flavonoids; antitumoral; comet assay; QSAR;
D O I
10.1016/j.bmc.2007.03.031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of synthetic chalcones, flavanones, and flavones has been synthesized and evaluated for antitumor activity against the human kidney carcinoma cells TK-10, human mammary adenocarcinoma cells MCF-7 (estrogen receptor-positive), and human colon adenocarcinoma cells HT-29. The most active series is the chalcone ones with the best results against TK-10 and HT-29 cells. Fourteen out of 53 analyzed compounds resulted very active against at least two of the studied tumoral cells. Alkaline single cell gel electrophoresis, comet assay, was performed as a study of the chromosomal aberrations promoted by the compounds on normal cells. Four active and two inactive chalcones were studied in the comet assay against normal human kidney cells (HK-2). A structure-activity relationship analysis of these compounds was performed and for 4- and 3,4-disubstituted derivatives a quantitative correlation was obtained in the case of anti-HT-29 activity. (c) 2007 Published by Elsevier Ltd.
引用
收藏
页码:3356 / 3367
页数:12
相关论文
共 67 条
[1]   Dietary flavonols: Chemistry, food content, and metabolism [J].
Aherne, SA ;
O'Brien, NM .
NUTRITION, 2002, 18 (01) :75-81
[2]   Novel 5-aminoflavone derivatives as specific antitumor agents in breast cancer [J].
Akama, T ;
Shida, Y ;
Sugaya, T ;
Ishida, H ;
Gomi, K ;
Kasai, M .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (18) :3461-3469
[3]   Synthesis, antibacterial and antifungal activity of some derivatives of 2-phenyl-chromen-4-one [J].
Alam, S .
JOURNAL OF CHEMICAL SCIENCES, 2004, 116 (06) :325-331
[4]   ANTICANCER AND ANTIOXIDANT ACTIVITY OF SYNTHETIC CHALCONES AND RELATED-COMPOUNDS [J].
ANTO, RJ ;
SUKUMARAN, K ;
KUTTAN, G ;
RAO, MNA ;
SUBBARAJU, V ;
KUTTAN, R .
CANCER LETTERS, 1995, 97 (01) :33-37
[5]   Synthesis, experimental and theoretical NMR study of 2'-hydroxychalcones bearing a nitro substituent on their B ring [J].
Barros, AIRNA ;
Silva, AMS ;
Alkorta, I ;
Elguero, J .
TETRAHEDRON, 2004, 60 (31) :6513-6521
[6]   CENTAUREIDIN, A CYTOTOXIC FLAVONE FROM POLYMNIA-FRUTICOSA, INHIBITS TUBULIN POLYMERIZATION [J].
BEUTLER, JA ;
CARDELLINA, JH ;
LIN, CM ;
HAMEL, E ;
CRAGG, GM ;
BOYD, MR .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1993, 3 (04) :581-584
[7]   1,2,5-oxadiazole N-oxide derivatives as potential anti-cancer agents:: synthesis and biological evaluation.: Part IV [J].
Boiani, M ;
Cerecetto, H ;
González, M ;
Risso, M ;
Olea-Azar, C ;
Piro, OE ;
Castellano, EE ;
de Ceráin, AL ;
Ezpeleta, O ;
Monge-Vega, A .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2001, 36 (10) :771-782
[8]  
Boiani Mariana, 2004, Farmaco (Lausanne), V59, P405, DOI 10.1016/j.farmac.2003.12.011
[9]   Ruthenium(II) nitrofurylsemicarbazone complexes:: new DNA binding agents [J].
Cabrera, E ;
Cerecetto, H ;
González, M ;
Gambino, D ;
Noblia, P ;
Otero, L ;
Parajón-Costa, B ;
Anzellotti, A ;
Sánchez-Delgado, R ;
Azqueta, A ;
de Ceráin, AL ;
Monge, A .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2004, 39 (04) :377-382
[10]   FLAVONOID INHIBITION OF AROMATASE ENZYME-ACTIVITY IN HUMAN PREADIPOCYTES [J].
CAMPBELL, DR ;
KURZER, MS .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1993, 46 (03) :381-388