2-[3-(Aziridin-1-yl)-2-hydroxypropyl]-5,5-dimethyl-2,5-dihydro-4H-benzo[e]isoindol-4-one (Cytotoxic Oxonaphthalene-Pyrroles, Part III)

被引:1
作者
Spreitzer, Helmut [1 ]
Puschmann, Christiane [1 ]
机构
[1] Univ Vienna, Fac Life Sci, Dept Drug & Nat Prod Synth, Althanstr 14, A-1090 Vienna, Austria
关键词
pyrrole; DNA-alkylation; anticancer;
D O I
10.3390/M772
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An hydroxypropyl-aziridine-containing side chain is attached to an oxonaphthalene-annelated pyrrole in expectation of DNA alkylating properties. The cytotoxicity is evaluated against two cell lines, KB-31 and KB-8511, respectively.
引用
收藏
页数:4
相关论文
共 18 条
[1]   HYDROXYACETOPHENONE-DERIVED ANTAGONISTS OF THE PEPTIDOLEUKOTRIENES [J].
BROWN, FJ ;
BERNSTEIN, PR ;
CRONK, LA ;
DOSSET, DL ;
HEBBEL, KC ;
MADUSKUIE, TP ;
SHAPIRO, HS ;
VACEK, EP ;
YEE, YK ;
WILLARD, AK ;
KRELL, RD ;
SNYDER, DW .
JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (04) :807-826
[2]  
GIANCASPRO GI, 1989, FARMACO, V44, P483
[3]   1,5-dimethyl-6H-pyridazino[4,5-b]carbazole, a 3-aza bioisoster of the antitumor alkaloid olivacine [J].
Haider, N ;
Sotelo, E .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2002, 50 (11) :1479-1483
[4]   Synthesis and In-vitro antitumor activity of 1-[3-(Indol-1-yl)prop-1-yn-1-yl]phthalazines and related compounds [J].
Haider, Norbert ;
Kabicher, Tamara ;
Kaeferboeck, Johann ;
Plenk, Angelika .
MOLECULES, 2007, 12 (08) :1900-1909
[5]   Synthesis of tetra- and pentacyclic carbazole-fused imides as potential antitumor agents [J].
Haider, Norbert ;
Jbara, Rami ;
Kaeferboeck, Johann ;
Traar, Ursula .
ARKIVOC, 2009, :38-47
[6]   Synthesis and Antitumor Evaluation of Novel Bis-Triaziquone Derivatives [J].
Huang, Cheng Hua ;
Kuo, Hsien-Shou ;
Liu, Jia-Wen ;
Lin, Yuh-Ling .
MOLECULES, 2009, 14 (07) :2306-2316
[7]   A study on inhibition mechanism of breast cancer cells by bis-type triaziquone [J].
Lin, Yuh-Ling ;
Su, Yi-Ting ;
Chen, Bing-Huei .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2010, 637 (1-3) :1-10
[8]   A DERIVATIVE OF STAUROSPORINE (CGP-41-251) SHOWS SELECTIVITY FOR PROTEIN-KINASE C INHIBITION AND INVITRO ANTI-PROLIFERATIVE AS WELL AS INVIVO ANTI-TUMOR ACTIVITY [J].
MEYER, T ;
REGENASS, U ;
FABBRO, D ;
ALTERI, E ;
ROSEL, J ;
MULLER, M ;
CARAVATTI, G ;
MATTER, A .
INTERNATIONAL JOURNAL OF CANCER, 1989, 43 (05) :851-856
[9]  
Motgomery J. A., 1995, CANC CHEMOTHERAPEUTI, P111
[10]   2-NITROIMIDAZOLE DUAL-FUNCTION BIOREDUCTIVE DRUGS - STUDIES ON THE EFFECTS OF REGIOISOMERISM AND SIDE-CHAIN STRUCTURAL MODIFICATIONS ON DIFFERENTIAL CYTOTOXICITY AND RADIOSENSITIZATION BY AZIRIDINYL AND OXIRANYL DERIVATIVES [J].
NAYLOR, MA ;
THREADGILL, MD ;
WEBB, P ;
STRATFORD, IJ ;
STEPHENS, MA ;
FIELDEN, EM ;
ADAMS, GE .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (19) :3573-3578