Literature DB >> 17376678

Synthesis and biological activity of 5-aza-ellipticine derivatives.

Deborah L Moody1, Marcin Dyba, Teresa Kosakowska-Cholody, Nadya I Tarasova, Christopher J Michejda.   

Abstract

Novel 5-aza-ellipticine derivatives were synthesized and tested as antitumor agents. The new compounds were prepared more readily than the analogous ellipticine derivatives, which are known to be potent anti-tumor agents Although the novel 5-aza-ellipticine derivatives are not as biologically active as their corresponding ellipticine analogues, the new compounds represent a new, readily accessible class of heteroaromatic catalytic inhibitors of topoisomerase II and possible anti-tumor agents.

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Year:  2006        PMID: 17376678      PMCID: PMC2262287          DOI: 10.1016/j.bmcl.2006.09.093

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  12 in total

Review 1.  Isolation and synthesis of biologically active carbazole alkaloids.

Authors:  Hans-Joachim Knölker; Kethiri R Reddy
Journal:  Chem Rev       Date:  2002-11       Impact factor: 60.622

Review 2.  Extending nature's leads: the anticancer agent ellipticine.

Authors:  Nichola C Garbett; David E Graves
Journal:  Curr Med Chem Anticancer Agents       Date:  2004-03

3.  Bisimidazoacridones induce a potent cytostatic effect in colon tumor cells that sensitizes them to killing by UCN-01.

Authors:  W M Cholody; T Kosakowska-Cholody; C J Michejda
Journal:  Cancer Chemother Pharmacol       Date:  2001-03       Impact factor: 3.333

4.  Stimulation of growth of a colon cancer cell line by gastrin.

Authors:  C J Kusyk; N O McNiel; L R Johnson
Journal:  Am J Physiol       Date:  1986-11

5.  A new synthetic agent with potent but selective cytotoxic activity against cancer.

Authors:  Wieslaw M Cholody; Teresa Kosakowska-Cholody; Melinda G Hollingshead; Humcha K Hariprakasha; Christopher J Michejda
Journal:  J Med Chem       Date:  2005-06-30       Impact factor: 7.446

6.  Synthesis of 6H-indolo[2,3-b][1,6]naphthyridines and related compounds as the 5-Aza analogues of ellipticine alkaloids.

Authors:  Q Zhang; C Shi; H R Zhang; K K Wang
Journal:  J Org Chem       Date:  2000-11-17       Impact factor: 4.354

7.  DNA-drug recognition and effects on topoisomerase II-mediated cytotoxicity. A three-mode binding model for ellipticine derivatives.

Authors:  M Monnot; O Mauffret; V Simon; E Lescot; B Psaume; J M Saucier; M Charra; J Belehradek; S Fermandjian
Journal:  J Biol Chem       Date:  1991-01-25       Impact factor: 5.157

8.  Structure-activity relationships in a series of newly synthesized 1-amino-substituted ellipticine derivatives.

Authors:  C Ducrocq; F Wendling; M Tourbez-Perrin; C Rivalle; P Tambourin; F Pochon; E Bisagni; J C Chermann
Journal:  J Med Chem       Date:  1980-11       Impact factor: 7.446

9.  Synthesis and evaluation of 4-amino-substituted 7-methoxy (and 7-hydroxy)- 11-methyl (and 5,11-dimethyl)-10H-pyrido [2,3-b] carbazoles and 4-amino- substituted 11-methyl (and 5,11-dimethyl)-10H-pyrido[3',4':4,5] pyrrolo [3,2-g] quinolines, two new series related to antitumor ellipticine derivatives.

Authors:  J Moron; M Rautureau; C Huel; A Pierré; L K Berthier; G Atassi; E Bisagni
Journal:  Anticancer Drug Des       Date:  1993-12

10.  Cytotoxic agents directed to peptide hormone receptors: defining the requirements for a successful drug.

Authors:  G Czerwinski; N I Tarasova; C J Michejda
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-29       Impact factor: 11.205

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  2 in total

Review 1.  Synthesis of indole derivatives as prevalent moieties present in selected alkaloids.

Authors:  Majid M Heravi; Zahra Amiri; Kosar Kafshdarzadeh; Vahideh Zadsirjan
Journal:  RSC Adv       Date:  2021-10-15       Impact factor: 4.036

2.  Efficient and simple synthesis of 6-aryl-1,4-dimethyl-9H-carbazoles.

Authors:  Anna Caruso; Anne Sophie Voisin-Chiret; Jean-Charles Lancelot; Maria Stefania Sinicropi; Antonio Garofalo; Sylvain Rault
Journal:  Molecules       Date:  2008-06-11       Impact factor: 4.411

  2 in total

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