Literature DB >> 11026546

Pyrazolo-triazoles as light activable DNA cleaving agents.

S Manfredini1, C B Vicentini, M Manfrini, N Bianchi, C Rutigliano, C Mischiati, R Gambari.   

Abstract

In view of the continuous interest in new DNA cleaving compounds, both for the development of new therapeutic agents and for the possible use as reagents in nucleic acids research, a few pyrazolo[3,4-d][1,2,3]triazole derivatives have been obtained and investigated for their antiproliferative activity and capability to cleave DNA, after light-activation. A possible in situ activation, i.e. in neoplastic tissues, of less cytotoxic derivatives, may lead to potential antitumor compounds endowed with high therapeutic indexes.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11026546     DOI: 10.1016/s0968-0896(00)00160-7

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  16 in total

1.  3'-(1,2,3-Triazol-1-yl)-3'-deoxythymidine analogs as substrates for human and Ureaplasma parvum thymidine kinase for structure-activity investigations.

Authors:  Jay Lin; Vincent Roy; Liya Wang; Li You; Luigi A Agrofoglio; Dominique Deville-Bonne; Tamara R McBrayer; Steven J Coats; Raymond F Schinazi; Staffan Eriksson
Journal:  Bioorg Med Chem       Date:  2010-03-15       Impact factor: 3.641

2.  1-{1-[2,8-Bis(trifluoro-meth-yl)-4-quin-olyl]-5-methyl-1H-1,2,3-triazol-4-yl}ethanone.

Authors:  H C Devarajegowda; S Jeyaseelan; V Sumangala; Suresh P Nayak
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-09-08

3.  2-({4-[4-(1H-Benzimidazol-2-yl)phen-yl]-1H-1,2,3-triazol-1-yl}meth-oxy)ethanol.

Authors:  Abdelaaziz Ouahrouch; Moha Taourirte; Hassan B Lazrek; Jan W Bats; Joachim W Engels
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-05-26

4.  N-[(E)-(5-Methyl-thio-phen-2-yl)methyl-idene]-1H-1,2,4-triazol-3-amine.

Authors:  Zahid H Chohan; Muhammad Hanif; M Nawaz Tahir
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-12-13

5.  (E)-N-Benzyl-idene-4H-1,2,4-triazol-4-amine.

Authors:  M Thenmozhi; T Kavitha; B Palakshi Reddy; V Vijayakumar; M N Ponnuswamy
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-02-06

6.  Ethyl 5-methyl-1-(4-nitro-phen-yl)-1H-1,2,3-triazole-4-carboxyl-ate.

Authors:  Hoong-Kun Fun; Ching Kheng Quah; Balakrishna Kalluraya
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-08-27

7.  N-(Naphthalen-1-yl-methyl-idene)-4H-1,2,4-triazol-4-amine.

Authors:  Pan Yang; Bin Ding; Gui-Xiang Du
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-09-22

8.  3-{[1-(2,3,5-Tri-O-benzoyl-β-d-ribofur-an-os-1-yl)-1H-1,2,3-triazol-4-yl]meth-yl}quin-a-zolin-4(3H)-one.

Authors:  Abdelaaziz Ouahrouch; Moha Taourirte; Mohamed El Azhari; Mohamed Saadi; Lahcen El Ammari
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-10-20

9.  Spectroscopic, Thermal, and Antimicrobial Studies of Co(II), Ni(II), Cu(II), and Zn(II) Complexes Derived from Bidentate Ligands Containing N and S Donor Atoms.

Authors:  Kiran Singh; Yogender Kumar; Parvesh Puri; Gulab Singh
Journal:  Bioinorg Chem Appl       Date:  2012-11-22       Impact factor: 7.778

10.  N'-[1-(4-Chloro-phen-yl)ethyl-idene]-5-methyl-1-(4-nitro-phen-yl)-1H-1,2,3-triazole-4-carbohydrazide.

Authors:  Hoong-Kun Fun; Ching Kheng Quah; Balakrishna Kalluraya; Shobhitha Shetty
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-06-23
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.