Literature DB >> 11858989

New 2-(1-adamantylcarbonyl)pyridine and 1-acetyladamantane thiosemicarbazones-thiocarbonohydrazones: cell growth inhibitory, antiviral and antimicrobial activity evaluation.

Antonios Kolocouris1, Kostas Dimas, Christophe Pannecouque, Myriam Witvrouw, George B Foscolos, George Stamatiou, George Fytas, Grigoris Zoidis, Nicolas Kolocouris, Graciela Andrei, Robert Snoeck, Erik De Clercq.   

Abstract

The new thiosemicarbazones and thiocarbonohydrazones derived from 2-(1-adamantylcarbonyl)pyridine and 1-acetyladamantane were synthesized and evaluated for their inhibitory effect on tumor cell proliferation and their antiviral and antimicrobial activity. Thiosemicarbazone inhibited tumor cell proliferation (GI50's range: 2.4-100 microM and mean GI50 43.9 microM against various human leukemic cell lines) while thiosemicarbazone and thiocarbonohydrazone 5d exhibited significant inhibition of tumor cell proliferation (GI50's range 2.3-23.6 microM and mean GI50 7.2 microM for and GI50's range 2.4-32.4 microM and mean GI50 12.8microM for ). These GI50 values are comparable to that of 2-acetylpyridine thiosemicarbazone an important lead in TSC's family. The compounds did not afford specific activity against any of the viruses tested when examined at non-toxic concentrations. A weak activity was found for thiocarbonohydrazones against Gram-(+) bacteria (MIC(50) 117.3 and 133 microM, respectively). Using a combination of molecular mechanics calculations and NOE spectroscopy it was shown that the parent compounds and have opposite configuration around C=N bond. Whether this difference in structure can be correlated with the biological activity will be investigated in future studies.

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Year:  2002        PMID: 11858989     DOI: 10.1016/s0960-894x(01)00838-1

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


  7 in total

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Journal:  Molecules       Date:  2014-03-11       Impact factor: 4.411

3.  Synthesis, Antimicrobial, and Anti-Proliferative Activities of Novel 4-(Adamantan-1-yl)-1-arylidene-3-thiosemicarbazides, 4-Arylmethyl N'-(Adamantan-1-yl)piperidine-1-carbothioimidates, and Related Derivatives.

Authors:  Aamal A Al-Mutairi; Monirah A Al-Alshaikh; Fatmah A M Al-Omary; Hanan M Hassan; Areej M El-Mahdy; Ali A El-Emam
Journal:  Molecules       Date:  2019-11-26       Impact factor: 4.411

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Authors:  Sara M Mostafa; Ashraf A Aly; Stefan Bräse; Martin Nieger; Sara Mohamed Naguib Abdelhafez; Walaa Yehia Abdelzaher; El-Shimaa M N Abdelhafez
Journal:  Molecules       Date:  2022-03-31       Impact factor: 4.927

5.  Bis-pharmacophore of cinnamaldehyde-clubbed thiosemicarbazones as potent carbonic anhydrase-II inhibitors.

Authors:  Asif Rasool; Zahra Batool; Majid Khan; Sobia Ahsan Halim; Zahid Shafiq; Ahmed Temirak; Mohamed A Salem; Tarik E Ali; Ajmal Khan; Ahmed Al-Harrasi
Journal:  Sci Rep       Date:  2022-09-27       Impact factor: 4.996

6.  Synthesis, spectroscopic, and antimicrobial studies on bivalent zinc and mercury complexes of 2-formylpyridine thiosemicarbazone.

Authors:  Sulekh Chandra; Shikha Parmar; Yatendra Kumar
Journal:  Bioinorg Chem Appl       Date:  2009-04-29       Impact factor: 7.778

7.  Adamantane derivatives as potential inhibitors of p37 major envelope protein and poxvirus reproduction. Design, synthesis and antiviral activity.

Authors:  Vadim A Shiryaev; Michael Yu Skomorohov; Marina V Leonova; Nikolai I Bormotov; Olga A Serova; Larisa N Shishkina; Alexander P Agafonov; Rinat A Maksyutov; Yuri N Klimochkin
Journal:  Eur J Med Chem       Date:  2021-04-29       Impact factor: 7.088

  7 in total

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