Literature DB >> 23964521

[Synthetic transformations of higher terpenoids. XXX. Synthesis and cytotoxic activity of betulonic acid amides with a piperidine or pyrrolidine nitroxide moiety].

A N Antimonova, N I Petrenko, E E Shults, Iu F Polienko, M M Shakirov, I G Irtegova, M A Pokrovskiĭ, K M Sherman, I A Grigor'ev, A G Pokrovskiĭ, G A Tolstikov.   

Abstract

The reaction of betulonic acid chloride with 4-amino-2,2,6,6-tetramethylpeperidine-1-oxyl, 3-amino-2,2,5,5-tetramethylpyrrolidine-1-oxyl and 3-aminomethyl-2,2,5,5-tetramethylpyrrolidine-1-oxyl gave corresponding triterpenoid amides. It was found that new derivatives exhibit cytotoxic activity against tumor cells CEM-13, U-937, MT-4. CCID50 value for most activity compound--N-[3-oxolup-20(29)-en-30-yl]-(2,2,6,6-tetramethylpiperidine-4-yl)-1-oxyl--was 5.7-33.1 microM.

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Year:  2013        PMID: 23964521     DOI: 10.1134/s1068162013020027

Source DB:  PubMed          Journal:  Bioorg Khim        ISSN: 0132-3423


  2 in total

1.  Access to New Cytotoxic Triterpene and Steroidal Acid-TEMPO Conjugates by Ugi Multicomponent-Reactions.

Authors:  Haider N Sultani; Ibrahim Morgan; Hidayat Hussain; Andreas H Roos; Haleh H Haeri; Goran N Kaluđerović; Dariush Hinderberger; Bernhard Westermann
Journal:  Int J Mol Sci       Date:  2021-07-01       Impact factor: 5.923

2.  4-Dialkylamino-2,5-dihydroimidazol-1-oxyls with Functional Groups at the Position 2 and at the Exocyclic Nitrogen: The pH-Sensitive Spin Labels.

Authors:  Dmitrii G Trofimov; Yuri I Glazachev; Artem A Gorodetsky; Denis A Komarov; Tatyana V Rybalova; Igor A Kirilyuk
Journal:  Gels       Date:  2021-12-23
  2 in total

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