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Synthesis, structure, and antitumor activity of 2,9-disubstituted perhydro 2,3a,7b,9,10a,14b-hexaazadibenzotetracenes
Catalytic methods for the synthesis of previously unknown 2,9-disubstituted 3bR*,7aR*,10bR*,14aR*-cis-14c,14d-perhydro-2,3a,7b,9,10a,14b-hexaazadibenzotetracenes have been developed. The structures were established by 1D ((1)H, (13)C) and 2D (COSY, HSQC, HMBC) NMR spectroscopy, MALDI TOF/TOF mass sp...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054349/ https://www.ncbi.nlm.nih.gov/pubmed/35518764 http://dx.doi.org/10.1039/d0ra03209c |
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author | Rakhimova, Elena B. Kirsanov, Victor Yu. Tret'yakova, Elena V. Khalilov, Leonard M. Ibragimov, Askhat G. Dzhemileva, Lilya U. D'yakonov, Vladimir A. Dzhemilev, Usein M. |
author_facet | Rakhimova, Elena B. Kirsanov, Victor Yu. Tret'yakova, Elena V. Khalilov, Leonard M. Ibragimov, Askhat G. Dzhemileva, Lilya U. D'yakonov, Vladimir A. Dzhemilev, Usein M. |
author_sort | Rakhimova, Elena B. |
collection | PubMed |
description | Catalytic methods for the synthesis of previously unknown 2,9-disubstituted 3bR*,7aR*,10bR*,14aR*-cis-14c,14d-perhydro-2,3a,7b,9,10a,14b-hexaazadibenzotetracenes have been developed. The structures were established by 1D ((1)H, (13)C) and 2D (COSY, HSQC, HMBC) NMR spectroscopy, MALDI TOF/TOF mass spectrometry, and X-ray diffraction analysis. Primary screening of the synthesized perhydro hexaazadibenzotetracenes for antitumor activity was carried out. |
format | Online Article Text |
id | pubmed-9054349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90543492022-05-04 Synthesis, structure, and antitumor activity of 2,9-disubstituted perhydro 2,3a,7b,9,10a,14b-hexaazadibenzotetracenes Rakhimova, Elena B. Kirsanov, Victor Yu. Tret'yakova, Elena V. Khalilov, Leonard M. Ibragimov, Askhat G. Dzhemileva, Lilya U. D'yakonov, Vladimir A. Dzhemilev, Usein M. RSC Adv Chemistry Catalytic methods for the synthesis of previously unknown 2,9-disubstituted 3bR*,7aR*,10bR*,14aR*-cis-14c,14d-perhydro-2,3a,7b,9,10a,14b-hexaazadibenzotetracenes have been developed. The structures were established by 1D ((1)H, (13)C) and 2D (COSY, HSQC, HMBC) NMR spectroscopy, MALDI TOF/TOF mass spectrometry, and X-ray diffraction analysis. Primary screening of the synthesized perhydro hexaazadibenzotetracenes for antitumor activity was carried out. The Royal Society of Chemistry 2020-06-04 /pmc/articles/PMC9054349/ /pubmed/35518764 http://dx.doi.org/10.1039/d0ra03209c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Rakhimova, Elena B. Kirsanov, Victor Yu. Tret'yakova, Elena V. Khalilov, Leonard M. Ibragimov, Askhat G. Dzhemileva, Lilya U. D'yakonov, Vladimir A. Dzhemilev, Usein M. Synthesis, structure, and antitumor activity of 2,9-disubstituted perhydro 2,3a,7b,9,10a,14b-hexaazadibenzotetracenes |
title | Synthesis, structure, and antitumor activity of 2,9-disubstituted perhydro 2,3a,7b,9,10a,14b-hexaazadibenzotetracenes |
title_full | Synthesis, structure, and antitumor activity of 2,9-disubstituted perhydro 2,3a,7b,9,10a,14b-hexaazadibenzotetracenes |
title_fullStr | Synthesis, structure, and antitumor activity of 2,9-disubstituted perhydro 2,3a,7b,9,10a,14b-hexaazadibenzotetracenes |
title_full_unstemmed | Synthesis, structure, and antitumor activity of 2,9-disubstituted perhydro 2,3a,7b,9,10a,14b-hexaazadibenzotetracenes |
title_short | Synthesis, structure, and antitumor activity of 2,9-disubstituted perhydro 2,3a,7b,9,10a,14b-hexaazadibenzotetracenes |
title_sort | synthesis, structure, and antitumor activity of 2,9-disubstituted perhydro 2,3a,7b,9,10a,14b-hexaazadibenzotetracenes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054349/ https://www.ncbi.nlm.nih.gov/pubmed/35518764 http://dx.doi.org/10.1039/d0ra03209c |
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