Synthesis of 2-Phenylazonaphtho[1,8-ef][1,4]diazepines and 9-(3-Arylhydrazono)pyrrolo[1,2-a]perimidines as Antitumor Agents

Two series of naphtho[1,8-ef][1,4]diazepines and pyrrolo[1,2-a]perimidines were prepared starting from 1,8-diaminonaphthalene and hydrazonoyl chlorides. The structures of the products were determined on the basis of their spectral data and elemental analyses. The mechanism of formation of such produ...

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Main Authors: Thoraya A. Farghaly, Eman M. H. Abbas, Kamal M. Dawood, Tarek B. A. El-Naggar
Format: Article
Language:English
Published: MDPI AG 2014-01-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/19/1/740
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author Thoraya A. Farghaly
Eman M. H. Abbas
Kamal M. Dawood
Tarek B. A. El-Naggar
author_facet Thoraya A. Farghaly
Eman M. H. Abbas
Kamal M. Dawood
Tarek B. A. El-Naggar
author_sort Thoraya A. Farghaly
collection DOAJ
description Two series of naphtho[1,8-ef][1,4]diazepines and pyrrolo[1,2-a]perimidines were prepared starting from 1,8-diaminonaphthalene and hydrazonoyl chlorides. The structures of the products were determined on the basis of their spectral data and elemental analyses. The mechanism of formation of such products was also discussed. The prepared compounds were screened for their antitumor activity against three cell lines, namely, MCF-7, TK-10 and UACC-62, and some derivatives showed promising activity.
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spelling doaj.art-1b38430ed971442f8a21e923721722f52022-12-21T19:49:58ZengMDPI AGMolecules1420-30492014-01-0119174075510.3390/molecules19010740molecules19010740Synthesis of 2-Phenylazonaphtho[1,8-ef][1,4]diazepines and 9-(3-Arylhydrazono)pyrrolo[1,2-a]perimidines as Antitumor AgentsThoraya A. Farghaly0Eman M. H. Abbas1Kamal M. Dawood2Tarek B. A. El-Naggar3Department of Chemistry, Faculty of Science, University of Cairo, Giza 12613, EgyptDepartment of Chemistry, Natural and Microbial Products, National Research Center, Dokki, Cairo 12622, EgyptDepartment of Chemistry, Faculty of Science, University of Cairo, Giza 12613, EgyptDepartment of Chemistry, Natural and Microbial Products, National Research Center, Dokki, Cairo 12622, EgyptTwo series of naphtho[1,8-ef][1,4]diazepines and pyrrolo[1,2-a]perimidines were prepared starting from 1,8-diaminonaphthalene and hydrazonoyl chlorides. The structures of the products were determined on the basis of their spectral data and elemental analyses. The mechanism of formation of such products was also discussed. The prepared compounds were screened for their antitumor activity against three cell lines, namely, MCF-7, TK-10 and UACC-62, and some derivatives showed promising activity.http://www.mdpi.com/1420-3049/19/1/7401,8-diaminonaphthalenenaphtho[1,8-ef][1,4]diazepinespyrrolo[1,2-a] perimidineshydrazonoyl chlorideantitumor activity
spellingShingle Thoraya A. Farghaly
Eman M. H. Abbas
Kamal M. Dawood
Tarek B. A. El-Naggar
Synthesis of 2-Phenylazonaphtho[1,8-ef][1,4]diazepines and 9-(3-Arylhydrazono)pyrrolo[1,2-a]perimidines as Antitumor Agents
Molecules
1,8-diaminonaphthalene
naphtho[1,8-ef][1,4]diazepines
pyrrolo[1,2-a] perimidines
hydrazonoyl chloride
antitumor activity
title Synthesis of 2-Phenylazonaphtho[1,8-ef][1,4]diazepines and 9-(3-Arylhydrazono)pyrrolo[1,2-a]perimidines as Antitumor Agents
title_full Synthesis of 2-Phenylazonaphtho[1,8-ef][1,4]diazepines and 9-(3-Arylhydrazono)pyrrolo[1,2-a]perimidines as Antitumor Agents
title_fullStr Synthesis of 2-Phenylazonaphtho[1,8-ef][1,4]diazepines and 9-(3-Arylhydrazono)pyrrolo[1,2-a]perimidines as Antitumor Agents
title_full_unstemmed Synthesis of 2-Phenylazonaphtho[1,8-ef][1,4]diazepines and 9-(3-Arylhydrazono)pyrrolo[1,2-a]perimidines as Antitumor Agents
title_short Synthesis of 2-Phenylazonaphtho[1,8-ef][1,4]diazepines and 9-(3-Arylhydrazono)pyrrolo[1,2-a]perimidines as Antitumor Agents
title_sort synthesis of 2 phenylazonaphtho 1 8 ef 1 4 diazepines and 9 3 arylhydrazono pyrrolo 1 2 a perimidines as antitumor agents
topic 1,8-diaminonaphthalene
naphtho[1,8-ef][1,4]diazepines
pyrrolo[1,2-a] perimidines
hydrazonoyl chloride
antitumor activity
url http://www.mdpi.com/1420-3049/19/1/740
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