Cargando…

Studies on the Reactivity of (9-Methyl-5,6-dihydronaphtho[1′,2′:4,5]-thieno[2,3-d]pyrimidin-11-yl)hydrazine Towards Some Reagents for Biological Evaluation

(9-Methyl-5,6-dihydronaphtho[1′,2′:4,5]thieno[2,3-d]pyrimidin-11-yl)hydrazine (1) was used as a precursor for preparation of some novel 1-(9-methyl-5,6-dihydronaphtho[1′,2′:4,5]thieno[2,3-d]pyrimidin-11-yl)-1H-pyrazoles 2–7, -1H-isoindole-1,3(2H)-dione 8, and -pyridazin-3(2H)-one 9. Moreover, the ac...

Descripción completa

Detalles Bibliográficos
Autores principales: Rashad, Aymn E., Shamroukh, Ahmed H., Abdel-Megeid, Randa E., Sayed, Hayam H., Abdel-Wahed, Nayera M.
Formato: Texto
Lenguaje:English
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002830/
https://www.ncbi.nlm.nih.gov/pubmed/21179366
http://dx.doi.org/10.3797/scipharm.0910-11
_version_ 1782193793291780096
author Rashad, Aymn E.
Shamroukh, Ahmed H.
Abdel-Megeid, Randa E.
Sayed, Hayam H.
Abdel-Wahed, Nayera M.
author_facet Rashad, Aymn E.
Shamroukh, Ahmed H.
Abdel-Megeid, Randa E.
Sayed, Hayam H.
Abdel-Wahed, Nayera M.
author_sort Rashad, Aymn E.
collection PubMed
description (9-Methyl-5,6-dihydronaphtho[1′,2′:4,5]thieno[2,3-d]pyrimidin-11-yl)hydrazine (1) was used as a precursor for preparation of some novel 1-(9-methyl-5,6-dihydronaphtho[1′,2′:4,5]thieno[2,3-d]pyrimidin-11-yl)-1H-pyrazoles 2–7, -1H-isoindole-1,3(2H)-dione 8, and -pyridazin-3(2H)-one 9. Moreover, the acyclic C-nucleosides 10 and 11 were prepared by treating compound 1 with D-glucose. The in vitro antimicrobial activity of the tested compounds was evaluated by measuring the zone diameters and some of the prepared products showed potent antimicrobial activity in compared with those of well known drugs (standard). In general, the non-acetylated sugar hydrazone derivative 10 showed the highest antibacterial and antifungal potency among the tested compounds and standard with IZ = 22, 21 and 22 mm and MIC = 62.5 and 31.25 μg/ml, respectively.
format Text
id pubmed-3002830
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Österreichische Apotheker-Verlagsgesellschaft
record_format MEDLINE/PubMed
spelling pubmed-30028302010-12-22 Studies on the Reactivity of (9-Methyl-5,6-dihydronaphtho[1′,2′:4,5]-thieno[2,3-d]pyrimidin-11-yl)hydrazine Towards Some Reagents for Biological Evaluation Rashad, Aymn E. Shamroukh, Ahmed H. Abdel-Megeid, Randa E. Sayed, Hayam H. Abdel-Wahed, Nayera M. Sci Pharm Original Papers (9-Methyl-5,6-dihydronaphtho[1′,2′:4,5]thieno[2,3-d]pyrimidin-11-yl)hydrazine (1) was used as a precursor for preparation of some novel 1-(9-methyl-5,6-dihydronaphtho[1′,2′:4,5]thieno[2,3-d]pyrimidin-11-yl)-1H-pyrazoles 2–7, -1H-isoindole-1,3(2H)-dione 8, and -pyridazin-3(2H)-one 9. Moreover, the acyclic C-nucleosides 10 and 11 were prepared by treating compound 1 with D-glucose. The in vitro antimicrobial activity of the tested compounds was evaluated by measuring the zone diameters and some of the prepared products showed potent antimicrobial activity in compared with those of well known drugs (standard). In general, the non-acetylated sugar hydrazone derivative 10 showed the highest antibacterial and antifungal potency among the tested compounds and standard with IZ = 22, 21 and 22 mm and MIC = 62.5 and 31.25 μg/ml, respectively. Österreichische Apotheker-Verlagsgesellschaft 2010 2009-12-11 /pmc/articles/PMC3002830/ /pubmed/21179366 http://dx.doi.org/10.3797/scipharm.0910-11 Text en © Rashad et al.; licensee Österreichische Apotheker-Verlagsgesellschaft m. b. H., Vienna, Austria. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Rashad, Aymn E.
Shamroukh, Ahmed H.
Abdel-Megeid, Randa E.
Sayed, Hayam H.
Abdel-Wahed, Nayera M.
Studies on the Reactivity of (9-Methyl-5,6-dihydronaphtho[1′,2′:4,5]-thieno[2,3-d]pyrimidin-11-yl)hydrazine Towards Some Reagents for Biological Evaluation
title Studies on the Reactivity of (9-Methyl-5,6-dihydronaphtho[1′,2′:4,5]-thieno[2,3-d]pyrimidin-11-yl)hydrazine Towards Some Reagents for Biological Evaluation
title_full Studies on the Reactivity of (9-Methyl-5,6-dihydronaphtho[1′,2′:4,5]-thieno[2,3-d]pyrimidin-11-yl)hydrazine Towards Some Reagents for Biological Evaluation
title_fullStr Studies on the Reactivity of (9-Methyl-5,6-dihydronaphtho[1′,2′:4,5]-thieno[2,3-d]pyrimidin-11-yl)hydrazine Towards Some Reagents for Biological Evaluation
title_full_unstemmed Studies on the Reactivity of (9-Methyl-5,6-dihydronaphtho[1′,2′:4,5]-thieno[2,3-d]pyrimidin-11-yl)hydrazine Towards Some Reagents for Biological Evaluation
title_short Studies on the Reactivity of (9-Methyl-5,6-dihydronaphtho[1′,2′:4,5]-thieno[2,3-d]pyrimidin-11-yl)hydrazine Towards Some Reagents for Biological Evaluation
title_sort studies on the reactivity of (9-methyl-5,6-dihydronaphtho[1′,2′:4,5]-thieno[2,3-d]pyrimidin-11-yl)hydrazine towards some reagents for biological evaluation
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002830/
https://www.ncbi.nlm.nih.gov/pubmed/21179366
http://dx.doi.org/10.3797/scipharm.0910-11
work_keys_str_mv AT rashadaymne studiesonthereactivityof9methyl56dihydronaphtho1245thieno23dpyrimidin11ylhydrazinetowardssomereagentsforbiologicalevaluation
AT shamroukhahmedh studiesonthereactivityof9methyl56dihydronaphtho1245thieno23dpyrimidin11ylhydrazinetowardssomereagentsforbiologicalevaluation
AT abdelmegeidrandae studiesonthereactivityof9methyl56dihydronaphtho1245thieno23dpyrimidin11ylhydrazinetowardssomereagentsforbiologicalevaluation
AT sayedhayamh studiesonthereactivityof9methyl56dihydronaphtho1245thieno23dpyrimidin11ylhydrazinetowardssomereagentsforbiologicalevaluation
AT abdelwahednayeram studiesonthereactivityof9methyl56dihydronaphtho1245thieno23dpyrimidin11ylhydrazinetowardssomereagentsforbiologicalevaluation