IDEAS home Printed from https://ideas.repec.org/a/adp/jomcij/v5y2018i4p101-106.html
   My bibliography  Save this article

Water Pollution

Author

Listed:
  • Evelyn U Godwin Nwakwasi

    (Department of Chemistry, Gregory University Uturu Abia State, Nigeria)

  • Uchechukwu C Okoro
  • Mercy A Ezeokonkwo

    (Department of Pure and Industrial Chemistry, University of Nigeria Nsukka, Nigeria)

  • Fidelia N Ibeanu

    (School of General Studies, Natural Science Unit, University of Nigeria Nsukka, Nigeria)

  • Ifeoma C Ugwu

    (Department of Veterinary Pathology and Microbiology, Faculty of Veterinary Medicine, University of Nigeria Nsukka, Nigeria)

Abstract

In a continued search for new biologically active angular phenothiazine compounds, novel non-linear polycyclic phenothiazine halogeno derivatives have been synthesized via coupling reactions. The coupling of equimolar mixture of 2-amino-5-bromopyrazine-3[4H]-thione and 6,7-dibromo-5,8-quninolinequinone under anhydrous condition, furnished two isomers, 6,9-dibromo-1, 8, 11-traiza-5H-benzo[a]phenothiazin-5-one and 6,9-dibromo-4, 8, 11-triaza-5H-benzo[a]phenothiazin-5-one. These compounds were screened for their antimicrobial activity against E. coli, Staphylococcus spp, Bacillus spp. and Pseudomonas aeruginosa at varying concentrations using Agar-well diffusion method and the results showed that these phenothiazine moieties had significant biological activity and inhibited the growth of these bacterial isolates even at low concentrations. Structures were assigned based on spectroscopic data and elemental analysis.

Suggested Citation

  • Evelyn U Godwin Nwakwasi & Uchechukwu C Okoro & Mercy A Ezeokonkwo & Fidelia N Ibeanu & Ifeoma C Ugwu, 2018. "Water Pollution," Organic & Medicinal Chemistry International Journal, Juniper Publishers Inc., vol. 5(4), pages 101-106, February.
  • Handle: RePEc:adp:jomcij:v:5:y:2018:i:4:p:101-106
    DOI: 10.19080/OMCIJ.2018.05.555666
    as

    Download full text from publisher

    File URL: https://juniperpublishers.com/omcij/pdf/OMCIJ.MS.ID.555666.pdf
    Download Restriction: no

    File URL: https://juniperpublishers.com/omcij/OMCIJ.MS.ID.555666.php
    Download Restriction: no

    File URL: https://libkey.io/10.19080/OMCIJ.2018.05.555666?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:adp:jomcij:v:5:y:2018:i:4:p:101-106. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Robert Thomas (email available below). General contact details of provider: .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.