Skip to main content
Log in

Synthesis, antibacterial and antifungal activity of 1, 3-di(2-substituted 10H-phenothiazin-10-yl)propan-1-one

  • Published:
Pharmaceutical Chemistry Journal Aims and scope

Aseries of 1,3-di(2-substituted 10H-phenothiazin-10-yl)propan-1-one (IVa – p) was synthesized by using the phenothiazine framework through a three-carbon atom chain by condensation of the different chlorides of 3-(10H-phenothiazin-10-y1)propionic acid (IIIa – d) with 2- substituted phenothiazines (Ia – d), and the structures of these compounds were confirmed by IR, 1H NMR, mass, and elemental analysis. The newly synthesized compounds were evaluated for antimicrobial activity.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. M. K. El-Said, Pharmazie, 36, 678 – 679 (1981).

    CAS  Google Scholar 

  2. S. R. Tilak, R. Tyagi, B. Goel, and K. K. Saxena, Indian Drugs, 35, 221 – 227(1998).

    Google Scholar 

  3. J. N. Dominguez, S. Lopez, J. Charris, et al., J. Med. Chem., 40, 2726 – 2733 (1997)

    Article  CAS  PubMed  Google Scholar 

  4. G. Lin, K. K. Midha, and E. M. Hawes, J. Heterocycl. Chem., 28, 215 – 219 (1991).

    CAS  Google Scholar 

  5. J. Raval and K. K. Desai, ARKIVOC, (XIII), 21 – 28 (2005).

    Google Scholar 

  6. M. Viveros and L. Amaral, Int. J. Antimicrob. Ag., 17, 225 – 228 (2001).

    Article  Google Scholar 

  7. L. Amaral and Kristiansen, Int. J. Antimicrob. Ag., 14, 173 – 180 (2000)

    Article  CAS  Google Scholar 

  8. A. Trivedi, A. Siddiqui, and V. Shah, ARKIVOC, (XII), 210 – 217 (2008).

    Google Scholar 

  9. N. Motohashi, M. Kawasa, S. Saito, and H. Sakagami, Curr. Drug Targets, 1, 237 – 240 (2000).

    Article  CAS  PubMed  Google Scholar 

  10. N. Motohashi, T. Kurihara, K. Satoh, et al., J. Anticancer Res., 19, 1837 – 1842 (1999).

    CAS  Google Scholar 

  11. T. Kurihara, N. Motohasho, G. L. Pang, et al., J. Anticancer Res., 16, 2757 – 2765 (1996).

    CAS  Google Scholar 

  12. D. Ledincer and L. A. Mitscher, The Organic Chemistry of Drug Synthesis, Wiley, New York (1976), Vol. 1, p. 372 – 392.

    Google Scholar 

  13. A. A. Borbely and M. Loepfe-Hinkkanen, Mod. Phamacol. Toxicol., 16, 403 – 426 (1979).

    CAS  Google Scholar 

  14. W. R. Reid, J. R. Wright, H. G. Kollofe, et al., J. Am. Chem. Soc., 70, 3100 – 3102 (1948).

    Article  CAS  PubMed  Google Scholar 

  15. I. Meiermed, Monatsh. Chem., 8, 397 – 399 (1954).

    Google Scholar 

  16. J. L. Vennerstrom, A. L. Ager, S. L. Andersen, et al., J. Med. Chem., 41, 4360 – 4367 (1998).

    Article  CAS  PubMed  Google Scholar 

  17. B. C. May, A. T. Fafarman, S. B. Hong, et al., Proc. Natl. Acad. Sci. U. S. A., 100, 3416 – 3421 (2003).

    Article  CAS  PubMed  Google Scholar 

  18. X. L. Smith, J. Org. Chem., 15, 1129 – 1130 (1950).

    Google Scholar 

  19. R. Cruickshank, J. P. Duguid, B. P. Marion, et al., Medicinal Microbiology. 12th ed., Churchill Livingstone, London (1975), Vol. II, p. 196 – 202.

  20. A. H. Collins (ed.), Microbiological Methods, 2nd ed., Butterworth, London (1976).

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to V. G. Dongre.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bansode, T.N., Dongre, P.M. & Dongre, V.G. Synthesis, antibacterial and antifungal activity of 1, 3-di(2-substituted 10H-phenothiazin-10-yl)propan-1-one. Pharm Chem J 43, 311–314 (2009). https://doi.org/10.1007/s11094-009-0297-9

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11094-009-0297-9

Keywords

Navigation