Skip to main content
Log in

Adenine and Uracil Derivatives with Antitubercular Activity

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

We have carried out the synthesis and investigated the antitubercular activity of adenine and 5-fluorouracil derivatives. It was found that a comparatively large, lipophilic fragment is needed in the active molecule to inhibit the tuberculosis pathogen.

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. S. L. Dax, Antibacterial Chemotherapeutic Agents, Blackie Academic and Professional, London (1997).

    Google Scholar 

  2. M. E. Wolf (editor), Burger's Medicinal Chemistry and Drug Discovery, 5th Edition, Vol. 2, Wiley Interscience (1996), p. 575.

  3. N. Ramzaeva, Yu. Gol'dberg, E. Alksnis, M. Lidak, and M. Shimanskaya, Zh. Org. Khim., 25, 1783 (1989).

    Google Scholar 

  4. N. Ramzaeva, Yu. Gol'dberg, E. Alksnis, M. Lidak, M. Yure, and E. Gudriniece, Zh. Org. Khim., 25, 1780 (1989).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Alksnis, E., Korneeva, D. & Lukevics, E. Adenine and Uracil Derivatives with Antitubercular Activity. Chemistry of Heterocyclic Compounds 37, 743–746 (2001). https://doi.org/10.1023/A:1011973514672

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1011973514672

Navigation