Skip to main content
Log in

Crystal structure and conformation of Linomide [N-methyl-N-phenyl-1,2-dihydro-4-hydroxy-1-methyl-2-oxo-quinoline-3-carboxamide]: A novel immunomodulator

  • Published:
Journal of Chemical Crystallography Aims and scope Submit manuscript

Abstract

Linomide [N-methyl-N-phenyl-1,2-dihydro-4-hydroxy-1-methyl-2-oxo-quinoline-3-carboxamide] is a new immunomodulator from Phamacia Laboratories, Helsingborg, Sweden. Linomide (LS-2616) has delayed hypersensitivity in rat skin, potentiates mouse natural killer cell activity, and stimulates polyclonal T-cell activation. It has been shown that LS-2616 abolishes the effects of continuous cyclosporine treatment in experimental models. Crystal structure of LS-2616 has been undertaken as a first step in the establishment of a possible structure–function relationship for the drug. Crystals of LS-2616 (C18H16N2O3) obtained from methylene chloride are monoclinic, of space group P21/a with the following crystallographic parameters: a = 8.793(1) Å, b = 22.349(3) Å, c = 7.808(1) Å, β = 92.96(1)°, V = 1532.3(6) Å3, ρobs = 1.34 Mg/m3, ρcalc = 1.337 Mg/m3, and Z = 4. The structure was solved with CAD-4 data using MULTAN programs and refined to a final R value of 0.041. The N-methyl carboxamide is in the cis configuration and is turned away from the quinoline ring by 87°. FK506 is a novel 23-membered macrolide lactone which is currently used for bone marrow and organ transplantations. The crystal structure of FK506 has been published. The absolute configuration of FK506 was established as a cis-amide which contains a L-pipecolic acid moiety. Preliminary modeling studies of FK506 with LS-2616 revealed that this cis conformation for the N-methyl carboxamide leads to a lower binding energy than the corresponding trans conformation. The plane of the phenyl group is inclined by 95° to the carboxamide plane. The molecule has the familiar herring-bone type of packing, characteristic of the polyphenyl molecules, stabilized by O–H ⋅ ⋅ ⋅ O and C–H ⋅ ⋅ ⋅ O hydrogen bonds involving the hydroxyl group and the ketone substituents on the quinoline ring and the N-methyl group of the carboxamide.

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. Srikrishnan, T. Anti-Cancer Drug Design 1990, 5, 213–220.

    Google Scholar 

  2. Srikrishnan, T.; Dasari, K.B.; Albini, B. Acta Crystallogr., Sect. A 1993, 49, 130.

    Google Scholar 

  3. Rooth, Walter.; Srikrishnan, T. J. Chem. Crystallogr. 1999, 29, 1187–1192.

    Google Scholar 

  4. Dasari, K. B.; Srikrishnan, T. J. Chem. Crystallogr. 2000, 30, 269–273.

    Google Scholar 

  5. Srikrishnan, T.; Dasari, K.B.; Zaleski, M.; Albini, B. In Proceedings of the XVI International Cancer Congress; Monduzzi Editore, Ed.; 1994, pp. 2817–2821.

  6. Stalhandske, T.; Eriksoo, E.; Sanbderg, B.M. Int. J. Immunopharmacol. 1982, 4, 336–339.

    Google Scholar 

  7. Stalhandske, T.; Kalland, T. Immunopharmacology 1986, 11, 87–92.

    Google Scholar 

  8. Tarkowski, A.; Gunnarsson, K.; Nillsson, L.A. Arthritis Rheum. 1986, 29, 1405–1409.

    Google Scholar 

  9. Tarkowski, A.; Gunnarsson, K.; Stalhandske, T. Immunology 1986, 59, 589–594.

    Google Scholar 

  10. Kalland, T.; Alm, G.; Stalhandske, T. J. Immunol. 1985, 134, 3956–3961.

    Google Scholar 

  11. Kalland, T. J. Immunol. 1990, 144, 4472–4476.

    Google Scholar 

  12. Larsson, E.-L.; Joki, A.; Stalhandske, T. Int. J. Immunopharmacol. 1987, 9, 425–431.

    Google Scholar 

  13. Kalland, T. Cancer Res. 1986, 46, 3018–3022

    Google Scholar 

  14. Enraf-Nonius Structure Determination Package; Enraf-Nonius: Delft, The Netherlands, 1979.

  15. Germain, G.; Main, P.; Woofson. M. M. Acta Crystallogr. Sect.A 1971, 27, 368–376.

    Google Scholar 

  16. Johnson, C.K. Report ORNL-3794; Oak Ridge National Laboratory: Tennessee, 1965.

    Google Scholar 

  17. Thomas, A.W. Immunol. Today 1989, 10, 6–9.

    Google Scholar 

  18. Tanaka, H. J. Am. Chem. Soc. 1987, 109, 5031–5033.

    Google Scholar 

  19. Starzl, T. Lancet 1989, 11, 1000–1004.

    Google Scholar 

  20. Tanak, H.; Kuroda, A.; Marusawa, H.; Hatanaka, F.; Kino, T.; Goto, T.; Hashimoto, M. J. Am. Chem. Soc. 1987, 109, 5031–5033.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to T. Srikrishnan.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dasari, K.B., Srikrishnan, T. Crystal structure and conformation of Linomide [N-methyl-N-phenyl-1,2-dihydro-4-hydroxy-1-methyl-2-oxo-quinoline-3-carboxamide]: A novel immunomodulator. Journal of Chemical Crystallography 32, 499–504 (2002). https://doi.org/10.1023/A:1021153011803

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1021153011803

Navigation