Issue 28, 2017

Synthesis and biological evaluation of N-arylated-lactam-type iminosugars as potential immunosuppressive agents

Abstract

Since the immunosuppressive agents currently used in clinics have significant side effects, it is very important to search for new effective and safe immunosuppressants. Iminosugars as a new class of immunosuppressants are less explored. In this report, 24 new N-arylated iminosugar derivatives, including D-talo and D-galacto epimers, were designed and synthesized, and their immunosuppressive effects were evaluated by MTT assay. The experimental data demonstrated that compound 20 showed the strongest inhibition effect (IC50 = 6.94 μM). Further studies revealed that the inhibitory effects on splenocyte proliferation may come from the suppression of both IFN-γ and IL-4 cytokines. The preliminary structure–activity relationship (SAR) analysis suggested that N-arylated D-galacto-type iminosugars showed better inhibitory activities than D-talo-type analogues. The SAR analysis also showed that the inhibition effect of iminosugars can be improved by decreasing the polarity or increasing the hydrophobicity. These results may be beneficial to the discovery of new iminosugar derivatives as immunosuppressive agents.

Graphical abstract: Synthesis and biological evaluation of N-arylated-lactam-type iminosugars as potential immunosuppressive agents

Supplementary files

Article information

Article type
Paper
Submitted
06 May 2017
Accepted
20 Jun 2017
First published
20 Jun 2017

Org. Biomol. Chem., 2017,15, 5912-5919

Synthesis and biological evaluation of N-arylated-lactam-type iminosugars as potential immunosuppressive agents

H. Liu, C. Song, Y. Niu, T. Li, Q. Li and X. Ye, Org. Biomol. Chem., 2017, 15, 5912 DOI: 10.1039/C7OB01110E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements