Literature DB >> 26733477

Novel carbocyclic nucleoside analogs suppress glomerular mesangial cells proliferation and matrix protein accumulation through ROS-dependent mechanism in the diabetic milieu. II. Acylhydrazone-functionalized pyrimidines.

Kamal H Bouhadir1, Ali Koubeissi2, Fatima A Mohsen3, Mira Diab El-Harakeh2, Rouba Cheaib2, Joan Younes4, Georges Azzi5, Assaad A Eid6.   

Abstract

We report herein the synthesis of a novel series of carbocyclic acylhydrazone derivatives of uracil, thymine and cytosine from the corresponding nucleic bases and their biological activity to treat diabetic nephropathy. Intriguingly, five derivatives significantly reduced high-glucose induced glomerular mesangial cells proliferation and matrix protein accumulation in vitro. The anti-oxidative effects displayed by these molecules suggest that their activity might involve a ROS-dependent mechanism.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Acylhydrazones; Carbocyclic nucleosides; Cytosine; Diabetic nephropathy; Thymine; Uracil

Mesh:

Substances:

Year:  2015        PMID: 26733477     DOI: 10.1016/j.bmcl.2015.12.042

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  XBP1 inhibits mesangial cell apoptosis in response to oxidative stress via the PTEN/AKT pathway in diabetic nephropathy.

Authors:  Yan Wang; Zhong He; Qiu Yang; Guangju Zhou
Journal:  FEBS Open Bio       Date:  2019-06-02       Impact factor: 2.693

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.