Literature DB >> 346364

Animal experiments on the compensation of the immunosuppressive action of cyclophosphamide by 2-[-2-cyanaziridinyl-(1)-]-2-[-2-carbamoylaziridinyl-(1)]-propane BM 12 531.

U Bicker, G Hebold, A E Ziegler, W Maus.   

Abstract

BM U2 531, the 2-[2-Cyanaziridinyl-(1)-]-2-[-2-carbamoylaziridinyl-(1)-]-propane, the further development of BM 06 002 is able to compensate the immunosuppressive action of Cyclophosphamide and to increase the carcinostatic action of Cyclophosphamide. These properties are demonstrated 1. by a leucocytosis induced after application of BM 12 531 in rats 2. by a quick restauration of leucocyte depression induced by Cyclophosphamide in rats and dogs 3. by an increase of resistance against an infection (candida albicans) in mice 4. by an increase of antitumour effect of Cyclophosphamide against a DS-carcinosarcoma in rats.

Entities:  

Mesh:

Substances:

Year:  1978        PMID: 346364     DOI: 10.1016/s0014-4908(78)80089-1

Source DB:  PubMed          Journal:  Exp Pathol (Jena)        ISSN: 0014-4908


  3 in total

1.  Reduction of acute toxicity of cyclophosphamide and X-rays by the new immunomodulating compound BM 12.531.

Authors:  U Bicker; K D Friedberg; G Hebold; K Mengel
Journal:  Experientia       Date:  1979-10-15

2.  The action of azimexone on the cells of the hemopoietic system in mice, especially after damage with X-rays.

Authors:  K D Friedberg; K Mengel; E Schlick
Journal:  Radiat Environ Biophys       Date:  1983       Impact factor: 1.925

3.  Effect of azimexon (BM 12.531) on mouse granulocyte-macrophage and monocyte-macrophage progenitor cells.

Authors:  J C Jeng; K F McCarthy; M A Chirigos; J F Weiss
Journal:  Experientia       Date:  1982-01-15
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.