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Synthesis of phosphoramide mustard analogues of daunomycin and carminomycin.

作者信息

Csorvási A, Kövér K E, Menyhárt M M, Sztaricskai F, Dobrynin Y V, Nikolaeva T G

机构信息

Research Group for Antibiotics of the Hungarian Academy of Sciences, L. Kossuth University, Debrecen, Hungary.

出版信息

Arch Pharm (Weinheim). 1998 Sep;331(9):265-8. doi: 10.1002/(sici)1521-4184(19989)331:9<265::aid-ardp265>3.0.co;2-n.

DOI:10.1002/(sici)1521-4184(19989)331:9<265::aid-ardp265>3.0.co;2-n
PMID:9793480
Abstract

New phosphoramide mustards (6-8) have been prepared from the antibiotics 2 and 3, and from 5. The mixture of cyclophosphamides could be separated by preparative layer and column chromatography. The assignments of configuration to the isomeric phosphoramidates was based on the magnetic anisotropy of the P = O bond. The synthesized compounds 6a,b-8a,b (mixture of isomers) were tested for inhibitory activity on the [3H]-thymidine incorporation into the DNA of tumor cells, using ovarian carcinoma cell line.

摘要

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