Sulfur base complexes of 4,6-dinitrobenzofuroxan. Isolation of the cysteine complex; Support for cellular thiol addition as a primary step in the inhibition of nucleic acid synthesis by nitrobenzofuroxans.-Reference-Cited by-同舟云学术

Sulfur base complexes of 4,6-dinitrobenzofuroxan. Isolation of the cysteine complex; Support for cellular thiol addition as a primary step in the inhibition of nucleic acid synthesis by nitrobenzofuroxans.

Published:1981-01 Issue:21 Volume:22 Page:1945-1948
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Strauss M.J.,DeFusco A.,Terrier F.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference10 articles.

1. Potential antileukemic and immunosuppressive drugs. Preparation and in vitro pharmacological activity of some 2,1,3-benzoxadiazoles (benzofurazans) and their N-oxides (benzofuroxans)

2. 4-nitrobenzofurazans and 4-nitrobenzofuroxans: a new class of thiol-neutralising agents and potent inhibitors of nucleic acid synthesis in leucocytes

3. Potential antileukemic and immunosuppressive drugs. 3. Effects of homocyclic ring substitution on the in vitro drug activity of 4-nitrobenzo-2,1,3-oxadiazoles (4-nitrobenzofurazans) and their N-oxides (4-nitrobenzofuroxans)

4. Mutagenicity of anti-cancer nitrobenzofuroxans

5. 4,6-Dinitrobenzofuroxan. I. Covalent Hydration1

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