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formamidoxime

 
National Institutes of Health

Papers overview

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2012
2012
The partial positive charge of amide protons is used to promote macrocyclization and form crown-ether analogs. Their… Expand
2004
2004
Various oxime derivatives were evaluated as nitric oxide (NO) donors in arteries. Relaxation of rat aortic rings was used for… Expand
2002
2002
The mechanisms of vasorelaxation elicited byN ω-hydroxy-l-arginine (l-NOHA) and other compounds bearing a C=NOH function and the… Expand
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1981
1981
Microsomal proteins from cultured chick embryo hepatocytes were separated by polyacrylamide gel electrophoresis and their rate… Expand
1978
1978
Hydroxyurea is an excellent selective agent for obtaining drug‐resistant mutants. At a frequency of approximately 1 × 10−5 it was… Expand
1978
1978
A series of amidoximes was prepared and evaluated for possible antitumor activity against L1210 leukemia. Three of the most… Expand
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1973
1973
Abstract Formamidoxime caused an inhibition of [3H]thymidine incorporation into DNA in regenerating liver and transplanted… Expand
1971
1971
Abstract Formamidoxime is a preferential inhibitor of bacterial and mammalian DNA synthesis. In bacteria, levels of formamidoxime… Expand
1971
1971
The prophage-inducing capability of hydroxylamine sulfate and 36 of its derivatives, and of hydrazine dihydrochloride and… Expand
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1971
1971
  • H. Bosmann
  • Chemico-biological interactions
  • 1971
  • Corpus ID: 38713661
Abstract The effects of formamidoxime and hydroxyurea over a 10 5 concentration range were studied on macromolecular synthesis in… Expand