Literature DB >> 5240831

5-Diazo-4-oxo-L-norvaline: reactive asparagine analog with biological specificity.

R E Handschumacher, C J Bates, P K Chang, A T Andrews, G A Fischer.   

Abstract

The L-asparagine analog, 5-diazo-4-oxo-L-norvaline, specifically inactivates L-asparaginase and inhibits the growth of L-asparagine-dependent or L-asparaginase-sensitive tumor cells in culture. With 5-(14)C-labeled compound, a biphasic incorporation into sensitive cells occurs, but the inhibition of cell multiplication is manifest much later than the rapid phase of incorporation of the analog.

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Year:  1968        PMID: 5240831     DOI: 10.1126/science.161.3836.62

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  5 in total

Review 1.  Diazo Compounds: Versatile Tools for Chemical Biology.

Authors:  Kalie A Mix; Matthew R Aronoff; Ronald T Raines
Journal:  ACS Chem Biol       Date:  2016-10-26       Impact factor: 5.100

2.  Utilization of the amide groups of asparagine and 2-hydroxysuccinamic Acid by young pea leaves.

Authors:  T C Ta; K W Joy; R J Ireland
Journal:  Plant Physiol       Date:  1984-07       Impact factor: 8.340

3.  De Novo Purine Biosynthesis in Intact Cells of Cucurbita pepo.

Authors:  C J Lovatt
Journal:  Plant Physiol       Date:  1983-11       Impact factor: 8.340

4.  Asparagine utilization in Escherichia coli.

Authors:  R C Willis; C A Woolfolk
Journal:  J Bacteriol       Date:  1974-04       Impact factor: 3.490

5.  High-resolution crystal structure of human asparagine synthetase enables analysis of inhibitor binding and selectivity.

Authors:  Wen Zhu; Ashish Radadiya; Claudine Bisson; Sabine Wenzel; Brian E Nordin; Francisco Martínez-Márquez; Tsuyoshi Imasaki; Svetlana E Sedelnikova; Adriana Coricello; Patrick Baumann; Alexandria H Berry; Tyzoon K Nomanbhoy; John W Kozarich; Yi Jin; David W Rice; Yuichiro Takagi; Nigel G J Richards
Journal:  Commun Biol       Date:  2019-09-17
  5 in total

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