An active puromycin analog derived from a non-nephrotoxic aminonucleoside
- 1 February 1976
- journal article
- research article
- Published by Elsevier in Life Sciences
- Vol. 18 (3) , 345-349
- https://doi.org/10.1016/0024-3205(76)90063-1
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Puromycin analogs. Ribosomal binding and peptidyl transferase substrate activity of a carbocyclic analog of 8-azapuromycinBiochemistry, 1974
- Puromycin analogs. Synthesis and biological activity of 5'-deoxypuromycin and its aminonucleoside, 6-dimethylamino-9-(3'-amino-3',5'-dideoxy-.beta.-D-ribofuranosyl)purineJournal of Medicinal Chemistry, 1973
- A detailed model of the active centre of Escherichia coli peptidyl transferaseBioorganic Chemistry, 1973
- Substrate Specificity of Ribosomal Peptidyl TransferaseEuropean Journal of Biochemistry, 1970
- Metabolism of puromycin aminonucleoside in the rat: Formation of nucleotide derivativesBiochemical Pharmacology, 1970
- Inhibition of aminonucleoside nephrosis in ratsToxicology and Applied Pharmacology, 1967
- Some Properties of Partially Purified Mammalian Adenosine KinaseJournal of Biological Chemistry, 1967
- Cellular Effects of Anticancer DrugsAnnual Review of Pharmacology and Toxicology, 1963
- Structural Requirements for Puromycin Inhibition of Protein SynthesisNature, 1963
- STUDIES ON THE MECHANISM OF PRODUCTION OF A NEPHROTIC SYNDROME IN RATS BY A NUCLEOSIDEPediatrics, 1960