A novel intramolecular hydrogen bond in the crystal structure of 5-hydroxymethyl-2'-deoxyuridine, an antiviral and antineoplastic nucleoside. Conformational analysis of the deoxyribose ring
- 1 June 1980
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 102 (12) , 4236-4241
- https://doi.org/10.1021/ja00532a041
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Synthetic inhibitors of Escherichia coli, calf thymus, and Ehrlich ascites tumor thymidylate synthetaseJournal of Medicinal Chemistry, 1976
- Nucleoside analogs with antiviral activityBiochemical Pharmacology, 1976
- Nonclassical Antimetabolites. XXV.1 Inhibitors of Thymidine Kinase. I. A New Spectrophotometric Assay. Inhibition by Nucleoside DerivativesJournal of Medicinal Chemistry, 1966
- The possible role of recombination in the infection of competent Bacillus subtilis by bacteriophage deoxyribonucleic acidVirology, 1964
- Nucleotide interconversions. VI. The enzymic formation of 5-methyluridylic acidArchives of Biochemistry and Biophysics, 1962
- Base pairing in DNAJournal of Molecular Biology, 1960
- The specific mutagenic effect of base analogues on Phage T4Journal of Molecular Biology, 1959
- VIRUS-INDUCED ACQUISITION OF METABOLIC FUNCTION .1. ENZYMATIC FORMATION OF 5-HYDROXYMETHYLDEOXYCYTIDYLATE1959
- VIRUS-INDUCED ACQUISITION OF METABOLIC FUNCTION .3. FORMATION AND SOME PROPERTIES OF THYMIDYLATE SYNTHETASE OF BACTERIOPHAGE-INFECTED ESCHERICHIA-COLI1959
- STUDIES ON THE BIOSYNTHESIS OF BACTERIAL AND VIRAL PYRIMIDINES .5. HYDROGENATION OF 5-HYDROXYMETHYLPYRIMIDINES1957