Zobrazeno 1 - 10 of 10 pro vyhledávání: '"DONALD C. CLAGETT"'
2
Specific Acylation of the Guanine Residues of Ribonucleic Acid
Autor: Robert Shapiro, Bertram I. Cohen, Donald C. Clagett
Publikováno v: Journal of Biological Chemistry. 245:2633-2639
Treatment of yeast RNA with Kethoxal (β-ethoxy-α-keto-butyraldehyde), followed by periodate cleavage, led to the specific introduction of α-ethoxypropionyl groups onto the guanine amino groups of the RNA. The extent of nitrous acid deamination of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3518a0b17482fb686f0be3a613cce125
https://doi.org/10.1016/s0021-9258(18)63117-5
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3
Ribonucleoside reactivities with singlet (1Δg) molecular oxygen
Autor: Donald C. Clagett, Theodore J. Galen
Publikováno v: Archives of Biochemistry and Biophysics. 146:196-201
An apparatus was developed for the external generation of singlet ( 1 Δg) molecular oxygen (singlet oxygen) for introduction into aqueous solutions of ribonucleosides and sodium ribonucleate (yeast). In contrast to previous conclusions on the specif
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::623825c6dc465b31f52e126085efd7a5
https://doi.org/10.1016/s0003-9861(71)80056-5
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6
Comptonia asplenifolia: low boiling components
Autor: W.P. Dubinsky, Donald C. Clagett, D. Przybyl
Publikováno v: Journal of pharmaceutical sciences. 62(3)
Room temperature, low pressure vacuum distillation of 920 g. of the fresh leaves from Comptonia asplenifolia Ait. typically yielded 3 mg. of methyl acetate, 1 mg. of ethyl acetate, 2 mg. of diisopropyl acetaldehyde acetal, and 5 mg. of cineol. Methyl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5e9efffb7d83b04617bd4ba4eab6294
https://pubmed.ncbi.nlm.nih.gov/4691715
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7
Molecular Orbital Studies of Antischistosomal Agents
Autor: Haven S. Aldrich, Donald C. Clagett
Publikováno v: Journal of Pharmaceutical Sciences. 65:1704-1705
Molecular orbital calculations were used to investigate the antischistosomal agent, niridazole, and an inactive derivative, 1-(5-nitro-2-thiazolyl)-2-ethylurea. The CNDO/2 calculations revealed that the inactive derivative had a preferred conformatio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fa103a868653d77522820bef05ee5fd
https://doi.org/10.1002/jps.2600651138
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