Arsenic - 75 nuclear magnetic resonance: A study of the interaction of arsenates with monosaccharides and gluconic acid.
โ Scribed by C.F.G.C. Geraldes; M.E. Saraiva; B.A. Dias
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 60 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0162-0134
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The proton magnetic resonance (PMR) and phosphorus magnetic resonance (PhMR) spectra of egg phosphatidylcholine in the presence of l-anilino-8-naphthalenesulfonate (ANS) have been studied. At low ratios of ANS to phospholipid, the spectra indicate that ANS molecules are in the lipid interface region
Deuterium nuclear magnetic resonance (2H-NMR) spectra have been determined for 50 wt% aqueous dispersions of 1 -palmitoyl(stearoyl)-2-[2H3, ]palmitoyl-sn -glycero-3-phosphocholinc (PC-d 3 I) containing 20 tool% of the isoprenoid compounds phytol or phytanic acid over the temperature range -5--55ยฐC.
Actinomycin D (ACD), Figure 1, is the most important member of a family of naturally occurring actinomycine whose primary biological function is the inhibition of DNA dependent RNA synthesis (5). If mechanisms propoaed for the biological activity of ACD ( 6) are to have a plausible structural basis,