## Abstract HIV‐1 integrase (IN) is a very promising and validated target for the development of therapeutic agents against AIDS. In an effort to design and synthesize biological isosteric analogs of β‐diketoacid‐containing inhibitors of IN, we prepared a series of substituted isoxazole carboxylic
Radioiodinated bleomycin: Stoichiometry of iodination and structural characterization by 1H-nuclear magnetic resonance
✍ Scribed by J.Richard Creekmore; Richard J. Kowalsky; Lester Kwock; Dale Eric Wurster
- Publisher
- Elsevier Science
- Year
- 1984
- Weight
- 466 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0020-708X
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