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Design, synthesis, and biological activity of anti-angiogenic hypoxic cell radiosensitizer haloacetylcarbamoyl-2-nitroimidazoles.
- H. Hori, C. Jin, M. Kiyono, S. Kasai, M. Shimamura, S. Inayama
- Chemistry, Medicine
- Bioorganic & medicinal chemistry
- 1 March 1997
The in vivo chick CAM angiogenesis assay showed that the strong bromoacetylcarbamoyl-2-nitroimidazole radiosensitizers, such as TX-1845 andTX-1846, were the strongest angiogenic inhibitors among them. Expand
Huang-Minlon Reduction of Acetylenic Keto Acids
[Hypotensive action of prostaglandin E1].
Inclusive production of protons in pp interactions at 6.94 GeV/c
Abstract We present an experimental study of inclusive production of protons in p p interactions at 6.94 GeV/ c . The distributions of the c.m. longitudinal and transverse momentum of protons show… Expand