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Target Specific Uptake of a Newly Synthesized Radiolabeled 5α-Reductase Inhibitor “Tc-99m-17-Oxo-17a-Aza-D-Homo-5-Androsten-3β-yl Phenoxyacetate (Tc-99m-17a-Aza Steroid)” in Rat Prostatic Neoplastic Lesions
OBJECTIVE: Considering the 5α-reductase (5AR) inhibitory activity of the oximes and the importance of the ester group in increasing the anti-androgenic property, we reasoned to synthesize a compound having a lactam group in ring D and an ester group at the 3 β position of the androsterone nucleus. T...
Autores principales: | Jan, Gowsia, Bhat, Swati, Chauhan, Monika, Dhawan, Devinder Kumar, Dhingra, Neelima, Chadha, Vijayta Dani |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380797/ https://www.ncbi.nlm.nih.gov/pubmed/35982808 http://dx.doi.org/10.4103/ijnm.ijnm_128_21 |
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