Cargando…
Synthesis and 5α-Reductase Inhibitory Activity of C(21) Steroids Having 1,4-diene or 4,6-diene 20-ones and 4-Azasteroid 20-Oximes
The synthesis and evaluation of 5α-reductase inhibitory activity of some 4-azasteroid-20-ones and 20-oximes and 3β-hydroxy-, 3β-acetoxy-, or epoxy-substituted C(21) steroidal 20-ones and 20-oximes having double bonds in the A and/or B ring are described. Inhibitory activity of synthesized compounds...
Autores principales: | Kim, Sujeong, Kim, Yong-ung, Ma, Eunsook |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268135/ https://www.ncbi.nlm.nih.gov/pubmed/22210173 http://dx.doi.org/10.3390/molecules17010355 |
Ejemplares similares
-
21-Hydroxypregna-1,4-diene-3,20-dione
por: Yousuf, S., et al.
Publicado: (2011) -
11,20-Dihydroxy-3-oxopregna-1,4-dien-21-oic acid monohydrate
por: Guo, Zhanqiang, et al.
Publicado: (2011) -
Synthesis and bioactivity evaluation of penta-1,4-diene-3-one oxime ether derivatives
por: Tang, Xu, et al.
Publicado: (2019) -
Catalytic, Regioselective 1,4‐Fluorodifunctionalization of Dienes
por: Yu, You‐Jie, et al.
Publicado: (2022) -
Synthesis of 2- and 7- Substituted C(19) Steroids Having a 1,4,6-Triene or 1,4-Diene Structure and Their Cytotoxic Effects on T47D and MDA-MB231 Breast Cancer Cells
por: Kim, Minwoo, et al.
Publicado: (2010)