Proxalutamide is an orally bioavailable androgen receptor (AR) antagonist with potential antineoplastic activity. Upon oral administration, proxalutamide binds to AR in target tissues, inhibits androgen-induced receptor activation, and facilitates the formation of inactive complexes that cannot translocate to the nucleus. This prevents binding to and transcription of AR-responsive genes that regulate prostate cancer cell proliferation. Additionally, proxalutamide induces AR downregulation, thereby further preventing AR-mediated signaling. This ultimately leads to an inhibition of growth in AR-expressing prostate cancer cells. AR is overexpressed in prostate cancer and plays a key role in prostate cancer cell proliferation. Its therapeutic use is listed as analgesics. The directory classifies it as a under development API with a synthetic source/manufacturing origin. Other names for this substance include Proxalutamide, 4-(4, 4-dimethyl-3-{6-[3-(1 and 3-oxazol-2-yl)propyl]pyridin-3-yl}-5-oxo-2-sulfanylideneimidazolidin-1-yl)-3-fluoro-2-(trifluoromethyl)benzonitrile. Its PubChem CID is 60194102.
Pruxelutamide
| CAS No | 1398046-21-3 |
|---|---|
| Molecular Formula | C24H19F4N5O2S |
| Molecular Weight | 517.5 g/mol |
| Synonyms | 4-[4,4-dimethyl-3-[6-[3-(1,3-oxazol-2-yl)propyl]-3-pyridinyl]-5-oxo-2-sulfanylideneimidazolidin-1-yl]-3-fluoro-2-(trifluoromethyl)benzonitrile |
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Frequently Asked Questions
Proxalutamide is an orally bioavailable androgen receptor (AR) antagonist with potential antineoplastic activity.
The listed CAS number is 1398046-21-3.
The listed molecular formula is C24H19F4N5O2S.
The listed molecular weight is 517.5 g/mol.
4-[4,4-dimethyl-3-[6-[3-(1,3-oxazol-2-yl)propyl]-3-pyridinyl]-5-oxo-2-sulfanylideneimidazolidin-1-yl]-3-fluoro-2-(trifluoromethyl)benzonitrile.
The source lists Proxalutamide, 4-(4, 4-dimethyl-3-{6-[3-(1 and 3-oxazol-2-yl)propyl]pyridin-3-yl}-5-oxo-2-sulfanylideneimidazolidin-1-yl)-3-fluoro-2-(trifluoromethyl)benzonitrile.