Bicalutamide
Chemical Name: N-[4-Cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide
Purity: ≥99%
Biological Activity
Bicalutamide is an orally active non-steroidal androgen receptor antagonist (IC50 = 190 nM). Displays peripheral selectivity and does not effect serum levels of LH and testosterone. Exhibits potent anticancer activity in vivo.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Additional Information
Background References
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ICI 176,334: a novel non-steroidal, peripherally selective antiandrogen.
Furr et al.
J.Endocrinol., 1987;113:R7 -
Nonsteroidal antiandrogens. Synthesis and structure-activity relationships of 3-substituted derivatives of 2-hydroxypropionanilides.
Tucker et al.
J.Med.Chem., 1988;31:954 -
The preclinical development of bicalutamide: pharmacodynamics and mechanism of action.
Furr and Tucker
Urology, 1996;47:13
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Citations for Bicalutamide
The citations listed below are publications that use Tocris products. Selected citations for Bicalutamide include:
4 Citations: Showing 1 - 4
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The Androgen Receptor Regulates PPARγ Expression and Activity in Human Prostate Cancer Cells.
Authors: Olokpa Et al.
J Cell Physiol 2016;231:2664
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TLR3 engagement induces IRF-3-dependent apoptosis in androgen-sensitive prostate cancer cells and inhibits tumour growth in vivo.
Authors: Gambara Et al.
J Cell Mol Med 2015;19:327
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Preclinical Development of ONC1-13B, Novel Antiandrogen for Prostate Cancer Treatment.
Authors: Ivachtchenko Et al.
PLoS One 2014;5:133
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Androgen deprivation promotes intratumoral synthesis of dihydrotestosterone from androgen metabolites in prostate cancer.
Authors: Ishizaki Et al.
Sci Rep 2013;3:1528
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