Bioanalytical Assay Development and Validation for the Pharmacokinetic Study of GMC1, a Novel FKBP52 Co-chaperone Inhibitor for Castration Resistant Prostate Cancer
Background: GMC1 (2-(1H-benzimidazol-2-ylsulfanyl)-<i>N</i>-[(Z)-(4-methoxyphenyl) methylideneamino] acetamide) effectively inhibits androgen receptor function by binding directly to FKBP52. This is a novel mechanism for the treatment of castration resistant prostate cancer (CRPC). Metho...
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Main Authors: | , , , , , , , , , |
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Format: | Book |
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MDPI AG,
2020-11-01T00:00:00Z.
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A1234.567 |
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