CAS Number 39962-28-2 ChemSpider 118991 Formula C14H12N2O3 | PubChem CID 135035 ChEMBL CHEMBL1710671 Molar mass 256.2567 g/mol | |
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Synonyms Ro 7-8117; N-(3,5-Dimethyl-4-isoxazolylmethyl)phthalimide |
DIMP (developmental code name Ro 7-8117), or N-(3,5-dimethyl-4-isoxazolylmethyl)phthalimide, is a non-steroidal antiandrogen (NSAA) structurally related to thalidomide (which also binds to and antagonizes the androgen receptor (AR)) that was first described in 1973 and was never marketed. Along with flutamide, it was one of the earliest NSAAs to be discovered, and for this reason, has been described as a "classical" NSAA. The drug is a selective, competitive, silent antagonist of the AR, although it is described as an "only relatively weak competitor". DIMP possesses no androgenic, estrogenic, progestogenic, or antigonadotropic activity, but it does reverse the antigonadotropic effects of testosterone, indicating that, like other pure AR antagonists, it is progonadotropic.
DIMP is the lead antiandrogen of the phthalimide group of non-steroidal AR ligands, and a variety of AR ligands with higher affinity for the AR have been derived from DIMP and thalidomide.