A number of cytochrome P450s are targets for compounds that are clinic
ally used or under clinical evaluation for treatment of patients with
mycotic infections, such as dermatophytosis, superficial and systemic
candidiasis, cryptococcosis and aspergillosis, with skin diseases, suc
h as psoriasis or ichthyosis, and other retinoid-sensitive malignancie
s, e.g., neuro-ectodermal glioma. Some of the P450 inhibitors are cand
idates for the treatment of hirsutism or prostate cancer, others are p
otent inhibitors of the P450 isomerase involved in the synthesis of th
romboxane A(2), a potent platelet aggregation inducer and vasoconstric
tor.