Chlornitrofen (CNP) was widely used in large quantities as a herbicide in rice paddy fields in Japan during 1965-1994. Recently, there has been concern that chemicals in the environment may disrupt the endocrine function of wildlife and humans, but little is known about the effect of CNP on endocrine function. We have developed reporter gene assays for human androgen receptor (hAR) and human estrogen receptor-alpha (hERalpha) using Chinese hamster ovary cells. Using this assay method, we measured CNP and its amino derivative (CNP-amino) for hAR and hERalpha agonist/antagonist activities, comparing them with several well-known AR antagonists or ER agonists. We found that CNP and CNP-amino have potent antiandrogenic activities as well as estrogenic activities. The order of their antiandrogenic activity was CNP > vinclozolin > o,p'-DDT = p,p'-DDE > CNP-amino, and the order of their estrogenic activity was o,p'-DDT > CNP-amino > p,p'-DDT > CNP. We investigated the binding ability of CNP and CNP-amino to hAR and hERa using a receptor competitive-binding assay. The. order of their binding potencies to hAR was CNP > o,p'-DDT = p,p'-DDE = CNP-amino > vinclozolin, and that of their binding potencies to hERa. was o,p'-DDT > CNP-amino > p,p'-DDT = CNP. These results suggest that both CNP and CNP-amino may act as endocrine disruptors via AR and ERalpha in humans and other animals. Our reporter gene assays are highly sensitive and specific and are suitable for screening AR and ERalpha agonist/antagonists among numerous environmental chemicals..