By B. Beek
The bioaccumulation of endocrine disruptors, continual natural chemical substances and different compounds of excessive environmental effect has turn into of accelerating curiosity in newest environmental learn, possibility research and toxicology. This quantity provides an up to date evaluate and introduces the reader to the hot thought of "internal impact focus" linking bioaccumulation and biomagnification within the meals chain to ecotoxicology and possibility evaluate.
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Extra resources for Bioaccumulation - New Aspects and Developments
However, Körner et al. [138a] found estrogenic potency of this chemical in the proliferation assay with the MCF-cell line (purity of TBBA: 97%). k Relative binding affinity (RBA) assay in serum-free medium determined by Nagel et al. . m n o p q r s t u v w x y z Relative estrogenic potency compared to 17b-estradiol (100) by molar mass determined with the recombinant yeast cell bioassay (RCBA) [138b]. Trade name. Laboratory model static ecosystem used by Metcalf . It is not possible to calculate “real” steady-state BCF values.
These antiandrogens can bind to the AR without activating it, and simultaneously prevent binding of natural androgens, such as 5a-dihydrotestosterone, testosterone, and/or 11-ketotestosterone. Examples of chemicals of antiandrogenic activity are the nonsteroidal pharmaceutical flutamide and its metabolite 2-hydroxyflutamide. The agricultural fungicides vinclozolin and procymidone with some of their metabolites, some phenylurea herbicides (PUHs), such as linuron and diuron and their metabolites 3,4-dichloroaniline and 3,4-dichloroacetanilide bind to the androgen receptor and prevent binding of natural androgens (Table 7).
This drug can bind to the estrogen receptor, thereby blocking activation by endogenous estrogens. The breast cancer adjuvant non-steroidal pharmaceutical agent tamoxifen and its metabolite, 4-hydroxy tamoxifen, exhibit both antiestrogenic and estrogenic activities [149, 294]. Raloxifene is a nonsteroidal estrogen receptor mixed agonist/antagonist depending on the tissue. This drug is useful in preventing further bone loss when the onset of osteoporosis has been detected in woman after menopause.