In vitro assay of hydrolysis and chlorohydroxy derivatives of bisphenol A diglycidyl ether for estrogenic activity

2002 ◽  
Vol 40 (12) ◽  
pp. 1827-1832 ◽  
Author(s):  
H Nakazawa ◽  
A Yamaguchi ◽  
K Inoue ◽  
T Yamazaki ◽  
K Kato ◽  
...  
Carbon ◽  
2004 ◽  
Vol 42 (5-6) ◽  
pp. 1195-1198 ◽  
Author(s):  
Bertrand Vileno ◽  
Andrzej Sienkiewicz ◽  
Małgorzata Lekka ◽  
Andrzej J. Kulik ◽  
László Forró

Toxicology ◽  
2005 ◽  
Vol 207 (2) ◽  
pp. 215-221 ◽  
Author(s):  
Hitomi Takemura ◽  
Jie Ma ◽  
Kazutoshi Sayama ◽  
Yoshiyasu Terao ◽  
Bao Ting Zhu ◽  
...  

2014 ◽  
Vol 28 (1) ◽  
pp. 70-75 ◽  
Author(s):  
Barbara Wozniak ◽  
Maria Minta ◽  
Sylwia Stypula-Trebas ◽  
Lidia Radko ◽  
Jan Zmudzki

2000 ◽  
Vol 162 (1) ◽  
pp. 22-33 ◽  
Author(s):  
N. Beresford ◽  
E.J. Routledge ◽  
C.A. Harris ◽  
J.P. Sumpter

1992 ◽  
Vol 3 (2) ◽  
pp. 79-84 ◽  
Author(s):  
C. McGuigan ◽  
B. C. N. M. Jones ◽  
S. M. Tollerfield ◽  
P. A. Riley

Novel phosphate triester derivatives of the antiviral drug araA and the anti-leukaemic agent araC have been prepared as membrane-soluble pro-drugs of the bio-active free nucleotides. In particular, novel trichloro- and trifluoroethyl phosphates have been prepared using phosphorochloridate chemistry, and are fully characterized. An in vitro assay indicates inhibition, by each of the compounds, of thymidine incor-portion by mammalian epithelial cells. It is notable that the trichloroethyl derivative is most active in each case, and in the case of araC its activity appears to exceed that of the parent nucleoside.


2004 ◽  
Vol 52 (5) ◽  
pp. 1410-1414 ◽  
Author(s):  
Hideo Kato ◽  
Toshio Iwata ◽  
Yoshinao Katsu ◽  
Hajime Watanabe ◽  
Yasuhiko Ohta ◽  
...  

2006 ◽  
Vol 80 (11) ◽  
pp. 748-755 ◽  
Author(s):  
Graciela Ramilo ◽  
Iago Valverde ◽  
Jorge Lago ◽  
Juan M. Vieites ◽  
Ana G. Cabado

1968 ◽  
Vol 20 (03/04) ◽  
pp. 384-396 ◽  
Author(s):  
G Zbinden ◽  
S Tomlin

SummaryAn in vitro system is described in which adhesion of blood platelets to washed and tannic acid-treated red cells was assayed quantitatively by microscopic observation. ADP, epinephrine and TAME produced a reversible increase in platelet adhesiveness which was antagonized by AMP. With Evans blue, polyanetholsulfonate, phthalanilide NSC 38280, thrombin and heparin at concentrations above 1-4 u/ml the increase was irreversible. The ADP-induced increase in adhesiveness was inhibited by sodium citrate, EDTA, AMP, ATP and N-ethylmaleimide. EDTA, AMP and the SH-blocker N-ethylmaleimide also reduced spontaneous platelet adhesion to red cells. No significant effects were observed with adenosine, phenprocoumon, 5-HT, phthalanilide NSC 57155, various estrogens, progestogens and fatty acids, acetylsalicylic acid and similarly acting agents, hydroxylamine, glucose and KCN. The method may be useful for the screening of thrombogenic and antithrombotic properties of drugs.


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