|1.||Hillard, Elizabeth A: 1 article (11/2014)|
|2.||Pigeon, Pascal: 1 article (11/2014)|
|3.||Rodrigues, Felipe A R: 1 article (11/2014)|
|4.||Goulart, Marilia O F: 1 article (11/2014)|
|5.||de Oliveira, Alane Cabral: 1 article (11/2014)|
|6.||Rocha, Danilo Damasceno: 1 article (11/2014)|
|7.||de Abreu, Fabiane C: 1 article (11/2014)|
|8.||da Rocha Ferreira, Fabrícia: 1 article (11/2014)|
|9.||da Silva, Emanuella Gomes: 1 article (11/2014)|
|10.||Costa-Lotufo, Letícia V: 1 article (11/2014)|
01/01/1988 - "A 1,1,2-triphenylbut-1-ene with a 4-OH group at one C-1 phenyl ring and a chlorocarbamate mustard moiety at the second C-1 ring (compound 3) was synthesized in order to obtain a "cytotoxic estrogen" with a specific antitumor effect on estrogen-receptor-containing tumors. "
11/01/2014 - "Both the organic analogue 1,1,2-triphenylbut-1-ene (2) and ferrocene were inactive against cancer and noncancer cell lines and did not react with DNA. "
08/01/1986 - "Catechol estrogens of the 1,1,2-triphenylbut-1-ene type: relationship between structure, estradiol receptor affinity, estrogenic and antiestrogenic properties, and mammary tumor inhibiting activities."
|1.||Estradiol Receptors (Estradiol Receptor)
|3.||DNA (Deoxyribonucleic Acid)