91444-11-0Relevant academic research and scientific papers
Antimitotic activities of 2-phenylindole-3-carbaldehydes in human breast cancer cells
Kaufmann, Doris,Pojarova, Michaela,Vogel, Susanne,Liebl, Renate,Gastpar, Robert,Gross, Dietmar,Nishino, Tsuyuki,Pfaller, Tobias,von Angerer, Erwin
, p. 5122 - 5136 (2008/03/27)
Small molecules such as indoles are attractive as inhibitors of tubulin polymerization. Thus a number of 2-phenylindole-3-carbaldehydes with lipophilic substituents in both aromatic rings was synthesized and evaluated for antitumor activity in MDA-MB 231
2-Phenylindoles. Relationship between Structure, Estrogen Receptor Affinity, and Mammary Tumor Inhibiting Activity in the Rat
Angerer, Erwin von,Prekajac, Jelica,Strohmeier, Josef
, p. 1439 - 1447 (2007/10/02)
A number of 2-phenylindole derivatives with one hydroxy group in the meta or para position of the phenyl ring and a second one in position 5, 6, or 7 of the indole nucleus were synthesized.In addition, different alkyl groups were introduced into positions
