Substituted 2-hydroxy-N-(arylalkyl) benzamides induce apoptosis in cancer cell lines

A Imramovský, R Jorda, K Pauk, E Řezníčková…

Index: European Journal of Medicinal Chemistry, , vol. 68, p. 253 - 259

Full Text: HTML

Citation Number: 7

Abstract

... Please enable JavaScript to use all the features on this page. European Journal of Medicinal Chemistry. ... a Institute of Organic Chemistry and Technology, Faculty of Chemical Technology, University of Pardubice, Studentská 573, 53210 Pardubice, Czech Republic; ...

Related Articles:

A Practical Synthesis of threo-3-Amino-2-hydroxycarboxylic Acids.

[Bulletin of the Chemical Society of Japan, , vol. 65, # 2 p. 360 - 365]

Optically active derivatives of imidazolines.. alpha.-Adrenergic blocking properties

[Journal of Medicinal Chemistry, , vol. 23, # 11 p. 1232 - 1235]

A facile method for the transformation of N-(tert-butoxycarbonyl) α-amino acids to N-unprotected α-amino methyl esters

[Journal of Organic Chemistry, , vol. 64, # 25 p. 9294 - 9296]

Unusual amino acids V. Asymmetric hydrogenation of (Z)-N-acylaminocinnamic acid derivatives bearing different protective groups

[Tetrahedron Asymmetry, , vol. 4, # 9 p. 2047 - 2051]

Chiral auxiliaries with a switching center: new tools in asymmetric synthesis. application to the synthesis of enantiomerically pure (R)-and (S)-α-amino acids

[Journal of Organic Chemistry, , vol. 63, # 23 p. 8094 - 8095]

More Articles...