Molecular Formula: C18H18Cl2N2O3
Molecular weight: 381.25312
InChi: InChI=1S/C18H18Cl2N2O3/c1-10(2)16(18(25)21-13-5-3-4-11(19)8-13)22-17(24)14-9-12(20)6-7-15(14)23/h3-10,16,23H,1-2H3,(H,21,25)(H,22,24)/t16-/m0/s1
InChi Key: IYCDUYRXILCPOP-INIZCTEOSA-N
SMILES: c1(C(=O)N[C@H](C(=O)Nc2cc(ccc2)Cl)C(C)C)c(ccc(c1)Cl)O
Chemical Name
(S)-5-chloro-N-(1-(3-chlorophenylamino)-3-methyl-1-oxobutan-2-yl)-2-hydroxybenzamide
Authors of compound
Ruzicka, Ales
Hanusek, Jiri
Lycka, Antonin
Imramovsky, Ales
Pauk, Karel
Jorda, Radek
Reznickova, Eva
Dusek, Jan
Krystof, Vladimir
Vinsova, Jarmila
Ferriz, Juana Monreal
Jampilek, Josef
Kratky, Martin
Palat, Karel
Ferriz, Juana M.
Stolarikova, Jirina
Pesko, Matus
Kralova, Katarina
Vejsova, Marcela
Articles
Hanusek, Jiri;
Imramovsky, Ales;
Pauk, Karel;
Jorda, Radek;
Reznickova, Eva;
Dusek, Jan;
Krystof, Vladimir,
Substituted 2-hydroxy-N-(arylalkyl)benzamides induce apoptosis in cancer cell lines.
European Journal of Medicinal Chemistry 2013,
68, 253 - 259,
10.1016/j.ejmech.2013.08.009 
.
Ruzicka, Ales;
Lycka, Antonin;
Imramovsky, Ales;
Vinsova, Jarmila;
Ferriz, Juana Monreal;
Kratky, Martin;
Palat, Karel,
An unprecedented rearrangement of salicylanilide derivatives: imidazolinone intermediate formation.
Tetrahedron Letters 2010,
51(1), 23 - 26,
10.1016/j.tetlet.2009.10.084 .
Imramovsky, Ales;
Vinsova, Jarmila;
Jampilek, Josef;
Stolarikova, Jirina;
Pesko, Matus;
Kralova, Katarina;
Vejsova, Marcela,
Investigating spectrum of biological activity of 4- and 5-Chloro-2-hydroxy-N-[2-(arylamino)-1-alkyl-2-oxoethyl]benzamides.
Molecules 2011,
16(3), 2414 - 2430,
10.3390/molecules16032414 .
