Perjési, P., Linnanto, J., Kolehmainen, E., Osz, E. and Virtanen, E. (2005) E-2-Benzylidenebenzocycloalkanones IV. Studies on Transmission of Substituent Effects on ¹³C NMR Chemical Shifts of E-2-(X-benzylidene)-1-tetralones, and -benzosuberones. Comparison with the ¹³C NMR Data of Chalcones and E-2-(X-benzylidene)-1-Indanones. Journal of Molecular Structure, 740, 81-89.
http://dx.doi.org/10.1016/j.molstruc.2004.10.013

has been cited by the following article:

• TITLE: (E)-2-Benzylidenecycloalkanones XII.* Kinetic Measurement of Bovine and Human Serum Albumine Interaction with Selected Chalcones and Their Cyclic Chalcone Analogues by UV Spectrophotometry

  AUTHORS: Beáta Veliká, Vladimíra Tomečková, Krisztina Fodor, Ivan Kron, Pál Perjési

  KEYWORDS: Chalcones, Cyclic Chalcone Analogues, UV Spectra, Kinetic Measurements, Binding Constant Bovine Serum Albumin, Human Serum Albumin

  JOURNAL NAME: Spectral Analysis Review, Vol.3 No.1, January 30, 2015

  ABSTRACT: UV-VIS spectroscopic investigations of interaction of bovine and human serum albumin with selected chalcones (1) and their cyclic chalcone analogues: (E)-2-(4’-X-benzylidene-1-tetralones (3), benzosuberones (4) with dimethylamino and methoxy substituents and (E)-2-(2’,4’-dimethox- ybenzylidene)-1-indanone (2) were performed in polar respiration medium. Absorption maxima of the tested compounds were investigated in the presence of bovine and human serum albumin at the 0, 10, 30 and 60 minute timepoints of the interaction. The absorbance of all studied compounds in the presence of proteins decreased after one hour of the reaction. Molecule 4a showed the strongest and fastest kinet initial interaction with both albumins.