[1] Calliste, CA, Le Bail, JC, Trouillas, P, Pouget, C, Habrioux, G, Chulia, AJ, Duroux, JL. (2001). Chalcones: structural requirements for antioxidant, estrogenic and antiproliferative activities. Anticancer Research, 21(6A),3949-3956.
[2] Allemão, GSB, Viana, AM, Bandeira, FJA, Matos. (2003). Analgesic and antiinflammatory effects of chalcones isolated from Myracrodruon urundeuva .Phytomedicine, 10 (2-3), 189-195.
[3] Lawrence, NJ, Patterson, RP, Ooi, LL, Cook, D, Ducki, S. (2006). Effects of α-substitutions on structure and biological activity of anticancer chalcones, Bioorganic & Medicinal Chemistry Letters, 16 (22), 5844–5848.
[4] Nowakowska, Z, Kędzia, B, Schroeder, G. (2008). Synthesis, physicochemical properties and antimicrobial evaluation of new (E)-chalcones, European Journal of Medicinal Chemistry, 43 (4), 707–713.
[5] Batovska, DI, Todorova, IT. (2010)..Trends in utilization of the pharmacological potential of chalcones. Current Clinical Pharmacology. 5(1), 1-29.
[6] Jeon, JH, Kim, SJ, Kim, CJ, Kim, JK, Jun, JG. (2012). Synthesis of Biologically Active Chalcones and their Anti-inflammatory Effects, Bulletin of Korean Chemical Society, 33 (3), 953-957.
[7] Mohammed, JH. (2015). Biological Activities Importance of Chalcone Derivatives, International Journal of Chemical and Biomolecular Science, 1( 3), 107-112.
[8] Diaz-Tielas, C, Grana, E, Reigosa, MJ, Sanchez-Moreiras, AM. (2016). Biological activities and novel applications of Chalcones. Planta Daninha, 34(3), http://dx.doi.org/10.1590/s0100-83582016340300022 ,.
[9] Ramkumar, V, Anandhi, S, Kannan , P, Gopalakrishnan, R. (2015). Substitution effect on chalcone based materials for corrosion and photocrosslinking applications, , RSC Adv., 5, 586-596.
[10] 10. Forkmann , G, Martens, S. (2001). Metabolic engineering and applications of flavonoids, Current Opinion in Biotechnology, 12(2), 155–160.
[11] Buytenhuys, FA. (1981). Ion chromatography of inorganic and organic ionic species using refractive index detection, Journal of Chromatography A, 218, 57-64.
[12] Clement , A, Yong, D, Brechet, C. (1992). Simultaneous Identification of Sugars by HPLC Using Evaporative Light Scattering Detection (ELSD) and Refractive Index Detection (RI). Application to Plant Tissues, Journal of Liquid Chromatography , 15 (5), 805-817.
[13] Strop, P, Brunger, AT. (2005). Refractive index-based determination of detergent concentration and its application to the study of membrane proteins, Protein Science, 14(8), 2207–2211.
[14] Ji, J. (1995). A Climate-Vegetation Interaction Model: Simulating Physical and Biological Processes at the Surface, Terrestrial Ecosystem Interactions with Global Change, Journal of Biogeography, 22( 2/3), 445-451.
[15] Owens, RM, Malliaras, GG. (2010). Organic Electronics at the Interface with Biology, MRS BULLETIN, 35, 449-456.
[16] Tunc, S, Duman, O. (2007). , Investigation of interactions between some anionic dyes and cationic surfactants by conductometric method , Fluid Phase Equilibria, 251(1), 1–7.
[17] Kubik, T, Bogunia-Kubik, K., Sugisaka, M.(2005). Nanotechnology on Duty in Medical Applications, Current Pharmaceutical Biotechnology, 6(1), 17-33.
[18] Muhammad-Tahir, Z, Alocilja, EC. (2003). A conductometric biosensor for biosecurity, Biosensors and Bioelectronics, 18,(5–6), 813–819.
[19] Nyamsi Hendji. AM, Jaffrezic-Renault. N, Claude Martelet, Shul'ga, AA, Dzydevich, SV, Soldatkin, AP, El'skaya. A.V. (1994). Enzyme biosensor based on a micromachined interdigitated conductometric transducer: application to the detection of urea, glucose, acetyl- andbutyrylcholine chlorides, Sensors and Actuators B: Chemical, 21(2),123-129,
[20] Joseph, A, Pai, A, Srinivasan, KK, Kedar, T, Thomas, AT, Jessy, EM, Singala, RK. (2010). Synthsis and anticancer activity of some novel 3-(1,3,4-thiadiazol-2-yl)-quinazolin-4-(3H)-ones, E. Journal of Chemistry., 2, 159-167.
[21] Ding, Z, Zhang, R, Long, B, Liu, L, Tu, H. (2010). Solubilities of m-phthalic acid in petroleum ether and its binary solvent mixture of alcohol + petroleum ether, Fluid Phase Equilibria, 292,96-103.
[22] Kuhs, M, Svard, M, Rasmuson, AC. (2013). Thermodynamics of fenoxycarb in solution, Journal of Chemical Thermodynamics. 66, 50–58.
[23] Seleem, HS, Shetary, BAE, Khalil, SME, Shebl, M. (2003). Potentiometric and spectrophotometric studies of the complexation of Schiff-base hydrazones containing the pyrimidine moiety, Journal of Serbian Chemical Society. 68, 729-748.
[24] Gorgiin, OC, Ozkutuk, K, Sakarya HC. (2009). Determination and evaluation of acid dissociation constants of some novel benzothiazole Schiff bases and their reduced analogs by spectroscopy, Arkivoc, 7, 197-209.
[25] Sanli,S, Altun,Y, Sanli, N, Alsancak, G, Beltran, ,JL. (2009). Solvent effects on pKa values of some substituted sulfonamides in acetonitrile-water binary mixtures by the UV-spectroscopy method, Journal of Chemical Engineering Data, 54, 3014–3021.
[26] Riddick, JA, Bunger, WB, Sakano, T. 1986. Organic Solvents-Physical Properties and Methods of Purification, Techniques of Chemistry, New York.
[27] Lorentz, HA, Lorentz, 1906. Theory of electronics, Leipzig.
[28] Apelblat, A, Manzurola, E. (1987). Solubility of oxalic, malonic, succinic, adipic, maleic, malic, citric, and tartaric acids in water from 278.15 to 338.15 K, Journal of Chemical Thermodynamics.19, 317–320.
[29] Glasstone, S. Textbook of Physical Chemistry. 2nd Edition. The Macmillan Press Ltd. P 828.
[30] Perlovich, GL, Kurkov, AN, Brandle, B. (2006). The difference between partitioning and distribution from a thermodynamic point of view. NSAIDs as an example.” European Journal of Pharma Biopharmaceutical, 27, 150-157.
[31] Szterner, P. (2008). Solubility in water of uracil and its halogenated derivatives. Journal of Chemical Engineering Data, 53, 1738-1744.
[32] Kalsi, PS. Organic Reactions and their Mechanisms. (2nd Edition), New Age International (P) Limited, 119.
[33] Turkoglu, G, Berber, H, Yaman Ozkutuk, M. (2014). Spectroscopic determination of acidity dissociation constants of symmetric Schiff base derivatives, Gazi Uni. J. Sci., 27(2), 771-783.