Search results for "MIDI"
showing 10 items of 1431 documents
CCDC 249686: Experimental Crystal Structure Determination
2005
Related Article: V.Niel, A.L.Thompson, A.E.Goeta, C.Enachescu, A.Hauser, A.Galet, M.C.Munoz, J.A.Real|2005|Chem.-Eur.J.|11|2047|doi:10.1002/chem.200400930
CCDC 249688: Experimental Crystal Structure Determination
2005
Related Article: V.Niel, A.L.Thompson, A.E.Goeta, C.Enachescu, A.Hauser, A.Galet, M.C.Munoz, J.A.Real|2005|Chem.-Eur.J.|11|2047|doi:10.1002/chem.200400930
CCDC 249689: Experimental Crystal Structure Determination
2005
Related Article: V.Niel, A.L.Thompson, A.E.Goeta, C.Enachescu, A.Hauser, A.Galet, M.C.Munoz, J.A.Real|2005|Chem.-Eur.J.|11|2047|doi:10.1002/chem.200400930
CCDC 249687: Experimental Crystal Structure Determination
2005
Related Article: V.Niel, A.L.Thompson, A.E.Goeta, C.Enachescu, A.Hauser, A.Galet, M.C.Munoz, J.A.Real|2005|Chem.-Eur.J.|11|2047|doi:10.1002/chem.200400930
CCDC 1490105: Experimental Crystal Structure Determination
2016
Related Article: B. Abu Thaher, D. Schollmeyer, S. Laufer|2016|IUCrData|1|x161081|doi:10.1107/S2414314616010816
CCDC 987580: Experimental Crystal Structure Determination
2014
Related Article: Isabel Castro, M. Luisa Calatayud, Wdeson P. Barros, José Carranza, Miguel Julve, Francesc Lloret, Nadia Marino, and Giovanni De Munno|2014|Inorg.Chem.|53|5759|doi:10.1021/ic500544n
CCDC 297276: Experimental Crystal Structure Determination
2006
Related Article: J.Pasan, J.Sanchiz, C.Ruiz-Perez, J.Campo, F.Lloret, M.Julve|2006|Chem.Commun.||2857|doi:10.1039/b602144a
CCDC 949552: Experimental Crystal Structure Determination
2013
Related Article: Pilar Amo-Ochoa, Oscar Castillo, Carlos J. Gómez-García, Khaled Hassanein, Sandeep Verma, Jitendra Kumar, and Félix Zamora|2013|Inorg.Chem.|52|11428|doi:10.1021/ic401758w
Design, Synthesis and Biological Evaluation of Novel Pyrazolo[1,2,4]triazolopyrimidine Derivatives as Potential Anticancer Agents
2021
Three novel pyrazolo-[4,3-e][1,2,4]triazolopyrimidine derivatives (1, 2, and 3) were designed, synthesized, and evaluated for their in vitro biological activity. All three compounds exhibited different levels of cytotoxicity against cervical and breast cancer cell lines. However, compound 1 showed the best antiproliferative activity against all tested tumor cell lines, including HCC1937 and HeLa cells, which express high levels of wild-type epidermal growth factor receptor (EGFR). Western blot analyses demonstrated that compound 1 inhibited the activation of EGFR, protein kinase B (Akt), and extracellular signal-regulated kinase (Erk)1/2 in breast and cervical cancer cells at concentrations…
Water Adsorption Properties of Free and Dehydrated β-Cyclodextrin Studied by near Infrared Spectroscopy and Gravimetry
2016
β-cyclodextrin, like other carbohydrates has a tendency to adsorb water molecules and the properties are attributed to the hydroxyl groups in the molecules. β-cyclodextrin, the cyclic oligomer of glucose has a hydrophobic interior and hydrophilic exterior. The cyclic structure favours the formation of hydrogen bonds between the OH groups on the adjacent glucose units and affects the formation of hydrogen bonds with water molecules. The hydoxyl groups engaged in hydrogen bondings can be eliminated at high temperatures and the adsorption properties of the dehydrated β-cyclodextrin will depend on the new functional groups formed. The aim of the report is to discuss the issue of the water adsor…