Search results for "Furan"
showing 10 items of 667 documents
CCDC 922164: Experimental Crystal Structure Determination
2022
Related Article: Liāna Orola, Anatoly Mishnev, Dmitrijs Stepanovs, Agris Bērziņš|2022|ChemRxiv|||doi:10.26434/chemrxiv-2022-rb0xk
CCDC 1421617: Experimental Crystal Structure Determination
2016
Related Article: Jakob Wudarczyk, George Papamokos, Vasilis Margaritis, Dieter Schollmeyer, Felix Hinkel, Martin Baumgarten, George Floudas, Klaus Müllen|2016|Angew.Chem.,Int.Ed.|55|3220|doi:10.1002/anie.201508249
CCDC 838880: Experimental Crystal Structure Determination
2012
Related Article: J.Barjau, J.Fleischhauer, G.Schnakenburg, S.R.Waldvogel|2011|Chem.-Eur.J.|17|14785|doi:10.1002/chem.201102722
CCDC 1474771: Experimental Crystal Structure Determination
2016
Related Article: Uğur Kaya, Pankaj Chauhan, Kristina Deckers, Rakesh Puttreddy, Kari Rissanen, Gerhard Raabe, Dieter Enders|2016|Synthesis|48|3207|doi:10.1055/s-0035-1561468
SYNTHESIS AND ANTITUMOR ACTIVITY OF 2,5-BIS(3'-INDOLYL)-FURANS AND 3,5-BIS(3'-INDOLIY)-ISOXAZOLES, NORTOPSENTIN ANALOGUES
2010
Abstract A series of novel 2,5-bis(3′-indolyl)furans and 3,5-bis(3′-indolyl)isoxazoles were synthesized as antitumor agents. The antiproliferative activity was evaluated in vitro toward diverse human tumor cell lines. Initially 5 isoxazoles and 3 furan derivatives were tested against a panel of 10 human tumor cell lines and the most active derivatives 3c and 4a were selected to be evaluated in an extended panel of 29 cell lines. By exhibiting mean IC50 values of 17.4 μg/mL (3a) and 20.5 μg/mL (4c), in particular 4c showed a high level of tumor selectivity toward the 29 cell lines.
CCDC 891057: Experimental Crystal Structure Determination
2012
Related Article: G.Bentabed-Ababsa, S.Hamza-Reguig, A.Derdour, L.R.Domingo, J.A.Saez, T.Roisnel, V.Dorcet, E.Nassar, F.Mongin|2012|Org.Biomol.Chem.|10|8434|doi:10.1039/c2ob26442k
CCDC 2077766: Experimental Crystal Structure Determination
2022
Related Article: Aija Trimdale, Anatoly Mishnev, Agris Bērziņš|2021|Pharmaceutics|13|734|doi:10.3390/pharmaceutics13050734
CCDC 1862873: Experimental Crystal Structure Determination
2018
Related Article: A. Zagidullin, D. Islamov, E. Oshchepkova, P. Lonnecke, V. Miluykov|2018|Acta Crystallogr.,Sect.E:Cryst.Commun.|74|1336|doi:10.1107/S2056989018011775
CCDC 1816139: Experimental Crystal Structure Determination
2018
Related Article: Aysun Çapcı Karagöz, Christoph Reiter, Ean-Jeong Seo, Lisa Gruber, Friedrich Hahn, Maria Leidenberger, Volker Klein, Frank Hampel, Oliver Friedrich, Manfred Marschall, Barbara Kappes, Thomas Efferth, Svetlana B. Tsogoeva|2018|Bioorg.Med.Chem.|26|3610|doi:10.1016/j.bmc.2018.05.041
Sensitivity of 3He NMR parameters to the proximity of heterocyclic rings. The helium–furan dimer
2014
The potential of NMR technique in probing the interaction between a noble gas atom (used as a spectroscopic probe) and five-membered heterocyclic systems was theoretically studied. Selected 3He NMR parameters of free noble gas atom and its dimer were calculated using density functional theory with three functionals (M06-2X, CAM-B3LYP, and APFD), combined with dedicated polarization-consistent basis sets, and critically compared with theoretical high level calculations from the literature. The change of sotropic nuclear magnetic shielding of free noble gas atom in the presence of furan (3He placed above he middle of the ring and used as NMR probe) increased with its proximity to the heterocy…