587-02-0Relevant articles and documents
HZSM-5-Catalyzed Isomerization of Alkylanilines
Weigert, F. J.
, p. 3296 - 3298 (1987)
Zeolite HZSM-5 catalyzes the equilibration of toluidines and ethylanilines by an intramolecular 1,2-shift mechanism.The three xylidines with the 1,2,4-substitution pattern are also interconverted by this catalyst.Larger methylanilines are neither formed nor consumed by the catalyst.
Development of LM98, a Small-Molecule TEAD Inhibitor Derived from Flufenamic Acid
Mélin, Léa,Abdullayev, Shuay,Fnaiche, Ahmed,Vu, Victoria,González Suárez, Narjara,Zeng, Hong,Szewczyk, Magdalena M.,Li, Fengling,Senisterra, Guillermo,Allali-Hassani, Abdellah,Chau, Irene,Dong, Aiping,Woo, Simon,Annabi, Borhane,Halabelian, Levon,LaPlante, Steven R.,Vedadi, Masoud,Barsyte-Lovejoy, Dalia,Santhakumar, Vijayaratnam,Gagnon, Alexandre
, p. 2982 - 3002 (2021/08/03)
The YAP-TEAD transcriptional complex is responsible for the expression of genes that regulate cancer cell growth and proliferation. Dysregulation of the Hippo pathway due to overexpression of TEAD has been reported in a wide range of cancers. Inhibition of TEAD represses the expression of associated genes, demonstrating the value of this transcription factor for the development of novel anti-cancer therapies. We report herein the design, synthesis and biological evaluation of LM98, a flufenamic acid analogue. LM98 shows strong affinity to TEAD, inhibits its autopalmitoylation and reduces the YAP-TEAD transcriptional activity. Binding of LM98 to TEAD was supported by 19F-NMR studies while co-crystallization experiments confirmed that LM98 is anchored within the palmitic acid pocket of TEAD. LM98 reduces the expression of CTGF and Cyr61, inhibits MDA-MB-231 breast cancer cell migration and arrests cell cycling in the S phase during cell division.
Zeolite-Encaged Isolated Platinum Ions Enable Heterolytic Dihydrogen Activation and Selective Hydrogenations
Dai, Weili,Deng, Xin,Guan, Naijia,Li, Landong,Liu, Runze,Ma, Ding,Qin, Bin,Qin, Xuetao,Wu, Guangjun
supporting information, p. 20898 - 20906 (2021/12/14)
Understanding the unique behaviors of atomically dispersed catalysts and the origin thereof is a challenging topic. Herein, we demonstrate a facile strategy to encapsulate Ptδ+ species within Y zeolite and reveal the nature of selective hydrogenation over a Pt@Y model catalyst. The unique configuration of Pt@Y, namely atomically dispersed Ptδ+ stabilized by the surrounding oxygen atoms of six-membered rings shared by sodalite cages and supercages, enables the exclusive heterolytic activation of dihydrogen over Ptδ+···O2- units, resembling the well-known classical Lewis pairs. The charged hydrogen species, i.e., H+ and Hδ-, are active reagents for selective hydrogenations, and therefore, the Pt@Y catalyst exhibits remarkable performance in the selective hydrogenation of α,β-unsaturated aldehydes to unsaturated alcohols and of nitroarenes to arylamines.
Pd-Nanoparticles immobilized organo-functionalized SBA-15: An efficient heterogeneous catalyst for selective hydrogenation of C–C double bonds of α,β-unsaturated carbonyl compounds
Burri, David Raju,Narani, Anand,Natte, Kishore,Reddy Kannapu, Hari Prasad
, (2020/10/05)
A novel PdNPs/SBA-NH2-LA catalyst has been prepared by a post-synthetic grafting approach via successive anchoring of propylamine (SBA-NH2) and lipoic acid (SBA-NH2-LA) functional groups followed by palladium nanoparticles immobilization. The Physico-chemical properties of the catalyst were extensively investigated by XRD, N2 adsorption-desorption, XPS, FT-IR, and TEM analysis. The PdNPs/SBA-NH2-LA catalyst is found to be highly selective for the hydrogenation of C–C double bonds of α, β-unsaturated carbonyl compounds. Excellent conversion (95–99 %) and selectivity (>99 %) with high turn over frequency (330?1065 h?1) achieved at room temperature under atmospheric hydrogen pressure within 30?90 min of reaction time. This kind of high activity is expected from its structural and textural integrity of the catalyst.
