Anticancer Agents Med Chem
July 2019
Background: In recent years, targeted cancer treatment methods at various molecular levels have been developed for Non-Small Cell Lung Cancer (NSCLC), one of two major subtypes of lung cancer. miRNAbased clinical trials are currently the preferred targeted therapeutic strategy. Also, ceRNAs (competing endogenous RNA) would be the newest and the most effective approach to uncover novel interactions between mRNAs and miRNAs in NSCLC carcinogenesis.
View Article and Find Full Text PDFActa Crystallogr Sect E Struct Rep Online
December 2007
In the centrosymmetric title complex, [Co(C(7)H(4)NO(3)S)(2)(C(6)H(15)N(3))(2)], the Co(II) ion is coordinated by two saccharinate (sac) anions and two neutral 2-piperazin-1-ylethanamine (ppzea) ligands, showing a distorted octa-hedral coordination. Sac is O-bonded via the carbonyl group, while ppzea acts as an N,N'-bidentate chelating ligand. The mol-ecules are connected by N-H⋯N and N-H⋯O hydrogen bonds, forming a linear chain running parallel to the crystallographic a axis.
View Article and Find Full Text PDFThe title complexes [M(sac)(2)(mpy)(2)] [sac is saccharinate (C(7)H(4)NO(3)S) and mpy is 2-pyridylmethanol (C(6)H(7)NO)], with M = Zn(II) and Cd(II), are isostructural and consist of neutral molecules. The Zn(II) or Cd(II) cations are octahedrally coordinated by the two neutral mpy and two anionic sac ligands. The mpy ligand acts as a bidentate donor through the amine N and hydroxyl O atoms.
View Article and Find Full Text PDFBis(pyridine-2,6-dimethanol-N,O,O')cobalt(II) disaccharinate dihydrate, [Co(C7H9NO2)2](C7H4NO3S)2*2H2O, (I), and bis(pyridine-2,6-dimethanol-N,O,O')copper(II) disaccharinate dihydrate, [Cu(C7H9NO2)2](C7H4NO3S)2*2H2O, (II), collectively [M(dmpy)2](sac)2*2H2O (where M is Co(II) or Cu(II), sac is the saccharinate anion and dmpy is pyridine-2,6-dimethanol), are isostructural. The [M(dmpy)2]2+ cations exhibit distorted octahedral geometry in which the two neutral dmpy species act as tripodal N,O,O'-tridentate ligands. The crystal packing is determined by hydrogen bonding, as well as by weak pyridine-saccharinate pi-pi-stacking interactions.
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