Results 71 to 80 of about 1,137 (169)

Synthesis and cytotoxic activity of organotin(IV) diallyldithiocarbamate compounds as anticancer agent towards colon adenocarcinoma cells (HT-29). [PDF]

Saudi J Biol Sci, 2021
Haezam FN, Awang N, Kamaludin NF, Mohamad R.   +3 more
europepmc   +1 more source

In Vitro Evaluation of Antiproliferative Properties of Novel Organotin(IV) Carboxylate Compounds with Propanoic Acid Derivatives on a Panel of Human Cancer Cell Lines. [PDF]

Molecules, 2021
Pantelić NĐ, Božić B, Zmejkovski BB, Banjac NR, Dojčinović B, Wessjohann LA, Kaluđerović GN.   +6 more
europepmc   +1 more source

NEW HALO- AND ORGANOTIN (IV) PHENYLARSENIATO ADDUCTS AND DERIVATIVES

Scientific Study & Research: Chemistry & Chemical Engineering, Biotechnology, Food Industry, 2013
Four new phenylarseniato adducts and organotin derivatives have been synthesized and studied by infrared. The suggested structures are polymeric, (SnX4; X = Cl, Br) and SnPh3Cl while being discrete for SnPh2Cl(PhAsO3H)2isoBu2NH2. When OH- - - Cl, NH - - -
BOCAR TRAORE, LIBASSE DIOP , MAMADOU SIDIBE   +2 more
doaj  

Synthetic, Structural, and Biochemical Studies of Organotin(IV) With Schiff Bases Having Nitrogen and Sulphur Donor Ligands

Bioinorganic Chemistry and Applications, 2006
Three bidentate Schiff bases having nitrogen and sulphur donor sequences were prepared by condensing S-benzyldithiocarbazate ( NH 2 NHCS 2 CH 2 C 6 H 5 ) with heterocyclic aldehydes.
doaj  

NEW [SnR2(C2O4)2]2- (R = Ph, Bu) MOIETY CONTAINING ADDUCTS AND COMPLEXES: SYNTHESIS, INFRARED AND MOSSBAUER STUDIES

Scientific Study & Research: Chemistry & Chemical Engineering, Biotechnology, Food Industry, 2015
New oxalato and hydrogenoxalato organotin (IV) derivatives containing mono- and bichelating oxalates or a monochelating hydrogenoxalate, have been synthesized and characterized by elemental analyses, infrared and Mossbauer spectroscopy.
YAYA SOW, LIBASSE DIOP
doaj  

NEW ORGANOTIN (IV) FORMIATO ADDUCTS. SYNTHESIS AND SPECTROSCOPIC STUDIES

Scientific Study & Research: Chemistry & Chemical Engineering, Biotechnology, Food Industry, 2011
Five new formiato complexes have been synthesized and studied by spectroscopic methods. The structures, when the cations are involved through hydrogen bonds, are supramolecular. The anion behaves as a monocoordinating ligand. The existence of tetrahedral
Seydi Mansour Sy Seck, Libasse Diop, Lorenzo Stievano   +2 more
doaj  

Síntese e caracterização de compostos organometálicos de estanho (IV)

Química Nova, 1999
Organotin(IV) derivatives containing bulky R groups have been synthesized and characterized. It is discussed how their syntheses depend on the reaction conditions, such as stoichiometry of starting materials, bulkiness of the organo group attached to the
Lima Geraldo Magela de
doaj  

Cytotoxic Activity of Organotin(IV) Derivatives with Triazolopyrimidine Containing Exocyclic Oxygen Atoms. [PDF]

Molecules, 2020
Attanzio A, D'Agostino S, Busà R, Frazzitta A, Rubino S, Girasolo MA, Sabatino P, Tesoriere L.   +7 more
europepmc   +1 more source

Heptacoordination in Organotin(IV) Complexes: Spectroscopic and Structural Studies of 2,6-Diacetylpyridine bis(thiosemicarbazone)di-n-butyltin(IV) Chloride Nitromethane Solvate, [nBu2Sn(H2daptsc)]Cl 2?MeNO2 and of 2,6-Diacetylpyridine bis(semicarbazone)dimethyltin(IV) trans-Tetrachlorodimethylstannate(IV), [Me2Sn(H2dapsc)][Me2 SnCl4]

Journal of the Brazilian Chemical Society, 2002
Two new cases of heptacoordination in organotin(IV) complexes are described. Both possess pentagonal bipyramidal geometry and show the organic groups on the axial positions, with the ligands forming five bonds to tin(IV) on the equatorial plane.
Sousa Gerimário F. de, Valdés-Martínez Jesús, Pérez Georgina E., Toscano Rubén A., Abras Anuar, Filgueiras Carlos A. L.   +5 more
doaj  

Synergistic Potential of Organotin(IV) Carbodithioate Derivatives with Vitamins D and E in MCF-7 and MDA-MB-231 Breast Cancer Cells. [PDF]

Pharmaceuticals (Basel)
Kanwal B, Shaheen F, Shah SS, Cheema Y, Ali S, Hanif R.   +5 more
europepmc   +1 more source