111514-29-5Relevant articles and documents
SYNTHESIS AND COMPLEXING PROPERTIES OF 1,5,8,12-TETRAKIS(DIHYDROXYPHOSPHORYLMETHYL)-1,5,8,12-TETRAAZACYCLOTETRADECANE, A CYCLOPENDANT PHOSPHORORGANIC COMPLEXON
Pisareva, S. A.,Bel'skii, F. I.,Medved', T. Ya.,Kabachnik, M. I.
, p. 372 - 376 (1987)
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Equilibrium and kinetic properties of CuII cyclophane complexes: The effect of changes in the macrocyclic cavity caused by changes in the substitution at the aromatic ring
Verdejo, Begona,Basallote, Manuel Garcia,Ferrer, Armando,Manez, Maria Angeles,Hernandez, Juan Carlos,Chadim, Martin,Hodacova, Jana,Llinares, Jose Miguel,Soriano, Conxa,Garcia-Espana, Enrique
experimental part, p. 1497 - 1507 (2009/02/07)
The o-B232, m-B232 and p-B232 cyclophanes result from attaching the terminal amine groups of 1,4,8,11-tetraazaundecane (232) to the benzylic carbons of the corresponding o-, m- or p-xylanes. The cavity size of these cyclophanes changes moderately as a con
Methods of preparing manganese complexes of nitrogen-containing macrocyclic ligands
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, (2008/06/13)
The present invention is directed to low molecular weight mimics of superoxide dismutase (SOD) represented by the formula: STR1 wherein R, R', R1, R'1, R2, R'2, R3, R'3, R4, R'4, R5, R'5, R6, R'6, R7, R'7, R8, R'8, R9, and R'9 and X, Y, Z and n are as defined herein, useful as therapeutic agents for inflammatory disease states and disorders, ischemic/reperfusion injury, stroke, atherosclerosis, hypertension and all other conditions of oxidant-induced tissue damage or injury.