130728-49-3Relevant articles and documents
Phenanthrolinic analogs of quinolones show antibacterial activity against M. tuberculosis
Coulibaly, Songuigama,Cimino, Mena,Ouattara, Mahama,Lecoutey, Cédric,Buchieri, Maria V.,Alonso-Rodriguez, Noelia,Briffotaux, Julien,Mornico, Damien,Gicquel, Brigitte,Rochais, Christophe,Dallemagne, Patrick
, (2020)
Several phenanthrolinic analogs of quinolones have been synthesized and their antibacterial activity tested against Mycobacterium tuberculosis, other mycobacterial species and bacteria from other genera. Some of them show high activity (of the range obser
Epimorphic Regeneration and Related Hidrogel Delivery Systems
-
Paragraph 0102, (2016/03/12)
Methods and compositions are described for enhancing tissue regeneration or wound repair in a mammalian subject comprising a composition comprising (a) a proline hydroxylase inhibitor component or molecule that increases or upregulates HIF1a and (b) a carrier component comprising a hydrogel.
Synthesis of a novel pentacycle: 8-Methyl-10-phenylpyrazolo[4′, 3′: 5,6]-pyrano[3,2-c]-[1,10]phenanthrolin-7(10H)-one
Eller,Habicht,Holzer
experimental part, p. 709 - 714 (2009/04/06)
The title compound - a derivative of a hitherto unknown pentacyclic ring system - results from the reaction of 3-methyl-1-phenyl-2-pyrazolin-5-one and 4-chloro-1,10-phenanthroline-3-carbonyl chloride in the presence of Ca(OH) 2 in boiling 1,4-dioxane.
The inhibition of factor inhibiting hypoxia-inducible factor (FIH) by β-oxocarboxylic acids
Banerji, Biswadip,Conejo-Garcia, Ana,McNeill, Luke A.,McDonough, Michael A.,Buck, Matthew R. G.,Hewitson, Kirsty S.,Oldham, Neil J.,Schofield, Christopher J.
, p. 5438 - 5440 (2008/01/27)
Cyclic β-oxocarboxylic acids inhibit factor inhibiting hypoxia-inducible factor via ligation to the active site iron. The Royal Society of Chemistry 2005.