Results 161 to 170 of about 6,458 (220)
Antimicrobial Activity of Gallium(III) Compounds: Pathogen-Dependent Targeting of Multiple Iron/Heme-Dependent Biological Processes. [PDF]
Choi SR +3 more
europepmc +1 more source
Binding of a Co(III) Metalloporphyrin to Amines in Water: Influence of the pKa and Aromaticity of the Ligand, and pH-Modulated Allosteric Effect. [PDF]
Milanesi L +3 more
europepmc +1 more source
Less is more: miniaturized heme enzymes with broad reactivity. [PDF]
Leone L +4 more
europepmc +1 more source
Porphyrin Aggregation under Homogeneous Conditions Inhibits Electrocatalysis: A Case Study on CO2 Reduction. [PDF]
Branch KL, Johnson ER, Nichols EM.
europepmc +1 more source
Metalloporphyrins based artificial olfactory receptors
Metalloporphyrins offer almost unique opportunities to design artificial receptors for chemical sensors. These molecules can be tailored, at the synthetic level, changing in a almost controlled way the sensor selectivity that can be oriented toward ...
Corrado Di Natale +2 more
exaly +2 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Supramolecular Chemistry of Metalloporphyrins
Chemical Reviews, 2009Aslan Tsivadze +2 more
exaly +4 more sources
Metalloporphyrin phototoxicity
Journal of Photochemistry and Photobiology B: Biology, 1990The phototoxicities of six metalloporphyrin dimethylesters (i.e. cobalt (Co), copper (Cu), manganese (Mn), nickel (Ni), tin (Sn) and zinc (Zn) were investigated. Hemolysis of human erythrocytes and inactivation of two enzymes (acetylcholinesterase and beta-galactosidase) were used to assess the phototoxic efficacy of these metal chelates.
J, Scott +4 more
openaire +2 more sources
Halogenation of metalloporphyrins
Russian Journal of Bioorganic Chemistry, 2000We found that thionyl chloride can chlorinate porphyrin complexes with transient metals (Pd, Ni, or Cu) at the free β andmeso-positions of the porphyrin macrocycle. A more prolonged or rigorous treatment also causes the chlorination of side alkyl substituents, mainly, methyl groups.
V. D. Rumyantseva +3 more
openaire +1 more source
Spectroelectrochemistry of metalloporphyrins
Pure and Applied Chemistry, 1990Abstract
K. M. Kadish, X. Mu
openaire +1 more source

