Abstract:
Methods for preventing or reducing the formation of scale in a wet-process phosphoric acid production process by intermixing a scale inhibiting reagent at one or more step of the phosphoric acid production process in an amount sufficient to prevent or reduce scale are provided.
Abstract:
The present disclosure encompasses pharmaceutically acceptable antimicrobial compositions of an amount of levulinic acid and sodium dodecyl sulfate effective in reducing the microbial population of an internal cranial cavity of a recipient human or animal subject. The disclosure also provides methods for reducing a microbial population of an internal cranial cavity of a recipient human or animal comprising contacting the oral cavity or sinuses of the subject with a composition comprising between about 0.5% to about 5% by weight per volume of levulinic acid and between about 0.05% to about 2% by weight per volume of sodium dodecyl sulfate (SDS) and for a period effective in reducing a microbial population of the oral cavity.
Abstract:
Provided herein are (8 S , 9 R )-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-lH-1,2,4-triazol-5- yl)-8,9-dihydro-2 H -pyrido[4,3,2- de ]phthalazin-3(7 H )-one tosylate salt forms, including crystalline forms, and methods of their preparation. Pharmaceutical compositions comprising a (8 S ,9 R )-5-fiuoro-8-(4-fluorophenyl)-9-(1-methyl-1 H -1,2,4-triazol-5-yl)-8,9-dihydro-2 H - pyrido[4,3,2- de ]phthalazin-3(7 H )-one tosylate salt are also provided, as are methods of using (8 S ,9 R )-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1 H -1,2,4-triazol-5-yl)-8,9-dihydro-2 H - pyrido[4,3,2- de ]phthalazin-3(7 H )-one tosylate salt to treat a disease or condition, such as a cancer.
Abstract:
The present invention relates generally to the field of brain health, brain protection, maintenance of cognitive function, prevention of cognitive decline and cognitive disorders. Neuronal cells in the brain can be protected. Also cognitive performance can be increased.
Abstract:
The present invention relates generally to the field of neuronal health and neuronal protection. One embodiment of the present invention relates to a composition that can be used for the protection of the enteric nervous system from neurodegeneration. Disorders linked to an impaired enteric nervous system can be treated or prevented by the administration of lactoferrin containing compositions according to the present invention.
Abstract:
A compound having the structure set forth in Formula (I) and Formula (II) wherein the substituents Y, Z, A, B, R1, R2, R3, R4 and R5 are as defined herein. Provided herein are inhibitors of poly(ADP-ribose)polymerase activity. Also described herein are pharmaceutical compositions that include at least one compound described herein and the use of a compound or pharmaceutical composition described herein to treat diseases, disorders and conditions that are ameliorated by the inhibition of PARP activity.
Abstract:
An electrostatic modification reagent as described herein. The electrostatic modification reagent may be used in an electric separation process for separating components from a mineral ore or sand.
Abstract:
Using NMRScore to generate an RMSD and evaluating whether the RMSD is below 1 ppm, in order to indicate that a docking software generated pose is a good match with the experimental assessment of a paradigm protein target and paradigm ligand, and therefore that the pose will be useful and accurate for the same target and similar ligands, or similar targets and the same ligands.
Abstract:
A method of improving learning and/or memory behavior in a mammal is described which involves administering to the mammal casein glycomacropeptide in an amount sufficient to improve learning and/or memory behavior in the mammal.
Abstract:
The invention relates to a process for the preparation of a polymer comprising at least aliphatic or aromatic hydrocarbyl C 2 - C 20 mono or multiolefins in the presence of a catalyst, an activator wherein the catalyst and the activator are combined in a catalyst system according to formula (I) wherein R, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 can independently be chosen from substituted or unsubstituted alkyl or aryl groups having 1 to 20 carbon atoms, M is a group 4, or 5 metal; with valency v, L a is a coordinating Lewis base with a = 0, 1, or 2, being the number of ligands L and, X i is an anionic ligand, with i = v-3, being the number of anionic ligands, the catalyst does not comprise boron and fluor atoms.