摘要:
The invention provides methods of reducing the severity of oral and gastrointestinal mucositis, involving administration of a toll-like receptor 4 antagonist.
摘要:
The invention provides methods for treating and/or preventing cognitive impairments, dementia, or neurodegenerative diseases and disorders (e.g., Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis) in patients by administering therapeutically effective amounts of an AMPA receptor antagonist (e.g., 1,2-dihydropyridine compounds) and therapeutically effective amounts of nootropics (e.g., cholinesterase inhibitors) to patients. The invention also provides combinations, commercial packages, and pharmaceutical compositions comprising therapeutically effective amounts of AMPA receptor antagonists (e.g., 1,2- dihydropyridine compounds) and therapeutically effective amounts nootropics (e.g., cholinesterase inhibitors). The 1,2-dihydropyridine compound may be, for example, 3- (2-cyanophenyl)-5-(2-pyridyl)-l-phenyl-l,2-dihydropyridin-2-one. The cholinesterase inhibitor may be, for example, donepezil.
摘要:
A method of detecting cell death which comprises quantitating cytochrome C in a bodily fluid and detecting cell death based on the value thus determined; a method of quantitating cytochrome C in a bodily fluid by the sandwich method; and a cytochrome C-assay reagent for quantitating cytochrome C in a bodily fluid by the sandwich method which contains an antibody against cytochrome C.
摘要:
The present invention provides macrocyclic compounds, synthesis of the same and intermediates thereto. Such compounds, and compositions thereof, are useful for treating or preventing proliferative disorders Formula (F-4).
摘要:
It is an object of the present invention to provide a capsule anti-sticking agent which can provide excellent anti-sticking effect on a soft capsule without impairing various properties such as water activity, disintegration property and safety, a coated soft capsule of high quality which is coated with the capsule anti-sticking agent and excels in anti-sticking effect, and an efficient method for manufacturing the coated soft capsule. The present invention includes a capsule anti-sticking agent containing an enzymatically decomposed lecithin, a coated soft capsule wherein a surface is coated with the capsule anti-sticking agent, and a method for manufacturing the coated soft capsule in which a surface of a soft capsule is coated with the capsule anti-sticking agent.
摘要:
The present invention provides compounds having formula (I), wherein R 1 , R 2 , R 3 and n are as described generally and in classes and subclasses herein, and additionally provides pharmaceutical compositions thereof, and methods for the use thereof in the treatment of inflammatory or autoimmune and proliferative disorders and as inhibitors of cell adhesion molecule expression and inflammatory cytokine signal transduction generally.
摘要:
The present invention provides a DNA participating in biological transformation of a macrolide compound 11107B. The present invention provides, paticularly, a DNA participating in biological transformation of a macrolide compound 11107B represented by the formula (I) into a 16-position hydroxy macrolide compound 11107D represented by the formula (II), the DNA encoding a protein having 16-position hydroxylating enzymatic activity or ferredoxin, to a method of isolating the DNA, to a protein encoded by the DNA, a plasmid carrying the DNA, a transformant obtained by transforming using the plasmid and a method of producing a 16-position hydroxy compound by using the transformant.
摘要:
A compound represented by the following general formula, its salt or hydrates thereof: (I) wherein R1 represents methoxy, methyltio, ethyl, etc.; R5 and R6 independently represent each cyclopropylmethyl, (4-tetrahydropyranyl)methyl, etc.; and two of R40, R41 and R42 are C1-6 alkoxy while the remainder is methoxymethyl, etc. The above compound has an excellent antagonism to a corticotropin-releasing factor receptor.
摘要:
No example of binding of magnetic particles to mesenchymal cell, chondrocyte and other cells whose use in regenerative medicine, etc. can be expected is known. Thus, whether or not cells having magnetic particles bound thereto after administration are retained in local by outside magnetism and whether or not the cells can exhibit the intrinsic activity are studied. In particular, there are provided magnetic cells comprising mesenchymal cells or chondral cultured cells having magnetic particles bound to the surface thereof, which magnetic cells are administered into a body. The magnetic cells can be retained in a seat of disease for a prolonged period of time by applying magnetic field from outside. Further, a drug delivery system can be constructed by causing the magnetic cells to contain drugs.