摘要:
The present disclosure provides a composition for the prophylaxis or treatment of diseases (e.g., infectious disease, allergy or autoimmune disease). The present disclosure provides a composition, a medicament, a kit, and the like for the prophylaxis or treatment of the disease of a test subject. The composition, medicament, kit, and the like contain a non-causative factor antigen component that is neither derived from nor cross-reactive with the causative factor of the disease, and is administered under conditions where a causative factor antigen component derived from and/or cross-reactive with a causative factor of the target disease is present in the target.
摘要:
The present disclosure provides a composition, a combination, a medical device, and the like, that use an extract from Mycobacterium tuberculosis and are a new modality for treating, preventing, or preventing the recurrence of a cancer or a tumor. The present disclosure provides a composition, a combination, and a medical device, that use an extract from Mycobacterium tuberculosis and are a new modality for treating, preventing, or preventing the recurrence of a cancer or a tumor, each of which comprises an immune checkpoint inhibitor and a dendritic cell direct activator or means.
摘要:
To provide an enteric coated tablet containing a large amount of medicinal ingredient and having sufficient impact resistance, without forming a thick enteric coating layer. The enteric coated tablet contains (A) a core tablet containing a medicinal ingredient and having a weight of 1,000 mg or more; (B) a coating layer containing a water-soluble polymer applied onto the surface of the core tablet; and (C) an enteric coating layer dissolving at pH 7 or higher which is applied onto the surface of the coating layer containing a water-soluble polymer, wherein the sum of the polymer amount of the coating layer (B) and the polymer amount of the coating layer (C) is 10 to 18 mg/cm 2 , the polymer amount of the coating layer (B) is 6 to 12 mg/cm 2 , and the polymer amount of the coating layer (C) is 3 to 6 mg/cm 2 .
摘要翻译:提供含有大量药用成分并且具有足够抗冲击性的肠溶衣片剂,而不形成厚的肠溶衣层。 肠溶片包含(A)含有药物成分并且重量为1,000mg以上的核心片剂; (B)涂布在芯片表面上的水溶性聚合物的涂层; 和(C)在pH7以上溶解的肠溶衣层,其涂布在含有水溶性聚合物的被覆层的表面上,其中,涂布层(B)的聚合物量与聚合物的量 涂层(C)为10〜18mg / cm 2,涂层(B)的聚合物的量为6〜12mg / cm 2,涂层(C)的聚合物量为3〜6mg / cm 2。
摘要:
Provided is a method for effectively producing a 4,5-dialkoxy-2-hydroxybenzoic acid from an inexpensive raw material. A method for producing a 2-bromo-4,5-dialkoxybenzoic acid represented by the following formula (2): (wherein each of R 1 and R 2 represents a lower alkyl group), the method including causing a 3,4-dialkoxybenzoic acid represented by the following formula (1): (wherein R 1 and R 2 have the same meanings as defined above) to react with bromine in concentrated hydrochloric acid.
摘要:
To provide a peroral tablet for bowel cleansing which leaves no remains in the intestinal tract after bowel cleansing, which exhibits a dissolution property equivalent to that of conventional sodium phosphate-containing tablets including crystalline cellulose, and which is a small-size agent readily taken by a subject. The peroral tablet for bowel cleansing containing the following ingredients (A) and (B): (A) 80 to 95 mass% of sodium phosphate, and (B) (B1) 7 to 11 mass% of hydroxypropyl cellulose which has such a particle size that ≥99% of the particles thereof pass through a mesh having an opening of 350 µm and whose 2-mass% aqueous solution has a viscosity of 2.0 to 10.0 mPa·s, (B2) 5 to 13 mass% of hydroxypropyl cellulose which has such a particle size that ≥99% of the particles thereof pass through a mesh having an opening of 150 µm and whose 2-mass% aqueous solution has a viscosity of 3.0 to 5.9 mPa·s, or (B3) 7 to 11 mass% of hydroxypropyl cellulose which has such a particle size that ≥99% of the particles thereof pass through a mesh having an opening of 150 µm and whose 2-mass% aqueous solution has a viscosity of 6.0 to 4,000 mPa·s, and having a water-insoluble ingredient content of 5 mass% or less.
摘要:
A novel carbazole derivative which has the excellent functions of reducing the weight of fat tissues and lowering the blood sugar level and the blood lipid level. It is useful as a preventive/therapeutic agent for fatty liver, obesity, lipid metabolism abnormality, visceral fat, diabetes, hyperlipemia, impaired glucose tolerance, hypertension, non-alcoholic fatty liver, or non-alcoholic steatohepatitis. It is a carbazole derivative represented by the following general formula (I). (In the formula (I), ring A represents phenyl, etc.; X represents -O-, etc.; Y represents =N-, etc.; a and b each represents methylene, etc.; V and Z each represents -O-, etc.; W represents C1-10 alkylene in which one or two hydrogen atoms may be replaced with phenyl or C1-5 alkyl, or represents 1,2-phenylene, 1,3-cyclohexyl, etc.; R1 represents methyl, etc.; R2 represents methoxy, etc.; and R3 represents carboxy, etc.)
摘要:
A production method of a compound represented by formula (2):
(wherein ring A represents a benzene ring or a 6-membered aromatic heterocycle; R 1 represents a hydrogen atom, a C 1-6 alkyl group, a halogen atom, a nitro group, an amino group, a mono-C 1-6 alkylamino group, or a di-C 1-6 alkylamino group; and at least one of R 2 , R 3 , and R 4 represents a methoxy group, and the rest each represents a hydrogen atom, a C 1-6 alkyl group, a halogen atom, a nitro group, an amino group, a mono-C 1-6 alkylamino group, or a di-C 1-6 alkylamino group), comprising reacting a compound represented by formula (1):
(wherein ring A and R 1 , R 2 , R 3 , and R 4 are the same as defined above) with a Lewis acid selected from BF 3 , TiCl 4 , and AlCl 3 in esteric, ketonic or amidic solvents selected from ethyl acetate, methyl acetate, butyl acetate, isobutyl acetate, acetone, 2-butane, cyclohexane, cyclopentane, dimethylformamide, and dimethylacetamide, with the proviso that when the Lewis acid is BF 3 , an alkali metal bromide or an alkali metal iodide coexists.
(wherein ring A represents a benzene ring or a 6-membered aromatic heterocycle; R 1 represents a hydrogen atom, a C 1-6 alkyl group, a halogen atom, a nitro group, an amino group, a mono-C 1-6 alkylamino group, or a di-C 1-6 alkylamino group; and at least one of R 2 , R 3 , and R 4 represents a methoxy group, and the rest each represents a hydrogen atom, a C 1-6 alkyl group, a halogen atom, a nitro group, an amino group, a mono-C 1-6 alkylamino group, or a di-C 1-6 alkylamino group).
摘要:
To provide a pharmaceutical agent or an antitumor agent useful for the treatment and/or prevention of gastrointestinal cancer, leukemia, pituitary tumor, small cell lung cancer, thyroid cancer, and neuroastrocytoma. The antitumor agent containing, as an active ingredient, a 1,5-benzodiazepine derivative represented by the following formula (1) : (wherein R 1 represents a C 1-6 alkyl group; R 2 represents a phenyl group or a cyclohexyl group; and Y represents a single bond or a C 1-4 alkylene group) or a pharmaceutically acceptable salt thereof.