180 results about "Pyrazoline" patented technology

Pharmaceutical compositions and compounds are provided. The compounds of the invention demonstrate anti-proliferative activity, and may promote apoptosis in cells lacking normal regulation of cell cycle and death. In one embodiment of the invention, pharmaceutical compositions of the compounds in combination with a physiologically acceptable carrier are provided. The pharmaceutical compositions are useful in the treatment of hyperproliferative disorders, which disorders include tumor growth, lymphoproliferative diseases, angiogenesis. The compounds of the invention are substituted pyrazoles and pyrazolines.

The present invention provides novel pyrazolines that are useful as cannabinoid receptor antagonists/inverse agonists and pharmaceutical compositions thereof and methods of using the same for treating obesity, diabetes, dyslipidemias, cardiovascular disorders, hepatic disorders, and a combination thereof.

The present invention relates to a photosensitive resin composition superior in sensitivity with respect to an exposure light source having the wavelength of 405+/-10 nm and resolution, having satisfactory tenting properties, and capable of being developed by an alkali aqueous solution, a photosensitive resin laminated body using the photosensitive resin composition, a method for forming a resist pattern on the substrate using the photosensitive resin stacked body, and the use of the resist pattern. The photosensitive resin composition contains: (a) a thermoplastic copolymer of 20-90% including alpha, beta-unsaturated carboxyl groups containing a monomer as a copolymerization component, and having an acid equivalent of 100-600 and weight average molecular weight of 5,000-500,000; (b) an addition polymerization monomer of 5-75% having a terminal ethylenic unsaturated group; (c) a photopolymerization initiator of 0.01-30%; and (d) a specific pyrazoline compound of 0.001-10%, and includes, (b) as the addition-polymerizable monomer containing addition-polymerizable monomer with specific structure.

The present invention discloses a kind of 1,3-aryl substituted pyrazoline whose delta-position contains ester group and its liquid phase synthesis method. In the organic solvent, in the presence of alkali the substituted acryloyl chlorine is coupled on the soluble resin, under the action of organic alkali the isoequivalent aromatic aldehyde and aromatic hydrazine hydrochloride are mixed to obtain the correspondent hydrazone, then the substituted acrylic ester loaded by soluble resin and oxidant are added, and the above-mentioned materials are undergone the ring-forming reaction of one-pot method so as to obtain the 1,3-aryl substituted pyrazoline whose delta-position contains ester group which is loaded on the resin. In the alcohol solvent and under the catalysis of correspondent alcohol sodium the pyrazoline can be separated from soluble resin so as to obtain the invented product with high yield rate and high purity. It can be developed into medicine, pesticide and light sensitive material.

The invention relates to application of an edaravone and borneol medicinal composition to preparation of a medicament for preventing and/or treating myocardial ischemia-reperfusion injury.

This invention is a wide-frequency vibration and high light sensitive azo or phthalocyanine compound single layer organic photoelectricity conductor and its process method, which belongs to organic photoelectricity conductor technique field. The material mainly adopts charge carrier generation material and charge carrier transmission material and resin and conductive base material with certain proportion to form organic photoelectricity coating liquid and adopts the dipping and coating method. And the charge carrier generation material is the compound material of oxazolyl bisazo or metal phthalocyanine and the charge carrier transmission material adopts compounds of triaryl amine and hydrazone compound, and pyrazoline compound.

The invention provides a burley tobacco nicotine extract product and an extraction technology for the same. The burley tobacco nicotine extract product is composed of the following components according to weight by percentage: 94 to 97% of nicotine, 0.4 to 0.6% of cotinine, 0.2 to 0.3% of N-methy pridine carboxamide, 0.1 to 0.2% of benzofuran, 0.1 to 0.2% of indol, 0.1 to 0.2% of 5.5-dimethyle pyrazoline, 0.05 to 0.15% of acetyl pridine, 0.05 to 0.1% of megastigmatrienone, 0.02 to 0.05% of hydroxide radical damascenone, 0.02 to 0.05% of palmitic acid and 0.01 to 0.04% of demethylation nicotine. The burley tobacco nicotine extract product has nigh nicotine content and has special flavor when prepared for electronic tobacco juice; electronic cigarette satisfaction can be enhanced; and the electronic cigarette can be closer to cigarette taste.

The invention provides pyrazoline sensitizer having a structure shown in the formula (I) as shown in the specification. The pyrazoline sensitizer has absorption waveband which is between 350nm and 440nm, is suitable for a light-curing system and particularly suitable for a system containing biimidazole photoinitiator. The pyrazoline sensitizer has ideal solubility and good light sensitivity improving effect. and a prepared film is good in resolution and adhesive force.

The invention relates to a compound having a structure as shown in a specification as well as a preparation method and application thereof. The preparation method comprises the steps of: reacting edaravone, sodium pyrosulfite and 1,2-propylene glycol; placing the solution of the reaction under an environment with the temperature of 35-55 DEG C for 96-168 hours and filtering for later use; and separating the edaravone solution by using a reversed phase high performance liquid chromatography method for preparing 4-(1-hydroxy-2-sulfo-propane-2-yl)-3-methyl-1-phenyl-2-pyrazoline-5-ketone. The compound can be used a comparison product of edaravone impurities and is convenient for controlling edaravone and the content of the edaravone in relevant preparations.

The invention relates to a concentrated softener for a dry cotton fabric. The concentrated softener comprises the following components in parts by mass: 50-65 parts of dihydrogenated tallow dimethyl ammonium chloride, 6-15 parts of ester quaternary ammonium salt, 0.7-1.5 parts of polyacrylamide, 2.5-8 parts of polyethylene glycol, 18-30 parts of isopropanol, 2-8 parts of coconut oil fatty acid diethanolamide, 0.8-1.5 parts of a pyrazoline fluorescent whitening agent and 0.2-0.6 part of fragrances. The concentrated softener provided by the invention is in a concentrated state; the number of use of the concentrated softener is more than that of an existing softener under the same volume; meanwhile, the treated dry cotton fabric is soft, fluffy, fresh and bright white, and does not cause yellowing and generate static electricity.

The invention relates to an anti-blue-ray system. The anti-blue-ray system is characterized in that an anti-blue-ray agent in the system has a pyrazoline compound structure as shown in a formula (I) which is described in the specification or/and a cinnamic acid compound structure as shown in a formula (II) which is described in the specification. The compound as shown in the formula (I) or/and thecompound as shown in the formula (II) can fully absorb short-wavelength blue light to protect the eye, and can also selectively absorb long-wavelength blue light so as to allow transmitted light to present particularly good visual perception. The anti-blue-ray system of the invention is applicable to products such as optical films, optical lenses, goggles, skin care products, lighting products, paints, adhesives and panels. The products have light-colored appearance and transmitted light presents particularly good visual perception.

The invention discloses an alkenyl-containing pyrazoline sensitizer as well as preparation method and application thereof. When used in a photocuring system, the alkenyl-containing pyrazoline sensitizer is very ideal in dissoluvability, free of odor and excellent in sensitivity improvement effect, and a film made of the alkenyl-containing pyrazoline sensitizer is very good in resolution ratio and adhesion property.

Processes are provided for inhibiting the formation of copper oxides on substantially oxide-free copper surfaces by contacting a substantially oxide-free copper surface with a pyrazoline ligand in an aqueous solution of pH 2-5. A thin layer of the ligand formed by coordination of 2-pyrazoline or 1-methyl-2-pyrazoline to the copper surface can be easily removed by exposure to a reducing plasma to regenerate a substantially oxide-free copper surface.

The invention belongs to the field of fluorescent dyes and laser dyes, and relates to coumarin fluorescent dyes and laser dyes, in particular to pyrazoline naphthyridine benzocoumarin fluorescent dye derivatives, a synthesis method of the same, and application of the same. The pyrazoline naphthyridine benzocoumarin fluorescent dye derivatives have longer emission wavelength and extremely high luminous efficiency, and the fluorescence quantum efficiency of the derivatives is approximately 100 percent; at the same time, a luminescent material of the derivatives has excellent thermo, photo and electrochemical stability, and can be used as fluorescent dyes, laser dyes, organic electroluminescent materials, fluorescent labeling materials, fluorescent chemosensitive materials and the like. The pyrazoline naphthyridine benzocoumarin fluorescent dye derivatives have a structure shown in a formula (I) or a formula (II).

The invention discloses a mechanochemical preparation method for a 1, 3, 5-triaryl-2-pyrazoline compound with a structure shown in a formula (III). The method comprises the following steps: a chalcone compound with a structure shown in a formula (I) and a phenyl hydrazine compound with a structure shown in a formula (II) are taken as raw materials, hydrosulfate is taken as a catalyst, and silica gel is taken as a grinding aid to perform a ball milling reaction in a closed ball milling tank; and after the reaction is finished, a reaction mixture is separated and purified to obtain the 1, 3, 5-triaryl-2-pyrazoline compound with the structure shown in the formula (III). The method has the advantages of safe and reliable production, simple and convenient operation, short reaction time, generally higher reaction yield, low production cost, simple post-treatment, small pollution and so on, and is the preparation method for the 1, 3, 5-triaryl-2-pyrazoline compound with better popularization and application prospects.

The invention relates to a new application of composition of 3-methyl-1-phenyl-2-pyrazoline-5-ketone and borneol, namely the application in preparation of medicine for preventing and/or treating psoriasis.

The invention discloses a new method for preparing 1-oxygen-4,5-diazepane easily and efficiently. The method comprises the steps that hydrazine salt and the equivalent amount of diglycol sulfonic ester are added into a solvent, then the equivalent amount of alkaline media are added, a condensation reaction is conducted, and 1-oxygen-4,5-diazepane is obtained directly; a reaction equation is as shown in a formula (2) defined in the description. The product can be used for preparing phenyl pyrazoline herbicide; compared with the method in original paper, the method has the advantages of being short in step, low in raw material cost, capable of obtaining raw materials easily, safe and mild in reaction condition, low in production cost and the like, and large-scale production popularization iseasy to achieve.

The invention relates to a compound of copper-bismuth double metal coordination polymer and graphene and a preparation method thereof. The compound is prepared from the following components in parts by mass: 1-2 parts of basic cupric carbonate, 2-6 parts of bismuth nitrate pentahydrate, 2-3 parts of 4,4'-dipyridyl, 3-5 parts of 3,5-pyrazoline diformic acid and smaller than 50 parts of graphene. The material can quickly degrade a rhodamine B solution under visible light and has a good photocatalytic property. In the preparation process of the material, no strong acids or strong alkali, strong oxidants or toxic reagents are used, so that the compound has the technical advantages of low cost, environment protection and the like.

The invention discloses a dimming function film, a dimming function assembly and a dimming function device. The dimming function film comprises an upper electrode layer, a dimming function layer and a lower electrode layer from top to bottom. The dimming function layer comprises a polymer dispersion liquid crystal base material and a UV blocking function compound dispersed in the polymer dispersion liquid crystal base material. The UV blocking function compound is selected from one or more of a viologen compound, dipyridine and a derivative thereof, anthraquinone and a derivative thereof, tetrathifulvalene and a derivative thereof, and pyrazoline and a derivative thereof. In the dimming function film, the compounds are dispersed in the polymer dispersion liquid crystal base material to form the dimming function layer. In the actual operation process, the compounds can be promoted to react by contorlling a direct current power source, and therefore controllable passing of ultraviolet light is achieved. The turning direction of liquid crystal molecules in a PDLC base layer is controlled by controlling the alternating current voltage, and therefore conversion between brightness and darkness is achieved.

The general structural formula of the arylpyrazoline light-emitting compound substituted by the 5-position condensed aromatic hydrocarbon is as follows: wherein, R1 is 4-nitrophenyl, 4-cyanophenyl, 4-esterylphenyl, 2-nitro Phenyl, 2-cyanophenyl, 2-esterylphenyl, 2,4-dinitrophenyl or hydrogen atom, R2 is 4-nitro, 4-cyano, 4-esteryl, 2-nitro Group, 2-cyano group, 2-ester group or 2,4-dinitro group, R3 is 9-anthracenyl group, 9-phenanthrenyl group or 1-pyrenyl group. The preparation method is as follows: firstly, condensing aromatic aldehydes with condensed rings and aromatic ketones substituted with electron-withdrawing groups on the benzene ring to generate chalcone intermediates, and then condensing with aromatic hydrazines substituted with electron-withdrawing groups on the benzene ring to form a ring; The generated pyrazoline molecule has two chromophores, the "arylpyrazoline" and the 5-position anthracycline, which enhance charge transfer in the molecule, and the luminescence spectrum of the 5-position aromatic condensed ring is compatible with the arylpyrazoline chromophore The absorption spectra overlap to produce effective energy transfer, improve the luminescence and two-photon fluorescence of pyrazoline molecules.

The invention relates to a concentrated laundry detergent for linen-cotton clothing and a preparation method thereof. The laundry detergent contains the following components by weight: 2.5-6 parts of magnesium dodecyl benzene sulfonate, 15-25 parts of sodium alkyl benzene sulfonate, 5-15 parts of polyoxyethylene lauryl ether sodium sulfate, 1.2-3 parts of organic siloxane, 3-9 parts of polyoxyethylene lauryl ether, 10-18 parts of ethanol, 4-8 parts of triethanolamine, 88-104 parts of sodium laureth sulfate, 0.3-0.5 part of a pyrazoline-type fluorescent whitening agent, 0.05-0.13 part of an essence and 50-70 parts of water. According to the concentrated laundry detergent for linen-cotton clothing and the preparation method thereof provided by the invention, the laundry detergent compared with an existing laundry detergent has the advantages of smaller usage amount for washing the same clothing, strong detergency, gentleness on the skin, no damage to clothing, easy biodegradability and good stability; and the clothing after washing gains bright color.