43 results about "Compound name" patented technology

The invention discloses a eudesmane typed sesquiterpene acid compound named 5alphaH-eudesmane-11 (13)-alkylene-12 acid, which is characterized by the following: inhibiting the replication of HBsAg and HBV-DNA; fitting for preparing prevention drug of virus B hepatitis; reducing the application in the hepatitis B surface antigen drug.

A method is presented for managing applications using application-based names. A naming service registers an alias name; the alias name represents a first compound name that includes an application name that is associated with an application and a deployment name that is associated with a deployment attribute that characterizes a deployment of an instance of the application. The naming service is also able to generate an application-based name associated with an application; the application-based name represents a context within a naming system, and the application-based name is a second compound name that includes the alias name. Applications are managed within a data processing system using application-based names. The first compound name can be associated with a first topology-based name that represents a first context for organizing files that are related to the instance of the application.

The invention relates to a cucurbituril and a synthetic method replacing the cucurbituril, which is an organic chemical heterocyclic compound, in particular to a compound named cucurbituril and a synthetic method replacing the cucurbituril. The synthetic method is that the glycolurils dimer is used as raw material and is heated and reacted with the epoxy glycolurils or the epoxy glycolurils derivatives and the formaldehyde in the hydrochloric acid medium under 90 DEG C. to 100 DEG C. for 1h to 2h; the cucurbituril is gained after condensation, filtration, separation and purification. The mixture is calculated based on the quantity of the material, and the glycolurils dimer : epoxy glycolurils or epoxy glycolurils derivatives : formaldehyde equals to 1 : 0 to 4 : 0 to 4, wherein, the epoxy glycolurils or epoxy glycolurils derivatives and the formaldehyde can not be zero at the same time, and the concentration of the hydrochloric acid is 3mol / L to 12mol / L. The invention can overcome the defect that the distribution of the cucurbituril in the product and the quantities and position of the substituent in the cucurbituril in the traditional synthetic method of the cucurbituril are difficult to control.

A method is presented for processing names by a naming service. A naming service obtains an application name for an application along with at least one deployment attribute for a deployment of an instance of the application within a data processing system. The naming service generates an application-based name for the instance of the application; the application-based name represents a context within a naming system that is supported by the naming service, and the application-based name is a compound name that includes the application name and at least one deployment name for a deployment attribute. A deployment attribute is a metadata value, such as a deployment identifier or version identifier, that characterizes a manner in which the instance of the application is deployed within the data processing system.

Provided is a system for helping an operator determine the target ion, collision energy and other analysis conditions. A chromatogram selected by an operator is displayed in a chromatogram display area of an MRM measurement parameter determination window. When the operator selects a point on this chromatogram, the name of a target compound which is registered in an event linked with a range of time including the selected point in time is displayed on a compound name display area. A plurality of mass spectra collected at that point in time are also displayed in a mass spectra display area in a vertically arranged form, using the same scale on the mass axis and the same scale on the intensity axis, with the scales of their mass axes aligned with each other in the vertical direction. The operator can then check whether the selected peak corresponds to the target compound.

The invention discloses a fluorescence probe rapidly responding to hydrogen sulfide and a preparation method and application thereof. The structural formula of the compound can be seen in the specification. The preparation method includes the step of making hydroxystyrene and 2,4-dinitrosalicylic bromobenzene react under the conditions of catalysts and heating to generate the compound named as TPE-NP. Probe molecules have large Stokes shift, self-absorption is effectively reduced, and imaging accuracy is improved. In addition, the fluorescence probe is quite sensitive to hydrogen sulfide, and fluorescence is enhanced by 40 times in the process of increasing the concentration of sodium bisulfide to 10 equivalent weights of the probe concentration from 0. The fluorescence probe has a high molar extinction coefficient (larger than 60000 M<-1>.CM<-1> except for water), has a good dyeing effect on living cells and nematode, and is short in dyeing time (15 min) and high in dyeing efficiency. After living cells and nematode are dyed, confocal imaging is directly conducted without conducting the washing process which must be conducted on other probes in the prior art, and the imaging operation process is greatly simplified.

The invention discloses a fluorescence labeling molecule with the compound name of (2Z, 2'Z)-3,3'-(2,5-bi(diphenylamino)-1,4-phenyl)bi(2-(3,5-bi(trifluoromethyl)phenyl)acrylonitrile and the molecular formula of C52H30F12N4, wherein the fluorescence labeling molecule can emit red fluorescence under the irradiation of an UV lamp with the wavelength of 365nm; nanoparticles in the prepared fluorescence labeling molecule are coated in a water solution by using Pluronic, and tumor cells are labeled in a region filled with near infrared light with the wavelength of larger than 650nm. The fluorescence labeling molecule has the advantages that the fluorescence labeling molecule has the characteristics of aggregation induced emission and high-aggregation light emission and is high in brightness and low in toxicity; and when being used for labeling tumor cells, the fluorescence labeling molecule is simple in operation, low in cost, good in specificity and capable of effectively avoiding autofluorescence interference of biological tissues and improving the fluorescence imaging sensitivity, and an available fluorescence labeling material is provided for researching a near infrared fluorescence labeling method for tumor cells.

The present invention relates to the development and utilization technology of radix radix sorbifolium, specifically a compound extracted from radix radix sorbiflora husk and stalk and its extraction method and application. The method is as follows: pulverize the sorbifolia fruit shell and / or fruit stalk, extract with a solvent, filter, recover the solvent to obtain a concentrated solution, pass the concentrated solution through a macroporous resin, elute with a solvent, recover the solvent to obtain a concentrate, evaporate to dryness, Obtain a brown solid, that is, total saponins. Dissolve the total saponins in water, extract with n-butanol, and dry to obtain a brown powder. After silica gel column chromatography, gradient elution is carried out with chloroform / methanol = 100:35-60, and the eluent is recovered , refined, to obtain the target compound pistachioside; the compound can be applied to the preparation of anti-tumor drugs for the treatment of brain diseases and health food for the prevention and treatment of brain diseases and tumors.

A method is presented for managing applications using application-based names. A naming service registers an alias name; the alias name represents a first compound name that includes an application name that is associated with an application and a deployment name that is associated with a deployment attribute that characterizes a deployment of an instance of the application. The naming service is also able to generate an application-based name associated with an application; the application-based name represents a context within a naming system, and the application-based name is a second compound name that includes the alias name. Applications are managed within a data processing system using application-based names. The first compound name can be associated with a first topology-based name that represents a first context for organizing files that are related to the instance of the application.

An insecticide used for garden flower cultivation and a preparing method thereof are disclosed. The insecticide is prepared from, by weight, 16-25 parts of turpentine, 8-14 parts of a compound named as Chinese characters 'Songzhisuantong' by the inventor, 6-11 parts of tobacco leaves, 7-11 parts of hot pepper, 3-5 parts of pirimiphos-methyl, 4-7 parts of mint, 2-6 parts of eucalyptus oil, 15-21 parts of ageratina adenophora, 7-12 parts of a stellera chamaejasme ketone extract and 6-12 parts of lobelia colorata. An effective ratio of the turpentine, the 'Songzhisuantong', the tobacco leaves, the hot pepper, the pirimiphos-methyl, the mint, the eucalyptus oil, the ageratina adenophora, the stellera chamaejasme ketone extract, and the like is adopted to prepare the insecticide. The insecticide and the method are efficient, highly targeted, environment-friendly, free of secondary toxicity, free of pollution, capable of keeping ecological balance and nuisanceless. A formula is reasonable. The preparing process is simple. The natural raw materials are adopted for preparation so that the insecticide has no toxicity, and has no influence on flowers after the insecticide is directly acted on the flowers. Effects are durable, insecticidal effects are good, and the insecticide effects quickly and is convenient to popularize and apply.

The invention relates to a structure and preparation method of a new phenolic acid compound and application in the antibacterial field. According to the invention, extraction of the sedum aizoon overground part, separation and purification are carried out to obtain a new compound named as sedumol A. Pharmacodynamic experiments show that sedumol A has strong inhibitory effect on Escherichia coli, Staphylococcus aureus and the like.

The invention discloses an amino-substituted staurosporin compound and a preparation method and the application thereof. The amino-substituted staurosporin compound is characterized by being named as12-N-methyl-k252c and being shown as a structural formula I. The amino-substituted staurosporin compound is obtained from an actinomycete through separation and purification, and is authenticated to be the amino-substituted staurosporin compound named as 12-N-methyl-k252c; experimental detections find that the amino-substituted staurosporin compound has relatively high activity on prostate cancercells, and has a relatively high inhibitory effect on Brd4 protein; the amino-substituted staurosporin compound has a good application prospect in preparation of medicines for treating tumors, HIV, leukemia and other diseases.

The invention discloses a natural medicine active component composition for preventing cerebral ischemia-reperfusion injury and an extraction method and applications thereof. The natural medicine active component comprises 3,4,5-trihydroxyl benzaldehyde, a compound named Temalisu II, and casuarictin. The composition is prepared by the following steps: cutting whole herb of dry geum aleppicum, adding a methanol / ethanol solution, carrying out extraction for many times by adopting a reflux extraction or impregnation extraction mode, filtering the extracts, merging the extracts, carrying out vacuum concentration, and recovering methanol / ethanol to obtain the active component composition. The preparation method is simple, the active component composition can relieve cell apoptosis caused by cerebral ischemia-reperfusion injury and recover the cerebral functions, and the development prospect is good.

The invention relates to a sterilization composition containing difenoconazole and a compound named as Chinese characters 'Fubenmixian'an' by the inventor. Effective components of the composition are the difenoconazole and the 'Fubenmixian'an' which are compounded. The mass ratio of the difenoconazole to the 'Fubenmixian'an' is 1-40:40-1. A preparation includes 1-80% by mass of the effective components which are the difenoconazole and the 'Fubenmixian'an', with the balance being auxiliary components allowable and acceptable in pesticides. The dosage form of the composition is an emulsifiable solution, a suspension, wettable powder, water dispersible granules, an emulsion in water, a microemulsion, granules and microcapsules. The composition can effectively prevent and treat late blight, downy mildew, scab of cucurbit, anthrachose of grape, white rot, alternaria leaf spot, powdery mildew, brown speckle disease, rust disease, stripe rust, scab, and the like, and has good effects on grape anthracnose and white rot.

Porcine reproductive and respiratory syndrome virus (PRRSV) causes serious economic losses in swine. The present invention determined that CD 151 is a susceptibility factor for PRRSV infection by transfecting a cell line which is not susceptible to PRRSV infection (BHK-21) with CD 151, which rendered the cell line susceptible. Because CD 151 can be accessed in cellular material including blood platelets and germplasm, the present invention provides a non-invasive method of screening different swine for susceptibility to PRRSV, thereby improving breeding plans. In the case of a valuable animal, results from such screening can indicate any offspring's susceptibility to PPRSV. Additionally, the viral RNA-CD 151 interaction possesses high affinity and can be used as a tool to detect anti-viral compounds which can be further improved by using combinatorial chemistry. Accordingly, anti-viral compounds that can block the viral RNA-CD 151 interaction can be developed. Advantageously, transfection of CD 151 into non-simian cell lines can confer susceptibility to PRRSV and these recombinant cell lines can be used for preparation of biologics that will avoid simian cell lines which could be a source of primate viruses in xenotransplanted organs from pigs. Finally, the present invention describes the basic mechanism by which the virus RNA enters a target cell. This novel class of proteins is termed viral RNA entry proteins and a novel class of compounds named anti-RNA Entry Proteins can be used to block the entry of viral RNA, thereby preventing viral infections.

The invention relates to a sterilization composition containing prothioconazole and a compound named as Chinese characters 'Fubenmixian'an' by the inventor. Effective components of the composition are the prothioconazole and the 'Fubenmixian'an' which are compounded. The mass ratio of the prothioconazole to the 'Fubenmixian'an' is 1-40:40-1. A preparation includes 1-80% by mass of the effective components which are the prothioconazole and the 'Fubenmixian'an', with the balance being auxiliary components allowable and acceptable in pesticides. The dosage form of the composition is an emulsifiable solution, a suspension, wettable powder, water dispersible granules, an emulsion in water and a microemulsion. The composition is mainly used for preventing and treating wheat rust disease, wheat powdery mildew, wheat banded sclerotial blight, rice banded sclerotial blight, rice sheath blight disease, green smut, cucumber powdery mildew, cucumber downy mildew, grape downy mildew, apple alternaria leaf spot, apple powdery mildew, banana leaf spot, tomato early blight, pear scab, strawberry powdery mildew, sunflower rust disease, and other diseases.

Peak information is collected from an MS / MS spectrum in which the product ions generated from ions originating from a plurality of compounds are mixed. Using one of the m / z values of a plurality of ion species as precursor-ion information and the peak information of the MS / MS spectrum as product-ion information, a database search is performed to find candidate compounds for each compound, and a standard MS / MS spectrum of each candidate compound is obtained. For each combination of the candidate compounds, a virtual MS / MS spectrum is created by integrating the standard MS / MS spectra of those candidate compounds, and the degree of similarity between the virtual MS / MS spectrum and the measured MS / MS spectrum is calculated. If the candidate compounds are correct compounds, the degree of similarity will be high. Accordingly, the compound names and other results are visually presented to users in descending order of the degree of similarity.

The invention belongs to traditional Chinese medicine-mineral matter organic fertilizer. The fertilizer is characterized by comprising, by weight, 0.5-1.5 parts of sweet wormwood herb, 0.5-1.5 parts of bitter apricot seed, 0.5-1.5 parts of myrrh, 2-4 parts of charred radix sanguisorbae, 0.5-1.5 parts of rosin, 0.5-1.5 parts of granular or hollow azurite, 0.5-1.5 parts of realgar, 1-3 parts of white-neck earthworm, 1-5 parts of wheat bran, 20-50 parts of rice straw, 10-20 parts of maifan stone powder, 130-170 parts of a compound named as Chinese characters 'Wuyanghuaergui', 750-780 parts of calcium carbonate, 1-5 parts of soybean and 40-46 parts of water. A beneficial effect of the fertilizer is that quality of various crops, vegetables and fruits can be greatly improved by applying the fertilizer. The fertilizer can loosen and regulate the soil structure, and can remove chemical toxic compounds in herbicides so that produced grains, vegetables and fruits are pollution-free green foods and are beneficial to human body health. The fertilizer has long fertility effects and is widely used.

The invention provides a compound named as 2-methyl-5-(3,4-dihydroxyphenyl)pyridine. The compound is capable of eliminating oxygen free radicals and has wide application prospects in the treatment of diseases relevant with cell breaking capacity of free radicals of a human body. The invention further provides an extraction method of 2-methyl-5-(3,4-dihydroxyphenyl)pyridine. The extraction method comprises the steps of firstly carrying out cold-soaked extraction on blaps rynehopetera fairmaire powder so as to obtain an extracting solution, and carrying out extraction, first silica gel column chromatography separation, second silica gel column chromatography separation, ODS reversed-phase column chromatography separation, third silica gel column chromatography separation and gel column chromatography separation, so as to obtain 2-methyl-5-(3,4-dihydroxyphenyl)pyridine. The extraction method has the beneficial effects that the steps are simple, the cost is low, the raw material sources are wide, and industrial production is easily realized.

The invention relates to a novel bacteriostatic compound named as Butein-0908, a preparing method thereof and applications of the bacteriostatic compound in aquatic products. When the mass percentage is 0.06%, the bacteriostatic compound can inhibit staphylococcus aureus, bacillus subtilis, salmonella bacillus, bacillus proteus and escherichia coli, has strong inhibiting functions for common pathogenic bacteria of the aquatic products, has obvious and rapid sterilization functions for aeromonas hydrophila, aeromonas sobria and non-O1 group vibrio cholerae, and can kill all bacteria in 12 h. Accordingly, the bacteriostatic compound is wide in antibacterial spectrum, few in side and toxic effects and high in bacteriostatic activity, is especially suitable for the common pathogenic bacteria of the aquatic products, and can be widely used as an economical and environmental friendly bacteriostatic agent for aquatic product bacteriostasis.

A method for preparing a dirt cleaning agent is disclosed. The cleaning agent includes, by weight, 3-5 parts of a compound named as Chinese characters 'Benerjia' by the inventor, 6-10 parts of calciumcarbonate, 1-3 parts of diatomite, 4-12 parts of essence, 5-15 parts of stearic acid and 50-150 parts of deionized water. The cleaning agent has simple components, is convenient to prepare, low in cost, good in cleaning effects, free of harm, and convenient to rinse, and does not need repeated rinsing, thus saving a large amount of labor and resources, and meeting demands of manufacturers better.

The invention discloses a chemical editor-based compound name generation method and device, and the method comprises the steps: obtaining a chemical structural formula of a to-be-named compound, and carrying out the disassembly of the chemical structural formula based on a preset rule, so as to obtain a plurality of connection components; respectively splitting each connecting component into a plurality of structure segments, and naming each structure segment to obtain the name of each structure segment; organizing the names of the structure fragments according to a preset strategy to generate names of the connection components corresponding to the structure fragments; sequentially connecting the names of the connecting components, and separating the names of two adjacent connecting components to generate the name of the compound to be named. The technical problems that in the prior art, chemical naming is difficult, and the naming error rate is high are solved.

The present invention discloses a compound named tinospora sinensis alkali. The present invention further discloses a preparation method for extracting and separating the tinospora sinensis alkali from tinospora sinensis. The preparation method comprises: extracting with an acidic alcohol, carrying out concentration redissolution, directly performing column chromatography, collecting the eluent, and re-crystallizing to obtain the high-purity tinospora sinensis alkali. According to the present invention, with the preparation method, palmatine having the purity of up to 90-95% and pseudopalmatine having the purity of up to 90-95% can be separated; and the preparation method has characteristics of simple process, good stability and good reproducibility, can concurrently obtain the pure compound products such as the tinospora sinensis alkali, the palmatine and the pseudopalmatine in one time, further has advantages of time saving and consumption reducing, is suitable for industrial production, provides positive significance for the acceleration of the comprehensive utilization and development of the tinospora sinensis herb resource, and has good application prospects.

A compound name-card-shaped proximity card holder includes: a main body that includes a first pocket, a plurality of interlayers, and a second pocket. The first pocket and the main body form a first receiving compartment. The second pocket and the main body form a second receiving compartment. The first receiving compartment and the second receiving compartment receive and hold therein various articles, such as cards and proximity cards. The interlayers are arranged in the interior of the main body and are fixed by a circular button to the main body to be rotatable out of the main body. The interlayers are each in the form of an open-end folder for insertion and storage of a single proximity card. The interlayers of the main body are formed of thin metal sheets or FAM films protect proximity cards placed inside and outside the interlayers from affecting and demagnetizing each other.

The invention relates to a process for processing ink for printers, comprising the steps of: uniformly mixing the following components according to parts by weight, and then passing through a 0.02 micron filter to obtain a finished product: 10-30 parts of black dye, 1-5 parts of ethylene glycol, 2-8 parts of alkoxylated alcohol, 1-6 parts of polyethylene glycol, 5-7 parts of sodium bicarbonate, 1-3 parts of sodium fatty alcohol ether sulfate, 1-3 parts of pyrrolidone, 2-5 parts of polyacrylic acid Ester emulsion, 1‑3 parts dipropylene glycol ether, 100‑150 parts deionized water. The ink prepared by the invention has good stability, and no flocculation and precipitation will occur after being placed for a long time.