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364results about How to "Strong growth inhibitory effect" patented technology

Preparation method of sargassum fusiforme selenium polysaccharide

The invention provides a preparation method of sargassum fusiforme selenium polysaccharide, and relates to a preparation method of polysaccharide, aiming at solving the technical problems that the existing selenium polysaccharide synthesizing method is complex to operate, the synthesized selenium polysaccharide is pungent in smell, and the used reagent is toxic. The method comprises the following steps of: 1, adding 1g of sargassum fusiforme polysaccharide into 100mL of 0.5% by volume HNO3 water solution to obtain a polysaccharide solution; 2, adding sodium selenite into the polysaccharide solution to obtain a mixed solution, wherein the mass ratio of sodium selenite to the sargassum fusiforme polysaccharide in the mixed solution is (0.4-1.2g):1g, reacting for 6-10hours at the temperature of 50DEG C-90DEG C, cooling, adding NaCO3 to adjust the pH value to 5-6, centrifuging, dialyzing till the red is not detected to be unavailable after ascorbic acid is added into dialyzate, heating and concentrating, and carrying out freeze drying to obtain the sargassum fusiforme selenium polysaccharide. The preparation method provided by the invention is simple to operate, and free of pungent smell, and the used reagent is non-toxic and environment-friendly.
Owner:HARBIN UNIV OF COMMERCE +1

Production of insect-proof sick wooden mold and its use

Production of anti-insect and disease-proof mold and its use are disclosed. The process includes taking hamycin, Agrobacterium tumefaciens AGL-1 and gene plasmid pPBH with thuricin bacillosporin stored in normal way, preparing conidiospore suspension, converting the obtained tumefaciens and pPBH plasmid, activation culturing, culturing the activated fungus liquid of conidiospore suspension, tumefaciens and pPBH plasmid mutually, converting, screening and purifying. It can be used to prepare anti-insect and disease-proof mold and insect prevention of plant.
Owner:杨谦

Compound of CDK7 small-molecule inhibitor, and application thereof

The invention belongs to the field of pharmacy and tumor diagnosis and treatment, and particularly relates to a compound serving as a cyclin-dependent kinase 7 (CDK7) inhibitor, and application of thecompound in treatment of proliferative diseases such as cancers including breast cancer, ovarian cancer, colon cancer, liver cancer, lung cancer and glioma. The CDK7 small-molecule inhibitor is a compound with the structural general formulas (I)-(X), or a stereoisomer, a pharmaceutically acceptable salt, solvate, hydrate, polymorph, co-crystal, tautomer, isotope labeled derivative or prodrug thereof. The small-molecule inhibitor provided by the invention is wide in anticancer spectrum; the compound has a good growth inhibition effect on various cancer cells such as liver cancer, stomach cancer, colorectal cancer, ovarian cancer, glioma, lung cancer and the like, provides an effective drug for preventing or treating proliferative diseases, especially cancers, in the aspects of structure and action mechanism, and has a good application prospect.
Owner:中国医科大学

Copper complex, preparation method and application thereof

The invention discloses a copper complex and the preparation method and application thereof, providing a cupric complex with 1, 10-phenanthroline, nitrate radical and N, N-dimethylfomamide. The preparation method of the cupric complex with 1, 10-phenanthroline is that nantokite, 1, 10-phenanthroline, nitrate radical and N, N-dimethylfomamide are mixed to react in solution to obtain the complex. The synthetic materials of the complex of the invention are easy to obtain and have low cost; the product precipitates in the form of crystalloid, thereby having a high purity and high production efficiency; besides, the complex can exist stably in natural states and has good water-solubility and fat-solubility; in addition, the complex of the invention has a good inhibiting effect on a plurality of cancer cells of lung cancer, liver cancer, adenocarcinoma of colon and so on, extensive effect and wide application range.
Owner:CAPITAL NORMAL UNIVERSITY

Aminoquinazolinone and aminoisoquinolinone derivatives and application thereof

The invention provides aminoquinazolinone and aminoisoquinolinone derivatives. Through multiple experiments, it is validated that the synthesized compounds have excellent PI3Kalpha and PI3Kgamma inhibition effects, and most of the compounds have a significant inhibition effect on PI3Kalpha, and show a potent growth inhibition effect on tumor cell lines such as a PIK3CA-mutated human breast cancercell line (MCF7). Therefore, the aminoquinazolinone and aminoisoquinolinone derivatives can be applied to preparing antitumor and anti-inflammatory drugs, and can be applied to drugs for the treatmentof human or animal cell proliferation-related tumors as a PI3Kalpha inhibitor. The drugs are prepared from any one or more of the derivatives, and pharmaceutically acceptable salt and solvate of thederivatives, and a pharmaceutically acceptable carrier. The general formulas a and b of the compounds are shown in the description.
Owner:ZHEJIANG UNIV +1
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