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37 results about "Berberine Chloride" patented technology

The orally bioavailable, hydrochloride salt form of berberine, a quaternary ammonium salt of an isoquinoline alkaloid and active component of various Chinese herbs, with potential antineoplastic, radiosensitizing, anti-inflammatory, anti-lipidemic and antidiabetic activities. Although the mechanisms of action through which berberine exerts its effects are not yet fully elucidated, upon administration this agent appears to suppress the activation of various proteins and/or modulate the expression of a variety of genes involved in tumorigenesis and inflammation, including, but not limited to transcription factor nuclear factor-kappa B (NF-kB), myeloid cell leukemia 1 (Mcl-1), B-cell lymphoma 2 (Bcl-2), B-cell lymphoma-extra large (Bcl-xl), cyclooxygenase (COX)-2, tumor necrosis factor (TNF), interleukin (IL)-6, IL-12, inducible nitric oxide synthase (iNOS), intercellular adhesion molecule-1 (ICAM-1), E-selectin, monocyte chemoattractant protein-1 (MCP-1), C-X-C motif chemokine 2 (CXCL2), cyclin D1, activator protein (AP-1), hypoxia-inducible factor 1 (HIF-1), signal transducer and activator of transcription 3 (STAT3), peroxisome proliferator-activated receptor (PPAR), arylamine N-acetyltransferase (NAT), and DNA topoisomerase I and II. The modulation of gene expression may induce cell cycle arrest and apoptosis, and inhibit cancer cell proliferation. In addition, berberine modulates lipid and glucose metabolism.

Berberine hydrochloride and fumaric acid eutectic substance as well as preparation method, composition and application thereof

ActiveCN110041326AAdvantages of good safety medicineNo crystallizationAntibacterial agentsOrganic active ingredientsDrugChemistry
The invention discloses a berberine hydrochloride and fumaric acid eutectic substance as well as a preparation method, composition and an application thereof, specifically discloses a novel berberinehydrochloride and fumaric acid eutectic substance with berberine hydrochloride as an active pharmaceutical ingredient and fumaric acid as a eutectic precursor, a preparation method of the berberine hydrochloride and fumaric acid eutectic substance as well as an application of the berberine hydrochloride and fumaric acid eutectic substance as the active pharmaceutical ingredient in preparation of drugs for preventing and treating cardiovascular diseases, resisting viruses and cancer, reducing blood fat and blood sugar and resisting inflammation, bacteria and infection.
Owner:INST OF MATERIA MEDICA AN INST OF THE CHINESE ACAD OF MEDICAL SCI

Biocompatible aggregation-induced luminogen and application thereof

The present subject material relates to the discovery of Berberine Chloride as aggregation induced emission (AIE) luminogen and use of this material in staining lipid droplets both in mammalian cellsand in living tissue slices. In particular, the present innovation is associated with proposing a new source to acquire more natural AIEgens with obvious advantages over artificial luminogens.
Owner:THE HONG KONG UNIV OF SCI & TECH

Berberine derivatives, their preparation method, pharmaceutical composition and anti-tumor application

The invention discloses berberine derivatives, their synthesis method and their application in the preparation of products for preventing, alleviating and / or treating tumors. Described berberine derivatives are 12-aminotetrahydroberberine derivatives shown in general formula I or their physiologically acceptable salts and 12-N, N-disubstituted amino tetrahydro berberine derivatives Berberine derivatives or their physiologically acceptable salts and 12-aminoberberine quaternary ammonium salt derivatives or their physiologically acceptable salts and 12-N, N-disubstituted Amino berberine quaternary ammonium derivatives or physiologically acceptable salts thereof. Compared with the raw material berberine chloride quaternary ammonium compounds, the solubility of these berberine derivatives in organic solvents has been significantly improved. The berberine derivatives have inhibitory activity on the growth of tumor cell lines, and the intensity of action may be significantly higher than that of the raw material of berberine quaternary ammonium salt, or equivalent to or higher than that of the positive control drug, and can be used to prepare Products for the prevention, mitigation and / or treatment of tumors.
Owner:INST OF MATERIA MEDICA CHINESE ACAD OF MEDICAL SCI

Extraction process for optimizing berberine hydrochloride in cortex phellodendri chinensis decoction pieces

The invention relates to the technical field of cortex phellodendri chinensis extraction, and provides an extraction process for optimizing berberine hydrochloride in cortex phellodendri chinensis decoction pieces, the extraction process for optimizing berberine hydrochloride in the cortex phellodendri chinensis decoction pieces comprises the following steps: taking the cortex phellodendri chinensis decoction pieces, naturally air-drying, and sieving the crushed powder to obtain berberine hydrochloride powder; adding water into dilute sulphuric acid, beta-glucanase and cellulase, and mixing for later use; respectively loading the cortex phellodendri chinense powder in the step 1 and sulfuric acid into a feeding device, adding into different extraction tanks, and carrying out reflux extraction; combining all filtrates, concentrating, and adjusting the pH with diluted hydrochloric acid; and cooling, adding a saturated NaCl solution, preserving overnight at 4 DEG C, carrying out suction filtration, and drying. According to the optimized extraction process for berberine hydrochloride in cortex phellodendri chinensis decoction pieces, the enzyme activity is improved through dilute sulphuric acid, plant cell walls are thoroughly damaged by beta-glucanase and cellulase, effective components are extracted more sufficiently, and therefore the effects of being capable of accelerating extraction, sufficient in extraction and high in extraction rate are achieved.
Owner:SICHUAN ACAD OF FORESTRY +1

Anti-streptococcus agalactiae traditional Chinese medicine extract effective part formula and production process thereof

The invention discloses an anti-streptococcus agalactiae traditional Chinese medicine extract effective part formula. The formula is composed of the following raw materials in parts by weight: 100-120parts of a rhubarb root and rhizome extract, 15-25 parts of berberine hydrochloride, 70-90 parts of a baical skullcap root extract, and 75-95 parts of a weeping forsythia capsule extract. Because theberberine hydrochloride content in the prescription is low and the baical skullcap root extract has poor fluidity, on the basis of previous experiments, a production process adopts a manner of performing pre-mixing of a small amount of a filling agent with berberine hydrochloride and the baical skullcap root extract, and then performing total mixing to increase the uniformity and ensure stable drug effects. The test shows that the minimum bacteriostatic concentration of the formula against streptococcus agalactiae is 5.625 [mu]g/mL; and the minimum bactericidal concentration is 31.25 [mu]g/mL, so that the formula shows good antibacterial effects. Therefore, the anti-streptococcus agalactiae traditional Chinese medicine extract with antibacterial effects, non-toxicity and no residue, and being capable of replace antibiotics, and a powder thereof have great significance and broad prospects.
Owner:GUANGXI UNIV

Berberine hydrochloride dimer as well as preparation method and application thereof

The invention provides a berberine hydrochloride dimer which has a chemical structure shown in the specification. The anti-tumor effect of the berberine hydrochloride dimer is remarkably superior to that of positive control berberine hydrochloride, and the berberine hydrochloride dimer has good anti-tumor activity and strong druggability; and as a novel anti-tumor compound, the compound has great development value. The invention also provides a preparation method of the berberine hydrochloride dimer.
Owner:PEKING UNIV SHENZHEN HOSPITAL
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