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36results about How to "Good anti-hepatic fibrosis effect" patented technology

Method for extracting C15H18O5 from Cichorium glandulosum Boiss.et Hout and application of C15H18O5

The invention relates to a method for separating and extracting C15H18O5 from Cichorium glandulosum Boiss.et Hout and use of C15H18O5 the English name of which is 11B, 13-Dihydrolacurin. The method is characterized by comprising the following steps: soaking the root of Cichorium glandulosum Boiss.et Hout by ethanol; collecting the percolate by a percolation method; obtaining a thick extract by a reduced pressure distillation device; passing the extract through a silicagel column, an octadecylsilyl column and a Sephadex LH-20 column; eluting; and drying the eluant by the reduced pressure distillation device to obtain dry powder which is the monomer C15H18O5, the English name of which is 11B, 13-Dihydrolacurin. The compound has the effect of preventing anti-hepatic fibrosis, namely, the compound inhibits activating and proliferating effect of hepatic stellate cells, so that the C15H18O5 with the English name of 11B, 13-Dihydrolacurin can be used as a lead compound for preventing anti-hepatic fibrosis.
Owner:SHIHEZI UNIVERSITY

Composition 67083001030512 and application of composition 67083001030512 to drug for resisting liver fibrosis

The invention relates to the fields of organic synthesis and medicinal chemistry, in particular to a composition 67083001030512, a preparation method of the composition 67083001030512, and application of the composition 67083001030512 to a drug for resisting liver fibrosis, and discloses the composition 67083001030512 and the preparation method. Pharmacological experiments show that the composition 67083001030512 plays a role in resisting liver fibrosis, thereby having a high value on development of the drug for resisting liver fibrosis.
Owner:苏州贺澳德生物医药科技有限公司

Derivative composition of imidazolyl and dihydroxyethylamino of Psiguadial A for anti-hepatic fibrosis

The invention relates to the field of organic synthesis and drug chemicals. The invention discloses a composition prepared from O-(imidazolyl)ethyl derivative (III) and O-(dihydroxyethylamino)ethyl derivative (IV) of Psiguadial A according to mass ratio of 15: 85 and a preparation method of the composition by mixing above compounds according to mass ratio of 15: 85. The pharmacological experiment indicates that the composition provided by the invention can significantly inhibit the NIH / 3T3 propagation and fibroblast propagation induced by transforming growth factor-beta 1 when its content is 20 ug / ml, and the composition has the anti-hepatic fibrosis effect; therefore, the invention further provides the application of thecomposition prepared from O-(imidazolyl)ethyl derivative (III) and O-(dihydroxyethylamino)ethyl derivative (IV) of Psiguadial A according to mass ratio of 15: 85 in preparing the anti-hepatic fibrosis drugs.
Owner:苏州贺澳德生物医药科技有限公司

Piperazinyl and dihydroxyethylamido derivative composition of Atropurpuran for anti-hepatic fibrosis

The invention relates to the field of organic synthesis and medicinal chemistry and discloses a composition composed of an O-(piperazinyl) ethyl derivative (III) and an O-(dihydroxyethylamido) ethyl derivative (IV) of Atropurpuran in a mass ratio of 70: 30 and a method of preparing the composition composed of the compounds in a mass ratio of 70: 30. A pharmacological experiment verifies that the composition provided by the invention can obviously inhibit NIH / 3T3 proliferation and fibroblast proliferation induced by a transforming growth factor-beta1 when the concentration of the composition is 20[mu]g / ml, and has the action of anti-hepatic fibrosis. Therefore, the composition provided by the invention also provides use of the composition composed of the O-(piperazinyl) ethyl derivative (III) and the O-(dihydroxyethylamido) ethyl derivative (IV) of Atropurpuran in the mass ratio of 70: 30 in preparing drugs for anti-hepatic fibrosis. The formula is as shown in the description.
Owner:NANJING FUHAIAOSAI PHARMA CO LTD

Application of composition of benzimidazolyl and bis(2-methylthioethyl) amino derivatives of Salviskinone A in anti-liver fibrosis drugs

The invention relates to the field of organic synthesis and medicinal chemistry and discloses a composition consisting of benzimidazolyl and bis(2-methylthioethyl) amino derivatives of Salviskinone A in a mass ratio of 55:45 and a method for mixing the compounds in a mass ratio of 55:45 to prepare the composition. Pharmacological experiments indicate that the composition provided by the invention in a concentration of 20mu g / ml can remarkably inhibit the NIH / 3T3 proliferation and the fibroblast proliferation induced by transforming growth factor-beta1, and realizes an anti-liver fibrosis effect; and therefore, the invention also provides an application of the composition consisting of benzimidazolyl and bis(2-methylthioethyl) amino derivatives of Salviskinone A in a mass ratio of 55:45 in preparing anti-liver fibrosis drugs.
Owner:NANJING FUHAIAOSAI PHARMA CO LTD

Application of composition of imidazolyl and dichloroethylamino derivatives of Atropurpuran to resistance of liver fibrosis

The invention relates to the field of organic synthesis and pharmaceutical chemistry and discloses application of a composition of imidazolyl and dichloroethylamino derivatives of Atropurpuran to resistance of liver fibrosis, namely a composition composed of an O-(imidazolyl) ethyl derivative (III) and an O-(dichloroethylamino) ethyl derivative (IV) of the Atropurpuran at the mass ratio of 70 to 30 and a method for preparing the composition by mixing the compounds at the mass ratio of 70 to 30. A pharmacology experiment shows that the composition provided by the invention can be used for remarkably inhibiting NIH / 3T3 proliferation and transforming growth factor-beta1 induced fibroblast proliferation when the concentration is 20mug / ml; the composition has the liver fibrosis resisting effect, so that the invention also provides application of the Atropurpuran to preparation of a medicine for resisting the liver fibrosis. (The formula (III) is shown in the description and the formula (IV) is shown in the description.).
Owner:NANJING FUHAIAOSAI PHARMA CO LTD

Application of composition of Schiglautone A derivatives in preparation of anti-hepatic fibrosis drugs

The invention relates to the field of organic synthesis and medicinal chemistry and discloses and provides a composition composed of Schiglautone A O-(1H-tetrazole)ethyl and O-(benzimidazolyl)ethyl derivatives according to a mass ratio of 65:35. Pharmacological experiments show that the composition provided herein can significantly inhibit NIH / 3T3 proliferation and transforming growth factor-induced fibroblast proliferation and can resist hepatic fibrosis; therefore, the invention also provides application of a composition composed Schiglautone A O-(1H-tetrazole)ethyl and O-(benzimidazolyl)ethyl derivatives according to the mass ratio of 65:35, in the preparation of anti-hepatic fibrosis drugs.
Owner:NANJING GUANGKANGXIE BIOLOGICAL MEDICAL TECH
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