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49 results about "Mapk signaling pathway" patented technology

Compositions and Methods for Modulating Cognitive Function

The present invention provides compositions and methods for modulating, e.g., enhancing, cognitive function. The methods involve modulation of translation, modulation of a MAPK signaling pathway, or both. The invention further provides screening methods useful in identifying compounds that modulate, e.g, enhance, cognitive function. The invention further provides method of treating a subject to modulate cognitive function.
Owner:MASSACHUSETTS INST OF TECH

Human cytokine and use thereof

The invention discloses a new secretive cytokine NS128 of human beings, which relates to a coding amino acid sequence of the cytokine or the polynucleotide of the cytokine fragment, containing a genetic engineering carrier and a host cell of the polynucleotide. The invention also relates to a production method of the amino acid sequence of the cytokine or the polypeptide of the cytokine fragment and the production method of the polypeptide as well as a small interference RNA, which suppresses the expression of the cytokine. The invention also relates to a salt which contains the polynucleotide or the salt of acceptable drugs, or a medical composition of the polypeptide or the salt of acceptable drugs. The invention further relates to applications of the polynucleotide of the cytokine, the polypeptide or the small interference RNA in preparation of prevention and / or treatment medicines for tumor, infection, hematopoietic disorder and autoimmune disease, etc., in particular having clinical implications for tumor, inflammation and nervous system disease and so on related to MAPK signal pathway. The invention also relates to a method of in vitro testing whether the expression of the polynucleotide or the polypeptide changes. The invention also relates to a monoclonal or polyclonal antibody which is specifically bound with the polypeptide or an active fragment of the polypeptide.
Owner:SINOGENOMAX +1

Purpose of polyether compound in medicine preparation and anti-tumor medicine screening method

InactiveCN107951879AOrganic active ingredientsBiological testingHippo signalingPi3k akt signaling
The invention discloses a purpose of a polyether compound in medicine preparation and an anti-tumor medicine screening method. The medicine is used for regulating and controlling at least one of the following signal channels: a calcium ion signal channel, a Wnt signal channel, a Hippo signal channel, a TNF signal channel, a VEGF signal channel, a p53 signal channel, an NF-kappa B signal channel, an Ras signal channel, an mTOR signal channel, an RNA degradation signal channel, a PPAR signal channel, a cAMP signal channel, an HIF-1 signal channel, an Insulin signal channel, an AMPK signal channel, an Rap1 signal channel, an apoptosis signal channel, a cell cycle signal channel, a cGMP-PKG signal channel, a DNA copying signal channel, an MAPK signal channel, a PI3K-Akt signal channel and an autophagy signal channel. The polyether compound provided by the invention can cause the tumor cell death through regulating and controlling various signal channels; and a better anti-cancer effect isachieved.
Owner:WUHAN J1 BIOTECH

Use of ursolic acid as colon tumor resistant medicament

InactiveCN101991579ABlock EGFR signaling pathwayOrganic active ingredientsAntineoplastic agentsSide effectApoptosis
The invention relates to use of ursolic acid as a colon tumor resistant medicament. The ursolic acid has the effects of inhibiting colon cancer / tumor cell proliferation and inducing apoptosis. In naked mouse in vivo experiments, the ursolic acid can effectively inhibit the proliferation of colon cancer transplanted tumor and inhibit the generation of tumor blood vessels, and has no obvious toxic or side effect on mice. The ursolic acid has the effect of inhibiting EGFR / MAPK signal channel phosphorylation of colon cancer cells, and the key target of the ursolic acid is to inhibit ERK1 / 2 protein phosphorylation. The ursolic acid which is synergetic with oxaliplatin serving as a clinical first-line chemotherapy medicament of the colon cancer has better curative effect. The ursolic acid has better proliferation inhibiting effect on the colon cancer cells of K-RAS gene mutation. The use of the ursolic acid as the colon tumor resistant medicament provides a new thought for treating the colon tumor.
Owner:ZHEJIANG UNIV

Application of hordenine in preparing drug for treating hypophysoma

ActiveCN110151742ASolving the plight of drug shortagesEnhanced inhibitory effectOrganic active ingredientsAntineoplastic agentsAdrenocorticotropic hormoneTLR4
The invention discloses application of hordenine in preparing a drug for treating hypophysoma, and relates to the technical field of biopharmacy. Specifically, in the application, the inventor finds that the hordenine can inhibit a TLR4 / NF-kB / MAPK signaling pathway, thereby being conductive to exerting the pharmaceutical effect on treating prolactinoma and adrenocorticotropic hormone adenoma, andsolving the problem of drug shortage for patients with the prolactinoma and the adrenocorticotropic hormone adenoma.
Owner:王雄 +1

Biomarker metabolic pathway, and analysis method and application

The invention belongs to the technical field of functional analysis methods of disease metabolism biomarkers, and provides a biomarker metabolic pathway and an analysis method. The metabolic biomarker is stearic acid, phytosphingosine, glycine, glutamine and phospholipids; an acting target spot of the metabolic biomarker is a target protein related to a depression nervous system, immune response and endocrine; and the metabolic pathway is a PI3K-Akt signaling pathway, an mTOR signaling pathway, an MAPK signaling pathway, an erbB signaling pathway, a neurenergen signaling pathway, an Rap1 signaling pathway and an Ras signaling pathway. A functional network analysis method suitable for depression characteristics is established, and the clinical application of these biomarkers helps to optimize the diagnosis of depression, and can provide some valuable clues for the subsequent depression network function researches.
Owner:SHANXI UNIV

Applications of cyanidin-3-O-glucoside in preparation of medicines treating diseases caused by 3-chloropropane-1,2-diol

InactiveCN107485616AImprove growth retardationAntagonistic destructionOrganic active ingredientsAccessory food factorsDiseaseEpithelium
Applications of cyanidin-3-O-glucoside in preparation of medicines treating and / or preventing diseases caused by 3-chloropropane-1,2-diol are provided. The cyanidin-3-O-glucoside (C3G) can improve rat ingestion decrease and growth retardation which are caused by 3-MCPD poisoning, can effectively resist rat antioxidant system damage caused by 3-MCPD poisoning, and can activate and adjust BTB structural functions of sustentacular cells through inhibiting an MAPK signaling pathway, thus relieving seminiferous epithelium injuries caused by the 3-MCPD, maintaining stability of a spermatogenic microenvironment, regulating spermatogenic cell proliferation and differentiation, and improving dyszoospermia. In addition, the C3G can improve sperm activity through adjusting sperm energy metabolism related enzymes. The C3G can regulate rat sex hormone secretion disorders caused by 3-MCPD poisoning and can maintain normal levels of sex hormone in serum and androgen in testis inner environments. The applications provide theoretical foundations for 3-MCPD reproduction toxicity nutritional intervention utilizing anthocyanin.
Owner:JINAN UNIVERSITY

Application of krait venom antibacterial peptide in preparation of medicine for resisting inflammatory factor

The invention relates to an application of krait venom antibacterial peptide in the preparation of a medicine for resisting inflammatory factor and belongs to the field of biomedical technology. A lot of researches show that the krait antibacterial peptide has an obvious effect of inhibiting inflammatory factor secretion induced by lipopolysaccharide in vitro and inhibits inflammatory factor secretion through inhibiting MAPK signal channels; the krait venom antibacterial peptide has a remarkable scavenging activity of DPPH and 2,2-azine-bis(3-ethylbenzothiazole-6-sulfoacid)diammonium salt (ABTS+)radical in vitro and has an obvious effect of inhibiting mice inflammation induced by a complete Freund adjuvant in vivo; and the krait venom antibacterial peptide can be applied in the preparation of a medicine for resisting inflammatory factor.
Owner:KUNMING INST OF ZOOLOGY CHINESE ACAD OF SCI

Application of chitosan oligosaccharide in preparation of medicaments for preventing and/or treating neurodegenerative diseases

The invention relates to a medicament for treating neurodegenerative diseases and particularly relates to an application of chitosan oligosaccharide in preparation of medicaments for preventing and / or treating neurodegenerative diseases, i.e., the chitosan oligosaccharide can be further applied to the medicaments for preventing and / or treating the neurodegenerative diseases. According to the medicament and the application thereof, with lipopolysaccharide (LPS) as an inducing factor and mouse microglia as a research object, a result shows that the chitosan oligosaccharide can remarkably restrict the expression of the activated microglia iNOS (Inducible Nitric Oxide Synthase) in mRNA (Messenger Ribonucleic Acid) and protein level, can restrict the generation of activated microglia NO (Nitric Oxide), can effectively restrict the generation of activated microglia ROS (Reactive Oxygen Species), can effectively restrict the activation of an MAPK (Mitogen Activated Protein Kinase) signal channel caused by LPS, and can effectively restrict the activation of transcription factor NF-kB (Nuclear Factor-Kappa B) and AP-1 (Activator Protein-1).
Owner:DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI

Application of MAPK signal pathway inhibitor to preparation of drugs for treating cystic echinococcosis

The invention relates to the technical field of an MAPK signal pathway inhibitor, in particular to application of the MAPK signal pathway inhibitor to preparation of drugs for treating cystic echinococcosis. The invention discloses for the first time the application of the MAPK signal pathway inhibitor to preparation of drugs for treating cystic echinococcosis, and further discloses for the first time application of Sorafenib Tosylate Tablets, U0126 or PD184352 in the MAPK signal pathway inhibitor to preparation of drugs for treating cystic echinococcosis. Pharmacodynamic experimental data show that the treating effect of Sorafenib Tosylate Tablets, U0126 or PD184352 on cystic echinococcosis is superior or equivalent to that of clinically commonly used albendazole on cystic echinococcosis, that is, the MAPK signal pathway inhibitor can serve as a novel anti-echinococcosis drug for cystic echinococcosis, especially Sorafenib Tosylate Tablets, U0126 or PD184352, which can serve as a novel anti-echinococcosis drug, so that a novel approach is provided for cystic echinococcosis treatment.
Owner:THE FIRST TEACHING HOSPITAL OF XINJIANG MEDICAL UNIVERCITY

Applications of small-molecular inhibitor MLN4924 in preparation of drug for inhibiting bleomycin-induced pulmonary fibrosis

The invention discloses an application of a small-molecular inhibitor MLN4924 in preparation of a drug for inhibiting bleomycin-induced pulmonary fibrosis. The invention also discloses an application of the small-molecular inhibitor MLN4924 in preparation of a drug for inhibiting an early inflammation process of bleomycin-induced pulmonary fibrosis. The invention also discloses an application of the small-molecular inhibitor MLN4924 in preparation of a drug for inhibiting activation of NF-[kappa]B and MAPK signal pathways in inflammatory reactions.
Owner:EAST CHINA NORMAL UNIV

Application of Lefty protein in restraining fibrosis lesion of organ

The invention discloses the application of a Lefty protein in prohibiting fibering pathologic change of organs, in basic research on preparing the medicine for antagonizing TGF-beta, Nodal, BMP, p38MAPK signal pathways, and in preparing the medicine for curing or preventing fibering pathologic change of organs and tissues of liver, kidney, lung, cardiac muscle, skin, etc. The invention has the functions of prohibiting signal pathways (such as TGF-beta / Smad, Nodal signal pathways) related to fibering diseases and activating protein hydrolytic ferment (such as MMP, gelatingase, etc) capable of prohibiting fibering, is a biological preparation with great potential clinical application value, and can help to further probe into the occurring mechanism of fibering diseases.
Owner:WUHAN UNIV

Application of strictosamide to preparation of anti-inflammatory drugs

The invention belongs to the technical field of medicines and in particular discloses application of strictosamide to preparation of anti-inflammatory drugs. The strictosamide is extracted and separated from nauclea officinalis medicinal materials. The strictosamide can achieve the effects of obviously inhibiting growth of inflammatory factors IL-1beta and TNF-alpha in LPS-stimulated RAW 264.7 cells and inhibiting expression of IL-1beta and TNF-alpha mRNA. Researches of anti-inflammatory mechanisms prove that the strictosamide can inhibit LPS-stimulated NF-kappaB and MAPK signal paths in RAW 264.7 cells.
Owner:JIANGSU PROVINCE INST OF TRADITIONAL CHINESE MEDICINE

Application of kaempferol to drugs for treating osteoarthritis

InactiveCN109453160AAlleviate the degeneration of articular cartilageAlleviate joint space narrowingOrganic active ingredientsSkeletal disorderSensory neuronNerve cells
The invention discloses application of kaempferol to drugs for treating osteoarthritis. Kaempferol decreases expression of anti-galectin-1 in sensory neurone by inhibiting NF-kappa B and MAPK signal pathway activated in the inflammatory environment, reducing expression of c-Fos, c-Jun and delta FosB in sensory neurone and inhibiting combination activity of transcription factor activator protein-1(AP-1) and DNA, expression of anti-galectin-1 in nerve cell is reduced, and accordingly development of osteoarthritis is relieved. The invention provides a new drug for clinic treatment of osteoarthritis, and meanwhile states the mechanism of the novel treatment drug. New thought and experiences are provided for better understanding the pathological process of osteoarthritis and developing the drugs for treating osteoarthritis in the future.
Owner:SHANGHAI NINTH PEOPLES HOSPITAL SHANGHAI JIAO TONG UNIV SCHOOL OF MEDICINE

Application of naucleamide G in preparation of anti-inflammatory drug

The invention relates to the technical field of medicines, in particular to a novel compound which is separated from a medicinal fathead tree and is named as naucleamide G, and application of the novel compound in preparation of an anti-inflammatory drug. The naucleamide G can obviously inhibit generation of inflammatory factors IL-1beta and TNF-alpha in an LPS-stimulated cell RAW 264.7 and also inhibit expression of IL-1beta and TNF-alpha mRNA. The research on an anti-inflammatory mechanism shows that the naucleamide G can inhibit NF-kB and MAPK signal channels stimulated by LPS in the cell RAW 264.7.
Owner:JIANGSU PROVINCE INST OF TRADITIONAL CHINESE MEDICINE

Application of NOD1 to preparation of products for inhibiting tumor SRC signal path

The invention belongs to the field of biological medicines, and particularly relates to application of NOD1 to preparation of products for inhibiting MAPK signal path. The products have the at least one of the following functions from A1) to A7): A1) combination with SRC; A2) inhibition of expression of p-SRC; A3) inhibition of MAPK signal path; A4) inhibition of expression of p-ERK; A5) inhibition of expression of p-CyclinD; A6) inhibition of expression of p-CyclinE; and A7) promotion of expression of p21. The invention firstly discovers NOD1 can inhibit p-SRC through target binding of SRC and further inhibit the MAPK signal path. The discovery provides a new target spot for screening drugs for treating diseases related to abnormal MAPK signal path.
Owner:SHANDONG UNIV

Application of soybean peptide in promoting osteogenic activity

The invention provides an application of a soybean peptide in promoting osteogenic activity, which comprises the following steps: detecting the proliferation level of osteoblasts, the activity of a marker ALP in the early stage of differentiation and a marker OCN in the later stage of differentiation, and detecting that the soybean peptide CBP promotes the proliferation and differentiation of the osteoblasts on the biochemical level; in the process of promoting osteoblast differentiation by the soybean peptide CBP, three classical signal pathways, namely ERK, JNK and p38 bypasses, of an MAPK signal pathway participate in the process and a key signal transduction step; the soybean peptide CBP promotes gene expression and phosphorylation level of a key factor Runx2 of an MAPK signal channel in osteoblasts.
Owner:YANTAI UNIV

Small interfering RNA for TRAPPC4 gene target point, and uses thereof

The present invention provides small interfering RNA for a TRAPPC4 gene target point, wherein a sense strand nucleotide sequence is represented by SEQIDNO:1, and an antisense strand nucleotide sequence is represented by SEQIDNO:2. The present invention further provides applications of the small interfering RNA for the TRAPPC4 gene target point in preparation of drugs for prevention or treatment of colorectal carcinoma. The present invention further provides a targeting molecule transport protein microparticle complex of the siRNA and applications of the targeting molecule transport protein microparticle complex in preparation of drugs for prevention or treatment of colorectal carcinoma. According to the present invention, experiment results show that: after the small interfering RNA for the TRAPPC4 gene target point is adopted to transfect human colorectal carcinoma cells to slice TRAPPC4 expression so as to inhibit ERK-MAPK signaling pathway activation, inhibit colorectal carcinoma proliferation and induce apoptosis, such that the small interfering RNA can be used for colorectal carcinoma treatment.
Owner:RENJI HOSPITAL AFFILIATED TO SHANGHAI JIAO TONG UNIV SCHOOL OF MEDICINE

1,2-dithiolane compounds useful in neuroprotection, autoimmune and cancer diseases and conditions

This invention provides compounds of the formula (I):wherein Y1, Y2, Z, X1, X2, and W′ are defined in the specification. These compounds are useful in the treatment of tyrosine kinases, MAPK signaling pathway kinases and PI3K / AKT / mTor signaling pathway kinases-mediated diseases or conditions, such as neurodegeneration, neuroprotection, cancer, autoimmune as well as other diseases and conditions associated with the modulation of tyrosine kinases selected from FYN, FYN Y531F, FLT3, FLT3-ITD, BRK, ITK, FRK, BTK, BMX, SRC, FGR, YES1, LCK, HCK, RET, CSK, LYN, and ROS1; MAPK pathway kinases selected from ARAF, BRAF, CRAF, ERK1 / 2, MEK1, MEK2, MEK3, MEK4, MEK5, MEK6, and MEK7; and PI3K / AKT / mTor pathway kinases: selected from mTor, PI3K α, PI3K β, PI3K γ, and PI3K δ.
Owner:SABILA BIOSCI LLC

Rat's IL-17RE span film region and cell inner region poly peptide and coding sequence, fusion protein and clone

The invention discloses white rat IL-17RE membrane crossing area and inside cell area polypeptide and the coding sequence, fusion albumen and cell line. The polypeptide is one sequence of the following aminoacid residue: SEQ ID No:2, the albumen relative to cell transferring of SEQ ID No:1 that has been replaced and / or lacking and / or adding one to ten aminoacid residue and passing RAS / MAPK signal channel path to take mitosis. Interfusing albumen of the polypeptide and the out area of the rat resource erythropoietin has one sequence of the following aminoacid residue: SEQ ID No:2, the albumen relative to cell transferring of SEQ ID No:1 that has been replaced and / or lacking and / or adding one to ten aminoacid residue and passing RAS / MAPK signal channel path to take mitosis. It has great actual value and wide application prospect.
Owner:TSINGHUA UNIV

Anguilla japonica liver expression antibacterial peptide LEP2 gene promoter and application thereof

The invention relates to an anguilla japonica liver expression antibacterial peptide LEP2 gene promoter and application thereof. The anguilla japonica liver expression antibacterial peptide LEP2 gene promoter sequence is successfully cloned, and the anguilla japonica liver expression antibacterial peptide LEAP2 gene promoter pGL3-LEAP2-pro luciferase reporter plasmid is successfully constructed; and experiments prove that the anguilla japonica liver expression antibacterial peptide LEAP2 gene promoter can be induced and activated by a virus simulant polyI:C, a Gram-negative bacterium important surface antigen LPS and aeromonas hydrophila. According to the invention, a good experimental system can be provided for researching an expression regulation mechanism of the anguilla japonica liver expression antibacterial peptide LEAP2 gene, a natural immune response mechanism of fish for resisting pathogenic bacterium infection, and particularly researching an important fish inflammation related NF-[kappa]B and MAPK signal path network regulation mechanism; and conditions are created for constructing an expression vector by using the promoter to efficiently express an exogenous gene or applying the promoter to transgenic fish construction.
Owner:JIMEI UNIV

Application of amygdalin in preparing knee osteoarthritis anti-inflammatory drug

ActiveCN109045048AReduce degenerationDoes not affect anti-inflammatory abilityOrganic active ingredientsAntipyreticAnaphylaxisSide effect
The invention discloses application of amygdalin in preparing a knee osteoarthritis anti-inflammatory drug. At an inflammatory state, AMD controls the expression of Dnmt3b by inhibiting a p38 / MAPK signal channel so as to retard the regression of cartilage cells. The AMD adjusts the metabolism of the cartilage cells by controlling the p38 / MAPK / Dnmt3b signal channel, so that the regression of OA isretarded. Therefore, AMD has good application prospect in clinically treating osteoarthritis. The existing anti-inflammatory pain alleviating drug generally has gastrointestinal reaction, anaphylacticreaction, renal damage and the like, the amygdalin can well control the side effect in an effective dose range and does not influence the improvement of the anti-inflammatory capability of cartilagecells.
Owner:浙江中医药大学附属第一医院

Application of rps9 protein in prediction of good response to superovulation in cynomolgus monkeys

ActiveCN113341152BImproved Prediction of Superovulation OutcomesPractical application valueDisease diagnosisBiological testingPhysiologySignalling pathways
The invention relates to the application of RPS9 protein in the prediction of good response to superovulation in cynomolgus monkeys, belonging to the technical field of superovulation. The method of proteomics is used to analyze the first day of superovulation success group and the fifth day of superovulation success group. , Superovulation failure group on day 1 and superovulation failure group on day 5 for bioinformatics analysis to obtain the differential protein among the groups. From the study of protein level, the changes of protein expression revealed in the blood of superovulated monkeys were explored. In superovulation in cynomolgus monkeys, RPS9 protein was expressed on day 5 in the superovulation success group, but not in the superovulation failure group on day 5. It is suggested that the down-regulation of PRS9 expression in the superovulation failure group affects the activation of MAPK signaling pathway and NK-κB pathway, thereby leading to cell apoptosis, cell cycle arrest and inhibition of proliferation. The down-regulation of PRS9 expression may lead to the activation of p53, resulting in the inhibition of cell proliferation, thereby affecting the formation of follicles and leading to the failure of superovulation response. Therefore, RPS9 protein has become a new molecule to predict the good response to superovulation in cynomolgus monkeys, and has practical application value.
Owner:SOUTH CHINA AGRI UNIV

Application of rhoifolin in preparation of drug for preventing and treating osteolytic diseases

The invention discloses an application of rhoifolin in preparation of a drug for preventing and treating osteolytic diseases. In-vitro experiments show that the rhoifolin can significantly inhibit theosteoclast formation and bone absorption induced by RANKL and also inhibit the expression of osteoclast-related genes. Western blotting experiments show that the rhoifolin can inhibit NF-[kappa]B andMAPK signaling pathways and two transcription factors of NFATc1 and c-fos; further studies show that the rhoifolin can inhibit P65 from entering nucleus and the activity of NFATc1 and NF-[kappa]B cells. In-vivo experiments show that the rhoifolin can reduce the number of TRAP-positive osteoclasts and bone destruction of skull in a titanium particle-induced skull model. Therefore, the rhoifolin can improve osteolysis induced by osteoclasts, and can become a potential drug for treatment of joint prosthesis loosening, and provides a new treatment option for aseptic loosening of prosthesis.
Owner:THE FIRST AFFILIATED HOSPITAL OF GUANGXI MEDICAL UNIV
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