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47 results about "Endothelial Growth Factor Receptor" patented technology

RNA interference mediated inhibition of vascular endothelial growth factor and vascular endothelial growth factor receptor gene expression using short interfering nucleic acid (siNA)

The present invention concerns methods and reagents useful in modulating vascular endothelial growth factor (VEGF, VEGF-A, VEGF-B, VEGF-C, VEGF-D) and / or vascular endothelial growth factor receptor (e.g., VEGFR1, VEGFR2 and / or VEGFr3) gene expression in a variety of applications, including use in therapeutic, diagnostic, target validation, and genomic discovery applications. Specifically, the invention relates to small nucleic acid molecules, such as short interfering nucleic acid (siNA), short interfering RNA (siRNA), double-stranded RNA (dsRNA), micro-RNA (miRNA), and short hairpin RNA (shRNA) molecules capable of mediating RNA interference (RNAi) against VEGF and / or VEGFr gene expression and / or activity. The small nucleic acid molecules are useful in the diagnosis and treatment of cancer, proliferative diseases, and any other disease or condition that responds to modulation of VEGF and / or VEGFr expression or activity.
Owner:SIRNA THERAPEUTICS INC

RNA interference mediated inhibition of vascular endothelial growth factor and vascular endothelial growth factor receptor gene expression using short interfering nucleic acid (siNA)

The present invention concerns methods and reagents useful in modulating vascular endothelial growth factor (VEGF, VEGF-A, VEGF-B, VEGF-C, VEGF-D) and / or vascular endothelial growth factor receptor (e.g., VEGFR1, VEGFR2 and / or VEGFr3) gene expression in a variety of applications, including use in therapeutic, diagnostic, target validation, and genomic discovery applications. Specifically, the invention relates to small nucleic acid molecules, such as short interfering nucleic acid (siNA), short interfering RNA (siRNA), double-stranded RNA (dsRNA), micro-RNA (mRNA), and short hairpin RNA (shRNA) molecules capable of mediating RNA interference (RNAi) against VEGF and / or VEGFr gene expression and / or activity. The small nucleic acid molecules are useful in the diagnosis and treatment of cancer, proliferative diseases, and any other disease or condition that responds to modulation of VEGF and / or VEGFr expression or activity.
Owner:SIRNA THERAPEUTICS INC

High concentration VEGF receptor fusion protein containing formulations

ActiveUS20190343918A1Long-term manufacturing and storage stabilityReduce dosageSenses disorderPeptide/protein ingredientsHigh concentrationVEGF receptors
The present invention provides ophthalmic formulations having high concentrations of vascular endothelial growth factor (VEGF) receptor fusion protein and high stability during storage. Methods for treating angiogenic eye disorders using the high concentration formulations are also provided.
Owner:REGENERON PHARM INC

Anti-cancer pharmaceutical compositions and methods for treating patients with cancer

Method of treating persons having carcinoma, sarcoma or hematopoietic cancer by administering (i) a compound of the formula (I)and (ii) an epidermal growth factor receptor (EGFR) inhibitor, a vascular endothelial growth factor receptor (VEGFR) inhibitor and pharmaceutical compositions for use in said method. A method for treating gastric cancer, colon cancer, lung cancer, breast cancer, pancreas cancer, kidney cancer, prostate cancer, medulloblastoma, rhabdomyosarcoma, Ewing sarcoma, liposarcoma, multiple myeloma and leukemia by administering a compound of the formula (I).
Owner:DAIICHI SANKYO CO LTD

Whole human source anti-vascular endothelial cell growth factor receptor 2 single chain antibody

The invention belongs to the technical field of genetic engineering antibodies and particularly relates to a whole human source single chain antibody which is designed and expressed by genetic engineering and has specific affinity towards human vascular endothelial growth factor receptor 2 (VEGFR-2). The invention also provides a nucleotide sequence of heavy chain variable region and light chain variable region immunoglobulin molecules, a nucleotide sequence which comprises the heavy chain variable region and light chain variable region immunoglobulin molecules, an amino acid sequence which comprises variable heavy chain and variable light chain immunoglobulin molecules, and a sequence which corresponds to CDR1, CDR2 and CDR3 of a complementary determining region. The invention also provides a method for generating and expressing the anti-VEGFR-2 single chain antibody, by cycling operations of gathering-elution-gathering, an antibody which has specific affinity towards the human vascular endothelial growth factor is screened, and then the single chain antibody is obtained through a prokaryotic cell secretion and expression system and an affinity purification system. The antibody can be coupled with a detectable substance and therapeutic agent.
Owner:CHINA PHARM UNIV

Charles ketone oxime and its composition , preparation method and uses

The related chalketoxime shown as the formula (1) is prepared by heating and reflux reacting the 2', 4'-dihydroxy -6'-methoxyl-3', 5'-dimethylchalcone and hydroxylamine hydrochloride in pyridine, which has well solvability, fit to direct inject for drug, restrains obviously all of the activity of blood vessel endothelium growth factor receptor, HER2 receptor and Tyr kinase as PDGFR receptor, the external growth of cells for breast cancer and liver cancer, and the phosphorylation of KDR in ECV304 cell, HER2 in MDA-MB-453 cell and PDGFR receptor in C6 cell, and benefit to treat tumor.
Owner:SOUTH CHINA BOTANICAL GARDEN CHINESE ACADEMY OF SCI +1

Topical administration of therapeutic agents and oligonucleotide formulations

Aspects of the invention relate to topical and ocular formulations of spherical nucleic acids (SNA), as well as methods of use thereof and compositions thereof. The formulations may include an inhibitor such as an inhibitor of tumour necrosis factor alpha (TNFa), platelet-derived growth factor subunit A (PDGFA), platelet-derived growth factor subunit B (PDGFB), platelet-derived growth factor subunit C (PDGFC), platelet-derived growth factor subunit D (PDGFD), platelet-derived growth factor receptor alpha (PDGFRA), platelet-derived growth factor receptor beta (PDGFRB), platelet-derived growth factor receptor like (PDGFRL), vascular endothelial growth factor A (VEGFA), vascular endothelial growth factor B (VEGFB), vascular endothelial growth factor C (VEGFC) vascular endothelial growth factor D (VEGFD), vascular endothelial growth factor receptor-1 (VEGFR1), vascular endothelial growth factor receptor-2 (VEGFR2), vascular endothelial growth factor receptor-3 (VEGFR3), beta-2 adrenergic receptor (ADRB2), connective tissue growth factor (CTGF), interleukin 1 beta (IL1 β), interleukin 1 receptor-1 (IL1 R1), interleukin 1 receptor-2 (IL1R2), and interleukin 1 receptor-3 (IL1R3). Aspects of the invention further relate to nanostructures comprising self-assembling therapeutic oligonucleotides, such as antisense oligonucleotides, that are linked to a molecular species, wherein the molecular species is positioned in a core of the nanostructure and the oligonucleotides extend radially from the core.
Owner:EXICURE INC

Targeted EGFR/KDR (Epidermal Growth Factor Receptor/Kinase Insert Domain Receptor) specific diabody

The invention belongs to the technical field of gene engineering antibodies, and in particular relates to a preparation method and an application of a bispecific diabody of an anti-tumor epidermal growth factor receptor (EGFR) and an anti-tumor vascular endothelial growth factor (VEGFR / KDR). The bispecific diabody formed by cross-linking and expressing heavy / light chain variable areas of an anti-EGFR high-affinity single-chain antibody E10 and an anti-KDR single-chain antibody AK404 by using genetic engineering technology can simultaneously act on EGFR with high expression on the surfaces of tumor cells and KDR with high expression on the surfaces of tumor angiogenesis vascular endothelial cells, and can achieve the purposes of simultaneously inhibiting or killing tumor cells or inhibiting or damaging tumor angiogenesis.
Owner:CHINA PHARM UNIV

Indolone compounds or derivatives thereof and applications thereof

The invention relates to indolone compounds shown as a general formula (a) or derivatives thereof and applications thereof. According to the invention, indolone compounds are substituted with deuterium to obtain deuterium-enriched indolone compounds; the indolone compounds can simultaneously act on the following three key receptor families involved in angiogenesis process: vascular endothelial growth factor receptor (VEGFR), fibroblast growth factor receptor (FGFR) and platelet-derived growth factor receptor (PDGFR), so as to inhibit angiogenesis and achieve the effect of treating cancers. The deuterated indolone compounds or the derivatives thereof have the advantage of high efficiency when used asdrugs. The general formula (a) is as shown in the specification.
Owner:SICHUAN UNIV

Human vascular endothelial growth factor specifically-binding antibody or antigen-binding fragment and application thereof

The invention brings forward a human vascular endothelial growth factor specifically-binding antibody or its antigen-binding fragment and an application thereof. The antibody or its antigen-binding fragment comprises a heavy-chain variable region having at least one of the following amino acid sequences: (1) an amino acid sequence as shown in SEQ ID NO:1; (2) an amino acid sequence as shown in SEQ ID NO:2; (3) an amino acid sequence as shown in SEQ ID NO:3; and (4) an amino acid sequence having more than one conserved amino acid mutations in comparison with the amino acid sequences in (1)-(3). According to the antibody or its antigen-binding fragment of the embodiment, human vascular endothelial growth factor can be specifically recognized, and binding of human vascular endothelial growth factor to its receptor can be effectively blocked so as to further block correlated signal pathways of the human vascular endothelial growth factor receptor such as VEGFR1 or 2. Thus, growth of cancer can be effectively inhibited.
Owner:WATERSTONE PHARMA WUHAN

Recombined vessel endothelium growth factor receptor, encoding genes thereof and application

The invention discloses a recombined vessel endothelium growth factor receptor, encoding genes thereof and application. The provided recombined blood vessel endothelium growth factor receptor is a fusion protein, and a structural domain 1-3 and an Fc section of a human IgG1 of the blood vessel endothelium growth factor receptor 1 are arranged sequentially from an amino terminal to a carboxyl terminal. An experiment proves that the fusion protein vessel endothelium growth factor receptor (VEGFR)-1 / Fc and a vessel endothelium growth factor (VEGF) have good affinity, the KD value reaches 265pm, the VEGFR-1 / Fc can inhibit proliferation and migration of vessel endothelium cells and chick embryo chorioallantoic membranes and vessel growth of naked mouse. The fusion protein VEGFR-1 / Fc has wide application in tumor therapy.
Owner:INST OF BIOENG ACAD OF MILITARY MEDICAL SCI OF THE CHINESE

N,N'-aryl substituted urea compound and application thereof

InactiveCN103288823AStrong inhibitory activityOrganic active ingredientsOrganic chemistryPlatelet-Derived Growth Factor Receptor AlphaWilms' tumor
The invention mainly relates to an N,N'-aryl substituted urea compound and an application thereof. The N,N'-aryl substituted urea compound is a compound shown in the formula I or a salt formed by the compound and a medicinal acid or alkali. The provided compound has the strong inhibitory activity for receptor protein kinases which comprise VEGFR2 (Endothelial Growth Factor Receptor 2), RGFR1 (Fibroblast Growth Factor Receptor 1) and PDGFR Alpha (Platelet Derived Growth Factor Receptor Alpha) and associated with the neogenesis of three kinds of tumor tissue blood vessels. Thus, the N,N'-aryl substituted urea compound can be used as a multi-target kinase inhibitor which is developed into a targeted anti-tumor medicine for treating solid tumors.
Owner:EAST CHINA UNIV OF SCI & TECH

A topical composition for treating rosacea and a method for treating rosacea with the same

A composition for use in the treatment of rosacea includes a multi-kinase inhibitor that inhibits both a Vascular Endothelial Growth Factor Receptor and a Fibroblast Growth Factor Receptor. A method for treating rosacea for a patient includes inhibiting a Vascular Endothelial Growth Factor Receptor of the patient; and inhibiting a Fibroblast Growth Factor Receptor of the patient.
Owner:ADS THERAPEUTICS LLC

LED treatment of dermatologic toxicities associated with vascular endothelial growth factor inhibitors

The present invention relates generally to methods of preventing or treating toxicities of the skin, hair, and / or nails, which are associated with administration of one or more vascular endothelial growth factor receptor inhibitors, with light-emitting diode photomodulation treatment, either alone or in combination with other agents.
Owner:DELAND M MAITLAND +1

Lervatinib-gallic acid eutectic crystal form and application thereof

The invention discloses a lenvatinib-gallic acid eutectic crystal form and application thereof. The eutectic crystal is composed of a compound as shown in a formula (I) and a compound as shown in a formula (II). The eutectic crystal can be used for inhibiting vascular endothelial growth factor receptors, fibroblast growth factor receptors, platelet-derived growth factor receptors and proto-oncogenes, and can be used for preventing and / or treating thyroid cancer or liver cancer.
Owner:NOVAGENESIS THERAPEUTIX SUZHOU LTD

Axitinib-loaded nanofiber membrane as well as preparation method and application thereof to surgical postoperative adhesion prevention

The invention discloses an application of a nanofiber membrane loaded with a small molecule drug for inhibiting a vascular endothelial growth factor and / or inhibiting a vascular endothelial growth factor receptor to preparation of a surgical postoperative anti-adhesion medical instrument. The nanofiber membrane has the advantages that the nanofiber membrane provided in the invention is good in biocompatibility, excellent in mechanical property, flexible and smooth after encountering water, good in air permeability and capable of effectively preventing the heart from adhering to surrounding tissues. In addition, the nanofiber membrane can also be applied to adhesion prevention in other surgical operations for abdominal cavities, pelvic cavities, tendons and the like.
Owner:SHANGHAI CHILDRENS MEDICAL CENT AFFILIATED TO SHANGHAI JIAOTONG UNIV SCHOOL OF MEDICINE

Use of vascular endothelial growth factor receptor 1+ cells in treating and monitoring cancer and in screening for chemotherapeutics

The present invention is directed to a method of inhibiting tumor formation in a cancer patient at a site remote from sites of prior tumor formation and to a method of preventing metastases. These methods involve administering to the cancer patient an inhibitor of vascular endothelial growth factor receptor 1+ bone marrow-derived cells under conditions effective either to inhibit tumor formation in the cancer patient at a site remote from sites of prior tumor formation or to prevent metastases. Candidate compounds useful for such purposes can be screened depending on whether they bind to vascular endothelial growth factor receptor 1+ bone marrow-derived cells and comparing the level of vascular endothelial growth factor receptor 1+ bone marrow-derived cells to prior levels.
Owner:CORNELL RES FOUNDATION INC

Use of vascular endothelial growth factor receptor 1+ cells in treating and monitoring cancer and in screening for chemotherapeutics

The present invention is directed to a method of inhibiting tumor formation in a cancer patient at a site remote from sites of prior tumor formation and to a method of preventing metastases. These methods involve administering to the cancer patient an inhibitor of vascular endothelial growth factor receptor 1+ bone marrow-derived cells under conditions effective either to inhibit tumor formation in the cancer patient at a site remote from sites of prior tumor formation or to prevent metastases. Candidate compounds useful for such purposes can be screened depending on whether they bind to vascular endothelial growth factor receptor 1+ bone marrow-derived cells. Metastases in a cancer patient can be monitored by evaluating a patient sample for detection and quantification of vascular endothelial growth factor receptor 1+ bone marrow-derived cells and comparing the level of vascular endothelial growth factor receptor 1+ bone marrow-derived cells to prior levels.
Owner:CORNELL RES FOUNDATION INC

Anticancer composition based on anti-angiogenesis medicine

Aiming at the prior art, the invention aims to provide an anticancer composition based on an anti-angiogenesis medicine. The anticancer composition comprises a vascular endothelial growth factor receptor protein kinase inhibition medicine, namely a VEGFR inhibition medicine; and furthermore, according to the characteristic of a molecular passageway, a targeted medicine deoxyverrucosidin and a medically accepted carrier or excipient thereof are selected to be combined with the VEGFR inhibition medicine and a medically accepted carrier or excipient thereof, so that the problem of medicine resistance of the VEGFR inhibition medicine is fundamentally solved; and the effect of treating cancers is greatly enhanced.
Owner:朱曙东

Polypeptide inhibitor modified with polyethylene glycol for inhibiting vascular endothelial growth factor receptors 2 tyrosine kinase and application thereof.

The invention relates to the field of medicines and particularly relates to polypeptide for inhibiting vascular endothelial growth factor receptors 2 tyrosine kinase and preventing and treating the rheumatoid arthritis. After the polypeptide is modified with polyethylene glycol and the sequence of the polypeptide is Mpeg-SC10k-Val-Cys-CyS-Ser-Thr-Arg-Glu which is an entirely-new sequence. The polypeptide can be used for treating the rheumatoid arthritis and has potential new-medicine development value.
Owner:NANTONG CHENGXIN AMINO ACID

Aromatic ring fused triazine derivatives and uses thereof

The invention belongs to pharmaceutical field. The invention relates to the compounds according to Formula I, including their optically active forms, pharmaceutically acceptable salts or hydrates, and the pharmaceutical composition comprising thereof as active ingredient; uses in the preparation of vascular endothelial growth factor receptor tyrosine kinase inhibitors, and uses in the preparation of medicament for the treatment and / or prevention of cancer.
Owner:SHENYANG PHARMA UNIVERSITY
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