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68 results about "Adenosine A2A receptor" patented technology

The adenosine A2A receptor, also known as ADORA2A, is an adenosine receptor, and also denotes the human gene encoding it.

Medical implants containing adenosine receptor agonists and methods for inhibiting medical implant loosening

The invention provides methods and compositions for reducing or inhibiting bone resorption, osteoclast differentiation and stimulation and the loosening of medical prostheses by administering a compound or agent that modulates an adenosine receptor such as the adenosine A2A receptor, in particular, an agonist of an adenosine A2A receptor. The invention also extends to pharmaceutical compositions comprising such an agent that modulates an adenosine receptor such as an adenosine A2A agonist and to prosthetic devices containing such an agent that modulates an adenosine receptor such as an A2A agonist on one or more surfaces or within the prosthetic device such as, for example, suspended in the cement forming the prosthetic device.
Owner:NEW YORK UNIV

Derivatives of triazoly-imidazopyridine and of the triazolypurines useful as ligands of the adenosine A2a receptor and their use as medicaments

InactiveUS20070249638A1BiocideNervous disorderDiseaseAryl
Compounds of formula (I) wherein: X is N; R1 is C1-C6 linear or branched alkyl or C1-C6 linear or branched alkenyl; R2 is hydrogen, C1-C6 linear or branched alkyl or C1-C6 linear or branched alkenyl, C6-C14 aryl or C6-C14 aryl(C1-C6) linear or branched alkyl or C6-C14 aryl(C1-C6) linear or branched alkenyl, with the aryl group optionally substituted by one or more substituents, either the same or different, selected from the group consisting of halogen, hydroxy, C1-C6 alkoxy linear or branched or C1-C6 alkenyloxy linear or branched, amino, optionally mono- or disubstituted with C1-C6 linear or branched alkyl; R3 is NH2, NHR4; R4 is C1-C6 alkyl or C1-C6 hydroxyalkyl, C1-C3 alkoxyalkyl, amino(C1-C6)alkyl, where the amino group is optionally substituted with one or two C1-C3 linear or branched alkyl groups, or with one or two C2-C3 alkenyl groups C6-C14 aryl or C6-C14 aryl(C1-C6)alkyl, with the aryl group optionally substituted by one or more substituents, either the same or different, selected from the group consisting by halogen, hydroxy, C1-C6 alkoxy linear or branched or C1-C6 alkenyloxy linear or branched, amino, mono- or di-substituted with C1-C6 alkyl linear or branched or C1-C6 alkenyl linear or branched; and their pharmaceutically acceptable salts. These compounds are antagonists of the adenosine A2a receptor and useful as medicaments, in particular for the treatment of Parkinson's disease.
Owner:SIGMA TAU IND FARMACEUTICHE RIUNITE SPA

Pharmaceutical compositions comprising an adenosine receptor agonist or antagonist

InactiveUS7064112B1Prevent proliferationInhibit proliferation and growth of tumor cellBiocideSugar derivativesSide effectLeukopenia
Adenosine receptor agonists, particularly an agonist which binds to the A3 adenosine receptor, are used for induction of production or secretion of G-CSF within the body, prevention or treatment of toxic side effects of a drug or prevention or treatment of leukopenia, particularly drug-induced leukopenias; and inhibition of abnormal cell growth and proliferation.
Owner:CAN-FITE BIOPHARMA LTD

Pharmaceutical administration of adenosine agonists

InactiveUS6638914B1Increase the molecule's A.sub.1 selectivityImprove biological activityBiocideSugar derivativesBone marrow cellBone marrow cell proliferation
The present invention relates to pharmaceutical compositions for use in inducing proliferation of the hematopoietic system, in particular, of bone marrow cells, comprising a pharmaceutically acceptable carrier, excipient or diluent and, as an active ingredient, an effective amount of an adenosine A1 receptor agonist. The pharmaceutical composition of the present invention may be used to induce proliferation of bone marrow cells, in a variety of clinical situations where such proliferation is therapeutically beneficial.The active ingredient within the pharmaceutical composition of the invention may be a compound of general formula (I) as described herein or any other compound or substance which specifically binds to and / or activates the A1 adenosine receptor and acts as an agonist to the receptor's natural ligand.
Owner:CAN-FITE BIOPHARMA LTD

Compounds specific to adenosine A3 receptor and uses thereof

This invention pertains to compounds which specifically inhibit the adenosine A3 receptor and the use of these compounds to treat a disease associated with A3 adenosine receptor in a subject, comprising administering to the subject a therapeutically effective amount of the compounds.
Owner:OSI PHARMA INC

Agonists of A2A adenosine receptors for treatment of diabetic nephropathy

ActiveUS7396825B2Prevent renal diabetic nephropathyGood effectBiocideSugar derivativesDiabetic kidneyDisease
The present invention provides a therapeutic method for treating diabetic kidney disease, e.g., diabetic nephropathy that includes the administration of an effective amount of an A2A adenosine receptor agonist. Optionally, the method includes administration of a type IV PDE inhibitor.
Owner:UNIV OF VIRGINIA ALUMNI PATENTS FOUND

Use of adenosine receptor signaling to modulate permeability of blood-brain barrier

InactiveUS20130224110A1Permeability of BBB is increasedFacilitates CNS entryBiocideHeavy metal active ingredientsMedicineBbb permeability
The present invention relates to a method of increasing blood brain barrier (“BBB”) permeability in a subject. This method involves administering to the subject an agent or agents which activate both of the A1 and A2A adenosine receptors. Also disclosed is a method to decrease BBB permeability in a subject. This method includes administering to the subject an agent which inhibits or blocks the A2A adenosine receptor signaling. Compositions relating to the same are also disclosed.
Owner:CORNELL UNIVERSITY

A1 adenosine receptor antagonists

Disclosed are novel methods of antagonizing the A1 adenosine receptor in a mammal, comprising administering to a mammal in need thereof a therapeutically effective dose of a compound of the formula: wherein R1 is optionally substituted C1-4 alkyl; Y is C1-4 alkylene; and Z is phenyl that is optionally substituted with halo, hydroxy, amino, cyano, or optionally substituted C1-4 alkyl or a pharmaceutically acceptable salt, ester, or prodrug thereof. The A1 adenosine receptors are antagonized in order to treat a disease state is chosen from renal failure, renal dysfunction, nephritis, hypertension, oedema, Alzheimers disease, stress, depression, cardiac arrhythmia, restoration of cardiac function, congestive heart failure, diabetes, asthma, respiratory disorders, ischaemia-induced injury of the brain, heart and kidney, and diarrhea.
Owner:CV THERAPEUTICS INC

A3 adenosine receptors as targets for the modulation of central serotonergic signaling

InactiveUS20090088403A1Reducing SERT activityEnhance SERT activityBiocideCarbohydrate active ingredientsSerotonin transporterIn vivo
The present invention relates to the use of adenosine type 3 receptor (A3R) modulators to modulate serotonin transporter (SERT) function in vivo. In particular, antagonists of A3R can be used to inhibit A3R-dependent upregulation of SERT, for example, as antidepressants.
Owner:VANDERBILT UNIV

Derivatives of triazolyl-imidazopyridine and of the triazolylpurines useful as ligandsof the adenosine a2a receptor and their use as medicaments

Compounds of formula (I)wherein: X is N;R1 is C1–C6 linear or branched alkyl or C1–C6 linear or branched alkenyl; R2 is hydrogen, C1–C6 linear or branched alkyl or C1–C6 linear or branched alkenyl, C6–C14 aryl or C6–C14 aryl(C1–C6) linear or branched alkyl or C6–C14 aryl(C1–C6) linear or branched alkenyl, with the aryl group optionally substituted by one or more substituents, either the same or different, selected from the group consisting of halogen, hydroxy, C1–C6 alkoxy linear or branched or C114 C6 alkenyloxy linear or branched, amino, optionally mono- or disubstituted with C1–C6 linear or branched alkyl; R3 is NH2, NHR4; R4 is C1–C6 alkyl or C1–C6 hydroxyalkyl, C1–C3 alkoxyalkyl, amino(C1–C6)alkyl, where the amino group is optionally substituted with one or two C1–C3 linear or branched alkyl groups, or with one or two C2–C3 alkenyl groups C6–C14 aryl or C6–C14 aryl(C1–C6)alkyl, with the aryl group optionally substituted by one or more substituents, either the same or different, selected from the group consisting by halogen, hydroxy, C1–C6 alkoxy linear or branched or C1–C6 alkenyloxy linear or branched, amino, mono- or di-substituted with C1–C6 alkyl linear or branched or C1–C6 alkenyl linear or branched; and their pharmaceutically acceptable salts. These compounds are antagonists of the adenosine A2a receptor and useful as medicaments, in particular for the treatment of Parkinson's disease.
Owner:SIGMA TAU IND FARMACEUTICHE RIUNITE SPA

Adenosine receptor stimulating agent and application thereof

The invention relates to an application HEA of N (6)-(2-hydroxyethyl)-adenosine (HEA) and derivatives thereof in medicine or food preparation as an adenosine A1 receptor stimulating agent as well as an application of the derivatives thereof in treating nervous system diseases, such as calming and hypnotizing, anti-convulsion, cerebral protection, Parkinson disease, drug addiction and the like, related to an adenosine receptor conditioner. The invention offers a new drug source for the prevention of nervous system diseases.
Owner:ZHEJIANG CHENGYI PAHRMACEUTICAL

Purine derivatives as A3 adenosine receptor-selective agonists

Disclosed are (N)-methanocarba adenine nucleosides, e.g., of formula (I) as highly potent A3 adenosine receptor agonists, pharmaceutical compositions comprising such nucleosides, and a method of use of these nucleosides, wherein R1-R6 are as defined in the specification. These nucleosides exhibit similar selectivities as agonists of the A3 versus the A1 receptor for both human and mouse adenosine receptors, and are contemplated for use in the treatment a number of diseases, for example, inflammation, cardiac ischemia, stroke, asthma, diabetes, and cardiac arrhythmias.
Owner:UNITED STATES OF AMERICA

Compounds antagonizing A3 adenosine receptor, method for preparing them, and medical-use thereof

ActiveUS10196396B2Preventing and ameliorating and treating glaucomaBiocideSenses disorderDiseaseGlaucoma
The present disclosure provides compounds useful in the amelioration, prevention or treatment of A3 adenosine receptor mediated diseases, such as glaucoma and glaucoma-related ocular disorders, having the structure of Formula I as defined in the detailed description; pharmaceutical compositions comprising at least one of the compounds; and methods for ameliorating, preventing or treating A3 adenosine receptor mediated diseases using the compound.
Owner:HANDOK INC

Small-molecular antagonist for A3 adenosine receptor

The invention discloses a small-molecular antagonist for an A3 adenosine receptor, and an application thereof in medicine synthesis, and concretely relates to a use of the small-molecular antagonist for the A3 adenosine receptor and pharmacologically available salts of the small-molecular antagonist for the A3 adenosine receptor as medicines for treating or preventing A3 adenosine receptor-mediated related diseases or symptoms.
Owner:NANKAI UNIV

Therapeutic agent for migraine

Provided are therapeutic and / or preventive agents for migraine which comprise, as an active ingredient, a compound having a selective adenosine A2A receptor antagonistic activity or a pharmaceutically acceptable salt thereof; therapeutic and / or preventive agents for migraine which comprise, as an active ingredient, a compound having a selective adenosine A2A receptor antagonistic activity, which has an affinity for the adenosine A2A receptor 10 times or higher than that for the adenosine A1 receptor, or a pharmaceutically acceptable salt thereof; and the like.
Owner:KYOWA HAKKO KIRIN CO LTD

Pharmaceutical use of adenosine agonists

The present invention relates to a method for inducing proliferation of the hematopoietic system, in particular, of bone marrow cells, comprising administering to a subject an effective amount of an adenosine A1 receptor agonist. The method of the invention may be utilized n a variety of clinical situations where such proliferation is therapeutically beneficial. The active ingredient within the pharmaceutical composition of the invention may be a compound of general formula (I) as described herein, or any other compound or substance which specifically binds to and / or activates the A1 adenosine receptor and acts as an agonist to the receptor's natural ligand.
Owner:CAN-FITE BIOPHARMA LTD

Synergy of dopamine d2 and adenosine a2 receptors activates pka signaling via beta/gamma dimers

This invention pertains to the discovery that a dopamine receptor agonist can activate PKA signaling and / or can act synergistically with an adenosine receptor to activate such signaling. In various embodiments, this invention exploits the synergy between the dopamine receptor pathway and an adenosine receptor pathway to provide methods of mitigating one or more symptoms produced by the chronic consumption of a substance of abuse or to mitigate one or more physiological and / or behavioral symptoms associated with cessation of chronic consumption of a substance of abuse. In certain embodiments, the methods involve administering to the mammal an effective amount of an adenosine receptor antagonist; and an effective amount of a dopamine receptor antagonist; where the effective amount of the adenosine receptor antagonist is lower than the effective amount of an adenosine receptor antagonist administered without said dopamine receptor antagonist.
Owner:RGT UNIV OF CALIFORNIA

Agitation micelle for treatment of cerebral arterial thrombosis

The invention belongs to the technical field of biology and relates to agitation micelle for treatment of cerebral arterial thrombosis as well as a preparation method and an application thereof. A drug delivery system comprises a functional group across BBB (blood brain barrier), a neuroprotection drug and a nano drug delivery system, wherein the functional group is an adenosine A2A receptor agitation group capable of reversibly regulating BBB permeability, and a micromolecular agonist is linked with a PEG end of the outer surface of a micelle drug carrier system in a chemical bond connectionmanner. The nano drug delivery system can enters the stroke area safely and initiatively across BBB, and the long-term neuroprotection function is provided through sustained and controlled release ofthe neuroprotection drug. The drug delivery system has great clinical significance in improving the treatment efficacy of patients suffering from cerebral arterial thrombosis and reducing the toxic and side effects of drugs used currently.
Owner:FUDAN UNIV

Method of screening adenosine A2A receptor ligands by Tag-lite and analytical experimental technique

The invention discloses a method of screening adenosine A2A receptor ligands by Tag-lite and an analytical experimental technique and belongs to the field of screening of adenosine A2A receptor ligands. The method herein comprises the steps of constructing a specific-tag-fused target cytomembrane surface protein expression vector; marking tag-fused cytomembrane surface proteins through an HTRF (homogeneous time-resolved fluorescence) fluorescent group donor covalently-bound tag-specific primer; incubating the marked cells or cytomembranes with binding ligands, detecting by HTRF, and calculating Kd or Ki value of a sample under test according to data results. The method herein has the advantages that the signals are strong, the results are reliable, and the new marking technique is employedso that the signals are stronger and more stable; binding condition of receptor ligands is truly reflected based on a cell homogenous detection system, and the results are reliable.
Owner:浠思(上海)生物技术有限公司

1-aminobenzo [4, 5] imidazo [1, 2-a] pyrazine-3-formamide compound and preparation and application thereof

The invention belongs to the technical field of medical chemistry, and particularly relates to a 1-aminobenzo [4, 5] imidazo [1, 2-a] pyrazine-3-formamide compound and preparation and application thereof.The structure of the compound is shown in the formula (I), and the compound is novel in structure, is an adenosine receptor inhibitor, and can be used for preparing a novel compound. The compound has good inhibitory activity on adenosine A2A receptors and good subtype selectivity, can be used as a targeted adenosine A2A receptor inhibitor for immunotherapy, and achieves the effect of treating tumors by inhibiting the activity of the adenosine A2A receptors and releasing the removal function of an immune system on tumor cells. Meanwhile, the preparation method of the compound is simple, the cheap and easily available compound is used as the raw material, the reaction condition is mild, the total yield and the purity are high, the production of dozens of grams can be realized, and the research of later clinical candidate adenosine A2A receptor inhibitors is supported.
Owner:SUN YAT SEN UNIV
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