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48 results about "MAO inhibitors" patented technology

MAO Inhibitors (also called MAOI's) work by interfering with the enzyme responsible for metabolizing seratonin, epinephrine, dopamine and norepinephrine.

Propargylamino indan derivatives and propargylamino tetralin derivatives as brain-selective mao inhibitors

The subject invention provides derivatives of propargylamino indan (PAI) and propargylamino tetralin that selectively inhibit monoamine oxidase (MAO) in the brain, having the structure:wherein R1 is OC(O)R9 and R2 is H,wherein R9 is branched or unbranched C1 to C6 alkyl, aryl, or aralkyl, orR1 is OC(O)R4 and R2 is OC(O)R4,wherein R4 is branched or unbranched C1 to C6 alkyl, aryl, aralkyl or NR5R6,wherein R5 and R6 are each independently H, C1 to C8 alkyl, C6 to C12 aryl, C6 to C12 aralkyl or C6 to C12 cycloalkyl, each optionally substituted;wherein R3 is H or C1 to C6 alkyl;wherein n is 0 or 1; andwherein m is 1 or 2,or a pharmaceutically acceptable salt thereof. Additionally, the subject invention provides methods of treating neurological disorders using these compounds, uses of these compounds for the manufacture of medicaments for treating neurological disorders and processes for synthesis of these compounds.
Owner:TEVA PHARMA IND LTD

As-needed administration of tricyclic and other non-SRI antidepressant drugs to treat premature ejaculation

A method is provided for treatment of premature ejaculation by administration of an antidepressant drug selected from tricyclic antidepressants, tetracyclic antidepressants, MAO inhibitors, azaspirone antidepressants, and atypical non-SRI antidepressants. In a preferred embodiment, administration is on as “as-needed” basis, i.e., the drug is administered immediately or at most several hours prior to sexual activity. Pharmaceutical formulations and packaged kits are also provided.
Owner:VIVUS

Monoamine oxidase inhibitors and methods for treatment and diagnosis of prostate cancer

ActiveUS20130039854A1Easy to switchMinimize background noiseBiocidePowder deliveryEpitheliumCancer cell
A mechanism of monoamine oxidases (MAOs) driven epithelium-to-mesenchymal transition (EMT) is disclosed. Also disclosed are methods for treating cancer by inhibiting or suppressing MAOs in cancer cells. Novel MAOs inhibitors, such as small molecules, siRNA, shRNA, antisense oligonucleotides, aptamers, decoys, and pharmaceutical compositions useful for treating cancer by disrupting the workings of MAOs are provided. In particular, a class of conjugates formed by covalently conjugating near infrared dye 783, IR-780, and MHI-148 to a MAO inhibitor, such as clorgyline, with and without encapsulation it in a nanoparticle is provided. Other aspects of the invention include methods for forming the nano-conjugates, method for monitoring treatment progress in a cancer patient by monitoring the changes in MAO activity, methods for screening patients who are at risk of cancer or differentiating different forms of cancer by assaying the level and location of MAO activity.
Owner:UNIV OF SOUTHERN CALIFORNIA

Monoamine oxidase (MAO) inhibitors and uses thereof

The present invention provides a group of tobacco alkaloids, tobacco extract, Yerbamaté extract, and an extract of chewing gum and lozenges which are modulators of monoamine oxidase (MAO) activity (i.e., compounds and substances which inhibit MAO enzyme and prevent its biological activity). The MAO inhibitors of the present invention can cause an increase in the level of norepinephrine, dopamine, and serotonin in the brain and other tissues, and thus can cause a wide variety of pharmacological effects mediated by their effects on these compounds. The MAO inhibitors of the present invention are useful for a variety of therapeutic applications, such as the treatment of depression, disorders of attention and focus, mood and emotional disorders, Parkinson's disease, extrapyramidal disorders, hypertension, substance abuse, smoking substitution, anti-depression therapy, eating disorders, withdrawal syndromes, and the cessation of smoking.
Owner:REGENT COURT TECH

Use of monoamine oxidase inhibitors to improve epithelial biology

The invention provides a method for improving hair biology, e.g., hair growth. The method comprises administering to a subject a monoamine oxidase inhibitor and a vasodilator, a zinc salt of a carboxylic acid, a xanthine compound, pyrithione or a salt thereof, saponin, tritapene, crataegolic acid, celastrol, asiatic acid, an inhibitor of 5-alpha-reductase, 1,4-methyl-4-azasteroid, an androgen receptor antagonist, azelaic acid or a derivate thereof, cyclosporin, triiodothyronine, diazoxide, retinoic acid, a prostaglandin analog, aminexil, carnitine tartrate, apigenin, procapil, or adenosine, in an amount effective to achieve a desired effect. The invention further provides a method of reducing or delaying the appearance of an age-related skin imperfection. The method comprises administering to the subject a composition comprising an MAO inhibitor. A kit for improving hair growth also is provided.
Owner:PROCTER & GAMBLE CO

Polypharmacophoric agents

One aspect of the present invention relates to polypharmacophoric compounds. In certain embodiments, the polyphamacophore compounds comprise individual pharmacophore units selected from the group consisting of D-1 agonists, D-2 agonists, D-3 agonists, D-4 agonists, irreversible monoamine inhibitors, reversible monoamine inhibitors, monoamine transporter inhibitors, COMT inhibitors, MAO inhibitors, and dopamine transporter inhibitors. Moreover, the present invention also relates to combinatorial libraries of polypharmacophoric compounds. Another aspect of the present invention relates to the use of a polypharmacophoric compound in a method of treating a mammal in need thereof. For example, a polypharmacophoric compound of the present invention may be used in a method of treating a mammal afflicted with Alzheimer's Disease, Huntington's Disease, depression, attention deficit disorder, autism, obesity, or inflammation.
Owner:MOLECULAR INSIGHT PHARMA

Propargyl imine compounds and use thereof in preparation of MAO inhibitor

The invention provides use of propargyl imine compounds in the preparation of a monoamine oxidase inhibitor and new propargyl imine compounds. The propargyl imine compounds have a structural formula (I). The invention has the advantages that: (1) equipment required for the preparation of the propargyl imine compounds is simple, the operation process is simple and convenient, the raw material sources are commercialized and readily available and the compounds serving as the monoamine oxidase inhibitor are stable in nature and high in purity (over 99 percent); and (2) compared with the traditional monoamine oxidase inhibitor, the monoamine oxidase inhibitor prepared from the new propargyl imine compounds has a simpler structure, a higher inhibition activity, higher MAO-A selectivity and higher MAO-B selectivity.
Owner:ZHEJIANG UNIV OF TECH

Methods of treating patients suffering from movement disorders

InactiveUS7727994B2Reducing and suppressing adverse effectiveness of L-DOPAShorten closing timeBiocideNervous disorderDisease patientAdenosine a
The present invention is directed to methods of treating movement disorders by administering an effective amount of one or more adenosine A2A receptor antagonists to a patient in need thereof. The present invention also provides methods of decreasing the adverse effects of L-DOPA in patients receiving L-DOPA therapy in the treatment of Parkinson's disease. The present invention further provides methods and compositions for treating Parkinson's disease patients with sub-clinically effective doses of L-DOPA by combining L-DOPA treatment with an effective amount of one or more adenosine A2A receptor antagonists (i.e., L-DOPA sparing effect). The present invention further provides methods of effective treatment of Parkinson's disease by co-administering at least one adenosine A2A receptor antagonist, L-DOPA and a dopamine agonist and / or a COMT inhibitor and / or a MAO inhibitor. The present invention further provides methods of prolonging effective treatment of Parkinson's disease by administering an adenosine A2A receptor antagonist singly or together with a dopamine agonist, and / or a COMT inhibitor, and / or a MAO inhibitor without prior or subsequent administration of L-DOPA, delaying or removing on-set of L-DOPA motor complication.
Owner:KYOWA HAKKO KIRIN CO LTD

MAO inhibitors and their conjugates as therapeutics for the treatment of brain cancer

A pharmaceutical composition and method for treating brain cancer are provided. The method includes administering to a patient in need thereof an effective amount of one or more compounds that include moclobemide, clorgyline, clorgyline's Near-infra-red dye Monoamine Oxidase Inhibitor (NMI), and MHI 148- clorgyline, and their salt thereof. The composition and method are particularly effective in reducing the size of glioblastomas that are temozolomide (TMZ) resistant.
Owner:UNIV OF SOUTHERN CALIFORNIA

Purpose of coumarin compound in preparation of monoamine oxidase inhibitor

InactiveCN108478568AMonoamine oxidase ACtiveNervous disorderHeterocyclic compound active ingredientsXanthine oxidase inhibitorMonoamine Oxidase A Gene
The invention discloses a purpose of a coumarin compound shown as a general formula (I) in preparation of a monoamine oxidase inhibitor, which belongs to the technical field of a medicine. Through in-vitro enzyme activity tests, the compound has good inhibition activity for monoamine oxidases A and B, and provides reference and novel thinking for developing the novel MAO inhibitor.
Owner:HUAZHONG AGRI UNIV

Polypharmacophoric agents

One aspect of the present invention relates to polypharmacophoric compounds. In certain embodiments, the polyphamacophore compounds comprise individual pharmacophore units selected from the group consisting of D-1 agonists, D-2 agonists, D-3 agonists, D-4 agonists, irreversible monoamine inhibitors, reversible monoamine inhibitors, monoamine transporter inhibitors, COMT inhibitors, MAO inhibitors, and dopamine transporter inhibitors. Moreover, the present invention also relates to combinatorial libraries of polypharmacophoric compounds. Another aspect of the present invention relates to the use of a polypharmacophoric compound in a method of treating a mammal in need thereof. For example, a polypharmacophoric compound of the present invention may be used in a method of treating a mammal afflicted with Alzheimer's Disease, Huntington's Disease, depression, attention deficit disorder, autism, obesity, or inflammation.
Owner:MOLECULAR INSIGHT PHARMA

Application of traditional Chinese medicine composition to preparation of monoamine oxidase MAO inhibitor

The invention provides application of a traditional Chinese medicine composition to preparation of a monoamine oxidase (MAO) inhibitor. The traditional Chinese medicine composition is prepared from 20 parts of delavay raspberry, 18 parts of galium verum, 12 parts of blumea balsamifera roots, 15 parts of wintersweet roots or stems and 10 parts of roots of multibract raspberry. Compared with the conventional monoamine oxidase MAO inhibitor, the monoamine oxidase MAO inhibitor provided by the invention has the advantages that the inhibitory activity and the selectivity on MAO-A and MAO-B of the monoamine oxidase MAO inhibitor are both greatly improved, that is, a great improvement is achieved.
Owner:臧孝国

Application of compound in preparing monoamine oxidase MAO inhibitor

The invention provides an application of a compound phyllanthoid A in preparing a monoamine oxidase (MAO) inhibitor. Compared with existing MAO inhibitors, the inhibiter has greatly improved inhibition activity and selectivity upon MAO-A and MAO-B. The application of phyllanthoid A in preparing the MAO inhibitor is disclosed for a first time, and the compound has high inhibition activity against MAO. The compound has outstanding substantive feature. The application has significant progress in treatments of diseases related to MAO disorder.
Owner:杨文君

Application of Chukrasone A in preparing MAO (Monoamine Oxidase) inhibitor medicines

The invention relates to an application of Chukrasone A in preparing MAO (Monoamine Oxidase) inhibitor medicines. Compared with existing MAO inhibitors, the MAO inhibitor provided by the invention is greatly improved in inhibitory activity and selectivity to MAO-A and MAO-B. The use of the Chukrasone A for preparing MAO inhibitor medicines provided by the invention is disclosed for the first time. As the framework type belongs to a brand-new framework type, and the inhibitory activity of the Chukrasone A to MAO is unimaginably strong, the probability of giving any enlightenment by other compounds does not exist. The Chukrasone A has remarkable substantial characteristics and meanwhile has remarkable progress for treating diseases associated to MAO disorder.
Owner:重庆西南制药二厂有限责任公司

Application of Norsampsone B in preparing MAO (monoamine oxidase) inhibitor

The invention provides application of Norsampsone B in preparing a MAO (monoamine oxidase) inhibitor, compared with the existing MAO inhibitor, the inhibitory activity and the selectivity of MAO-A and MAO-B of the Norsampsone B are greatly improved. The application of the Norsampsone B in preparing the MAO inhibitor is disclosed for the first time, and the inhibitory activity to the MAO is high, the Norsampsone B has outstanding substantive features, and obviously has remarkable improvement for treating diseases relevant to imbalance of the MAO at the same time.
Owner:ZIBO DINGLI PATENT INFORMATION CONSULTING CO LTD

Application of Kadcoccitones A in preparing monoamine oxidase (MAO) inhibitor

The invention provides application of Kadcoccitones A in preparing a monoamine oxidase (MAO) inhibitor. Compared with the existing MAO inhibitor, the Kadcoccitones A has greatly higher activity and selectivity for MAO-A and MAO-B. The application of the Kadcoccitones A in preparing the MAO inhibitor is disclosed for the first time; and the Kadcoccitones A has high activity for inhibiting MAO, has the characteristic of outstanding materiality, and apparently has marked progresses when being used for treating MAO maladjustment related diseases.
Owner:NANJING ZHENGLIANG MEDICAL TECH

Application of Aphanamgrandiol A in preparing monoamine oxidase (MAO) inhibitor

The invention provides an application of Aphanamgrandiol A in preparing a monoamine oxidase (MAO) inhibitor. Compared with existing MAO inhibitors, the inhibiting activity and the selectivity to MAO-A and MAO-B of Aphanamgrandiol A are greatly improved. The use of Aphanamgrandiol A for preparing the MAO inhibitor provided by the invention is disclosed for the first time. As the framework type belongs to a brand-new framework type, and the inhibiting activity of Aphanamgrandiol A to MAO is unexpectedly strong, the probability of giving any indication by other compounds does not exist, so that Aphanamgrandiol A has remarkable substantive characteristics and meanwhile obviously has remarkable progress for treating MAO disorder related diseases.
Owner:HUAIAN UNIV SCI PARK MANAGEMENT CO LTD

Application of lathyranone A to preparation of monoamine oxidase (MAO) inhibitor

The invention provides the application of Lathyranone A. in the preparation of monoamine oxidase (MAO) inhibitors. Compared with the existing monoamine oxidase inhibitors, its inhibitory activity and selectivity to MAO‑A and MAO‑B are greatly improved. The use of Lathyranone A. involved in the present invention in the preparation of monoamine oxidase (MAO) inhibitors is disclosed for the first time. Since the skeleton type belongs to a new skeleton type, and its inhibitory activity against monoamine oxidase is unexpectedly strong, there is no inspiration from other compounds It is possible, has outstanding substantive features, and at the same time, it is obviously a significant progress in the treatment of diseases related to monoamine oxidase disorders.
Owner:ZIBO DINGLI PATENT INFORMATION CONSULTING CO LTD

Application of triazine compound in preparation of monoamine oxidase inhibitor

The invention discloses the application of a triazine compound shown as a structural formula (I) in the preparation of a monoamine oxidase inhibitor. Through in vitro enzyme activity experimental measurement, the compound has good inhibitory activity for monoamine oxidase-B, so that reference is provided for developing a novel MAO inhibitor, and a new thought is inspired.
Owner:HUAZHONG AGRI UNIV

Applications of Ternatusine A in preparing monoamine oxidase MAO inhibitor

The invention provides applications of Ternatusine A in preparing a monoamine oxidase (MAO) inhibitor. Compared with conventional monoamine oxidase inhibitors, the inhibitory activity of the monoamine oxidase (MAO) inhibitor, and the selectivity of the monoamine oxidase (MAO) inhibitor on MAO-A and MAO-B are increased greatly. The applications of Ternatusine A in preparing the monoamine oxidase (MAO) inhibitor are disclosed for the first time, the skeleton type of the monoamine oxidase (MAO) inhibitor is new, inhibition activity of the monoamine oxidase (MAO) inhibitor on monoamine oxidase is unexpectedly high, no revelation is provided by other compounds, prominent substantive features are achieved, and obvious progress is achieved when the monoamine oxidase (MAO) inhibitor is used for treating monoamine oxidase disorder related diseases.
Owner:ZIBO DINGLI PATENT INFORMATION CONSULTING CO LTD

Application of Gypensapogenin B to preparation of MAO (monoamine oxidase) inhibitor

The invention provides application of Gypensapogenin B to preparation of a MAO (monoamine oxidase) inhibitor. Compared with the existing MAO inhibitor, the MAO inhibitor provided by the invention has greatly improved inhibitory activity and selectivity on MAO-A and MAO-B. The application of Gypensapogenin B to preparation of the MAO inhibitor is firstly publicized; and as a framework type belongs to a brand-new framework type, the framework type has unexpectedly strong inhibitory activity on the MAO inhibitor without any possibility shown by other compounds, and has outstanding substantial characteristics and remarkable progress for treating the diseases related to MAO unbalance at the same time.
Owner:吴俊华

Application of ieodoglucomides B to prepare monoamine oxidase (MAO) inhibitor

The invention provides application of ieodoglucomides B to prepare a monoamine oxidase (MAO) inhibitor, and compared with a known monoamine oxidase inhibitor, the monoamine oxidase (MAO) inhibitor is greatly improved in inhibition activity and selectivity on MAO-A and MAO-B. The related purpose of ieodoglucomides B to prepare the monoamine oxidase (MAO) inhibitor is disclosed for the first time. Because the l type belongs to a brand-new framework type and the inhibition activity of the inhibitor on monoamine oxidase (MAO) is unexpected, there is not the possibility that other compounds give any enlightenment, the technical scheme possesses prominent substantive features, and also treatment on monoamine oxidase (MAO) imbalance related diseases obviously possesses notable progress.
Owner:ZIBO DINGLI PATENT INFORMATION CONSULTING CO LTD

Application of Aphanamgrandiol A in preparing monoamine oxidase (MAO) inhibitor

The invention provides an application of Aphanamgrandiol A in preparing a monoamine oxidase (MAO) inhibitor. Compared with existing MAO inhibitors, the inhibiting activity and the selectivity to MAO-A and MAO-B of Aphanamgrandiol A are greatly improved. The use of Aphanamgrandiol A for preparing the MAO inhibitor provided by the invention is disclosed for the first time. As the framework type belongs to a brand-new framework type, and the inhibiting activity of Aphanamgrandiol A to MAO is unexpectedly strong, the probability of giving any indication by other compounds does not exist, so that Aphanamgrandiol A has remarkable substantive characteristics and meanwhile obviously has remarkable progress for treating MAO disorder related diseases.
Owner:HUAIAN UNIV SCI PARK MANAGEMENT CO LTD

Use of Daphnilongeranin A in preparation of monoamine oxidase (MAO) inhibitor

The invention relates to a novel use of Daphnilongeranin A in preparation of a monoamine oxidase (MAO) inhibitor. Compared with the exciting monoamine oxidase inhibitor, the Daphnilongeranin A has higher inhibition activity and MAO-A and MAO-B selectivity. The use of Alistonitrine A in preparation of a MAO inhibitor is disclosed first. The skeleton type of the Daphnilongeranin A belongs a novel skeleton type, the Daphnilongeranin A has unexpected monoamine oxidase inhibition activity, is free of any enlightenment provided by other compounds and has prominent substantive features, and the use of Daphnilongeranin A in treatment on monoamine oxidase disorder-related diseases has substantial progress.
Owner:ZIBO DINGLI PATENT INFORMATION CONSULTING CO LTD
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