CAS: 156-51-4; Phenelzine Hydrogen Sulphate

该化合物是一种化学化合物,主要用作单胺氧化酶抑制剂(MAOI),用于治疗抑郁和焦虑症,是一种氢氨衍生物,其特点是能够抑制酶单胺氧化酶,造成脑中诸如血清素,无肾上腺素和多巴胺等...

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    专利号:US-12295961-B2
    优先权日:2009-12-31
    标 题:Modulation of solubility, stability, absorption, metabolism, and pharmacokinetic profile of lipophilic drugs by sterols
    发明人:DHINGRA OM
    权利人:MARIUS PHARMACEUTICALS INC
    摘要:A formulation for drug delivery, providing enhanced modulation of solubility, stability, absorption, metabolism, and/or pharmacokinetic profile of a lipophilic therapeutic agent by formulation with sterols and/or sterol esters, resulting in higher bioavailability of a therapeutic agent administered to a subject in need of such therapeutic agent. The formulation contains a therapeutic agent and a sterol or sterol ester, and can, optionally, further contain a solubilizer and/or an enhancing agent. Also described are pharmaceutical compositions containing the formulations and methods of making and methods of using the formulations and pharmaceutical compositions. Formulations of the disclosure can be constituted to minimize the synthesis of dihydrotestosterone when the therapeutic agent includes testosterone or testosterone esters.

    专利号:US-2011040105-A1
    优先权日:2008-04-16
    标题 :Processes useful for the synthesis of (r)-1--2-methyl-pyrrolidine
    发明人:HUBER CHRISTIAN H; KHULMAN YOUNG MI; TANDEL SAGUN K; JOHANNSEN STEPHEN R; WANG TINGMIN; ANGELL PAUL
    权利人:ARENA PHARM INC
    摘要:Processes useful for making a pharmaceutically useful compound according to Formula (I), forms of such a compound, and intermediates useful in such processes are described.

    专利号:WO-2024061972-A1
    优先权日:2022-09-20
    标 题:Methods and platform for chemical synthesis
    发明人:CRONIN LEE; MANZANO SEBASTIÃ?N; ZALESSKIY SERGEY; KITSON PHILIP; WANG HSIN
    权利人:UNIV GLASGOW COURT
    摘要:The invention relates to a method and apparatus for performing and characterising a chemical synthesis, such as those performed with an automated chemical synthesis platform, including such that are portable platforms, the method comprising the steps of: performing a chemical synthesis in a chemical synthesiser; recording analytical data during the chemical synthesis, and developing a profile for the analytical data recorded over time; and comparing the profile for the chemical synthesis against a reference profile, which reference profile is the analytical data recorded over time for a reference chemical synthesis, wherein the chemical synthesis and the reference chemical synthesis share at least the same reagents and method steps for the same intended product, such as the chemical synthesis and the reference chemical synthesis sharing the same instruction set. The method and apparatus are for intended for use in replication of approved, chemical syntheses based on common reaction platforms.

    专利号:US-11617758-B2
    优先权日:2009-12-31
    标 题 :Emulsion formulations
    发明人:DHINGRA OM; BERNSTEIN JAMES S
    权利人:MARIUS PHARMACEUTICALS LLC
    摘要:A SEDDS or SMEDDS or SNEDDS formulation for drug delivery of a lipophilic therapeutic agent, providing enhanced modulation of solubility, stability, absorption, metabolism, and/or pharmacokinetic profile of the therapeutic agent by formulation with a lipophilic surfactant, a hydrophilic surfactant, one or more solubilizers and, optionally, digestible oils, resulting in higher bioavailability of the therapeutic agent administered to a subject in need of such therapeutic agent. Also described are pharmaceutical compositions containing the formulations and methods of making and methods of using the formulations and pharmaceutical compositions. Formulations of the disclosure can be constituted to minimize the synthesis of dihydrotestosterone when the therapeutic agent includes testosterone or testosterone esters.

    专利号:US-2013303495-A1
    优先权日:2009-12-31
    标题:Emulsion formulations
    发明人:DHINGRA OM; BERNSTEIN JAMES S
    权利人:SOV THERAPEUTICS; DIFFERENTIAL DRUG DEV ASSOCIATES LLC
    摘要:A SEDDS or SMEDDS or SNEDDS formulation for drug delivery of a lipophilic therapeutic agent, providing enhanced modulation of solubility, stability, absorption, metabolism, and/or pharmacokinetic profile of the therapeutic agent by formulation with a lipophilic surfactant, a hydrophilic surfactant, one or more solubilizers and, optionally, digestible oils, resulting in higher bioavailability of the therapeutic agent administered to a subject in need of such therapeutic agent. Also described are pharmaceutical compositions containing the formulations and methods of making and methods of using the formulations and pharmaceutical compositions. Formulations of the disclosure can be constituted to minimize the synthesis of dihydrotestosterone when the therapeutic agent includes testosterone or testosterone esters.

    专利号:US-9751877-B2
    优先权日:2012-09-21
    标题 :Substituted pyrido[1,2-a]pyrazines for the treatment of neurodegenerative and neurological disorders
    发明人:PETTERSSON MARTIN YOUNGJIN; JOHNSON DOUGLAS SCOTT; SUBRAMANYAM CHAKRAPANI; O'DONNELL CHRISTOPHER JOHN; AM ENDE CHRISTOPHER WILLIAM; GREEN MICHAEL ERIC; PATEL NANDINI CHATURBHAI; STIFF CORY MICHAEL; TRAN TUAN PHONG; KAUFFMAN GREGORY WAYNE; STEPAN ANTONIA FRIEDERIKE; VERHOEST PATRICK ROBERT
    权利人:PFIZER
    摘要:Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I n nas defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

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    主要参考文献


    1: Beechinor RJ, Tyson R, Roth ME. Phenelzine and Morphine Drug-Drug Interaction? A Literature Review. J Pharm Pract. 2021 Oct;34(5):818-823. doi: 10.1177/0897190020970752. Epub 2020 Dec 3. 41(1):53-6. doi: 10.1111/j.1365-2044.1986.tb12704.x. 47(1):81-89. doi: 10.1080/01480545.2023.2217696. Epub 2023 May 29.
    6:107-10. doi: 10.2147/CPAA.S67271. Retraction in: Clin Pharmacol. 2021 Mar 03;13:39. doi: 10.2147/CPAA.S308255.
    5: Phenelzine and phenelzine sulphate. IARC Monogr Eval Carcinog Risk Chem Hum. 1980;24:175-84. 164(3):e211-22. Italian. doi: 10.7417/CT.2013.1571. 1(6072):1353. doi: 10.1136/bmj.1.6072.1353-a.

    合成参考文献


    摘要:Journal of Medicinal Chemistry., 18(20), 1975
    摘要:American Journal of Medicine., 80(689), 1986 []
    摘要:Anaesthesia., 41(53), 1986 []
    参考文献:10.1007/s11920-004-0068-y
    摘要:Raj YP. Psychopharmacology of borderline personality disorder. Curr Psychiatry Rep. 2004 Jun;6(3):225–31. doi: 10.1007/s11920-004-0068-y.
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