CAS: 23109-05-9; α-Amanitin

该化合物是一种循环八氯化物,是RNA聚合酶II的强大抑制剂,产自某些阿曼尼塔蘑菇物种,其主要机制涉及对高特异酶的约束,有效阻止在eukaryatic细胞中合成氨氨,这种特性使α-阿马尼丁成为分子生物学研究转录机制和吸附的一种宝贵工具.由于其毒性高,α-阿马尼丁还被用于研究肝毒性和细胞应激反应.其明确界定的结构和连贯的生物活性确保实验应用的可靠性.适当处理由于其极端毒性,要求实验室遵守严格的安全规定,因此至关重要.

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    专利号:US-2022298204-A1
    优先权日:2019-07-05
    标题 :Synthesis of a-amanitin and its derivatives
    发明人:SIEGERT MARY-ANN; KNITTEL CAROLINE HERTA; SÜSSMUTH RODERICH
    权利人:PURE BIOORGANICS SIA
    摘要:The present invention relates to the chemical synthesis of α-amanitin and its derivatives. The present invention also relates to intermediate products of the α-amanitin synthesis.

    专利号:EP-3792250-A1
    优先权日:2019-09-13
    标题:Synthesis of alpha-amanitin and its derivatives
    发明人:SIEGERT MARY-ANN; KNITTEL CAROLINE HERTA; SÜSSMUTH RODERICH
    权利人:PURE BIOORGANICS SIA
    摘要:The present invention relates to the chemical synthesis of α-amanitin and its derivatives. The present invention also relates to intermediate products of the α-amanitin synthesis.

    专利号:US-7459443-B2
    优先权日:1999-04-08
    标 题 :Synthesis of biologically active compounds in cells
    发明人:SERGEEV PAVEL
    权利人:SERGEEV PAVEL
    摘要:This invention relates to a new method of synthesis of biologically active substances of determined structure directly in the cells of living organisms containing specific RNA or DNA molecules of determined sequence. The method is based on the hybridization of two or more oligomers bound with biologically inactive precursors of biologically active substances to specific RNA or DNA in vivo in the cells of living organisms. After hybridization of the oligomers to RNA or DNA the biologically inactive precursors bound to the 5′ and/or 3′ ends of the oligomers can interact with each other to make biologically active form of the substances. This changing of properties is due to chemical reactions which bind the biologically inactive precursors through a chemical bond into a biologically active form of the whole compound.

    专利号:US-12378196-B2
    优先权日:2018-12-11
    标 题 :Synthesis of (S)-6-hydroxytryptophan and derivatives thereof
    发明人:SIMON WERNER; WERNER-SIMON SUSANNE; MüLLER CHRISTOPH
    权利人:HEIDELBERG PHARMA RES GMBH
    摘要:The present invention relates to novel methods and compounds for synthesizing amanitin derivatives. The invention in particular relates to methods for synthesizing (S)-6-hydroxy-tryptophan derivatives which can be used as building blocks for synthesizing amanitin derivatives or amatoxin drug conjugates. The invention further relates to intermediate compounds of said synthesis pathways for use in amanitin derivative and amatoxin drug conjugate synthesis, and to the use of particular catalysts suited for mediating said synthesis pathways.

    专利号:US-11851651-B2
    优先权日:2017-06-19
    标 题 :Automated methods for scalable, parallelized enzymatic biopolymer synthesis and modification using microfluidic devices
    发明人:BANAL JAMES; BERLEANT JOSEPH DON; SHEPHERD TYSON; BATHE MARK
    权利人:MASSACHUSETTS INST TECHNOLOGY
    摘要:Methods for the automated template-free synthesis of user-defined sequence controlled biopolymers using microfluidic devices are described. The methods facilitate simultaneous synthesis of up to thousands of uniquely addressed biopolymers from the controlled movement and combination of regents as fluid droplets using microfluidic and EWOD-based systems. In some forms, biopolymers including nucleic acids, peptides, carbohydrates, and lipids are synthesized from step-wise assembly of building blocks based on a user-defined sequence of droplet movements. In some forms, the methods synthesize uniquely addressed nucleic acids of up to 1,000 nucleotides in length. Methods for adding, removing and changing barcodes on biopolymers are also provided. Biopolymers synthesized according to the methods, and libraries and databases thereof are also described. Modified biopolymers, including chemically modified nucleotides and biopolymers conjugated to other molecules are described.

    专利号:US-10815194-B2
    优先权日:2016-11-14
    标题 :Process for the preparation of mono-protected α,ω-diamino alkanes
    发明人:MENGE WIRO MICHAEL PETRUS BERNARDUS
    权利人:BYONDIS BV
    摘要:The present invention relates to a process for the synthesis of mono-protected α,ω-diamino alkanes, the use of said process in a process for the synthesis of a linker drug comprising an α,ω-diamino alkane moiety and the use of the process of the present invention in a process for preparing an antibody-drug conjugate comprising an α,ω-diamino alkane moiety.

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    合成参考文献


    参考文献:10.1186/1471-230x-11-79
    摘要:Thiel K, Schenk M, Etspüler A, Schenk T, Morgalla MH, Königsrainer A, Thiel C. A simple dummy liver assist device prolongs anhepatic survival in a porcine model of total hepatectomy by slight hypothermia. BMC Gastroenterol. 2011 Jul 14;11():79.
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