CAS: 53910-25-1; (R)-3-((2R,4S,5R)-4-Hydroxy-5-(Hydroxymethyl)Tetrahydrofuran-2-yl)-3,4,7,8-Tetrahydroimidazo[4,5-D][1,3]Diazepin-8-Ol

该化合物是纯核素核素的模拟, 具有强效抗乳性, 主要用于治疗某些种类的白血病和淋巴瘤, 特别是毛细胞白血病. Pentostatain 功能, 抑制对纯素新陈代谢至关重要的醋酸酶; 这种抑制导致甘油细胞中有毒代谢物的累积, 最终导致恶性细胞中的流行性硬化. 该化合物通常通过静脉注射施用, 并由于潜在副作用而有特定的剂量疗法, 其中可包括乳房抑制, 胃肠扰动和免疫抑制. Pentostatain 的特征是分子配方, 其结构反映了它作为改良的纯素的结构, 并且众所周知, 它的溶性相对较低. 它的治疗功效经常在临床环境中被评估, 并且它被归类为抗血代谢剂. 任何关键的治疗剂都通过对抗热剂进行审慎的检测来评估.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号69195-91-1 2-氨基-1-[5-氨基-1-... | CAS号69195-97-7 2-硝基-1-[5-硝基-1-... | CAS号69196-02-7 3-(2-deoxy-3,5-... | CAS号69195-92-2 2-氨基-1-(5-氨基-1H...

合成工艺路线路线简述

    苯酚 反应生成 脱氧助间型霉素
    参考文献:Chlorination Process,Alkylation Of Products Of Said Process And Some
    标题:Chlorination Process,Alkylation Of Products Of Said Process And Some
    摘要:具有酸性质子和能够共轭碱离子的电子密度离域的分子结构(目标化合物)通过将这些化合物与高氯烷和水溶性碱以及存在相转移催化剂(四烷基铵羟基)接触而被氯化.产生氯化产物,优选产生宝石二氯化合物.这些宝石二氯化合物可用于芳香化合物的烷基化.例如,萘被氯化形成9,9-二氯萘,然后与酚或苯胺等化合物反应,形成9,9-双(羟基苯基)萘,9,9-双(氨基苯基)萘或9-氨基苯基-9-氯萘等化合物.

    海关参考信息

    专利信息


    专利号:US-2004242897-A1
    优先权日:2002-07-31
    标题 :Universal support media for synthesis of oligomeric compounds
    发明人:GUZAEV ANDREI P; MANOHARAN MUTHIAH
    摘要:Compounds for the synthesis of oligomeric compounds, particularly oligonucleotides and oligonucleotide mimetics, are provided. In addition, methods for functionalizing a support medium with a first monomeric subunit and methods for the synthesis of oligomeric compounds utilizing the novel compounds bound to support media are provided.

    专利号:WO-2004011474-A1
    优先权日:2002-07-31
    标题:Universal support media for synthesis of oligomeric compounds
    发明人:GUZAEV ANDREI P; MANOHARAN MUTHIAH; RAVIKUMAR VASULINGA T; KUMAR RAJU K
    权利人:ISIS PHARMACEUTICALS INC; GUZAEV ANDREI P; MANOHARAN MUTHIAH; RAVIKUMAR VASULINGA T; KUMAR RAJU K
    摘要:Compounds for the synthesis of oligomeric compounds, particularly oligonucleotide and oligonucleotide mimetics, are provided. In addition, methods for functionalizing a support medium with a first monomeric subunit and methods for the synthesis of oligomeric compounds utilizing the novel compounds bound to support media are provided.

    专利号:US-6653468-B1
    优先权日:2002-07-31
    标 题 :Universal support media for synthesis of oligomeric compounds
    发明人:GUZAEV ANDREI P; MANOHARAN MUTHIAH
    权利人:ISIS PHARMACEUTICALS INC
    摘要:Compounds for the synthesis of oligomeric compounds, particularly oligonucleotides and oligonucleotide mimetics, are provided. In addition, methods for functionalizing a support medium with a first monomeric subunit and methods for the synthesis of oligomeric compounds utilizing the novel compounds bound to support media are provided.

    专利号:US-11603382-B2
    优先权日:2015-12-11
    标题 :Diastereoselective synthesis of phosphate derivatives
    发明人:KOTALA MANI BUSHAN; DAMMALAPATI VENKATA LAKSHMI NARASIMHA RAO
    权利人:NuCana plc
    摘要:The present invention provides a method for the preparation of intermediates useful in the synthesis of gemcitabine-[phenyl-benzoxy-L-alaninyl)]-phosphate. It also provides a method of preparing gemcitabine-[phenyl-benzoxy-L-alaninyl)]-phosphate.

    专利号:US-10925977-B2
    优先权日:2006-10-05
    标 题 :Efficient synthesis of chelators for nuclear imaging and radiotherapy: compositions and applications
    发明人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S
    权利人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S; CEIL POINT LLC; UNIV TEXAS
    摘要:Novel methods of synthesis of chelator-targeting ligand conjugates, compositions comprising such conjugates, and therapeutic and diagnostic applications of such conjugates are disclosed. The compositions include chelator-targeting ligand conjugates optionally chelated to one or more metal ions. Methods of synthesizing these compositions in high purity are also presented. Also disclosed are methods of imaging, treating and diagnosing disease in a subject using these novel compositions, such as methods of imaging a tumor within a subject and methods of diagnosing myocardial ischemia.

    专利号:US-2021220331-A1
    优先权日:2016-05-03
    标题:Inhibitors of ires-mediated protein synthesis
    发明人:GERA JOSEPH F; LICHTENSTEIN ALAN; JUNG MICHAEL E; LEE JIHYE; HOLMES BRENT; BENAVIDES-SERRATO ANGELICA
    权利人:UNIV CALIFORNIA; THE UNITED STATE GOVERNMENT REPRESENTED BY THE DEPT OF VETERANS AFFAIRS
    摘要:This disclosure relates to inhibitors of IRES-mediated protein synthesis, compositions comprising therapeutically effective amounts of these compounds, and methods of using those compounds and compositions in treating hyperproliferative disorders, e.g., cancers. This disclosure also relates to compositions comprising inhibitors of IRES-mediated protein synthesis and mTOR inhibitors, and to methods of treating cancer by conjoint administration of inhibitors of IRES-mediated protein synthesis and mTOR inhibitors.
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    主要参考文献


    1: Paillassa J, Maitre E, Belarbi Boudjerra N, Madani A, Benlakhal R, Matthes T, Van Den Neste E, Cailly L, Inchiappa L, Bekadja MA, Tomowiak C, Troussard X. Recommendations for the Management of Patients with Hairy-Cell Leukemia and Hairy-Cell Leukemia-like Disorders: A Work by French-Speaking Experts and French Innovative Leukemia Organization (FILO) Group. Cancers (Basel). 2024 Jun 10;16(12):2185. doi: 10.3390/cancers16122185.
    2: Zeng J, Zhou Y, Lyu M, Huang X, Xie M, Huang M, Chen BX, Wei T. Cordyceps militaris: A novel mushroom platform for metabolic engineering. Biotechnol Adv. 2024 Sep;74:108396. doi: 10.1016/j.biotechadv.2024.108396. Epub 2024 Jun 19. 1993–2024.
    13:1302038. doi: 10.3389/fonc.2023.1302038.

    合成参考文献


    参考文献:10.1080/10428190500282019
    摘要:Braiteh F, Ng C, Kurzrock R. Refractory Hodgkin lymphoma responds to pentostatin (2'-deoxycoformycin). Leuk Lymphoma. 2006 Feb;47(2):373–5. doi: 10.1080/10428190500282019.
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