CAS: 35943-35-2; (2R,3R,4S,5R)-2-(3-Amino-5-Methyl-1,4,5,6,8-Pentaazaacenaphthylen-1(5H)-yl)-5-(Hydroxymethyl)Tetrahydrofuran-3,4-Diol

该化合物是一种合成化合物,主要研究其潜在的治疗用途,特别是在肿瘤学方面.它被公认为一种蛋白质血酶抑制剂,具体针对在细胞生存和扩散中具有关键作用的Akt路径.三硅基苯基苯基苯基丙基丙基苯,因其在细胞生存和生物利用率方面的能力受到调查.该化合物的特性是复杂的分子的特性,而其研究仍在继续进行中,其研究,安全性和治疗性研究的特性是全部的立体研究.

结构式图片

上下游产品

CAS号699011-59-1 4-(1-methylhydr... | CAS号6974-32-9 1-乙酰氧基-2,3,5-三苯... | CAS号699011-57-9 6-bromo-4-chlor... | CAS号699011-58-0 6-bromo-5-cyano... | CAS号24391-39-7 6-bromo-4-chlor... | CAS号24391-40-0 6-Bromo-4-oxo-4... | CAS号19393-83-0 4-氨基-6-溴-7H-吡咯并... | CAS号35943-36-3 4-(N-methyl-hyd...

合成工艺路线路线简述

    📜6-Bromo-4-Chloro-5-Cyano-7-[2,3,5-Tri-O-Benzoyl-β-D-Ribofuranosyl]Pyrrolo[2,3-D]Pyrimidine置于palladium On Activated Charcoal Sodium Methylate,Ammonium Formate体系中,用 甲醇,乙醇,氯仿 用作溶剂,化学反应 20.5H,反应生成曲西瑞宾
    参考文献:Triciribine 的改进全合成:具有抗肿瘤和抗病毒特性的三环核苷
    标题:Triciribine 的改进全合成:具有抗肿瘤和抗病毒特性的三环核苷
    摘要:我们描述了从 4-氨基-6-溴-5-氰基吡咯并[2,3-D]嘧啶开始,高效全合成曲西瑞宾,一种具有抗肿瘤和抗病毒特性的三环核苷.†为了纪念和庆祝 Leroy B. Townsend 教授 70 岁生日.
    Doi:10.1081/ncn-120027815

    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-12391691-B2
    优先权日:2018-11-16
    标题:Synthesis of key intermediate of KRAS G12C inhibitor compound
    发明人:PARSONS ANDREW THOMAS; COCHRAN BRIAN MCNEIL; POWAZINIK IV WILLIAM; CAPORINI MARC ANTHONY
    权利人:AMGEN INC
    摘要:The present invention relates to an improved, efficient, scalable process to prepare intermediate compounds, such as compound 5M, having the structure n nuseful for the synthesis of compounds that target KRAS G12C mutations, such as

    专利号:US-2025206736-A1
    优先权日:2019-11-14
    标题 :Synthesis of kras g12c inhibitor compound
    发明人:CORBETT MICHAEL THOMAS; CAILLE SEBASTIEN
    权利人:AMGEN INC
    摘要:The present disclosure relates to an improved, efficient, scalable process to prepare intermediate compounds, such as 2-isopropyl-4-methylpyridin-3-amine, useful for the synthesis of compounds, such as Compound 9, for the treatment of KRAS G12C mutated cancers.

    专利号:US-4123524-A
    优先权日:1977-06-08
    标题:Synthesis of 6-amino-4-methyl-8-(β-D-ribofuranosyl)pyrrolo[4,3,2-de]pyrimido[4,5-C]pyridazine-5'-phosphate as a novel compound and its utility against L-1210 mouse leukemia
    发明人:TOWNSEND LEROY B; LEWIS ARTHUR F; ROTI ROTI LINDA W
    权利人:US HEALTH EDUCATION & WELFARE
    摘要:The compound 6-amino-4-methyl-8-(β-D-ribofuranosyl)pyrrolo[4,3,2-de]pyrimido[4,5-c]pyridazines-5'-phosphate (a nucleotide) as a new compound and its method of synthesis by phosphorylation of the known 6-amino-4-methyl-8-(β-D-ribofuranosyl)pyrrolo[4,3,2-de]pyrimido[4,5-c]pyridazine (a nucleoside). The 5'-phosphate ester has utility against L-1210 mouse leukemia and has superior solubility over the parent compound which gives it a broader use pattern relative to dosage. This novel nucleotide also shows advantage in utilization as to pH over, for example, the hydrochloride salt which gives in solution a pH of 4 and is too acid for use.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Sato-Nagaoka Y, Suzuki S, Suzuki S, Takahashi S. Combination of triciribine and p38 MAPK inhibitor PD169316 enhances the differentiation effect on myeloid leukemia cells. PLoS One. 2024 Dec 31;19(12):e0312406. doi: 10.1371/journal.pone.0312406.
    2: Yang JP, Toughiri R, Gounder AP, Scheibe D, Petrus M, Fink SJ, Vallee S, Kenniston J, Papaioannou N, Langston S, Gavva NR, Horman SR. Identification of small molecule agonists of fetal hemoglobin expression for the treatment of sickle cell disease. PLoS One. 2024 Nov 6;19(11):e0307049. doi: 10.1371/journal.pone.0307049.
    3: Curcio AG, Ribeiro TIS, Gomes HF, Carvalho CSP, Bussiere MCC, Dias AJB. Increased in vitro production of bovine embryos resulting from oocyte maturation in the presence of triciribine, a specific inhibitor of AKT. Theriogenology. 2025 Jan 1;231:222-227. doi: 10.1016/j.theriogenology.2024.10.024. Epub 2024 Oct 24. 25(15):8069. doi: 10.3390/ijms25158069.

    合成参考文献


    摘要:National Cancer Institute Screening Program Data Summary, Developmental Therapeutics Program., JAN1986
    参考文献:10.1210/en.2012-1836
    摘要:Wang Q, Leader A, Tsang BK. Inhibitory roles of prohibitin and chemerin in FSH-induced rat granulosa cell steroidogenesis. Endocrinology. 2013 Feb;154(2):956–67. doi: 10.1210/en.2012-1836.
    参考文献:10.1081/ncn-120026873
    摘要:Porcari AR, Ptak RG, Borysko KZ, Breitenbach JM, Drach JC, Townsend LB. Synthesis and antiviral activity of 2-substituted analogs of triciribine. Nucleosides Nucleotides Nucleic Acids. 2003 Dec;22(12):2171–93. doi: 10.1081/ncn-120026873.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知