CAS: 174-78-7; 2-Oxa-6-Azaspiro[3.3]Heptane

该化合物是一种环绕化合物,其特点是将氧和氮结合在硬性双环框架内的独特混合环环结构,其松散的环环系统和双功能性使其成为药用化学和药物发现的宝贵建筑块,特别是用于设计受整形限制的药用药用植物.该化合物的螺旋中心增强三维多样性,能够精确控制分子几何测量,这有利于优化结合性和选择性.其合成多功能性可以进一步实现功能化,促进新型生物活性分子的开发.由于它具有创建结构界定的聚合物和超分子组件的潜力,这对材料科学也具有兴趣.

结构式图片

相似化合物

1045709-32-7 1159599-99-1 1263285-88-6

欧盟法规

C&L通报

上下游产品

CAS号13573-28-9 6-(对甲苯磺酰)-2-氧杂-... | CAS号1159599-99-1 2-氧杂-6-氮杂-螺[3,3...

合成工艺路线路线简述

    三溴新戊醇置于potassium Carbonate,Magnesium体系中,用 甲醇,乙醇 用作溶剂,化学反应 94.0H,反应生成2-氧杂-6-氮杂-螺[3,3]庚烷
    参考文献:新型3,5,7-三取代吡唑并[1,5-A]嘧啶的合成及生物活性评价
    标题:新型3,5,7-三取代吡唑并[1,5-A]嘧啶的合成及生物活性评价
    摘要:Flt3 蛋白激酶的突变通常与急性髓性白血病中细胞增殖失调有关,抑制该激酶是一种潜在的治疗策略.我们报告了一系列新的 3,5,7-三取代吡唑并 [1,5-A ] 嘧啶,旨在研究它们的生物活性,特别是对 Flt3-Itd 及其下游调节剂以及对 Cdk2 和 Cdk9 的生物活性.衍生物10B能够强烈抑制所有激酶,其在 Flt3-Itd 表达细胞系 Molm13 和 Mv4-11 中的选择性与 Flt3-Itd 抑制作用一致.进一步的生化分析和分子对接证实 Flt3 是10B的细胞靶标.
    Doi:10.1016/j.Bmcl.2022.129096

    海关参考信息

    专利信息


    专利号:US-11897914-B2
    优先权日:2021-11-29
    标题 :Synthesis of 2′ protected nucleosides
    发明人:POON WING C; ZOU RUIMING; LAU ALDRICH N K; YU DAVID; Du Gengyu; YAO YUN-CHIAO; ZHAO GANG
    权利人:HONGENE BIOTECH CORP
    摘要:Embodiments of the present application relate to the preparation of 2′-O-protected nucleoside phosphoramidites and conjugation of the 2′-O-protected nucleoside to a solid support. More specifically, the present application relates to nucleosides having a hydroxy protecting group at the 2′ position that reduces migration to the 3′ position during RNA (e.g., mRNA) synthesis and can be readily removed under mild conditions without the use of toxic metal-containing reagents. Methods of using the nucleosides described herein in RNA synthesis are also disclosed.

    专利号:US-2023119227-A1
    优先权日:2020-02-24
    标 题:Oligonucleotide synthesis on solid support
    发明人:JI AN; MARVIN MICHAEL; MARKS KEVIN; ANDERSON DAVID
    权利人:INTEGRATED DNA TECH INC
    摘要:Functionalized solid supports are useful in the synthesis of oligonucleotides. The functionalized solid supports contain an extended linker to a terminal functional group or a first nucleotide or nucleoside moiety. The extended linker permits oligonucleotide synthesis to take place at a greater distance from the solid support with greater efficiency.

    专利号:US-12180182-B2
    优先权日:2021-12-01
    标题 :(Di)amination of activated allene compounds, derivatives thereof, and methods for synthesis of the same
    发明人:DAI MINGJI
    权利人:PURDUE RESEARCH FOUNDATION
    摘要:One-pot synthesis methods for producing amines from activated allenes and derivatives thereof are provided, as well as the compounds produced thereby.

    专利号:US-11691135-B2
    优先权日:2020-10-15
    标 题:Synthesis of alkynones via carbonylative Sonogashira coupling reactions catalyzed by Pd(II)-N-Heterocyclic carbene-pyridine complexes
    发明人:EL ALI BASSAM; MANSOUR WASEEM; FETTOUHI MOHAMMED
    权利人:UNIV KING FAHD PET & MINERALS; SAUDI ARABIAN OIL CO
    摘要:This disclosure relates to N-substituted Pd(II)-N-heterocyclic carbene-pyridine complexes, methods of preparing the complexes, and methods of using the complexes in Sonogashira coupling reactions.

    专利号:US-11142545-B2
    优先权日:2016-06-24
    标 题 :Synthesis of thiolated oligonucleotides without a capping step
    发明人:SHI XIANGLIN; YANG JIMIN; KIESMAN WILLIAM F; FILLON YANNICK
    权利人:BIOGEN MA INC
    摘要:The invention herein describes a solid-phase synthetic method for preparing thiolated oligonucleotides without needing a capping step. The methods of the invention comprises repetition of a three-reaction per cycle, namely detritylation, coupling and sulfurization, without a capping step. In some embodiments, the synthetic methods of the present invention can be used for preparing an anti-sense oligonucleotide.

    专利号:US-11192912-B1
    优先权日:2020-10-15
    标 题 :Synthesis of biaryl ketones and biaryl diketones via carbonylative Suzuki-Miyaura coupling reactions catalyzed by bridged bis(N-heterocyclic carbene)palladium(II) catalysts
    发明人:EL ALI BASSAM; MANSOUR WASEEM; FETTOUHI MOHAMMED
    权利人:UNIV KING FAHD PET & MINERALS; SAUDI ARABIAN OIL CO
    摘要:This disclosure relates to bridged bis(N-heterocyclic carbene)palladium(II) complexes, methods of preparing the complexes, and methods of using the complexes in Suzuki-Miyaura coupling reactions.
    常州市力仁医药科技有限公司
    ⚠️ 未注册 · 未认证企业
    ⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
    数据来源于公开网络搜索,平台未作核实,请自行辨别。
    🏢敬请 企业认领
    🏬开设公司展台
    📢获取免费会员权益
    🎖️点亮专属注册企业标签
    📇展现公司完整信息 样本查看立即注册认领 →
    网址: http://www.lirenchem.com
    企业联系电话:0519-85859058,13915836899👤
    📞常州市力仁医药科技有限公司 ⚠️参考联系方式
    联系人:黄经理
    电话:0519-85859058,13915836899
    手机:13915836899
    传真:0519-85852385,QQ:3003793626
    邮箱:liren_medicine@163.com
    通信地址: 江苏省常州市天宁区东仓桥弄1号
    邮编: 213000
    🆔 联系时候可告知是从"百琢研"平台获取的信息.
    ⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

    地址:江苏省常州市天宁区东仓桥弄1号
    ⚠️ 未注册 · 未认证企业
    注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
    ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
    第 1 / 1 页
    现货

    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

    合成参考文献


    参考文献:10.1007/978-981-15-8002-4_3
    摘要:Patel MV, Bhagwat SS, Deshpande PK. Indian Discovery Effort in the Quest of Novel Antibiotics. 2021. In: Drug Discovery and Drug Development.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知