CAS: 186698-58-8; H-D-Tyr(Tbu)-Oh

化学文摘社编号为186698-58-8,便于在化学数据库中识别.它作为浸化物化学的一个建筑块,在生物化学的制药和研究中发挥着关键作用.该化合物在标准实验室条件下一般稳定,但与许多氨基酸衍生物一样,应小心避免降解或不必要反应.

结构式图片

相似化合物

118488-18-9 18822-59-8 47375-34-8

欧盟法规

C&L通报

上下游产品

N-Benzyloxycarbonyl-O-tert.-butyl-L-tyrosin-(4-nitro-benzylester) N-α-benzyloxycarbamoyl-O-t-butyl-L-tyrosine dicyclohexylammonium salt Z-L-Tyr-OH isobutene(S)-3-(4-tert-Butoxy-phenyl)-2-(2-methanesulfonyl-ethoxycarbonylamino)-propionic acid (S)-2-((S)-2-Benzyloxycarbonylamino-3-carbamoyl-propionylamino)-3-(4-tert-butoxy-phenyl)-propionic acid N-benzoyl-O-tert-butyl-L-tyrosine N-benzoyl-O-tert-butyl-L-tyrosine methyl ester

合成工艺路线路线简述

    海关参考信息

    专利信息


    专利号:US-9574189-B2
    优先权日:2005-12-01
    标题:Enzymatic encoding methods for efficient synthesis of large libraries
    发明人:FRANCH THOMAS; LUNDORF MIKKEL DYBRO; JACOBSEN SØREN NYBOE; OLSEN EVA KAMPMANN; ANDERSEN ANNE LEE; HOLTMANN ANETTE; HANSEN ANDERS HOLM; SØRENSEN ANDERS MALLING; GOLDBECH ANNE; DE LEON DAEN; KALDOR DITTE KIEVSMOSE; SLØK FRANK ABILDGAARD; HUSEMOEN GITTE NYSTRUP; DOLBERG JOHANNES; Jensen Kim Birkebæ; PEDERSEN LENE; NØRREGAARD-MADSEN MADS; GODSKESEN MICHAEL ANDERS; GLAD SANNE SCHRØDER; NEVE SØREN; THISTED THOMAS; KRONBORG TINE TITILOLA AKINLEMINU; SAMS CHRISTIAN KLARNER; FELDING JAKOB; FRESKGÃ…RD PER-OLA; GOULIAEV ALEX HAAHR; PEDERSEN HENRIK
    权利人:FRANCH THOMAS; LUNDORF MIKKEL DYBRO; JACOBSEN SØREN NYBOE; OLSEN EVA KAMPMANN; ANDERSEN ANNE LEE; HOLTMANN ANETTE; HANSEN ANDERS HOLM; SØRENSEN ANDERS MALLING; GOLDBECH ANNE; DE LEON DAEN; KALDOR DITTE KIEVSMOSE; SLØK FRANK ABILDGAARD; HUSEMOEN GITTE NYSTRUP; DOLBERG JOHANNES; Jensen Kim Birkebæ; PEDERSEN LENE; NØRREGAARD-MADSEN MADS; GODSKESEN MICHAEL ANDERS; GLAD SANNE SCHRØDER; NEVE SØREN; THISTED THOMAS; KRONBORG TINE TITILOLA AKINLEMINU; SAMS CHRISTIAN KLARNER; FELDING JAKOB; FRESKGÃ…RD PER-OLA; GOULIAEV ALEX HAAHR; PEDERSEN HENRIK; NUEVOLUTION AS
    摘要:Disclosed is a method for obtaining a bifunctional complex comprising a molecule linked to a single stranded identifier oligonucleotide, wherein a nascent bifunctional complex comprising a chemical reaction site and a priming site for enzymatic addition of a tag is a) reacted at the chemical reaction site with one or more reactants, and b) reacted enzymatically at the priming site with one or more tag(s) identifying the reactant(s).

    专利号:US-11702652-B2
    优先权日:2005-12-01
    标题:Enzymatic encoding methods for efficient synthesis of large libraries

    专利号:US-2009264300-A1
    优先权日:2005-12-01
    标题 :Enzymatic encoding methods for efficient synthesis of large libraries

    专利号:US-2020216836-A1
    优先权日:2005-12-01
    标题 :Enzymatic encoding methods for efficient synthesis of large libraries

    专利号:EP-1957644-B1
    优先权日:2005-12-01
    标 题 :Enzymatic encoding methods for efficient synthesis of large libraries

    专利号:US-2019330618-A1
    优先权日:2005-12-01
    标题 :Enzymatic encoding methods for efficient synthesis of large libraries
    上海吉尔多肽有限公司
    ⚠️ 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.glbiochem.com
    电话: 86-21-61263309👤
    📞上海吉尔多肽有限公司 ⚠️参考联系方式

    销售电话:86-21-61263309
    邮箱:ymbetter@glbiochem.com
    🆔 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→

    ⚠️ 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

    主要参考文献

    参考标题:Diastereoselective Synthesis Of Highly Functionalized Fluoroalkene Dipeptide Isosteres And Its Application To Fmoc-Based Solid-Phase Synthesis Of A Cyclic Pentapeptide Mimetic
    作者:Tetsuo Narumi,Kenji Tomita,Eriko Inokuchi,Kazuya Kobayashi,Shinya Oishi,Hiroaki Ohno,Nobutaka Fujii |发布日期:2008.5
    摘要:A Diastereoselective And Divergent Method For Synthesis Of A Highly Functionalized (Z)-Fluoroalkene Dipeptide Isosteres Has Been Developed. The Key Feature Of This Synthetic Method Is An Efficient One-Pot Reaction Involving Reduction/asymmetric Alkylation Via Transmetalation, Which Produces Trans-Amide Type (Z)-Fluoroalkenes Flanking Two Stereogenic Centers In High Yields, With Excellent (Z)-Selectivity

    合成参考文献

    合成方法参考DOI号:10.1007/s00726-013-1625-7
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知