CAS: 198544-94-4; (R)-2-((((9H-Fluoren-9-yl)Methoxy)Carbonyl)Amino)-6-((Diphenyl(P-Tolyl)Methyl)Amino)Hexanoic Acid

该化合物是常见于peptide合成的受保护氨酸衍生物."Fmoc"(9-氟甲基苯氧碳基)组是氨基功能的保护组,允许在peptide组装过程中有选择地作出反应."D-Lys"表示氨酸是碱的D-抗omer,在Peptide立体化学中非常重要."Mtt"(4-甲基三丁基)组是另一种保护性动物的动物,专门用来保护侧链的甘酸矿,使与特定序列和功能相结合.该化合物通常用于固相的peptide合成(SPS)中,因为对功能组的保护和减少保护对于成功组装配peptide至关重要.在各种反应条件下,其有机溶剂中的溶液和稳定性使得它成为特别是生物化学和生物化学领域的重要化学材料.

结构式图片

相似化合物

167393-62-6 111061-54-2 1272755-60-8

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    专利信息


    专利号:US-2024209034-A1
    优先权日:2021-04-12
    标题:Engineering peptides for a a vb6 integrin binding and related methods of use and synthesis
    发明人:SELLERS DREW; CARDLE IAN; PUN SUZIE HWANG
    权利人:UNIV WASHINGTON; SEATTLE CHILDRENS HOSPITAL D/B/A SEATTLE CHILDRENS RES INSTITUTE
    摘要:Embodiments of the claimed invention are directed to synthetic peptides comprising an amino acid sequence of X 1 X 2 VX 3 NLRGDLQVLX 4 QKVCX 5 T (SEQ ID NO:18), wherein at least one of X 1 and X 2 is a cysteine, and wherein one or more of X 3 , X 4 , and X 5 is a non-natural amino acid. Also described are methods of using the claimed embodiments for inhibiting growth of a cancer cell overexpressing integrin αvβ6. Additionally, also described are methods of using the claimed embodiments for detecting a cancer cell overexpressing integrin αvβ6.

    专利号:CN-107056894-B
    优先权日:2017-05-26
    标 题:A kind of method for fragment method solid-phase synthesis of ganirelix acetate

    专利号:CN-107056894-A
    优先权日:2017-05-26
    标 题 :A kind of method for the solid-phase synthesis of ganirelix acetate by fragment method

    专利号:WO-2022221144-A1
    优先权日:2021-04-12
    标题 :Engineered peptides for αvβ6 integrin binding and related methods of use and synthesis

    专利号:US-10610608-B2
    优先权日:2013-08-01
    标题 :Modular imaging agents containing amino acids and peptides
    发明人:SCHMITTHENNER HANS F; BEACH STEPHANIE; BARRETT TAYLOR; WEIDMAN CHELSEA
    权利人:SCHMITTHENNER HANS F; BEACH STEPHANIE; BARRETT TAYLOR; WEIDMAN CHELSEA; ROCHESTER INSTITUTE TECH
    摘要:Targeted molecular imaging agents (TMIAs) are derived from coupling together pre-formed amino acids with imaging agents attached to their side chains. These peptide-based imaging agents may synthesized from a single or multiple preformed amino acids containing multi-modal, multi-chelated metal, multi-dye imaging agents, or combinations of these, on the side chains of resultant peptides. These imaging amino acids or peptides may be conjugated directly, or activated, or attached to linkers to which targeting groups, such as peptides, proteins, antibodies, aptamers, or small molecule inhibitors, may be conjugated in the final steps of the synthesis to form a wide variety of TMIAs.

    专利号:WO-2022221144-A9
    优先权日:2021-04-12
    标题 :Engineered peptides for αvβ6 integrin binding and related methods of use and synthesis
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