CAS: 14620-72-5; Dimethyl Adipimidate Dihydrochloride

该化合物是一个化学化合物,其特点是硅酸结构,有两种隐化功能组,该化合物一般是白色至非白色固体,由于盐酸碱存在,极地溶液中溶解,这增加了其在水中的溶解性;二甲基酯组的存在表明,它有两个甲基酯功能,有助于其在有机合成中的再活性和潜在应用;作为盐,它显示出碘化合物的典型特性,例如与自由基质形式相比,稳定性和处理便利性增强;经常探讨乙烷二酰酸衍生物在制药,农用化学品和有机合成中作为中间体的潜在用途;在处理和储存方面,应参考安全数据,与所有化学物质一样,以确保采取适当的防范措施.

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欧盟法规

ECHA物质C&L通报REACH预注册

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    专利信息


    专利号:US-2017283878-A1
    优先权日:2015-12-11
    标题:Modulation of globoseries glycosphingolipid synthesis and cancer biomarkers
    发明人:WONG CHI-HUEY; WU CHUNG-YI; CHEUNG SARAH K C; CHUANG PO-KAI; HSU TSUI-LING
    权利人:ACADEMIA SINICA
    摘要:The present disclosure relates to methods and compositions which can modulate the globoseries glycosphingolipid synthesis. Particularly, the present disclosure is directed to glycoenzyme inhibitor compound and compositions and methods of use thereof that can modulate the synthesis of globoseries glycosphingolipid SSEA-3/SSEA-4/GloboH in the biosynthetic pathway; particularly, the glycoenzyme inhibitors target the alpha-4GalT; beta-4GalNAcT-I; or beta-3GalT-V enzymes in the globoseries synthetic pathway. Additionally, the present disclosure is also directed to vaccines, antibodies, and/or immunogenic conjugate compositions targeting the SSEA-3/SSEA-4/GLOBO H associated epitopes (natural and modified) which elicit antibodies and/or binding fragment production useful for modulating the globoseries glycosphingolipid synthesis. Moreover, the present disclosure is also directed to the method of using the compositions described herein for the treatment or detection of hyperproliferative diseases and/or conditions. Furthermore, the instant disclosure also relates to cancer stem cell biomarkers for diagnostic and therapeutic uses.

    专利号:US-2008267981-A1
    优先权日:2004-06-30
    标题:Compositions and Methods for Delivery of Antitumor Agents
    发明人:JANDA KIM D; WIRSCHING PETER; BOGER DALE L
    权利人:SCRIPPS RESEARCH INST
    摘要:Methods for treating a neoplastic disease with an antibody-cytotoxin conjugate molecule, methods of synthesizing an antibody-cytotoxin conjugate molecule are provided. Compounds that are useful as antibody-cytotoxin conjugate molecule or useful in the synthesis of these molecules are also provided.

    专利号:US-7635749-B2
    优先权日:1999-12-24
    标题 :Methods and compositions for prolonging elimination half-times of bioactive compounds
    发明人:DENNIS MARK S; LOWMAN HENRY B; DELANO WARREN L
    权利人:GENENTECH INC
    摘要:Peptide ligands having affinity for IgG or for serum albumin are disclosed. Also disclosed are hybrid molecules comprising a peptide ligand domain and an active domain. The active domain may comprise any molecule having utility as a therapeutic or diagnostic agent The hybrid molecules of the invention may be prepared using any of a number techniques including production in and purification from recombinant organisms transformed or transfected with an isolated nucleic acid encoding the hybrid molecule, or by chemical synthesis of the hybrid. The hybrid molecules have utility as agents to alter the elimination half-times of active domain molecules. Elimination half-time is altered by generating a hybrid molecule of the present invention wherein the peptide ligand has binding affinity for a plasma protein. In a preferred embodiment, a bioactive molecule having a short elimination half-time is incorporated as or into an active domain of the hybrid molecules of the invention, and the binding affinity of the peptide ligand domain prolongs the elimination half-time of the hybrid as compared to that of the bioactive molecule.

    专利号:WO-2009056955-A1
    优先权日:2007-10-30
    标题 :Amine-bearing phospholipids (abps), their synthesis and use
    发明人:ZUMBUEHL ANDREAS
    权利人:UNIV BASEL; ZUMBUEHL ANDREAS
    摘要:Disclosed herein are amine-bearing phospholipids (ABP). The ABPs display many properties and functionalities of naturally occurring phospholipids, but also new properties and functionalities, such as the ability to polymerize while maintaining structural integrity, that may supplement or expand the functionalities of naturally occurring phospholipids.

    专利号:US-4259233-A
    优先权日:1979-10-23
    标题 :β-Galactosyl-umbelliferone-labeled protein and polypeptide conjugates
    发明人:CARRICO ROBERT J; NGO THAT T
    权利人:MILES LAB
    摘要:A β-galactosyl-umbelliferone-labeled conjugate of the formula: ##STR1## wherein --NH)L is a protein or polypeptide, such as an immunoglobulin, bound through an amino group thereof, n is an integer from 2 through 10, m is an integer from 1 through 10, and p is on the average from 1 to the number of available amino groups in L. An intermediate in the synthesis of such labeled conjugate is also provided. The labeled conjugates are useful as reagents in specific binding assays (e.g., immunoassays) for determining the conjugated protein or polypeptide, or a specific binding analog or partner thereof, in liquid media.

    专利号:US-4261974-A
    优先权日:1979-11-13
    标题:Valproic acid immunogen conjugates and antibodies thereto
    发明人:BUCKLER ROBERT T; BURD JOHN F; WONG RAPHAEL C
    权利人:MILES LAB
    摘要:Reagents for use in binding assays, particularly immunoassays, to determine valproic acid in liquid media such as serum. Such reagents include antibody to valproic acid and β-galactosyl-umbelliferone-valproic acid conjugates. Also provided are compounds used to prepare such reagents, including valproic acid immunogen conjugates and intermediates in the synthesis of such immunogen conjugates and β-galactosyl-umbelliferone-labeled conjugates.

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    合成参考文献


    参考文献:10.1007/978-1-4939-1363-3_15
    摘要:Lefrançois P, Gallagher JE, Snyder M. Global analysis of transcription factor-binding sites in yeast using ChIP-Seq. Methods Mol Biol. 2014;1205():231–55.
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