CAS: 222530-33-8; Cis-3-((Tert-Butoxycarbonyl)Amino)Cyclohexanecarboxylic Acid

该化合物是一家以其环环结构为特征的手性化合物,有助于其立体化学;二甲基乙氧碳基化合物组的存在表明,该产品有一个在有机合成中常用的保护性组,特别是在浸泡物化学中;该化合物的特征是氨基氨基酸组和一个箱状酸功能组,使其成为氨基硫酸衍生物;其立声化学配置(1R,3S)建议其替代体的具体空间安排,这可能影响其生物活动和相互作用;这些化合物由于具有模拟天然氨基乙酸的能力,常常被研究其在制药中的潜在应用,特别是在药物设计和开发中.该化合物溶性,稳定性和再活性可根据其功能组和立体化而变化,使其在合成化学和药化学中都具有利益.

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tert-butyl dicarbonatedi-tert-butyl dicarbonate 3-amin°Cyclohexanecarboxylic acid tert-butyldicarbonate ethyl (1R,3S)-3-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylatetert-butyl (3-formylcyclohexyl)carbamate tert-butyl [3-(hydroxymethyl)cyclohexyl]carbamate (1S,3R)-3-((tert-butoxycarbonyl)amino)cyclo hexane-1-carboxylic acid

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    专利信息


    专利号:US-2023295613-A1
    优先权日:2020-02-14
    标 题:Long chain carbon and cyclic amino acids substrates for genetic code reprogramming
    发明人:JEWETT MICHAEL C; LEE JOONGOO; MOORE JEFFREY S; SCHWARZ KEVIN J
    权利人:UNIV NORTHWESTERN; UNIV ILLINOIS
    摘要:Abstract: Disclosed are methods, systems, components, and compositions for synthesis of sequence defined polymers. The methods, systems, components, and compositions may be utilized for incorporating novel substrates that include non-standard amino acid monomers and non-amino acid monomers into sequence defined polymers. As disclosed herein, the novel substrates may be utilized for acylation of tRNA via flexizyme catalyzed reactions. The tRNAs thus acylated with the novel substrates may be utilized in synthesis platforms for incorporating the novel substrates into a sequence defined polymer.

    专利号:US-11814621-B2
    优先权日:2018-06-01
    标题 :Expanding the chemical substrates for genetic code reprogramming
    发明人:JEWETT MICHAEL CHRISTOPHER; LEE JOONGOO; MOORE JEFFREY S; SCHWIETER KENNETH E; SCHWARZ KEVIN JEROME
    权利人:UNIV NORTHWESTERN; UNIV ILLINOIS
    摘要:Disclosed are methods, systems, components, and compositions for synthesis of sequence defined polymers. The methods, systems, components, and compositions may be utilized for incorporating novel substrates that include non-standard amino acid monomers and non-amino acid monomers into sequence defined polymers. As disclosed herein, the novel substrates may be utilized for acylation of tRNA via flexizyme catalyzed reactions. The tRNAs thus acylated with the novel substrates may be utilized in synthesis platforms for incorporating the novel substrates into a sequence defined polymer.

    专利号:WO-2023091726-A1
    优先权日:2021-11-18
    标题:Inhibitors of cyclin‑dependent kinase 12 (cdk12)
    发明人:BENOIT GUILLAUME; CARULLI JOHN; CHEN FEI; CHUAQUI CLAUDIO; CIBLAT STEPHANE; COOPER ELLIOT; DAGENAIS ROBIN; HU SHANHU; KABRO ANZHELIKA; LAPLACA DEREK; MARINEAU JASON; MOEBIUS DAVID; MOON DIANE; SOLODININ ANDREI; WHITMORE KENNETH
    权利人:SYROS PHARMACEUTICALS INC
    摘要:The present invention provides chemical compounds that inhibit one or more families of kinases (e.g., serine/threonine kinases, including one or more of the families of CDK proteins, and in particular, CDK12). More specifically, the present invention provides CDK12 inhibitors, of formula (I), pharmaceutically acceptable salts and isotopically labeled derivatives thereof, pharmaceutical compositions containing the compounds/inhibitors, and methods of their synthesis and use in treating proliferative diseases (e.g., a bladder cancer, a breast cancer, Ewing's sarcoma, a gastric cancer, a gastrointestinal cancer, a hematologic cancer, a lung cancer (e.g., small cell lung cancer (SCLC)), an ovarian cancer (e.g., a high grade serous ovarian cancer), a pancreatic cancer (e.g., pancreatic ductal adenocarcinoma (PDAC)), a brain cancer (e.g., glioblastoma), or a prostate cancer), alone or in combination with a second therapeutic agent. The proliferative disease can be a cancer, benign neoplasm, or pathologic angiogenesis, and any of the therapeutic methods or uses described herein can include a step of diagnosing the patient's disease. In other embodiments of the invention, the compositions described herein (e.g., the compounds, pharmaceutical compositions, and kits containing them) are used for the treatment of myotonic dystrophy (type 1 or type 2).
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    合成参考文献


    参考文献:10.1007/s11164-017-2973-9
    摘要:Hamama WS, Ibrahim ME, Metwalli AE, Zoorob HH. Recent synthetic aspects on the chemistry of aminocoumarins. Research on Chemical Intermediates. 2017 Jul 07;43(11):5943–83. doi: 10.1007/s11164-017-2973-9.
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