CAS: 475108-18-0; 1-(2-Chloro-4-((6,7-Dimethoxyquinolin-4-yl)Oxy)Phenyl)-3-(5-Methylisoxazol-3-yl)Urea

该化合物是一个小分子气管结骨酶抑制剂,主要用于治疗肾细胞癌,有选择性地抑制血管内皮生长因子受体(VEGFR-1,VEGFR-2和VEGFR-3),这些受体在血管产生过程中起着关键作用,即新血管从原有血液中形成的过程,这种抑制会干扰肿瘤的血液供应,从而限制肿瘤的生长和转移.Tivozanib的特点是其高能性和选择性,有助于其治疗效果,并有可能尽量减少目标外影响.该化合物一般是口服的,具有有利的药用植物基因特征,包括长半衰期,允许一次性服用.常见的副作用可能包括高血压,疲劳和胃肠扰动.作为调查药物,Tivozanib在各种临床试验中进行了评估,显示出改善高肾细胞癌病人结果的希望.

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CAS号1072-67-9 3-氨基-5-甲基异恶唑 | CAS号1885-14-9 氯甲酸苯酯 | CAS号286371-44-6 2-氯-4-((6,7-二甲氧... | CAS号682745-43-3 1-[2-chloro-4-(...

合成工艺路线路线简述

    1-(4,5-二甲氧基-2-硝基苯基)乙酮置于吡啶,Potassium Tert-Butylate,氢气,三氯氧磷体系中,用 四氢呋喃,N,N-二甲基乙酰胺,甲苯 作为反应溶剂,5.0~115.0 °C,101.33 Kpa 条件下,反应 27.5H,反应生成 N-[2-氯-4-[(6,7-二甲氧基-4-喹啉基)氧基]苯基]-N'-(5-甲基-3-异恶唑基)脲
    参考文献:A New And Practical Synthesis Of Tivozanib
    标题:A New And Practical Synthesis Of Tivozanib
    摘要:New And Improved Synthetic Route Of Tivozanib Is Described On A Hectogram Scale. An Reduction Cyclization Process To Prepare The Key Intermediate 6,7-Dimethoxyquinolin-4-Ol From The 3-(Dimethylamino)-1-(2-Nitrophenyl)Prop-2-En-L-One Compound At H-2/ni Condition Is Adopted In Good Result. Commercially Available Materials,Simple Reaction And Operation Are Used,Including Nitration,Condensation,Hydrogenation,Chlorination And So On,To Give The Final Product In 28.7% Yield Over Six Steps And 98.9% Purity (HPLC).
    DOI:10.3987/com-16-13555

    海关参考信息

    专利信息


    专利号:US-12383499-B2
    优先权日:2018-01-01
    标题:Scale up synthesis of silicasome nanocarriers
    发明人:NEL ANDRE E; MENG HUAN; LIU XIANGSHENG
    权利人:UNIV CALIFORNIA
    摘要:In order to facilitate the approval and commercialization of silicasome drug delivery systems (e.g. irinotecan silicasomes) it is necessary to scale up synthesis of the drug-loaded silicasomes. In this regard, it was discovered that the synthesis protocols used for laboratory synthesis of drug-loaded silicasomes (e.g., 500 mg/batch) do not scale to large scale silicasome production, because the resulting products were too heterogeneous for use as pharmaceuticals. Accordingly, new methods are provided herein that effectively afford the large-scale production of mesoporous silica nanoparticles (MSNPs) and lipid bilayer coated MSNPs (silicasomes).

    专利号:US-10973847-B2
    优先权日:2017-06-30
    标题 :Core-to-surface polymerization for the synthesis of star polymers and uses thereof
    发明人:JOHNSON JEREMIAH A; GOLDER MATTHEW R
    权利人:MASSACHUSETTS INST TECHNOLOGY
    摘要:Disclosed are methods, compositions, reagents, systems, and kits to prepare star polymers, as well as compositions and uses thereof. Various embodiments show that synthesis of these polymers contain low metal concentration to provide polymers for diverse biomedical applications including in vivo applications.

    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-2022233673-A1
    优先权日:2019-06-04
    标 题:METHODS OF PRODUCING SHIGA TOXIN B-SUBUNIT (STxB) MONOMERS AND OLIGOMERS, AND USES THEREOF
    发明人:BILLET ANNE; SCHMIDT FRÉDÉRIC; JOHANNES LUDGER; SERVENT DENIS; MOURIER GILLES; TARTOUR ÉRIC; KAY MICHAEL; FULCHER JAMES M
    权利人:INST CURIE; CENTRE NAT RECH SCIENT; INST NAT SANTE RECH MED; COMMISSARIAT A LENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES CEA; APHP ASSIST PUBLIQUE HOPITAUX DE PARIS; UNIV PARIS; UNIV OF UTAH RESEARCH FOUDATION; UNIV UTAH RES FOUND
    摘要:A method of producing a monomer of a Shiga toxin B-subunit (STxB) protein or of a variant thereof by peptide chemical synthesis, as well as to a method of producing a pentamer of the STxB protein or of the variant thereof. The methods are particularly advantageous as they overcome major issues typically observed in peptide chemical synthesis, including solubility and purity issues.

    专利号:WO-2025128098-A1
    优先权日:2023-12-13
    标 题 :Solid oral dosage forms, kits, and methods of using the same
    发明人:LI YING; LANGER ROBERT; TRAVERSO CARLO
    权利人:MASSACHUSETTS INST TECHNOLOGY; BRIGHAM & WOMENS HOSPITAL INC
    摘要:Provided herein are solid oral dosage forms, methods, and kits useful, e.g, for the extension of the residence time of active pharmaceutical agents in vivo by the synthesis of a polymer in situ in a subject. In particular, the solid oral dosage forms, methods, and kits disclosed herein are particularly useful for drugs that require more than once daily administration (e.g, drugs that have short half-lives).

    专利号:US-2025289827-A1
    优先权日:2022-12-02
    标 题:Morphic forms of a mutant braf degrader and methods of manufacture thereof
    发明人:YU ROBERT T; HE MINSHENG; SCHNADERBECK MATTHEW J; KREGER BRIDGET; POLLOCK ROY MACFARLANE; JIANG SIYI; LI MEIQI; CHEN BOLU; LU JIANNAN
    权利人:C4 THERAPEUTICS INC
    摘要:Advantageous isolated morphic forms of (3R)-3-[6-[2-cyano-3-[[ethyl(methyl)sulfamoyl]amino]-6-fluorophenoxy]-4-oxoquinazolin-3-yl]-8-[2-[1-[3-(2,4-dioxo-1,3-diazinan-1-yl)-5-fluoro-1-methylindazol-6-yl]-4-hydroxypiperidin-4-yl]acetyl]-1-oxa-8-azaspiro[4.5]decane (Compound 1), which is a mutant BRAF degrader, and methods to prepare Compound 1 morphic forms for therapeutic applications are provided in the invention. The invention also provides improved methods for the synthesis of Compound 1, new pharmaceutical compositions comprising Compound 1, and new uses of Compound 1.
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    主要参考文献


    1: Mehta A, Sonpavde G, Escudier B. Tivozanib for the treatment of renal cell carcinoma: results and implications of the TIVO-1 trial. Future Oncol. 2014 Aug;10(11):1819-26. doi: 10.2217/fon.14.120. doi: 10.1016/j.juro.2014.07.054. Epub 2014 Jul 18. doi: 10.2217/fon.13.253. Epub 2013 Dec 3. doi: 10.1200/JCO.2012.47.4940. Epub 2013 Sep 9. doi: 10.1200/JCO.2013.51.4869. Epub 2013 Sep 9. Erratum in: J Clin Oncol. 2013 Dec 1;31(34):4383. doi: 10.1007/s10549-013-2632-9. Epub 2013 Jul 19. doi: 10.2147/DDDT.S31442. Print 2013. Review.
    8: Hepgur M, Sadeghi S, Dorff TB, Quinn DI. Tivozanib in the treatment of renal cell carcinoma. Biologics. 2013;7:139-48. doi: 10.2147/BTT.S32958. Epub 2013 Jun 11.
    9: Wong HH, Eisen T. Tivozanib for the treatment of metastatic renal cancer. Expert Rev Anticancer Ther. 2013 Jun;13(6):649-60. doi: 10.1586/era.13.40. Review. doi: 10.1016/j.ejca.2013.04.019. Epub 2013 May 28. doi: 10.1358/dot.2013.49.5.1960218. Review. doi: 10.1016/j.exer.2013.05.006. Epub 2013 May 20. doi: 10.1111/cas.12197. Epub 2013 Jun 21. doi: 10.1634/theoncologist.2012-0378. Epub 2013 Apr 11.

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    摘要:https://www.mybiosource.com/inhibitor/tivozanib-av-951/384260
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