CAS: 453562-69-1; N-(3,3-Dimethylindolin-6-yl)-2-((Pyridin-4-Ylmethyl)Amino)Nicotinamide

该化合物是一个小分子,主要作为抗抑郁性血管血管酶抑制剂,针对与血管成形和肿瘤生长有关的各种受体强力强力结流体,特别注意到它针对血管内皮生长因子受体(VeGFRs),小盘生长因子受体(PDGFRs)和纤维增生因子受体(FGFRs)的活动.Motesanib因其在治疗各种癌症(包括非小型细胞肺癌和其他固态肿瘤)方面的潜在治疗应用而受到调查.该化合物的特点是能够抑制肿瘤血管血管化,从而限制对肿瘤的营养和氧供应.就其化学结构而言,Motesanib具有有助于其生物活动的复杂安排,尽管此处没有提供具体的结构细节.与许多调查药物一样,Motesanib的药,功效和安全特征一直是临床研究的课题,其肿瘤发育结果各不相同.

结构式图片

欧盟法规

C&L通报

上下游产品

N-(1-乙酰基-3,3-二甲基-6-基)-2-((吡啶-4-基甲基)氨基)烟酰胺 N-(1-Acetyl-3,3-Dimethylindolin-6-yl){2-[(4-Pyridylmethyl)-Amino](3-Pyridyl)}-Carboxamide 453562-74-8

合成工艺路线路线简述

    N-(1-乙酰基-3,3-二甲基-6-基)-2-((吡啶-4-基甲基)氨基)烟酰胺 反应生成 莫特塞尼
    参考文献:Substituted Alkylamine Derivatives And Methods Of Use
    标题:Substituted Alkylamine Derivatives And Methods Of Use
    摘要:选择的胺类化合物对于预防和治疗疾病,如介导血管反应生成的疾病,具有有效性.该发明涵盖了新颖的化合物,类似物,前药及其药用可接受的盐,用于预防和治疗涉及癌症等疾病和其他疾病或病况的药物组合物和方法.该发明还涉及制备这类化合物的方法,以及在这类方法中有用的中间体.

    海关参考信息

    专利信息


    专利号:US-12391691-B2
    优先权日:2018-11-16
    标题:Synthesis of key intermediate of KRAS G12C inhibitor compound
    发明人:PARSONS ANDREW THOMAS; COCHRAN BRIAN MCNEIL; POWAZINIK IV WILLIAM; CAPORINI MARC ANTHONY
    权利人:AMGEN INC
    摘要:The present invention relates to an improved, efficient, scalable process to prepare intermediate compounds, such as compound 5M, having the structure n nuseful for the synthesis of compounds that target KRAS G12C mutations, such as

    专利号:US-2025206736-A1
    优先权日:2019-11-14
    标题 :Synthesis of kras g12c inhibitor compound
    发明人:CORBETT MICHAEL THOMAS; CAILLE SEBASTIEN
    权利人:AMGEN INC
    摘要:The present disclosure relates to an improved, efficient, scalable process to prepare intermediate compounds, such as 2-isopropyl-4-methylpyridin-3-amine, useful for the synthesis of compounds, such as Compound 9, for the treatment of KRAS G12C mutated cancers.

    专利号:US-11649285-B2
    优先权日:2016-08-03
    标题 :Identification of VSIG3/VISTA as a novel immune checkpoint and use thereof for immunotherapy
    发明人:KALABOKIS VASSILIOS; WANG JINGHUA; WU GUOPING; BAZAN JOSE FERNANDO; VALLEY CHRISTOPHER CARLIN
    权利人:BIO TECHNE CORP
    摘要:The ligand for VISTA is identified (VSIG3) as well as the use of this ligand and receptor interaction in the identification or synthesis of a VSIG3 agonist or antagonist compounds, preferably antibodies, polypeptides and fusion proteins which agonize or antagonize the effects of VSIG3 and/or VISTA and/or the VSIG3/VISTA interaction. These antagonists may be used to suppress VSIG3/VISTA's suppressive effects on T cell immunity, and more particularly used in the treatment of cancer, or infectious disease. These agonist compounds may be used to potentiate or enhance VSIG3/VISTA's suppressive effects on T cell immunity and thereby suppress T cell immunity, such as in the treatment of autoimmunity, allergy or inflammatory conditions. Screening assays for identifying these agonists and antagonist compounds are also provided.

    专利号:US-10370455-B2
    优先权日:2014-12-05
    标题 :Identification of VSIG8 as the putative VISTA receptor (V-R) and use thereof to produce VISTA/VSIG8 agonists and antagonists
    发明人:MOLLOY MICHAEL; GUO YALIN; ROTHSTEIN JAY; ROSENZWEIG MICHAEL
    权利人:IMMUNEXT INC
    摘要:The receptor for VISTA is identified (VSIG8) as well as the use of this receptor in the identification or synthesis of agonist or antagonist compounds, preferably antibodies, polypeptides and fusion proteins which agonize or antagonize the effects of VSIG8 and/or VISTA and/or the VSIG8/VISTA binding interaction. These antagonists may be used to suppress VISTA's suppressive effects on T cell immunity, and more particularly used in the treatment of cancer, or infectious disease. These agonist compounds may be used to potentiate or enhance VISTA's suppressive effects on T cell immunity and thereby suppress T cell immunity, such as in the treatment of autoimmunity, allergy or inflammatory conditions. Screening assays for identifying these agonists and antagonist compounds are also provided.

    专利号:US-2024400576-A1
    优先权日:2021-09-03
    标 题:Nitrogen-containing derivatives of salinomycin, synthesis and uses thereof
    发明人:RODRIGUEZ RAPHAËL; CZERWONKA DOMINIKA; ANTOSZCZAK MICHAL; HUCZYNSKI ADAM
    权利人:CENTRE NAT RECH SCIENT; INST CURIE; INST NAT SANTE RECH MED; ADAM MICKIEWICZ UNIV
    摘要:The present invention relates to nitrogen-containing derivatives of salinomycin having the formula (I), as well as pharmaceutically acceptable salt thereof, and synthesis and uses thereof, in particular for the treatment and/or prevention of cancer including for preventing cancer metastasis and/or for preventing cancer recurrence and/or for decreasing resistance to a chemotherapy in a subject.

    专利号:US-2025250280-A1
    优先权日:2021-09-03
    标 题 :Nitrogen-containing derivatives of narasin, synthesis and uses thereof
    发明人:RODRIGUEZ RAPHAËL; CAÑEQUE TATIANA; MÜLLER SEBASTIAN; ANTOSZCZAK MICHAL
    权利人:CENTRE NAT RECH SCIENT; INST NAT SANTE RECH MED; INST CURIE
    摘要:The present invention relates to nitrogen-containing derivatives of narasin having the formula (I), as well as synthesis and uses thereof, in particular for the treatment and/or prevention of cancer. Also disclosed are medicaments including the nitrogen-containing derivatives of narasin, which include medicaments for preventing cancer metastasis and/or for preventing cancer recurrence and/or for decreasing resistance to a chemotherapy in a subject.
    台州市科瑞生物技术有限公司
    ⚠️ 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.pharm-intermediates.com
    企业联系电话:0576-88813233👤
    📞台州市科瑞生物技术有限公司 ⚠️参考联系方式
    联系人:金崇光
    电话:0576-88813233
    手机:13396860566
    传真:0576-88813233
    邮箱:sales@pharm-intermediates.com
    通信地址: 台州市开发大道东段288号
    邮编: 318000
    🆔 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→

    地址:台州市开发大道东段288号
    ⚠️ 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


    1: Çelenk M, Yıldırım H, Tektemur A, Balbaba M, Erdağ M. Effect of topical motesanib in experimental corneal neovascularization model. Int Ophthalmol. 2023 Aug;43(8):2989-2997. doi: 10.1007/s10792-023-02685-3. Epub 2023 Mar 27. 41(4):2482-2490. doi: 10.3892/or.2019.7005. Epub 2019 Feb 11.
    166:244-251. doi: 10.1016/j.jpba.2019.01.023. Epub 2019 Jan 14. 35(32):3662-3670. doi: 10.1200/JCO.2017.72.7297. Epub 2017 Sep 13. 95(37):e4645. doi: 10.1097/MD.0000000000004645.
    6: Gosselin NH, Mouksassi MS, Lu JF, Hsu CP. Population pharmacokinetic modeling of motesanib and its active metabolite, M4, in cancer patients. Clin Pharmacol Drug Dev. 2015 Nov;4(6):463-72. doi: 10.1002/cpdd.196. Epub 2015 Jul 23. 17(3):1103-10. doi: 10.7314/apjcp.2016.17.3.1103. 10(3):e0121162. doi: 10.1371/journal.pone.0121162. Erratum for: PLoS One. 2014 Oct 14;9(10):e108048. doi: 10.1371/journal.pone.0108048.

    合成参考文献


    参考文献:10.4061/2011/678357
    摘要:Prazeres H, Torres J, Rodrigues F, Couto JP, Vinagre J, Sobrinho-Simões M, Soares P. How to Treat a Signal Current Basis for RET-Genotype-Oriented Choice of Kinase Inhibitors for the Treatment of Medullary Thyroid Cancer. Journal of Thyroid Research. 2011;2011():1–10. doi: 10.4061/2011/678357.
    参考文献:10.4061/2011/762905
    摘要:Burrows N, Babur M, Resch J, Williams KJ, Brabant G. Hypoxia-Inducible Factor in Thyroid Carcinoma. Journal of Thyroid Research. 2011;2011():1–17. doi: 10.4061/2011/762905.
    参考文献:10.1155/2011/982879
    摘要:Elferink LA, Resto VA. Receptor-Tyrosine-Kinase-Targeted Therapies for Head and Neck Cancer. Journal of Signal Transduction. 2011 Jun 07;2011():1–11. doi: 10.1155/2011/982879.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知