CAS: 85977-49-7; Tauromustine

该化合物是一种合成化合物,属于专门设计用于癌症治疗的烷基制剂类别,是氮芥子的衍生物,其特点是能够形成与DNA的共价联系,导致DNA复制和转录的交叉联系并随后中断.这一行动机制使其对迅速分裂的癌症细胞有效.陶鲁穆素素通常在临床环境中进行,并被调查其治疗各种恶性肿瘤的潜力.其化学结构包括一种酸盐混合物,可能会影响其药用植物和毒性特征.已知该化合物具有一系列副作用,许多乳胶类制剂都常见,包括我的乳房压抑和胃肠紊乱.正在进行的研究旨在更好地了解其功效,最佳剂量疗法和可能的组合疗法,以提高其治疗效果,同时尽量减少不利影响.

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Ls 3114 91893-26-4

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    📜Ls 3114 反应生成 牛磺莫司汀
    参考文献:Novel N-Nitroso Compounds,Compositions Containing Such Compounds And Processes For Their Preparation
    标题:Novel N-Nitroso Compounds,Compositions Containing Such Compounds And Processes For Their Preparation

    海关参考信息

    专利信息


    专利号:US-8734846-B2
    优先权日:2008-06-16
    标 题 :Methods for the preparation of targeting agent functionalized diblock copolymers for use in fabrication of therapeutic targeted nanoparticles
    发明人:ALI MIR M; HRKACH JEFF; ZALE STEPHEN E; ALVAREZ DE CIENFUEGOS LUIS
    权利人:BIND BIOSCIENCES INC
    摘要:This application provides nanoparticles and methods of making nanoparticles using pre-functionalized poly(ethylene glycol)(also referred to as PEG) as a macroinitiator for the synthesis of diblock copolymers. Ring opening polymerization yields the desired poly(ester)-poly (ethylene glycol)-targeting agent polymer that is used to impart targeting capability to therapeutic nanoparticles. This “polymerization fromâ€? approach typically employs precursors of the targeting agent wherein the reactivity of functional groups of the targeting agent is masked using protecting groups. Also described is a “coupling toâ€? that utilized the poly(ethylene glycol)-targeting agent conjugate where the targeting agent remains in its native un-protected form. This method uses “orthogonalâ€? chemistry that exhibit no cross reactivity towards functional groups typically found within targeting agents of interest.

    专利号:US-2013035307-A1
    优先权日:2010-01-26
    标 题:Methods for treating or preventing the spread of cancer using semi-synthetic glycosaminoglycosan ethers
    发明人:PRESTWICH GLENN D; KENNEDY THOMAS P
    权利人:UNIV UTAH RES FOUND; PRESTWICH GLENN D; KENNEDY THOMAS P
    摘要:Described herein are methods for the treatment and prevention of tumor metastasis using alkylated and fluoroalkylated semi-synthetic glycosaminoglycan ethers (“SAGEsâ€?). The synthesis of sulfated alkylated and fluoroalkylated SAGEs is also described.

    专利号:US-2008214827-A1
    优先权日:2004-02-03
    标 题:Synthesis of Cyanoimino-Benzoimidazoles
    发明人:GOEHRING R RICHARD; WHITEHEAD JOHN; SHAO BIN
    权利人:EURO CELTIQUE SA
    摘要:Disclosed in certain embodiments is a process for synthesizing a compound of formula (V) and salts thereof.

    专利号:US-9220714-B2
    优先权日:2006-03-16
    标 题 :Nitrofuran compounds for the treatment of cancer and angiogenesis
    发明人:SAULNIER SHOLLER GISELLE L; SWAMY NARASIMHA; KALKUNTE STAYAN; SINGH RAKESH K; BRARD LAURENT; KIM KYU KWANG
    权利人:WOMEN AND INFANTS HOSPITAL OF RHODE ISLAND; UNIV BROWN; WOMEN AND INFANTS HOSPITAL RHODE ISLAND
    摘要:The invention is directed to the synthesis and use of nitrofuran compounds, especially Nifurtimox, as medicaments to treat cancer, especially neuroblastoma, and to inhibit angiogenesis. The invention also provides compositions, unit dosage forms, and kits comprising the compounds.

    专利号:US-6787668-B2
    优先权日:2000-04-13
    标 题 :2-amino-4,5 heptenoic acid derivatives useful as nitric oxide synthase inhibitors
    发明人:PITZELE BARNETT S; SIKORSKI JAMES A; WEBBER RONALD KEITH
    权利人:PHARMACIA CORP
    摘要:The present invention is directed to a compound of formula I:or a pharmaceutically acceptable salt thereof, wherein:R1 is selected from the group consisting of H and methyl; andR2 is selected from the group consisting of H and methyl.The compounds possess useful nitric oxide synthetase inhibiting activity, and are expected to be useful in the treatment or prophylaxis of a disease or condition in which the synthesis or over synthesis of nitric oxide forms a contributory part.

    专利号:US-2024382626-A1
    优先权日:2023-05-16
    标题 :Irradiation amenable liposomal dye aggregates and methods of synthesis and use thereof
    发明人:PORTER TYRONE; STERN NOAH; TUNNELL JAMES; SHRESTHA BINITA
    权利人:UNIV TEXAS
    摘要:The present invention provides lipid nanoparticles that are amenable to an irradiation at a wavelength at or above 850 nm, have an absorption peak from about 850 to 1100 nm wavelength, and comprise a high transition temperature lipid and a dye (e.g., a J-aggregate of a dye). In some embodiments, the dye (e.g., J-aggregate of the dye) is encapsulated in the lipid nanoparticle. In various embodiments, the present invention also relates to compositions comprising said lipid nanoparticles and methods of generating said lipid nanoparticles and compositions thereof. The present invention further relates to methods relating to the said lipid nanoparticles for imaging, detection, and treatment of diseases or disorders (e.g., phototherapy) in a subject.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Gregor A, Rampling R, Aapro M, Malmström P, Whittle IR, Rye R, Stewart M, Sellar R, Demierre B, Ironside JW, et al. Phase II study of tauromustine in malignant glioma. Eur J Cancer. 1992;28A(12):1959-62.

    合成参考文献


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    摘要:Johansson CJ. Pharmacokinetic rationale for chemotherapeutic drugs combined with intra-arterial degradable starch microspheres (Spherex). Clin Pharmacokinet. 1996 Sep;31(3):231–40. doi: 10.2165/00003088-199631030-00006.
    参考文献:10.1007/s004320050295
    摘要:Paulsen F, Hoffmann W, Becker G, Belka C, Weinmann M, Classen J, Kortmann R, Bamberg M. Chemotherapy in the treatment of recurrent glioblastoma multiforme: ifosfamide versus temozolomide. Journal of Cancer Research and Clinical Oncology. 1999 Jun 02;125(7):411–8. doi: 10.1007/s004320050295.
    参考文献:10.1007/bf02307174
    摘要:Bien E, Vick K, Skorka G. Effects of exogenous factors on the cerebral glutathione in rodents. Arch Toxicol. 1992;66(4):279–85. doi: 10.1007/bf02307174.
    参考文献:10.1023/a:1015768225145
    摘要:Grant R, Walker M, Hadley D, Barton T, Osborn C. Imaging response to chemotherapy with RMP-7 and carboplatin in malignant glioma: size matters but speed does not. J Neurooncol. 2002 May;57(3):241–5. doi: 10.1023/a:1015768225145.
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