CAS: 56605-16-4; Spiromustine

该化合物是属于氮芥子类的合成烷基剂,其主要特征是其独特的结构,包括有助于其生物活动的环球运动,Spiromustine表现出抗沙素特性,并因其在癌症治疗中的潜在用途,特别是在治疗各种恶性肿瘤方面的潜在用途而受到调查.复合功能是与DNA形成共价联系,导致DNA复制和转录的交叉联系和随后的中断,最终导致癌症细胞的流行.其药用动力学和毒性特征是其治疗应用中的重要考虑因素,与许多化学化学剂一样.此外,该化合物的溶性,稳定性和再活性是影响其临床环境中的功效和安全的关键因素.持续的研究继续探索其在肿瘤学方面的潜在好处和局限性.

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3-<2-'-Hydroxyethyl)Amino>-Ethyl>-5,5-Pentamethylen-Hydantoin 56605-11-9

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    📜3-<2-'-Hydroxyethyl)Amino>-Ethyl>-5,5-Pentamethylen-Hydantoin 以51的收率获得产物螺莫司汀
    参考文献:J. Med. Chem. 1975,18,846-849
    标题:J. Med. Chem. 1975,18,846-849

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    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-2021275545-A1
    优先权日:2018-11-21
    标 题 :Method of treating cancer preferably characterized by expression of a fusion protein comprising a member of the e-twenty-six family by administering an agent that inhibits the synthesis and/or activity of cortisol
    发明人:YARDEN YOSEF; SRIVASTAVA SWATI
    权利人:YEDA RES & DEV
    摘要:A method of treating a cancer selected from the group consisting of a myeloid malignancy, a lymphoid malignancy and Ewing's sarcoma is disclosed. The method comprises administering to the subject a therapeutically effective amount of an agent that inhibits the synthesis and/or activity of cortisol.

    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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    合成参考文献


    摘要:National Cancer Institute Screening Program Data Summary, Developmental Therapeutics Program., JAN1986
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