CAS: 68247-85-8; Peplomycin

该化合物是一种从细菌脊椎炎杆菌发酵中衍生出来的抗沙素抗生素,它属于被称为骨髓类类似物的化合物,主要用于癌症治疗,特别是治疗某些类型的肿瘤,包括睾丸癌和淋巴瘤;该化合物展示了一种独特的行动机制,它涉及通过形成自由基体来诱导DNA链断裂,最终导致细胞死亡;Peplomycin的特点是,它与其他乳胶化剂相比,其毒性较低,使其成为混合疗法中的一种宝贵的选择;其结构具有一种可塑胶细胞的灵敏性,有助于其生物活动;此外,Peplomycin是通过注射施用,其致癌性能因配方和病人因素而不同;许多乳胶化剂,监测潜在的副作用,如肺毒性和皮肤反应,在治疗期间至关重要.

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      专利信息


      专利号:US-10925977-B2
      优先权日:2006-10-05
      标 题 :Efficient synthesis of chelators for nuclear imaging and radiotherapy: compositions and applications
      发明人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S
      权利人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S; CEIL POINT LLC; UNIV TEXAS
      摘要:Novel methods of synthesis of chelator-targeting ligand conjugates, compositions comprising such conjugates, and therapeutic and diagnostic applications of such conjugates are disclosed. The compositions include chelator-targeting ligand conjugates optionally chelated to one or more metal ions. Methods of synthesizing these compositions in high purity are also presented. Also disclosed are methods of imaging, treating and diagnosing disease in a subject using these novel compositions, such as methods of imaging a tumor within a subject and methods of diagnosing myocardial ischemia.

      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-2024173256-A1
      优先权日:2022-11-29
      标 题:Hdl mimicking targeted drug delivery system for the treatment of solid tumors
      发明人:SABNIS NIRUPAMA; LACKO ANDRAS; FUDALA RAFAL
      权利人:UNIV OF NORTH TEXAS HEALTH SCIENCE CENTER
      摘要:The present disclosure is directed to an SR-B1-targeting nanomicelle and compositions, methods of synthesis and methods of use thereof. The nanomicelle may be an HDL-mimetic drug delivery system and may be cross-linked with DSS. The composition may contain a therapeutic agent with the ability to treat cancers, especially sarcomas.

      专利号:US-2016318862-A1
      优先权日:2013-09-25
      标 题:Synthesis of delta 12-pgj3 and related compounds
      发明人:NICOLAOU KYRIACOS C; HERETSCH PHILIPP; HALE CHRISTOPHER R H; EL GHZAOUI ABDELLATIF EL MARROUNI; PULUKURI KIRAN KUMAR; YU RUOCHENG; GROVE CHARLES
      权利人:UNIV RICE WILLIAM M
      摘要:In one aspect, the present invention provides novel derivatives of Δ 12 -PGJ 3 and modular synthetic pathways to obtaining Δ 12 -PGJ 3 and derivatives thereof. In some aspects, the present derivatives of Δ 12 -PGJ 3 are useful as chemotherapeutic agents. The present disclosure also describes compositions of these derivatives as well as methods of use of the derivatives thereof.

      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.

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      主要参考文献


      1: Carter SK, Ultmann J. Peplomycin. Cancer Treat Rev. 1984 Dec;11(4):303-5. doi: 10.1016/0305-7372(84)90028-8. 150(6):1213-4. doi: 10.1111/j.1365-2133.2004.05969.x. 49(8):984-992. doi: 10.1016/j.ijom.2020.01.024. Epub 2020 Feb 16. 19(7):664-668. doi: 10.1002/cbic.201700643. Epub 2018 Feb 12. 12(1-3):247-55. 18(10):1613-9. Japanese. 30(3):377-82. Japanese. 45(5):627-31. doi: 10.1111/j.1365-4632.2005.02647.x. 25(12):1698-704. 73 Suppl
      2:188-90. Japanese.

      合成参考文献


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