CAS: 22006-84-4; Denopterin

该化合物是一种复杂的有机化合物,其独特结构包括一种甘酸碱和一种丙烯衍生物.该化合物具有多种功能组,包括一种矿,一种碳基和氨基酸,有助于其潜在的生物活动.由于存在来自谷酸的碳酸组,极地溶剂有可能表现出溶性.石酸环系统可能具有其他特性,例如能够参与各种生物化学途径.该化合物可能具有医学化学方面的兴趣,特别是针对特定生物过程的药品开发.该化合物的复杂结构表明它可能与生物巨型分子发生相互作用,因此它有可能成为对药物设计和开发进行进一步研究的场所.然而,熔点,沸点和再活性等具体特性需要经验确定或文献参考精确的特征.

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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-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-10590158-B2
      优先权日:2015-06-29
      标题:Total synthesis of shishijimicin A and analogs thereof
      发明人:NICOLAOU KYRIACOS C; LI RUOFAN; LU ZHAOYONG; SOHN TE-IK; WOODS JAMES; PITSINOS EMMANOUIL N
      权利人:UNIV RICE WILLIAM M
      摘要:In one aspect, the present disclosure provides shishijimicin analogs of the formula: wherein the variables are as defined herein. In another aspect, the present disclosure also provides methods of preparing the compounds disclosed herein. In another aspect, the present disclosure also provides pharmaceutical compositions and methods of use of the compounds disclosed herein. Additionally, antibody drug conjugates of the compounds are also provided.

      专利号:US-11465997-B2
      优先权日:2017-06-22
      标 题 :Synthesis of disorazoles and analogs thereof as potent anticancer agents
      发明人:NICOLAOU KYRIACOS C; BELLAVANCE GABRIEL; BUCHMAN MAREK; PULUKURI KIRAN KUMAR; RIGOL STEPHAN
      权利人:UNIV RICE WILLIAM M
      摘要:In one aspect, the present disclosure provides disorazole analogs of the formula: Formula (I) wherein the variables are as defined herein. In another aspect, the present disclosure also provides methods of preparing the compounds disclosed herein. In another aspect, the present disclosure also provides pharmaceutical compositions and methods of use of the compounds disclosed herein. Additionally, drug conjugates with cell targeting moieties of the compounds are also provided.

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      主要参考文献


      1: Whyte MP, Lim E, McAlister WH, Gottesman GS, Trinh L, Veis DJ, Bijanki VN, Boden MG, Nenninger A, Mumm S, Buchbinder D. Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized Osteosclerosis. J Bone Miner Res. 2018 Jun 22. doi: 10.1002/jbmr.3532. [Epub ahead of print] doi: 10.1212/NXI.0000000000000467. eCollection 2018 Jul.
      3: Kırmızıbekmez H, İnan Y, Reis R, Sipahi H, Gören AC, Yeşilada E. Phenolic compounds from the aerial parts of Clematis viticella L. and their in vitro anti-inflammatory activities. Nat Prod Res. 2018 Mar
      12:1-4. doi: 10.1080/14786419.2018.1448815. [Epub ahead of print] doi: 10.1080/15622975.2017.1355473. Epub 2017 Aug 9. doi: 10.2147/IJNRD.S131869. eCollection 2017. Review.

      合成参考文献


      参考文献:10.1021/jm800656v
      摘要:Santana L, González-Díaz H, Quezada E, Uriarte E, Yáñez M, Viña D, Orallo F. Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors. J Med Chem. 2008 Nov 13;51(21):6740–51. doi: 10.1021/jm800656v.
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