CAS: 928134-65-0; Lci699

该化合物是一个化学化合物,其结构复杂,包括一个闪烁[1-2(c)imidazole meety和氟苯丙烯聚醚组.该化合物通常具有中等溶解性,并具有潜在的生物活性,因此对医药化学具有兴趣.氟甲醇原子的存在可以增强脂性,影响化合物与生物目标的相互作用.闪烁[1-2-c]imdazole框架因其在各种药用活动中的作用而闻名,包括潜在的抗癌和抗炎作用.此外,硝酸盐组可能助长化合物的再活性和形成氢联结的能力,这对于其生物活动至关重要.

结构式图片

合成工艺路线路线简述

  • 合成目标产物 Lci699 主要起始原料 1H-Imidazole-1-Acetic Acid, α-(4-Cyano-2-Fluorophenyl)-5-(2-Hydroxyethyl)-, Methyl Ester
  • (文献来源)合成步骤主要原料 1H-Imidazole-1-Acetic Acid, α-(4-Cyano-2-Fluorophenyl)-5-(2-Hydroxyethyl)-, Methyl Ester

海关参考信息

专利信息


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-2024066133-A1
优先权日:2020-03-06
标 题 :Therapeutic agents and conjugates thereof
发明人:SONG YUNTAO; LI ANRONG; LI HUI; LI XIANFENG; YANG JUNBAO
权利人:BEIJING XUANYI PHARMASCIENCES CO LTD
摘要:The present disclosure provides a class of conjugates of general formula (X), a class of TLR9 agonist derivatives, such as formula (I), (XX), and (XXI), certain diastereomers of STING agonists, a class of STING agonist derivatives, such as formula (XXVIV), a class of heterocyclic compounds of general formula (II), a class of heterocyclic compounds of general formula (III), as defined herein. A 1 , A 2 , T, Z 1 , Z 2 , Z 3 , b 1 , and b 2 , in formula (X) are defined herein. The conjugate provides unique properties that are based upon the properties of the therapeutic agents that are part of the conjugate. Also provided are methods of synthesis and use of compounds.

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✅ COA系统入驻 | 共享模式

主要参考文献


1: Castinetti F, Bertherat J, Chanson P, Raverot G, Young J, Tabarin A. Use of osilodrostat in a block-and-replace and titration strategy for cushing's syndrome: a position paper by French experts. Rev Endocr Metab Disord. 2026 Feb 28. doi: 10.1007/s11154-026-10020-1. Epub ahead of print. 21(2):89-102. doi: 10.1080/17446651.2026.2615346. Epub 2026 Feb 20. 73(1):87-92. doi: 10.1507/endocrj.EJ25-0150. Epub 2025 Oct 25.
4: Osilodrostat for Cushing syndrome. Aust Prescr. 2025 Apr;48(2):67-68. doi: 10.18773/austprescr.2025.010.
5: Fleseriu M, Auchus RJ, Bancos I, Biller BMK. Osilodrostat Treatment for Adrenal and Ectopic Cushing Syndrome: Integration of Clinical Studies With Case Presentations. J Endocr Soc. 2025 Feb 14;9(4):bvaf027. doi: 10.1210/jendso/bvaf027.

合成参考文献


摘要:Caron, S.; Lee, J.; Liu, Y.; Nguyen, T. N.; Piper, J. L.; Vicini, A. C., Science of Synthesis: Modern Strategies in Organofluorine Chemistry, (2025) 2.
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