1-(2-chloropyridin-4-yl)-3-(pyridin-4-yl)urea

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 1-(2-chloropyridin-4-yl)-3-(pyridin-4-yl)urea
• 英文别名: 1-(2-Chloropyridin-4-yl)-3-pyridin-4-ylurea；1-(2-chloropyridin-4-yl)-3-pyridin-4-ylurea
• 化学式: C₁₁H₉ClN₄O
• 分子量: 248.672
• InChiKey: HFIPFTAKXMECCX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  17
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  66.9
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  4-氨基吡啶 、 2,2,2-trichloroethyl (2-chloropyridin-4-yl)carbamate 在 三乙胺 作用下， 以 N-甲基吡咯烷酮 为溶剂， 反应 72.0h， 以40 mg的产率得到1-(2-chloropyridin-4-yl)-3-(pyridin-4-yl)urea
  参考文献：
  名称：

  [EN] UREA DERIVATIVES FOR USE AGAINST PROLIFERATIVE DISEASES
  [FR] DÉRIVÉS D'URÉE

  摘要：

  公开号：

  WO2020126968A3

文献信息

• [EN] SMARCA DEGRADERS AND USES THEREOF<br/>[FR] AGENTS DE DÉGRADATION DE SMARCA ET LEURS UTILISATIONS
  申请人：KYMERA THERAPEUTICS INC

  公开号：WO2020251971A1

  公开（公告）日：2020-12-17

  The present invention provides compounds, pharmaceutically acceptable compositions thereof, and methods of using the same for the modulation of one or more SWI/SNF-related matrix associated actin dependent regulator of chromatin subfamily A (SMARCA) and/or polybromo-1 (PB-1) protein via ubiqitination and/or degradation by compounds. The compounds are bifunctional molecules that link a cereblon-binding moiety to a ligand that binds SMARCA and/or PB1 proteins.

  本发明提供化合物、其药学上可接受的组合物，以及利用这些化合物调控一个或多个SWI/SNF相关基质相关肌动蛋白依赖的染色质亚家族A（SMARCA）和/或聚溴-1（PB-1）蛋白通过化合物的泛素化和/或降解的方法。这些化合物是双功能分子，将结合到cereblon的部分与结合到SMARCA和/或PB1蛋白的配体连接在一起。
• Discovery of Orally Active Inhibitors of Brahma Homolog (BRM)/SMARCA2 ATPase Activity for the Treatment of Brahma Related Gene 1 (BRG1)/SMARCA4-Mutant Cancers
  作者：Julien P. N. Papillon、Katsumasa Nakajima、Christopher D. Adair、Jonathan Hempel、Andriana O. Jouk、Rajeshri G. Karki、Simon Mathieu、Henrik Möbitz、Rukundo Ntaganda、Troy Smith、Michael Visser、Susan E. Hill、Felipe Kellermann Hurtado、Gregg Chenail、Hyo-Eun C. Bhang、Anka Bric、Kay Xiang、Geoffrey Bushold、Tamara Gilbert、Anthony Vattay、Julie Dooley、Emily A. Costa、Isabel Park、Ailing Li、David Farley、Eugen Lounkine、Q. Kimberley Yue、Xiaoling Xie、Xiaoping Zhu、Raviraj Kulathila、Daniel King、Tiancen Hu、Katarina Vulic、John Cantwell、Catherine Luu、Zainab Jagani

  DOI：10.1021/acs.jmedchem.8b01318

  日期：2018.11.21

  SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin subfamily A member 2 (SMARCA2), also known as Brahma homologue (BRM), is a Snf2-family DNA-dependent ATPase. BRM and its close homologue Brahma-related gene 1 (BRG1), also known as SMARCA4, are mutually exclusive ATPases of the large ATP-dependent SWI/SNF chromatin-remodeling complexes involved in transcriptional regulation of gene expression. No small molecules have been reported that modulate SVVI/SNF chromatin-remodeling activity via inhibition of its ATPase activity, an important goal given the well-established dependence of BRG1-deficient cancers on BRM. Here, we describe allosteric dual BRM and BRG1 inhibitors that downregulate BRM-dependent gene expression and show antiproliferative activity in a BRG1-mutant-lung-tumor xenograft model upon oral administration. These compounds represent useful tools for understanding the functions of BRM in BRG1-loss-of-function settings and should enable probing the role of SWI/SNF functions more broadly in different cancer contexts and those of other diseases.
• METHODS OF TREATING CANCERS
  申请人：Foghorn Therapeutics Inc.

  公开号：US20220016083A1

  公开（公告）日：2022-01-20

  The present invention relates to methods and compositions for the treatment of BAF-related disorders such as melanoma, prostate cancer, breast cancer, bone cancer, renal cell carcinoma, and hematologic cancer.
• [EN] UREA DERIVATIVES<br/>[FR] DÉRIVÉS D'URÉE
  申请人：BAYER AG

  公开号：WO2020126968A2

  公开（公告）日：2020-06-25

  The present invention covers urea compounds of general formula (I) in which R1, A and B are as defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds and the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular of hyperproliferative disorders, as a sole agent or in combination with other active ingredients.