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5-Fluoro-6-methyl-2,1,3-benzothiadiazole

中文名称
——
中文别名
——
英文名称
5-Fluoro-6-methyl-2,1,3-benzothiadiazole
英文别名
5-fluoro-6-methyl-2,1,3-benzothiadiazole
5-Fluoro-6-methyl-2,1,3-benzothiadiazole化学式
CAS
——
化学式
C7H5FN2S
mdl
——
分子量
168.19
InChiKey
ALWOWESAZDDJQN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    54
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF INTERLEUKIN-1 RECEPTOR-ASSOCIATED KINASE 4 POLYPEPTIDES
    申请人:Arvinas, Inc.
    公开号:US20190151295A1
    公开(公告)日:2019-05-23
    The present disclosure relates to bifunctional compounds, which find utility as modulators of Interleukin-1 Receptor-Associated Kinase 4 (IRAK-4); the target protein). In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a Von Hppel-Lindau, cereblon, ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds the target protein, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aggregation or accumulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.
    本公开涉及双功能化合物,其作为白细胞介素-1受体相关激酶4(IRAK-4;目标蛋白)的调节剂具有实用性。具体而言,本公开涉及包含一端结合E3泛素连接酶的Von Hppel-Lindau、cereblon配体的双功能化合物,另一端结合目标蛋白的部分,使得目标蛋白靠近泛素连接酶以实现目标蛋白的降解(和抑制)。本公开展示了与目标蛋白的降解/抑制相关的广泛药理活性。本公开的化合物和组合物用于治疗或预防由目标蛋白聚集或积累导致的疾病或紊乱。
  • [EN] BICYCLIC HETEROCYCLE SUBSTITUTED PYRIDYL COMPOUNDS USEFUL AS KINASE MODULATORS<br/>[FR] COMPOSÉS PYRIDYLES À SUBSTITUTION PAR HÉTÉROCYCLE BICYCLIQUE UTILES EN TANT QUE MODULATEURS DE KINASE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2014074657A1
    公开(公告)日:2014-05-15
    Compounds having the following formula (I) or a stereoisomer or a pharmaceutically-acceptable salt thereof, wherein R2 is a bicyclic heterocycle, and R1, R3, R4, R5 and R6 are as defined herein, that are useful as kinase modulators, including IRAK-4 modulation.
    具有以下式(I)的化合物或其立体异构体或药用盐,其中R2是双环杂环,R1、R3、R4、R5和R6如本文所定义,这些化合物可用作激酶调节剂,包括IRAK-4调节。
  • BICYCLIC HETEROCYCLE SUBSTITUTED PYRIDYL COMPOUNDS USEFUL AS KINASE MODULATORS
    申请人:BRISTOL-MYERS SQUIBB COMPANY
    公开号:US20150274696A1
    公开(公告)日:2015-10-01
    Compounds having the following formula (I) or a stereoisomer or a pharmaceutically-acceptable salt thereof, wherein R 2 is a bicyclic heterocycle, and R 1 , R 3 , R 4 , R 5 and R 6 are as defined herein, that are useful as kinase modulators, including IRAK-4 modulation.
    具有以下式(I)或其立体异构体或药物可接受的盐的化合物,其中R2是双环杂环,R1、R3、R4、R5和R6如此定义,可用作激酶调节剂,包括IRAK-4调节剂。
  • Compounds and methods for the targeted degradation of interleukin-1 receptor- associated kinase 4 polypeptides
    申请人:Arvinas Operations, Inc.
    公开号:US11065231B2
    公开(公告)日:2021-07-20
    The present disclosure relates to bifunctional compounds, which find utility as modulators of Interleukin-1 Receptor-Associated Kinase 4 (IRAK-4); the target protein). In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a Von Hppel-Lindau, cereblon, ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds the target protein, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aggregation or accumulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.
    本公开涉及双功能化合物,这些化合物可作为白细胞介素-1受体相关激酶4(IRAK-4)(靶蛋白)的调节剂。特别是,本公开涉及双功能化合物,其一端含有与 E3 泛素连接酶结合的 Von Hppel-Lindau(脑龙)配体,另一端含有与靶蛋白结合的分子,从而使靶蛋白靠近泛素连接酶,以实现对靶蛋白的降解(和抑制)。本公开物具有与降解/抑制靶蛋白相关的广泛药理活性。本公开的化合物和组合物可以治疗或预防因目标蛋白聚集或积聚而导致的疾病或失调。
  • ORGANIC SEMICONDUCTOR MATERIAL AND THIN-FILM TRANSISTOR
    申请人:Au Optronics Corporation
    公开号:US20140312317A1
    公开(公告)日:2014-10-23
    An organic semiconductor material is provided. The organic semiconductor material includes a compound represented by formula (1): wherein r and s each independently represent a positive integer of 1 to 20; n represents a positive integer of 2 to 10000; X 1 , X 2 and X 3 each independently represent O, S, Se, Te, NR, RCR, RSiR, RGeR or RSnR; Y 1 and Y 2 each independently represent H, F, Cl, CF 3 , haloalkyl, CN, R, OR, SR, COOR or COR; and Z 1 , Z 2 , Z 3 and Z 4 each independently represent H, F, Cl, CF 3 , haloalkyl, CN, R, OR, SR, COOR or COR, wherein R represents alkyl group.
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