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2-tertiary butyl-4-(2-pyridyl)thiazole | 1244554-06-0

中文名称
——
中文别名
——
英文名称
2-tertiary butyl-4-(2-pyridyl)thiazole
英文别名
2-Tert-butyl-4-pyridin-2-yl-1,3-thiazole
2-tertiary butyl-4-(2-pyridyl)thiazole化学式
CAS
1244554-06-0
化学式
C12H14N2S
mdl
——
分子量
218.323
InChiKey
ASIIXVRGJFNHHX-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):
    3.3
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    54
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • ARYL HYDROCARBON RECEPTOR MODULATOR
    申请人:Ariagen, Inc.
    公开号:US20190307731A1
    公开(公告)日:2019-10-10
    Disclosed is an aryl hydrocarbon receptor modulator of formula (I), and a pharmaceutically acceptable salt thereof, wherein R′ is H, CN, CH 2 (OH)R 0 , C m H 2m+1 , C n H 2n-1 , C n H 2n-3 , two R a are independently H or two R a together form ═O or ═N—W 3 —R 1 ; A is a C 6 to C 10 aromatic ring unsubstituted or substituted with 1 to 3 R, or a C 2 -C 10 heteroaromatic ring interrupted by 1 to 5 heteroatoms selected from N, O, and S or a 4 to 7 membered nonaromatic heterocyclic ring containing C═N and interrupted by 1 to 3 heteroatoms selected from N, O, and S, with either one unsubstituted or substituted with 1 to 3 R; Q is R, or is a C 6 to C 10 aromatic ring or a C 2 to C 10 heteroaromatic ring unsubstituted or substituted with 1 to 3 R and interrupted by 1 to 5 heteroatoms selected from N, O, and S; and R is R c which is C-attached or R N which is N-attached. The compounds of formula (I) of the present invention can regulate AhR activity, and can be used to inhibit the growth of cancer cells and inhibit the metastasis and invasion of tumor cells.
    本发明揭示了一种化学式(I)的芳香烃受体调节剂及其药用可接受盐,其中R′为H、CN、CH2(OH)R0、CmH2m+1、CnH2n-1、CnH2n-3,两个Ra独立地为H或两个Ra共同形成═O或═N—W3—R1;A为未取代或取代1至3个R的C6至C10芳香环,或由N、O和S中选择的1至5个杂原子中断的C2-C10杂芳环,或含有C═N并由N、O和S中选择的1至3个杂原子中断的4至7个成员的非芳杂环,其中一个未取代或取代1至3个R;Q为R,或者是未取代或取代1至3个R并由N、O和S中断的C6至C10芳香环或C2至C10杂芳环;R为C-连接的Rc或N-连接的RN。本发明的化合物可以调节AhR活性,可用于抑制癌细胞的生长,以及抑制肿瘤细胞的转移和侵袭。
  • Quinuclidine Compounds as Alpha-7 Nicotinic Acetylcholine Receptor Ligands
    申请人:Cook, II James H.
    公开号:US20100099684A1
    公开(公告)日:2010-04-22
    The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic α7 receptor and may be useful for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.
    本公开提供公式I的化合物,包括其盐,以及使用这些化合物的组合物和方法。这些化合物是尼古丁α7受体的配体,可能对中枢神经系统的各种疾病,特别是情感和神经退行性疾病的治疗有用。
  • THIAZOLE DERIVATIVE AND PROCESS FOR PRODUCING SAME
    申请人:Gifu University
    公开号:EP2388253B1
    公开(公告)日:2015-02-11
  • ARYL HYDROCARBON RECEPTOR MODULATORS
    申请人:SHENZHEN IMMUNOVA PHARMACEUTICAL CO., LTD.
    公开号:US20190330201A1
    公开(公告)日:2019-10-31
    The disclosure discloses an aryl hydrocarbon receptor modulators of formula (I), and pharmaceutically acceptable salts, R′ is H, CN, CH 2 (OH)R 0 , C m H 2m+1 , C n H 2n-1 , C n H 2n-3 , two R a is independently H, or two R a together form ═O or ═N—W 3 —R 1 ; A is a C 6 to C 10 aromatic ring, or a C 2 to C 10 heteroaromatic ring containing 1 to 5 heteroatom from N, O and S, or 4 to 7 membered non-aromatic heterocyclic ring containing 1 to 3 heteroatom from N, O and S and C═N, which are with no substituent or substituted by 1 or 3 R; Q is R, or a C 6 to C 10 aromatic ring or a C 2 to C 10 heteroaromatic ring containing 1 to 5 heteroatom selected from N, O and S, which are with no substituent or substituted by 1 or 3 R; R is R c connected with C or R N connected with N.
  • US8309577B2
    申请人:——
    公开号:US8309577B2
    公开(公告)日:2012-11-13
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