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5-tert-butylfuranacetic acid | 222554-03-2

中文名称
——
中文别名
——
英文名称
5-tert-butylfuranacetic acid
英文别名
2-(5-Tert-butylfuran-2-yl)acetic acid
5-tert-butylfuranacetic acid化学式
CAS
222554-03-2
化学式
C10H14O3
mdl
——
分子量
182.219
InChiKey
PYQJKUCHXFODNJ-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):
    2.2
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    50.4
  • 氢给体数:
    1
  • 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。
  • CYCLIC KETONE DERIVATIVE AND PHARMACEUTICAL USE THEREOF
    申请人:TORAY INDUSTRIES, INC.
    公开号:EP0962456A1
    公开(公告)日:1999-12-08
    The present invention relates to cyclic ketones represented by the following formula and to drugs in which an effective component is such a cyclic ketone or a pharmacologically acceptable salt thereof. The cyclic ketones of the present invention encourage the production of blood platelets, leukocytes and erythrocytes, and can be employed in the prevention or treatment of cytopaenia brought about by cancer chemotherapy, radiotherapy or drug therapy, or by immunological abnormality, anaemia and the like.
    本发明涉及下式所代表的环酮 以及有效成分为这种环酮或其药理学上可接受的盐的药物。 本发明的环酮能促进血小板、白细胞和红细胞的生成,可用于预防或治疗因癌症化疗、放疗或药物治疗,或因免疫异常、贫血等引起的细胞减少症。
  • 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.
  • US6184245B1
    申请人:——
    公开号:US6184245B1
    公开(公告)日:2001-02-06
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