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3-(2-methylthiazol-4-yl)phenol

中文名称
——
中文别名
——
英文名称
3-(2-methylthiazol-4-yl)phenol
英文别名
3-(2-methyl-thiazol-4-yl)-phenol;3-(2-methyl-1,3-thiazol-4-yl)phenol
3-(2-methylthiazol-4-yl)phenol化学式
CAS
——
化学式
C10H9NOS
mdl
——
分子量
191.254
InChiKey
XUTSREOVBGWBPA-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):
    2.7
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    61.4
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    Compounds enhancing antitumor activity of other cytotoxic agents
    摘要:
    这项发明涉及某些杂环化合物及其药用可接受的盐,这些化合物对于使多药耐药肿瘤细胞对抗癌药物和多药耐药形式的疟疾、结核病、利什曼病和阿米巴痢疾对化疗药物具有敏感性是有用的。这些化合物及其药用可接受的盐还是人类MDR1基因编码的P-糖蛋白的活性药物转运能力的抑制剂,以及来自真核和原核生物(例如,来自疟原虫的pfmdr,以及小鼠mdr1和mdr3基因产物)的某些其他相关的ATP结合盒转运蛋白的抑制剂。
    公开号:
    US06130217A1
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文献信息

  • [EN] BENZOFURAN AND BENZOTHIOPHENE DERIVATIVES USEFUL IN THE TREATMENT OF HYPER-PROLIFERATIVE DISORDERS<br/>[FR] DERIVES DE BENZOFURANE ET DE BENZOTHIOPHENE UTILISES DANS LE TRAITEMENT DE TROUBLES HYPERPROLIFERATIFS
    申请人:BAYER PHARMACEUTICALS CORP
    公开号:WO2003072561A1
    公开(公告)日:2003-09-04
    This invention relates to novel benzofuran and benzothiophene derivatives of the general formula and their use for the treatment of hyper-proliferative disorders.
    这项发明涉及一般式的新型苯并呋喃苯并噻吩生物及其用于治疗高增殖性疾病的用途。
  • [EN] AROMATIC SULFONAMIDE DERIVATIVES<br/>[FR] DÉRIVÉS DE SULFONAMIDE AROMATIQUE
    申请人:BAYER PHARMA AG
    公开号:WO2016198374A1
    公开(公告)日:2016-12-15
    Substituted aromatic sulfonamides of formula (I) pharmaceutical compositions and combinations comprising said compounds and the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease.
    公式(I)的取代芳香磺胺类化合物,包括所述化合物的药物组合物和组合物,以及利用所述化合物制造用于治疗或预防疾病的药物组合物。
  • [EN] HETEROCYCLIC COMPOUNDS AS CLASS II PHOSPHOINOSITIDE 3-KINASE INHIBITORS<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES EN TANT QU'INHIBITEURS DE PHOSPHOINOSITIDE 3-KINASE DE CLASSE II
    申请人:FORSCHUNGSVERBUND BERLIN EV
    公开号:WO2019234237A1
    公开(公告)日:2019-12-12
    The present application relates to compounds of formula (1) and their use as medicament, in particular for the treatment of a medical condition associated with defective PI3K signalling.
    本申请涉及式(1)化合物及其作为药物的用途,特别是用于治疗与缺陷PI3K信号传导相关的医疗状况。
  • MODULATORS OF GLUCOCORTICOID RECEPTOR, AP-1, AND/OR NF-kB ACTIVITY AND USE THEREOF
    申请人:Yang Bingwei Vera
    公开号:US20100063051A1
    公开(公告)日:2010-03-11
    Novel non-steroidal compounds are provided which are useful in treating diseases associated with modulation of the glucocorticoid receptor, AP-1, and/or NF-κB activity including inflammatory and immune diseases, obesity and diabetes having the structure of formula (I) an enantiomer, diastereomer, tautomer, solvate (e.g. a hydrate), or a pharmaceutically-acceptable salt, thereof, wherein: M is selected from alkyl, substituted alkyl, cycloalkyl, aryl, heterocyclo, and heteroaryl, provided that if M is alkyl then R 6 and R 7 taken together with the carbon atom to which they are both attached are selected from a group other than cycloalkyl; Q is selected from (i) hydrogen, C 1 -C 4 alkyl, and substituted C 1 -C 4 alkyl; or (ii) Q and R 6 are combined with the carbon atoms to which they are attached to form a 3- to 6-membered cycloalkyl; or (iii) Q and M a M are combined with the carbon atom(s) to which they are attached to form a 3- to 7-membered ring containing 1-2 heteroatoms which are independently selected from the group consisting of O, S, SO 2 , and N which ring may be optionally substituted with 0-2 R 5 groups or carbonyl; Z is selected from cycloalkyl, heterocyclo, aryl, or heteroaryl; and M a , Z a , R 1 , R 2 , R 3 , R 4 , R 6 , R 7 , and R 22 are as defined herein. Also provided are pharmaceutical compositions and methods of treating metabolic and inflammatory- or immune-associated diseases or disorders using said compounds.
    提供了一些新型非类固醇化合物,其在治疗与糖皮质激素受体、AP-1和/或NF-κB活性调节相关的疾病中非常有用,包括炎症和免疫性疾病、肥胖症和糖尿病,具有以下结构公式(I)的对映体、顺反异构体、互变异构体、溶剂化物(例如合物)或其医药上可接受的盐,其中:M选自烷基、取代烷基、环烷基、芳基、杂环烷基和杂芳基,但如果M是烷基,则R6和R7与它们都连接的碳原子一起选自环烷基之外的一组;Q选自(i)氢、C1-C4烷基和取代的C1-C4烷基;或(ii)Q和R6与它们连接的碳原子结合形成3-到6-成员的环烷基;或(iii)Q和MaM与它们连接的碳原子结合形成1-2个杂原子(独立于O、S、SO2和N组成)的3-到7-成员的环,该环可以选择性地用0-2个R5基团或羰基取代;Z选自环烷基、杂环烷基、芳基或杂芳基;而Ma、Za、R1、R2、R3、R4、R6、R7和R22如本文所定义。还提供了制药组合物和使用所述化合物治疗代谢和炎症或免疫相关疾病或紊乱的方法。
  • Benzofuran and benzothiophene derivatives useful in the treatmint of hyper-proliferative disorders
    申请人:Zhang Chengzhi
    公开号:US20050139814A1
    公开(公告)日:2005-06-30
    This invention relates to novel benzofuran and benzothiophene derivatives of the general table formula and their use for the treatment of hyper-proliferative disorders.
    本发明涉及通表式的新型苯并呋喃苯并噻吩生物,以及它们在治疗过度增殖性疾病中的用途。
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