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(2-phenyloxazol-4-yl)(3,4,5-trimethoxyphenyl)methanone | 1202518-65-7

中文名称
——
中文别名
——
英文名称
(2-phenyloxazol-4-yl)(3,4,5-trimethoxyphenyl)methanone
英文别名
(2-Phenyl-4-oxazolyl)(3,4,5-trimethoxyphenyl)methanone;(2-phenyl-1,3-oxazol-4-yl)-(3,4,5-trimethoxyphenyl)methanone
(2-phenyloxazol-4-yl)(3,4,5-trimethoxyphenyl)methanone化学式
CAS
1202518-65-7
化学式
C19H17NO5
mdl
——
分子量
339.348
InChiKey
YSZWUFPOMPOSSS-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):
    3.6
  • 重原子数:
    25
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    70.8
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

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文献信息

  • Design, Synthesis, and SAR Studies of 4-Substituted Methoxylbenzoyl-aryl-thiazoles Analogues as Potent and Orally Bioavailable Anticancer Agents
    作者:Yan Lu、Chien-Ming Li、Zhao Wang、Jianjun Chen、Michael L. Mohler、Wei Li、James T. Dalton、Duane D. Miller
    DOI:10.1021/jm2003427
    日期:2011.7.14
    In a continued effort to improve upon the previously published 4-substituted methoxybenzoyl-aryl-thiazole (SMART) template, we explored chemodiverse “B” rings and “B” to “C” ring linkage. Further, to overcome the poor aqueous solubility of this series of agents, we introduced polar and ionizable hydrophilic groups to obtain water-soluble compounds. For instance, based on in vivo pharmacokinetic (PK)
    为了继续改进之前发表的 4-取代甲氧基苯甲酰基-芳基-噻唑 (SMART) 模板,我们探索了化学多样性的“B”环和“B”到“C”环的连接。此外,为了克服该系列试剂水溶性差的问题,我们引入了极性和可离子化的亲水基团以获得水溶性化合物。例如,基于体内药代动力学 (PK) 研究,设计并合成了一种口服生物可利用的苯基-氨基-噻唑 (PAT) 模板,其中在化合物1 的“A”和“B”环之间插入了一个氨基键. PAT 模板通过抑制微管蛋白聚合保持了对癌细胞系的纳摩尔 (nM) 范围效力,并且在体外不易受到 P-糖蛋白介导的多药耐药性的影响,与 SMART 模板相比,溶解度和生物利用度显着提高 ( 45a – c (PAT)与1(智能))。
  • COMPOUNDS FOR TREATMENT OF CANCER
    申请人:Miller Duane D.
    公开号:US20090326020A1
    公开(公告)日:2009-12-31
    Compounds according to formula (I) are disclosed where Q is S, N, or O; X is optional, and can be O═, S═, ═N—NH 2 , ═N—OH, or —OH; Y is optional and can be —N(H)—, O, or C 1 to C 20 hydrocarbon; and R 1 and R 2 are each independently substituted or unsubstituted single-, fused- or multiple-ring aryl or (hetero)cyclic ring systems. Methods of making these compounds, pharmaceutical compositions containing the compounds, and their use, particularly for treating or preventing cancer, are also disclosed.
    根据公式(I)披露的化合物如下:其中Q为S、N或O;X为可选,可以是O═、S═、═N—NH2、═N—OH或—OH;Y为可选,可以是—N(H)—、O或C1至C20碳氢化合物;而R1和R2分别独立地为取代或未取代的单环、融合环或多环芳基或(杂)环烷基环系统。还披露了制备这些化合物的方法、含有这些化合物的药物组合物,以及它们的用途,特别是用于治疗或预防癌症。
  • COMPOUND FOR TREATMENT OF CANCER
    申请人:University of Tennessee Research Foundation
    公开号:EP2959900A1
    公开(公告)日:2015-12-30
    A compound, wherein the compound is (2-(1H-indol-3-yl)imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone. A pharmaceutical composition comprising the compound is (2-(1H-indol-3-yl)imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone and a pharmaceutically acceptable carrier. The compound (2-(1H-indol-3-yl)imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone for use in treating prostate cancer, breast cancer, ovarian cancer, skin cancer, lung cancer, colon cancer, leukemia, renal cancer or CNS cancer, or a combination thereof.
    一种化合物,其中化合物为(2-(1H-吲哚-3-基)咪唑-4-基)(3,4,5-三甲氧基苯基)甲酮。 一种药物组合物,包含化合物 (2-(1H-吲哚-3-基)咪唑-4-基)(3,4,5-三甲氧基苯基)甲酮和药学上可接受的载体。 (2-(1H-吲哚-3-基)咪唑-4-基)(3,4,5-三甲氧基苯基)甲酮化合物用于治疗前列腺癌、乳腺癌、卵巢癌、皮肤癌、肺癌、结肠癌、白血病、肾癌或中枢神经系统癌症,或它们的组合。
  • Compounds for treatment of cancer
    申请人:University of Tennessee Research Foundation
    公开号:US10301285B2
    公开(公告)日:2019-05-28
    The present invention relates to a compound of formula XXII and a compound of formula 17ya, which are defined as anywhere in the specification, to a composition comprising the same, and to a method of using thereof in the treatment of various forms of cancer.
    本发明涉及一种式 XXII 化合物和一种式 17ya 化合物(在说明书的任何地方都有定义),涉及一种包含这些化合物的组合物,还涉及一种将其用于治疗各种癌症的方法。
  • COMPOUNDS FOR THE TREATMENT OF CANCER
    申请人:University of Tennessee Research Foundation
    公开号:EP2303021A2
    公开(公告)日:2011-04-06
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