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3-(4-羟基苯基)-2-苯基喹唑啉-4-酮 | 37856-23-8

中文名称
3-(4-羟基苯基)-2-苯基喹唑啉-4-酮
中文别名
——
英文名称
3-(4-hydroxyphenyl)-2-phenylquinazolin-4(3H)-one
英文别名
3-(4-Hydroxyphenyl)-2-phenyl-quinazoline-4(3H)-one;4(3H)-Quinazolinone, 3-(4-hydroxyphenyl)-2-phenyl-;3-(4-hydroxyphenyl)-2-phenylquinazolin-4-one
3-(4-羟基苯基)-2-苯基喹唑啉-4-酮化学式
CAS
37856-23-8
化学式
C20H14N2O2
mdl
——
分子量
314.343
InChiKey
AGCPREGHUBUQTJ-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):
    3.4
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    52.9
  • 氢给体数:
    1
  • 氢受体数:
    3

SDS

SDS:0314cccd27305e41dade13a28e78a803
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-(4-羟基苯基)-2-苯基喹唑啉-4-酮正丁基锂甲烷磺酸N-环己基异丙基胺 作用下, 以 四氢呋喃 为溶剂, 反应 9.0h, 生成 (S)-4-(4-oxo-2-phenylquinazolin-3(4H)-yl)phenyl 2-methylbutanoate
    参考文献:
    名称:
    通过潜在的 AKT 抑制合成、计算机模拟和体外评估作为抗癌剂的新型喹唑啉酮
    摘要:
    合成了一系列新型喹唑啉酮衍生物 (2-13),并在 MTT 试验中检测了它们对 HepG2、MCF-7 和 Caco-2 的细胞毒性。在这些衍生物中,化合物 4 和 9 对 Caco-2、HepG2 和 MCF-7 癌细胞表现出显着的细胞毒活性。化合物4对Caco-2、HepG2和MCF-7细胞系的抑制作用比化合物9更显着,IC50值分别为23.31±0.09、53.29±0.25和72.22±0.14μM。AKT 通路是人类癌症最常见的失调信号之一。AKT 在人类癌症中也过度表达,例如神经胶质瘤、肺癌、乳腺癌、卵巢癌、胃癌和胰腺癌。进行分子对接研究以分析新合成的喹唑啉酮衍生物对智人 AKT1 蛋白的抑制作用。发现分子对接模拟符合体外研究,因此支持生物活性。结果表明,如对接研究所述,化合物 4 和 9 可通过其对 AKT1 的潜在抑制作用作为癌症治疗的候选药物。
    DOI:
    10.3390/molecules25204780
  • 作为产物:
    描述:
    参考文献:
    名称:
    Design, synthesis and in vivo screening of some novel quinazoline analogs as anti-hyperlipidemic and hypoglycemic agents
    摘要:
    A novel series of substituted quinazoline derivatives were designed, synthesized and evaluated for their hypolipidemic activity in cholesterol induced hyperlipidemic rats. In vivo screening concluded that compounds A-4, C-5 and C-6 have shown potent antihyperlipidemic activity by decreasing the plasma level of triglycerides (TG), very low density lipoprotein (VLDL), low density lipoprotein (LDL), followed by increase in level of high density lipoprotein (HDL). (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2015.12.037
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文献信息

  • Synthesis and Antimicrobial Evaluation of Quinazoline-4[3H]-one Derivatives
    作者:Cheenu Chaudhary、Sushil Kumar、Surendra Kumar、S. Riaz Hashim
    DOI:10.2174/1570178617999200818205800
    日期:2021.7
    <p>The present investigation aimed to synthesize quinazoline-4(3H)-one derivatives (B1-10) and evaluated their antimicrobial activity. The test compounds (B1-10) were obtained by reaction of 2- phenyl-4H-benzo[d] [1, 3]oxazin-4-one (1) with 4-aminophenol (2) to afford 3-(4-hydroxyphenyl)-2- phenylquinazoline-4(3H)-one (3) which were further reacted with different N-phenylacetamide (4) in the presence of anhydrous potassium carbonate and a catalytic amount of potassium iodide in ethylmethylketone. The test compounds (B1-10) were characterized by the spectroscopic method and evaluated for their antimicrobial activity using the cup plate method by measuring the zone of inhibition. Among the compounds, compound B1, B2, B4, B6, and B8 showed maximum zone of inhibition as compared to standard drug ciprofloxacin and fluconazole against Bacillus subtilis, Escherichia coli and Aspergillus niger. Molecular docking was also performed for test compounds to predict their binding affinities in the target protein and results showed good drug-like properties.</p> </sec></div> <div class="value-text ch">本研究旨在合成喹唑啉-4(3H)-酮衍生物(B1-10)并评估它们的抗菌活性。试验化合物(B1-10)是通过将2-苯基-4H-苯并[d][1,3]噁嗪-4-酮(1)与4-氨基苯酚(2)反应得到3-(4-羟基苯基)-2-苯基喹唑啉-4(3H)-酮(3),然后在无水碳酸钾和少量碘化钾的催化下在乙基甲基酮中与不同的N-苯乙酰胺(4)进一步反应而获得的。试验化合物(B1-10)通过光谱方法进行表征,并使用杯培法测量抑菌圈直径评估它们的抗菌活性。在这些化合物中,化合物B1、B2、B4、B6和B8对枯草杆菌、大肠杆菌和黑曲霉的抑菌效果最好,与标准药物环丙沙星和氟康唑相比。此外,还对试验化合物进行了分子对接以预测它们在靶蛋白中的结合亲和力,结果显示具有良好的药物样性能。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Pandey; Kumar, Jitendra; Saxena, Journal of the Indian Chemical Society, 2007, vol. 84, # 6, p. 593 - 597</div> <div class="value"> <div class="value-text"> <span>作者:</span>Pandey、Kumar, Jitendra、Saxena、Mukesh、Joshi、Bajpai </div> <div class="value-text"> <span>DOI:</span>—— </div> <div class="value-text"> <span>日期:</span>—— </div> <div class="value-text en"></div> <div class="value-text ch"></div> </div> </li> <li class="feature-list-item"> <div class="content-title">Makino; Suzuki; Nakanishi, Synlett, 2000, # 11, p. 1670 - 1672</div> <div class="value"> <div class="value-text"> <span>作者:</span>Makino、Suzuki、Nakanishi、Tsuji </div> <div class="value-text"> <span>DOI:</span>—— </div> <div class="value-text"> <span>日期:</span>—— </div> <div class="value-text en"></div> <div class="value-text ch"></div> </div> </li> <li class="feature-list-item"> <div class="content-title">Syntheses Of New Heterocycles Derived From 2-Phenyl-3,1 - Benzoxazin-4-One And Their Antibacterial And Antifungal Activity</div> <div class="value"> <div class="value-text"> <span>作者:</span>Freddy H. Havaldar、Abhay R. Patil </div> <div class="value-text"> <span>DOI:</span>10.1515/hc.2009.15.4.251 </div> <div class="value-text"> <span>日期:</span>2009.1 </div> <div class="value-text en">A series of novel substituted N-(6-substituted-4H-benzo[e][1,3]oxazin-3-yl)- 2-[4-(4-oxo-2-phenyl-4H-quinazolin-3-yl)-phenoxy]-acetamides (9a-b) and N-(6-substituted-2-thione-4H-benzo[e][1,3]oxazin-3-yl)-2-[4-(4-oxo-2-phenyl-4H-quinazolin-3- -yl)-phenoxy]-acetamides (10a-b) were designed and synthesized. The structures of the newly synthesized compounds have been confirmed by IR, H-1 NMR and mass spectra. The compounds have also been screened for their biological activity.</div> <div class="value-text ch"></div> </div> </li> <li class="feature-list-item"> <div class="content-title">SYNTHESES OF SOME NOVEL [4-(4-OXO-2-PHENYL-4H-QUINAZOLIN-3-YL)-PHENOXY]-ACETIC ACID [1-SUBSTITUTED AMINOMETHYL-2-OXO-1,2-DIHYDRO-INDOL-3-YLIDENE]-HYDRAZIDE DERIVATIVES AND THEIR POTENTIAL BIOLOGICAL ACTIVITY</div> <div class="value"> <div class="value-text"> <span>作者:</span>Freddy H. Havaldar、Abhay R. Patil </div> <div class="value-text"> <span>DOI:</span>10.1515/hc.2008.14.1-2.107 </div> <div class="value-text"> <span>日期:</span>2008.1 </div> <div class="value-text en"></div> <div class="value-text ch"></div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=3101677r307ce5ca54M0&inchikey=AGCPREGHUBUQTJ-UHFFFAOYSA-N" target="_blank" rel="nofollow" class="view-more">查看更多</a> </div> <div class="module" id="tongleihuahewu"> <h3 class="module-title"><i class="iconfont icon-tongleihuahewu"></i>同类化合物</h3> <div class="compounds-list"> <a target="_blank" href="https://www.molaid.com/MS_199" class="compound-item" title="(12羟基吲[2,1-b〕喹唑啉-6(12H)-酮)">(12羟基吲[2,1-b〕喹唑啉-6(12H)-酮)</a> <a target="_blank" href="https://www.molaid.com/MS_334" class="compound-item" title="黑暗猝灭剂BHQ-3,BHQ-3NHS">黑暗猝灭剂BHQ-3,BHQ-3NHS</a> <a target="_blank" href="https://www.molaid.com/MS_657" class="compound-item" title="鸭嘴花酚碱">鸭嘴花酚碱</a> <a target="_blank" 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