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3,5-bis(4-hydroxy-3-methoxystyryl)-1H-pyrazole-1-carbothioamide | 1196987-70-8

中文名称
——
中文别名
——
英文名称
3,5-bis(4-hydroxy-3-methoxystyryl)-1H-pyrazole-1-carbothioamide
英文别名
3,5-bis[(E)-2-(4-hydroxy-3-methoxy-phenyl)vinyl]pyrazole-1-carbothioamide;3,5-bis[(E)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]pyrazole-1-carbothioamide
3,5-bis(4-hydroxy-3-methoxystyryl)-1H-pyrazole-1-carbothioamide化学式
CAS
1196987-70-8
化学式
C22H21N3O4S
mdl
——
分子量
423.492
InChiKey
DUXNRXKYPKOEJD-FCXRPNKRSA-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

物化性质

  • 沸点:
    667.9±65.0 °C(Predicted)
  • 密度:
    1.29±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    135
  • 氢给体数:
    3
  • 氢受体数:
    6

反应信息

点击查看最新优质反应信息

文献信息

  • Structure activity relationship, cytotoxicity and evaluation of antioxidant activity of curcumin derivatives
    作者:Pramod K. Sahu、Praveen K. Sahu、Puran L. Sahu、Dau D. Agarwal
    DOI:10.1016/j.bmcl.2015.12.013
    日期:2016.2
    compound 3c, (IC50 value 6.25 μM) has shown better cytotoxicity effect against three cell lines. According to results of SAR study, it was found that 4H-pyrimido[2,1-b]benzothiazole derivatives (2e and 2f), pyrazoles (3a, 3b, 3c and 3d) benzylidenes (4d) exhibited better antioxidant activity than curcumin. A correlation of structure and activities relationship of these compounds with respect to drug
    设计了一系列姜黄素衍生物/类似物,并描述了其合成的有效方法。筛选所有合成的化合物的细胞毒性并评估其抗氧化活性。已经通过MTT测定法评估了针对三种细胞系Hep-G2,HCT-116和QG-56的细胞毒性作用。结构活性关系表明,特别是化合物3c(IC50值为6.25μM)对三种细胞系表现出更好的细胞毒性作用。根据SAR研究的结果,发现4H-嘧啶并[2,1-b]苯并噻唑衍生物(2e和2f),吡唑(3a,3b,3c和3d)亚苄基(4d)具有比姜黄素更好的抗氧化活性。
  • Synthesis and evaluation of antimicrobial activity of 4H-pyrimido[2,1-b]benzothiazole, pyrazole and benzylidene derivatives of curcumin
    作者:Pramod K. Sahu、Praveen K. Sahu、S.K. Gupta、D. Thavaselvam、D.D. Agarwal
    DOI:10.1016/j.ejmech.2012.05.020
    日期:2012.8
    A novel, one-pot, simple, efficient procedure for 4H-pyrimido[2,1-b]benzothiazole (4a-h), pyrazole (6a-d) and benzylidene (7a-d) derivatives of curcumin under solvent and solvent free conditions in microwave with good yield is have been synthesized. The synthesized compounds were evaluated for their antibacterial activity against gram-positive and gram-negative bacteria viz. Staphylococcus aureus, Pseudomonas aeruginosa, Salmonella typhi, Escherichia coli, Bacillus cereus and Providencia rettgeri and antifungal activity against fungi viz Aspergillus niger, Aspergillus fumigates, Aspergillus flavus. Detailed mechanistic study shows reaction proceeds through Knoevenagel type intermediate 3a which has been suggested as key intermediate for reaction (Fig. 3). (C) 2012 Elsevier Masson SAS. All rights reserved.
  • 10.1016/j.jics.2024.101193
    作者:Kamrani, Seyyedeh Negin、Sharifzadeh, Bahman、Barazandehdoust, Maryam、Mirmasoudi, Seyyedeh Sahra
    DOI:10.1016/j.jics.2024.101193
    日期:——
  • Design and Synthesis of New Curcuminoid Compounds and their Derivatives as Antioxidant Agents
    作者:Rehab Abood、Tahseen Alsalim、Einas Abood
    DOI:10.21608/ejchem.2021.49070.3005
    日期:2021.1.24
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