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{4-[(E)-(3-Phenyl-acryloyl)]-phenyl}-acetic acid

中文名称
——
中文别名
——
英文名称
{4-[(E)-(3-Phenyl-acryloyl)]-phenyl}-acetic acid
英文别名
{4-[(2E)-3-phenyl-2-propenoyl]phenyl}acetic acid;2-[4-[(E)-3-phenylprop-2-enoyl]phenyl]acetic acid
{4-[(E)-(3-Phenyl-acryloyl)]-phenyl}-acetic acid化学式
CAS
——
化学式
C17H14O3
mdl
——
分子量
266.296
InChiKey
FUBIEIGQPXUXNV-DHZHZOJOSA-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):
    2.5
  • 重原子数:
    20
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    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:
    参考文献:
    名称:
    SHRIDHAR, D. R.;SASTRY, C. V. REDDY;BANSAL, O. P.;SINGH, P. P.;RAO, C. SE+, INDIAN J. CHEM., 1981, 20, N 5, 401-403
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    与姜黄素有关的芳族烯酮的合成及生物学评价。
    摘要:
    姜黄素是从香料姜黄中分离得到的天然产物,已显示出广泛的药理活性,包括某些抗癌特性。它已被明确地证明是在体外和体内血管生成的有效抑制剂。使用姜黄素作为抗血管生成类似物设计的先导化合物,已经合成了一系列利用取代的查尔酮骨架的结构相关化合物,并通过已建立的SVR细胞增殖测定法进行了测试。结果产生了范围广泛的化合物,这些化合物等于或超过姜黄素体外抑制内皮细胞生长的能力。由于它们的商业可获得性和相当简单的合成制备方法,这些低分子量化合物是开发未来血管生成抑制剂的诱人线索。
    DOI:
    10.1016/j.bmc.2005.03.054
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文献信息

  • Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states
    申请人:Bowen Phillip J.
    公开号:US20050148599A1
    公开(公告)日:2005-07-07
    The present invention relates to chalcone and chalcone derivatives and analogs which are useful as angiogenesis inhibitors. The present compounds, which are inexpensive to synthesize, exhibit unexpectedly good activity as angiogenesis inhibitors. The present invention also relates to the use of chalcone and its analogs as antitumor/anticancer agents and to treat a number of conditions or disease states in which angiogenesis is a factor, incluidng angiongenic skin diseases such as psoriasis, acne, rosacea, warts, eczema, hemangiomas, lymphangiogenesis, among numerous others, as well as chronic inflammatory disease such as arthritis.
    本发明涉及查尔酮和查尔酮衍生物及类似物,其可用作抗血管生成抑制剂。这些化合物成本低廉且表现出意外的良好抗血管生成活性。本发明还涉及使用查尔酮及其类似物作为抗肿瘤/抗癌剂以及治疗许多条件或疾病状态,其中血管生成是一个因素,包括血管生成性皮肤病如银屑病、痤疮、酒渣鼻、疣、湿疹、血管瘤、淋巴管生成等等,以及慢性炎症性疾病如关节炎。
  • Light Activated Shape Memory Co-Polymers
    申请人:Tong Hung Tat
    公开号:US20080021166A1
    公开(公告)日:2008-01-24
    The present discovery uses monomers which contain reversible photo-crosslinkable groups in addition to primary polymerizable groups. The mechanical properties of these materials and the reversibility of the photo-activated shape memory effect demonstrate the effectiveness of using photo-irradiation to effect change in modulus and shape memory effect. In the preferred embodiment the reaction mixture includes a photo-reactive monomer comprising a photo reactive group and a polymerizable group; a second monomer, which is more preferably a mixture of monomers, which are acrylate based; a multi-functional crosslinking agent, preferably 1,6 hexanediol diacrylate (HDODA); an initiator, preferably a free radical initiator; and a fifth, optional, component which is a modifying polymer. The mixture of the second monomer, crosslinking agent, and initiator comprise the base polymer matrix into which the photo-reactive monomer is incorporated. The polymeriziable group of the photo reactive monomer allows the photo reactive monomer to polymerize with the base polymer matrix.
  • US6462075B1
    申请人:——
    公开号:US6462075B1
    公开(公告)日:2002-10-08
  • US6906105B2
    申请人:——
    公开号:US6906105B2
    公开(公告)日:2005-06-14
  • US7432303B2
    申请人:——
    公开号:US7432303B2
    公开(公告)日:2008-10-07
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