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methyl 2-acetyl-3,5-dimethoxybenzoate | 35773-92-3

中文名称
——
中文别名
——
英文名称
methyl 2-acetyl-3,5-dimethoxybenzoate
英文别名
——
methyl 2-acetyl-3,5-dimethoxybenzoate化学式
CAS
35773-92-3
化学式
C12H14O5
mdl
——
分子量
238.24
InChiKey
LUWXCCCGOWDRJL-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

物化性质

  • 沸点:
    374.2±42.0 °C(Predicted)
  • 密度:
    1.151±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.4
  • 重原子数:
    17
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    61.8
  • 氢给体数:
    0
  • 氢受体数:
    5

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

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文献信息

  • Molecular modeling studies and <i>in vitro</i> screening of dihydrorugosaflavonoid and its derivatives against <i>Mycobacterium tuberculosis</i>
    作者:Ninad V. Puranik、Pratibha Srivastava、Sagar Swami、Amit Choudhari、Dhiman Sarkar
    DOI:10.1039/c8ra00636a
    日期:——

    Novel drug regimens against tuberculosis (TB) are urgently needed and may be developed by targeting essential enzymes of Mtb that sustain the pathogenicity of tuberculosis. Dihydrorugosaflavonoid interacted with the active pocket of MabA and PanK.

    对结核病(TB)的新药方案迫切需要,并且可以通过针对维持结核病致病性的Mtb的关键酶来开发。二氢橙黄素与MabA和PanK的活性口袋发生相互作用。
  • [EN] ANTIVIRAL COMPOUNDS AND THEIR USE<br/>[FR] COMPOSÉS ANTIVIRAUX ET LEUR UTILISATION
    申请人:SALUT PRODUCTS PTY LTD
    公开号:WO2021062482A1
    公开(公告)日:2021-04-08
    The invention relates to compounds that have antiviral activity, particularly 4-oxochromane derivatives that have antiviral activity against viruses of the Family Flaviviridae. Methods of treating viruses with the 4-oxochromane compounds, particularly viruses of the Family Flaviviridae, are also described.
    这项发明涉及具有抗病毒活性的化合物,特别是具有针对黄病毒科病毒的抗病毒活性的4-氧代色酮衍生物。还描述了使用4-氧代色酮化合物治疗病毒的方法,特别是黄病毒科病毒。
  • Rational design of inhibitors of VirA–VirG two-component signal transduction
    作者:Justin Maresh、Jin Zhang、Yih-Ling Tzeng、Nora A. Goodman、David G. Lynn
    DOI:10.1016/j.bmcl.2007.04.018
    日期:2007.6
    VirA-VirG two-component system regulates the vir (virulence) operon in response to specific host factors (xenognosins) in the plant pathogen Agrobacterium tumefaciens. Using whole cell assays, stable inhibitors inspired by the labile natural benzoxazinone inhibitor HDMBOA are developed. It is found that aromatic aldehydes represent a minimal structural unit for activity. In particular, 3-hydroxy-4,6-dimethoxy-3H-isobenzofuran-1-one (HDI) was found to have the highest activity, making it the most potent developed inhibitor of virulence gene expression in Agrobacterium. (c) 2007 Elsevier Ltd. All rights reserved.
  • Enantiomerically homogeneous intermediates toward the synthesis of descarbamoylcalicheamicinone
    作者:Dennis S. Yamashita、Vincent P. Rocco、Samuel J. Danishefsky
    DOI:10.1016/s0040-4039(00)93570-6
    日期:1991.11
    Enzymatically mediated kinetic resolution of racemic 12 with lipase PS-30 provides a practical route to the aglycones of descarbamoylcalicheamicin.
  • Ramachandran P. Veeraraghavan, Gong Baoqing, Brown Herbert C., Tetrahedron Lett, 35 (1994) N 14, S 2141-2144
    作者:Ramachandran P. Veeraraghavan, Gong Baoqing, Brown Herbert C.
    DOI:——
    日期:——
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