(3-pentylphenyl)methanol | 475208-94-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (3-pentylphenyl)methanol
• 英文别名: m-pentylbenzyl alcohol
• CAS: 475208-94-7
• 化学式: C₁₂H₁₈O
• 分子量: 178.274
• InChiKey: CGQLRXROISZUSF-UHFFFAOYSA-N

物化性质

• 沸点：
  266.6±8.0 °C(Predicted)
• 密度：
  0.960±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  13
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (3-pentylphenyl)methanol 在 manganese oxide 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 以886 mg的产率得到m-pentylbenzaldehyde
  参考文献：
  名称：

  Development of Novel EDG3 Antagonists Using a 3D Database Search and Their Structure−Activity Relationships

  摘要：

  Sphingosine-1-phosphate (SIP) is an intracellular second messenger and an extracellular mediator through endothelial differentiation gene (EDG) receptors, which are a novel class of G-protein-coupled receptors. Although EDG has attracted much attention because of its various roles, no selective agonists or antagonists have yet been developed. This could account for the delay in clarifying the physiological roles of members of the EDG family. Because precise structural information on EDG receptors is not yet available, pharmacophore models were generated based on structural information for SIP using the rational drug design software Catalyst. Novel antagonists, 2-alkylthiazolidine-4-carboxylic acids, were retrieved from a three-dimensional database search using the pharmacophore models, and these showed activity for EDG3. On the basis of their nonphosphoric acid structure, more potent antagonists, 2-(m- or p-heptylphenyl)thiazolidine-4-carboxylic acid, were developed.

  DOI：

  10.1021/jm020080c
• 作为产物：
  描述：

  methyl 5-(pent-1-yn-1-yl)benzoate 在 lithium aluminium tetrahydride 、 palladium 10% on activated carbon 、 氢气 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 生成 (3-pentylphenyl)methanol
  参考文献：
  名称：

  Role of the CAI-1 Fatty Acid Tail in the Vibrio cholerae Quorum Sensing Response

  摘要：

  Quorum sensing is a mechanism of chemical communication among bacteria that enables collective behaviors. In V. cholerae, the etiological agent of the disease cholera, quorum sensing controls group behaviors including virulence factor production and biofilm formation. The major V. cholerae quorum-sensing system consists of the extracellular signal molecule called CAI-1 and its cognate membrane bound receptor called CqsS. Here, the ligand binding activity of CqsS is probed with structural analogues of the natural signal. Enabled by our discovery of a structurally simplified analogue of CAI-1, we prepared and analyzed a focused library. The molecules were designed to probe the effects of conformational and structural changes along the length of the fatty acid tail of CAI-1. Our results, combined with pharmacophore modeling, suggest a molecular basis for signal molecule recognition and receptor fidelity with respect to the fatty acid tail portion of CAI-1. These efforts provide novel probes to enhance discovery of antivirulence agents for the treatment of V. cholerae.

  DOI：

  10.1021/jm300908t

文献信息

• New enzymes and prodrugs for ADEPT
  申请人：THE WELLCOME FOUNDATION LIMITED

  公开号：EP0728018B1

  公开（公告）日：2003-08-06
• THERAPY
  申请人：THE WELLCOME FOUNDATION LIMITED

  公开号：EP0728018A1

  公开（公告）日：1996-08-28
• US6140100A
  申请人：——

  公开号：US6140100A

  公开（公告）日：2000-10-31
• US6319702B1
  申请人：——

  公开号：US6319702B1

  公开（公告）日：2001-11-20
• [EN] THERAPY<br/>[FR] THERAPIE
  申请人：——

  公开号：WO1995013095A2

  公开（公告）日：1995-05-18

  [EN] The present invention relates to improvements in targetted enzyme prodrug therapy including antibody-directed enzyme prodrug therapy (ADEPT), it particularly relates to novel enzymes and prodrugs for use in ADEPT.
  [FR] La présente invention se rapporte à des améliorations apportées à la thérapie par promédicament à base d'enzyme ciblée, notamment la thérapie par promédicament à base d'enzyme dirigée contre des anticorps (ADEPT); l'invention se rapporte à des nouveaux promédicaments et enzymes destinés à être utilisés dans la thérapie ADEPT.