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methyl 8-hydroxy-5-octynoate | 85924-38-5

中文名称
——
中文别名
——
英文名称
methyl 8-hydroxy-5-octynoate
英文别名
8-hydroxy-oct-5-ynoic acid methyl ester;Methyl 8-hydroxyoct-5-ynoate
methyl 8-hydroxy-5-octynoate化学式
CAS
85924-38-5
化学式
C9H14O3
mdl
——
分子量
170.208
InChiKey
PLHUQXLGDPCPPU-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):
    0.7
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    46.5
  • 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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Synthesis of three potential inhibitors of leukotriene biosynthesis
    作者:Juerg R. Pfister、D. V. Krishna Murthy
    DOI:10.1021/jm00362a002
    日期:1983.8
    and 5,6-benzoarachidonic acid (3), potential substrate analogue inhibitors of leukotriene biosynthesis, are described. Two of these compounds (1 and 2) apparently stimulated, while 3 inhibited, the activity of lipoxygenase from intact human polymorphonuclear leukocytes in vitro when stimulated with Ca2+ and calcium ionophore A23187 in the presence of BSA and arachidonic acid.
    描述了7,7-二甲基-(1),10,10-二甲基-(2)和5,6-苯并花生四烯酸(3)的合成,这是白三烯生物合成的潜在底物类似物抑制剂。当在BSA和花生四烯酸存在下用Ca2 +和钙离子载体A23187刺激时,其中的两种化合物(1和2)在体外明显刺激了完整人多形核白细胞中脂氧合酶的活性。
  • 12-HETrE analogs and methods of use thereof
    申请人:——
    公开号:US20020151734A1
    公开(公告)日:2002-10-17
    The present invention to 12-HETrE analogs which are agonists and antagonists of 12-HETrE. The compositions may be formulated in pharmaceutically acceptable formulations. The invention also includes methods and products for treating inflammatory conditions, neovascularization, tumor growth, cancer, ischemic cardiovascular diseases, and ocular conditions.
    本发明涉及12-HETrE类似物,其为12-HETrE的激动剂和拮抗剂。这些组合物可以制成药学上可接受的制剂。本发明还包括用于治疗炎症、新生血管形成、肿瘤生长、癌症、缺血性心血管疾病和眼部疾病的方法和产品。
  • Design and synthesis of hydroxy-alkynoic acids and their methyl esters as novel activators of BK channels
    作者:Shivaputra Patil、Anna N. Bukiya、Wei Li、Alejandro M. Dopico、Duane Miller
    DOI:10.1016/j.bmcl.2008.03.080
    日期:2008.6
    Physiological and pharmacological agents that activate large conductance, voltage-, and calcium- gated potassium (BK) channels located in the smooth muscle are effective vasodilators. Thus, activators of smooth muscle BK channels may be potential therapeutic tools to treat cardiovascular disease associated with vasoconstriction and/or impaired dilation, such as cerebrovascular spasm and constriction. We previously showed that lithocholic acid (LC) and other cholane derivatives activated smooth muscle BK channels and, thus, caused endothelium-independent cerebral artery dilation. However, clinical use of these cholane derivatives could be limited by the actions of these steroids, such as elevation of intracellular calcium and induction of apoptosis. Using LC as template, we designed and synthesized a series of hydroxy-alkynoic acids and corresponding methyl esters, as putative, nonsteroid BK channel activators. Indeed, the newly synthesized compounds effectively and reversibly activated rat cerebrovascular myocyte BK channel at concentrations similar to those found effective with LC. Among all the novel compounds tested, C-10 hydroxy-alkynoic acid methyl ester appears to be the most effective activator of vascular myocyte BK channels. (c) 2008 Elsevier Ltd. All rights reserved.
  • Palladium-mediated transannular cyclizations of medium-ring olefinic enolsilanes
    作者:Andrew S. Kende、Clara E. Mota Nelson、Sébastien Fuchs
    DOI:10.1016/j.tetlet.2005.09.125
    日期:2005.11
    Medium-ring olefinic ketone and lactone enolsilanes were subjected to palladium(II)-mediated cycloalkenylation conditions. Diverse bicyclic ring products were obtained in moderate to good yields. The effect of olefin geometry and ring size is discussed. (c) 2005 Elsevier Ltd. All rights reserved.
  • Ethanoarachidonic acids. A new class of arachidonic acid cascade modulators. 1. Monoethano compounds
    作者:K. C. Nicolaou、N. A. Petasis、W. S. Li、T. Ladduwahetty、J. L. Randall、S. E. Webber、P. E. Hernandez
    DOI:10.1021/jo00174a061
    日期:1983.12
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