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EPA | 391921-07-6

中文名称
——
中文别名
——
英文名称
EPA
英文别名
eicosapentaenoic acid;cis-5,8,11,14,17-eicosapentaenoic acid;(5E,8E,11E,14E,17E)-icosa-5,8,11,14,17-pentaenoic acid
EPA化学式
CAS
391921-07-6
化学式
C20H30O2
mdl
——
分子量
302.457
InChiKey
JAZBEHYOTPTENJ-RCHUDCCISA-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):
    5.6
  • 重原子数:
    22
  • 可旋转键数:
    13
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

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

  • 作为反应物:
    描述:
    EPA 生成 methyl 4-[3-[(2E,5E,8E,11E)-tetradeca-2,5,8,11-tetraenyl]oxiran-2-yl]butanoate
    参考文献:
    名称:
    SHEVCHENKO, V. P.;NAGAEV, I. YU.;MYASOEDOV, N. F.;KUKLEV, D. V.;IMBO, A. +, SINTEZ I ISSLED. PROSTAGLANDINOV, MINSK,(1989) S. 83
    摘要:
    DOI:
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文献信息

  • [EN] LYMPHATIC SYSTEM-DIRECTING LIPID PRODRUGS<br/>[FR] PROMÉDICAMENTS LIPIDIQUES ORIENTANT VERS LE SYSTÈME LYMPHATIQUE
    申请人:ARIYA THERAPEUTICS INC
    公开号:WO2019046491A1
    公开(公告)日:2019-03-07
    The present invention provides lymphatic system-directing lipid prodrugs, pharmaceutical compositions thereof, methods of producing such prodrugs and compositions, as well as methods of improving the bioavailability or other properties of a therapeutic agent that comprises part of the lipid prodrug. The present invention also provides methods of treating a disease, disorder, or condition such as those disclosed herein, comprising administering to a patient in need thereof a provided lipid prodrug or a pharmaceutical composition thereof.
    本发明提供了淋巴系统定向脂质前药,其制药组合物,制备这种前药和组合物的方法,以及改善作为脂质前药一部分的治疗剂的生物利用度或其他性质的方法。本发明还提供了治疗疾病、紊乱或症状的方法,包括向需要的患者施用所提供的脂质前药或其制药组合物。
  • FATTY ACID ANTIVIRAL CONJUGATES AND THEIR USES
    申请人:Catabasis Pharmaceuticals, Inc.
    公开号:US20160129122A1
    公开(公告)日:2016-05-12
    The invention relates to fatty acid antiviral conjugates; compositions comprising an effective amount of a fatty acid antiviral conjugate; and methods for treating or preventing a viral infection comprising the administration of an effective amount of a fatty acid antiviral conjugate.
    这项发明涉及脂肪酸抗病毒共轭物;包含有效量脂肪酸抗病毒共轭物的组合物;以及治疗或预防病毒感染的方法,包括给予有效量脂肪酸抗病毒共轭物。
  • BIOPASSIVATING MEMBRANE STABILIZATION BY MEANS OF NITROCARBOXYLIC ACID-CONTAINING PHOSPHOLIPIDS IN PREPARATIONS AND COATINGS
    申请人:Dietz Ulrich
    公开号:US20140099354A1
    公开(公告)日:2014-04-10
    The present invention relates to nitro-carboxylic acid (s)-containing phospholipids, to be used for coating of medical devices such as stents, catheter balloons, wound pads or surgical suture material and for bio-passivating compositions, such as rinses, waterproofing solutions, coating solutions, cryoprotection solutions, cold preservation media, lyoprotection solutions, contrast media solutions, preservation and reperfusion solutions containing these compounds as well as preparing solutions thereof and coating medical devices as well as their uses.
    本发明涉及一种含硝基羧酸(s)的磷脂,用于涂覆医疗器械,如支架、导管球囊、伤口垫或外科缝合材料,以及用于生物钝化组合物,如漱口液、防水溶液、涂层溶液、冷冻保护溶液、冷藏介质、冻干保护溶液、造影介质溶液、含有这些化合物的保存和再灌注溶液,以及制备这些溶液和涂覆医疗器械以及它们的用途。
  • METHOD FOR PREPARING CARBOXYLIC ACIDS BY OXIDATIVE CLEAVAGE OF A VICINAL DIOL
    申请人:Lemaire Marc
    公开号:US20130131379A1
    公开(公告)日:2013-05-23
    The present invention relates to a method for preparing carboxylic acids, in particular mono- and dicarboxylic acids, by oxidative cleavage of a vicinal diol. According to the invention, said method consists of reacting a vicinal diol of formula I: where: p is an integer comprised between 1 and 6; R1 and R2 are, separately: an alkyl or hydroxyl group having 1 to 12 carbon atoms; a —(CH 2 ) n —C0 2 M group where n, which can be identical or different in R1 and R2, is an integer comprised between 1 and 11 and M is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms or an alkaline cation; or R1 and R2 jointly form an alkylene —(CH 2 )m- group where m is an integer comprised between 2 and 10, preferably between 2 and 6; with industrial-grade sodium hypochlorite (or bleach), in the absence of an organic solvent and without adding a catalyst, preferably at room temperature. The invention can be used for recycling natural vegetable oils.
    本发明涉及一种制备羧酸的方法,特别是通过对邻二醇进行氧化裂解制备单羧酸和二羧酸。 根据本发明,所述方法包括将式I的邻二醇进行反应: 其中: p是介于1和6之间的整数; R1和R2分别是: 具有1至12个碳原子的烷基或羟基基团; 一个—(CH 2 ) n —C0 2 M基团,其中n在R1和R2中可以相同也可以不同,是介于1和11之间的整数,M是氢原子或具有1至4个碳原子的烷基基团或碱性阳离子; 或者R1和R2共同形成一个亚烷基—(CH 2 )m-基团,其中m是介于2和10之间的整数,优选在2和6之间; 使用工业级次氯酸钠(或漂白剂),在无机溶剂的情况下且不添加催化剂的情况下,最好在室温下进行。该发明可用于回收天然植物油。
  • PROCESS FOR PREPARING A CARBOXYLIC ACID FROM A DIOL OR FROM AN EPOXIDE BY OXIDATIVE CLEAVAGE
    申请人:SOCIETE INTEROLEAGINEUSE D'ASSISTANCE ET DE DEVELOPPEMENT (S.I.A.)
    公开号:US20150210623A1
    公开(公告)日:2015-07-30
    A process for preparing a carboxylic acid, by oxidative cleavage of at least one vicinal diol, or an epoxide, wherein the reaction is carried out in the presence of a catalyst and of an oxidizing agent and in the absence of solvent.
    通过氧化裂解至少一个邻二醇或环氧化物来制备羧酸的方法,其中反应在催化剂和氧化剂的存在下,在无溶剂的情况下进行。
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