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trans 5-tetradecenoic acid | 5684-69-5

中文名称
——
中文别名
——
英文名称
trans 5-tetradecenoic acid
英文别名
(Z)-5-tetradecenoic acid;tetradec-5E-enoic acid;tetradec-5-enoic acid;Tetradec-5-ensaeure;5-Tetradecenoic acid;(E)-tetradec-5-enoic acid
trans 5-tetradecenoic acid化学式
CAS
5684-69-5
化学式
C14H26O2
mdl
MFCD18642142
分子量
226.359
InChiKey
AFGUVBVUFZMJMX-MDZDMXLPSA-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

  • 物理描述:
    Solid

计算性质

  • 辛醇/水分配系数(LogP):
    5.1
  • 重原子数:
    16
  • 可旋转键数:
    11
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.785
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2916190090

SDS

SDS:aeed5456afa1468e62e94d7f238918dd
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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:
    trans 5-tetradecenoic acid二氯甲烷 为溶剂, 生成 5,6-dichlorotetradecanoic acid
    参考文献:
    名称:
    Hostmark, Arne T.; Lystad, Einar; Jebens, Einar, Pharmacology and Toxicology, 1999, vol. 85, # 4, p. 162 - 168
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    1H-Nuclear magnetic resonance spectroscopic studies of saturated, acetylenic and ethylenic triacylglycerols
    摘要:
    DOI:
    10.1016/0009-3084(95)02463-s
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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。
  • [EN] LIPID PRODRUGS OF PREGNANE NEUROSTEROIDS AND USES THEREOF<br/>[FR] PROMÉDICAMENTS LIPIDIQUES DE NEUROSTÉROÏDES DE PRÉGNANE ET LEURS UTILISATIONS
    申请人:PURETECH HEALTH LLC
    公开号:WO2020028787A1
    公开(公告)日:2020-02-06
    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 disclosed lipid prodrug or a pharmaceutical composition thereof.
    本发明提供了淋巴系统定向脂质前药,以及其制药组合物、生产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述的脂质前药或其制药组合物。
  • METHOD FOR SYNTHESIZING AN OMEGA-AMINO ACID OR ESTER FROM A MONOUNSATURATED FATTY ACID OR ESTER
    申请人:Couturier Jean-Luc
    公开号:US20140187808A1
    公开(公告)日:2014-07-03
    A method for synthesizing ω-amino-alkanoic acids or the esters thereof from natural unsaturated fatty acids passing through an intermediate ω-unsaturated nitrile compound. The method is simple to implement and, relative to known methods, avoids the environmental constraints and economic disadvantages resulting from the reaction by-products. The method includes synthesizing an ω-amino acid (ester) of formula R3OOC—(CH2) q —CH2NH2, in which R3 is H or an n-butyl radical and q is an integral index of between 2 and 13, from a monounsaturated fatty acid (ester) of formula (R1-CH═CH—(CH2)p-COO) xR2, in which x represents 1, 2 or 3, R1 is H or a hydrocarbon radical comprising from 4 to 11 carbon atoms and, where appropriate, a hydroxyl function, R2 is H or an alkyl radical comprising from 2 to 4 carbon atoms, and may contain one or more heteroatoms, and p is an integral index of between 2 and 11, including a reaction step of ammoniation.
    一种从天然不饱和脂肪酸通过中间体ω-不饱和腈化合物合成ω-氨基-烷酸或其酯的方法。该方法实施简单,与已知方法相比,避免了由反应副产物导致的环境限制和经济劣势。该方法包括从公式为(R1-CH═CH—(CH2)p-COO)xR2的单不饱和脂肪酸(酯)合成公式为R3OOC—(CH2)q—CH2NH2的ω-氨基酸(酯),其中R3是H或n-丁基基团,q是2到13之间的整数指数,x代表1、2或3,R1是H或含4到11个碳原子的烃基团,适当情况下还含有羟基,R2是H或含2到4个碳原子的烷基基团,可包含一个或多个杂原子,p是2到11之间的整数指数,包括氨化反应步骤。
  • METHOD FOR THE SYNTHESIS OF OMEGA-AMINO-ALKANOIC ACIDS
    申请人:Dubois Jean-Luc
    公开号:US20100168453A1
    公开(公告)日:2010-07-01
    The invention relates to a method for the synthesis of amino acids/esters of general formula NH 2 —(CH 2 ) n —COOR in which n is an integer between 5 and 14, and R is either H or an alkyl radical including from 1 to 4 carbon atoms, from natural long-chain mono-unsaturated fatty acids or esters including at least 10 adjacent carbon atoms per molecule, said method comprising: first converting, if necessary, said natural long-chain fatty acid or ester into a monounsaturated fatty acid/ester of general formula R 1 —(CH 2 ) m —CH═CH—(CH 2 ) p —COOR in which R 1 is H, CH 3 or a COOR radical, m is an integer between 0 and 14 and p is an integer between 2 and 11, then submitting the latter to a crossed catalytic metathesis reaction with a compound of formula R 2 —CH═CH—R 3 in which R 2 is either H or CN and R 3 is CN or CH 2 NH 2 , provided that if R 2 is CN, R 3 can be only CN, and finally converting the resulting product of the general formula R 3 —CH═CH—(CH 2 ) p —COOR into an amino-acid, either by hydrogenation, or by hydrogenation of the triple terminal bond, or by amination of the double terminal bond.
    本发明涉及一种合成通式为NH2—(CH2)n—COOR的氨基酸/酯的方法,其中n为5至14之间的整数,R为H或包括1至4个碳原子的烷基基团,所述方法包括:首先,如果必要,将天然长链脂肪酸或酯转化为通式为R1—(CH2)m—CH═CH—(CH2)p—COOR的单不饱和脂肪酸/酯,其中R1为H,CH3或COOR基团,m为0至14之间的整数,p为2至11之间的整数;然后,将后者与通式为R2—CH═CH—R3的化合物进行交叉催化复分解反应,其中R2为H或CN,R3为CN或CH2NH2,如果R2为CN,则R3只能为CN;最后,将得到的通式为R3—CH═CH—(CH2)p—COOR的产品转化为氨基酸,可以通过氢化,或通过氢化末端的三键,或通过末端的双键的氨基化来实现。
  • COSMETIC OR DERMATOLOGICAL COMPOSITION COMPRISING A POLYMER BEARING JUNCTION GROUPS, AND COSMETIC TREATMENT PROCESS
    申请人:Chodorowski-Kimmes Sandrine
    公开号:US20100239509A1
    公开(公告)日:2010-09-23
    The present patent application relates to a cosmetic or dermatological composition comprising, in a cosmetically or dermatologically acceptable medium, a polymer comprising: (a) a polymer backbone that may be obtained by reaction: of a polyol comprising 3 to 6 hydroxyl groups; of a monocarboxylic acid containing 6 to 32 carbon atoms; of a polycarboxylic acid comprising at least two carboxylic groups COOH, and/or of a cyclic anhydride such as a polycarboxylic acid and/or of a lactone comprising at least one carboxylic group COOH; and (b) at least one junction group linked to the said polymer backbone and capable of establishing H bonds with one or more partner junction groups, each pairing of a junction group involving at least three H (hydrogen) bonds. The patent application also concerns a cosmetic treatment process using the said composition.
    本专利申请涉及一种化妆品或皮肤科学组合物,包括在化妆品或皮肤科学上可接受的介质中,包含以下聚合物的组合物:(a) 由以下反应得到的聚合物骨架:含有3至6个羟基的多元醇;含有6至32个碳原子的一元羧酸;至少含有两个羧基COOH的多元羧酸,和/或类似多元羧酸的环酐和/或至少含有一个羧基COOH的内酯;以及(b) 至少一个连接到所述聚合物骨架的连接基团,并能够与一个或多个配对连接基团建立H键,每个连接基团的配对涉及至少三个H(氢)键。该专利申请还涉及使用所述组合物的化妆品处理过程。
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