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2-dodecanoylamino-succinic acid 4-methyl ester

中文名称
——
中文别名
——
英文名称
2-dodecanoylamino-succinic acid 4-methyl ester
英文别名
(2S)-2-(dodecanoylamino)-4-methoxy-4-oxobutanoic acid
2-dodecanoylamino-succinic acid 4-methyl ester化学式
CAS
——
化学式
C17H31NO5
mdl
——
分子量
329.437
InChiKey
MICZVYPBUROXRF-AWEZNQCLSA-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):
    4.2
  • 重原子数:
    23
  • 可旋转键数:
    15
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    92.7
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    2-dodecanoylamino-succinic acid 4-methyl esterN-羟基丁二酰亚胺1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 生成 2-dodecanoylamino-succinic acid 1-(2,5-dioxopyrrolidin-1-yl) ester 4-methyl ester
    参考文献:
    名称:
    Polymeric and dendrimeric pyridoxal enzyme mimics
    摘要:
    Pyridoxal was covalently attached to polyethylenimine polymers, but the resulting materials were found to degrade rapidly. In comparison, the dendrimeric pyridoxals, which possess only one pyridoxal unit at the core of every dendrimer molecule were found to be relatively stable compounds. A total of 12 poly(amidoamine) type dendrimers were synthesized. They range from G1 to G6 with either NMe2 or NHAc termini. The NMe2-terminated pyridoxal dendrimers racemize alpha-amino acids 50-100 times faster than does simple pyridoxal, while the NHAc-terminated pyridoxal dendrimers racemize alpha-amino acids only 3-5 times faster than does simple pyridoxal. Both the NMe2- and NHAc-terminated pyridoxal dendrimers decarboxylate 2-amino-2-phenyl-propionic acid 1-3 times faster than simple pyridoxal. The interior polarity in the pyridoxal dendrimers is similar to that of 85:15 water-DMFsolution. Furthermore we successfully incorporated eight lauryl groups to the G5 pyridoxal dendrimer at known positions. The laurylated dendrimer exhibits lower racemization and decarboxylation rates than do the unlaurylated ones, in contrast to the positive rate effects of laurylation in polyethylenimine-pyridoxamines in our previous transamination studies. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2004.03.062
  • 作为产物:
    参考文献:
    名称:
    Polymeric and dendrimeric pyridoxal enzyme mimics
    摘要:
    Pyridoxal was covalently attached to polyethylenimine polymers, but the resulting materials were found to degrade rapidly. In comparison, the dendrimeric pyridoxals, which possess only one pyridoxal unit at the core of every dendrimer molecule were found to be relatively stable compounds. A total of 12 poly(amidoamine) type dendrimers were synthesized. They range from G1 to G6 with either NMe2 or NHAc termini. The NMe2-terminated pyridoxal dendrimers racemize alpha-amino acids 50-100 times faster than does simple pyridoxal, while the NHAc-terminated pyridoxal dendrimers racemize alpha-amino acids only 3-5 times faster than does simple pyridoxal. Both the NMe2- and NHAc-terminated pyridoxal dendrimers decarboxylate 2-amino-2-phenyl-propionic acid 1-3 times faster than simple pyridoxal. The interior polarity in the pyridoxal dendrimers is similar to that of 85:15 water-DMFsolution. Furthermore we successfully incorporated eight lauryl groups to the G5 pyridoxal dendrimer at known positions. The laurylated dendrimer exhibits lower racemization and decarboxylation rates than do the unlaurylated ones, in contrast to the positive rate effects of laurylation in polyethylenimine-pyridoxamines in our previous transamination studies. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2004.03.062
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文献信息

  • Cosmetics comprising an n-acylamino acid ester
    申请人:KASHIMA OIL COMPANY
    公开号:EP0839515A2
    公开(公告)日:1998-05-06
    There are disclosed cosmetics which comprise esters of N-acylamino acids containing acyl groups having odd-numbered carbon atoms, and esters of N-acylamino acids containing acyl groups having carbon atoms in an odd number in the range of 13 to 17. The above esters are used for the foregoing cosmetics, which have excellent hair growth promoting effect, humectant action, subcutaneous blood flow rate increasing action, etc. and thus are well suited for hair growth, skin care and the like.
    已公开的化妆品包括含有碳原子数为奇数的酰基的 N-酰基氨基酸的酯,以及含有碳原子数为 13 至 17 的奇数的酰基的 N-酰基氨基酸的酯。上述酯类用于上述化妆品,具有良好的促进头发生长效果、保湿作用、增加皮下血流量作用等,因此非常适合用于头发生长、皮肤护理等。
  • BIODEGRADABLE CORROSION INHIBITORS
    申请人:THE ASSOCIATED OCTEL COMPANY LIMITED
    公开号:EP1080067A1
    公开(公告)日:2001-03-07
  • US6010708A
    申请人:——
    公开号:US6010708A
    公开(公告)日:2000-01-04
  • [EN] BIODEGRADABLE CORROSION INHIBITORS<br/>[FR] INHIBITEURS DE CORROSION BIODEGRADABLES
    申请人:THE ASSOCIATED OCTEL COMPANY LIMITED
    公开号:WO1999059958A1
    公开(公告)日:1999-11-25
    (EN) Compounds of formula (I), wherein R is the $g(a)-side chain of an amino acid, R1 is a straight or branched chain alkyl or alkenyl residue containing 1 to 30 carbon atoms or a cycloalkyl or aryl residue having from 5 to 12 carbon atoms; R2 is hydrogen or aryl or a straight chain alkyl or alkenyl residue having from 1 to 30 carbon atoms or together with R is the $g(a)-side chain of an amino acid; X is a linking moiety and Y is a suitable backbone moiety on which to append the N-acylated amino acid moieties via X linkages; and n is a number between 1 and the total number of available reactive substituents on Y; are corrosion inhibitors and/or scale inhibitors.(FR) L'invention porte sur des composés de formule (I) dans laquelle: R est la chaîne latérale $g(a) d'un acide aminé; R1 est un groupe alkyle ou alcényle C1-30 à chaîne droite ou ramifiée, ou un groupe cycloalkyle ou aryle C5-12; R2 est H ou aryle ou un groupe alkyle ou alcényle C1-30 à chaîne droite ou ramifiée ou forme avec R la chaîne latérale $g(a) d'un acide aminé; X est un fragment de liaison; Y est un fragment de squelette sur lequel peuvent se fixer les fragments d'acides aminés N-acétylés par l'intermédiaire de liaisons X; et n est un nombre compris entre 1 et le nombre total des substituants réactifs disponibles sur Y. Lesdits composés sont des inhibiteurs de corrosion et/ou des inhibiteurs scalaires.
  • Polymeric and dendrimeric pyridoxal enzyme mimics
    作者:Lei Liu、Ronald Breslow
    DOI:10.1016/j.bmc.2004.03.062
    日期:2004.6
    Pyridoxal was covalently attached to polyethylenimine polymers, but the resulting materials were found to degrade rapidly. In comparison, the dendrimeric pyridoxals, which possess only one pyridoxal unit at the core of every dendrimer molecule were found to be relatively stable compounds. A total of 12 poly(amidoamine) type dendrimers were synthesized. They range from G1 to G6 with either NMe2 or NHAc termini. The NMe2-terminated pyridoxal dendrimers racemize alpha-amino acids 50-100 times faster than does simple pyridoxal, while the NHAc-terminated pyridoxal dendrimers racemize alpha-amino acids only 3-5 times faster than does simple pyridoxal. Both the NMe2- and NHAc-terminated pyridoxal dendrimers decarboxylate 2-amino-2-phenyl-propionic acid 1-3 times faster than simple pyridoxal. The interior polarity in the pyridoxal dendrimers is similar to that of 85:15 water-DMFsolution. Furthermore we successfully incorporated eight lauryl groups to the G5 pyridoxal dendrimer at known positions. The laurylated dendrimer exhibits lower racemization and decarboxylation rates than do the unlaurylated ones, in contrast to the positive rate effects of laurylation in polyethylenimine-pyridoxamines in our previous transamination studies. (C) 2004 Elsevier Ltd. All rights reserved.
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