N-propyldodecanamide | 110790-31-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: N-propyldodecanamide
• 英文别名: N-propyllauroylamide
• CAS: 110790-31-3
• 化学式: C₁₅H₃₁NO
• mdl: MFCD01357827
• 分子量: 241.417
• InChiKey: AUYWNLPGKFYZFF-UHFFFAOYSA-N

物化性质

• 熔点：
  142-146 °C(Solv: ethanol (64-17-5))
• 沸点：
  316.1±10.0 °C(Predicted)
• 密度：
  0.855±0.06 g/cm3(Predicted)
• 保留指数：
  1962

计算性质

• 辛醇/水分配系数(LogP)：
  5.6
• 重原子数：
  17
• 可旋转键数：
  12
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.933
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  N-propyldodecanamide 在 ruthenium(IV) oxide 、 sodium periodate 作用下， 以 乙酸乙酯 为溶剂， 反应 72.0h， 以92%的产率得到N-propanoyldodecanamide
  参考文献：
  名称：

  Tanaka, Ken-Ichi; Yoshifuji, Shigeyuki; Nitta, Yoshihiro, Chemical and pharmaceutical bulletin, 1987, vol. 35, # 1, p. 364 - 369

  摘要：

  DOI：
• 作为产物：
  描述：

  月桂酸 在 氯化亚砜 作用下， 以 乙醚 为溶剂， 生成 N-propyldodecanamide
  参考文献：
  名称：

  Dodecanoic acid derivatives: Synthesis, antimicrobial evaluation and development of one-target and multi-target QSAR models

  摘要：

  In this study a series of dodecanoic acid derivatives (1-30) were synthesized and evaluated for in vitro antimicrobial activity against the panel of Gram positive, Gram negative bacterial and fungal strains. 4-Nitro phenyl dodecanoate (4) and quinolin-8-yl dodecanoate (5) emerged as most effective antibacterial agents, and 1-(4-benzylpiperazin-1-yl) dodecan-1-one (15) was found to be the most effective antifungal agent amongst the synthesized dodecanoic acid derivatives. Quantitative structure activity relationship (QSAR) studies performed by the development of one-target and multi-target models indicated that multi-target model was effective in describing the antimicrobial activity of dodecanoic acid derivatives as well demonstrated the importance of topological parameter, zero-order molecular connectivity index ((0)chi).

  DOI：

  10.1007/s00044-010-9383-5

文献信息

• Effects of synthetic alkamides on Arabidopsis fatty acid amide hydrolase activity and plant development
  作者：Lionel Faure、Ronaldo Cavazos、Bibi Rafeiza Khan、Robby A. Petros、Peter Koulen、Elison B. Blancaflor、Kent D. Chapman

  DOI：10.1016/j.phytochem.2014.11.011

  日期：2015.2

  hydrolase (FAAH) has been described as a key contributor to NAE hydrolysis; however, no enzyme has been associated with alkamide degradation in plants. Herein reported is synthesis of 12 compounds structurally similar to a naturally occurring alkamide (N-isobutyl-(2E,6Z,8E)decatrienamide or affinin) with different acyl compositions more similar to plant NAEs and various amino alkyl head groups. These "hybrid"

  烷酰胺和 N-酰基乙醇胺 (NAE) 是影响植物发育的生物活性、酰胺连接的脂质。烷基酰胺仅限于高等植物的几个科和一些真菌，而 NAE 是植物和动物中广泛存在的信号分子。脂肪酸酰胺水解酶 (FAAH) 已被描述为 NAE 水解的关键因素；然而，没有酶与植物中的烷酰胺降解有关。本文报道了 12 种结构类似于天然存在的烷酰胺（N-异丁基-（2E，6Z，8E）十碳三烯酰胺或亲和素）的化合物的合成，具有不同的酰基组成，更类似于植物 NAE 和各种氨基烷基头基。测试了这些“混合”合成烷酰胺对重组拟南芥 FAAH 的活性及其对植物发育的影响（即，子叶扩张和初生根长度）。在一些合成的烷酰胺（如 N-乙基月桂酰胺）存在下，在体外发现 FAAH 对 NAE 的活性显着增加 (4)。发现这种“增强”效应至少部分是由于乙醇胺对 FAAH 产物抑制的缓解，而不是由于 FAAH 酶的寡聚化状态的改变。对于这些醇酰胺中的一些，观察到幼苗生长的抑制，FAAH
• Surfactant cocamide monoethanolamide causes eye irritation by activating nociceptor TRPV1 channels
  作者：Fang Zhao、Shuangyan Wang、Yan Li、Jin Wang、Yujing Wang、Chunlei Zhang、Yong Li、Longjiang Huang、Ye Yu、Jie Zheng、Boyang Yu、Isaac N. Pessah、Zhengyu Cao

  DOI：10.1111/bph.15491

  日期：2021.9

  monoethanolamide (CMEA) is commonly used as a surfactant-foam booster in cosmetic formulations. Upon contact with the eye or other sensitive skin areas, CMEA elicits stinging and lasting irritation. We hypothesized a specific molecular interaction with TRPV1 channels by which CMEA caused eye irritation.

  椰油酰胺单乙醇酰胺 (CMEA) 通常用作化妆品配方中的表面活性剂泡沫促进剂。接触眼睛或其他敏感皮肤区域后，CMEA 会引起刺痛和持久刺激。我们假设 CMEA 与 TRPV1 通道存在特定的分子相互作用，从而引起眼睛刺激。
• NOVEL 1,3-BENZOXAZOL-2(3H)-ONES AND THEIR USE AS MEDICAMENTS AND COSMETICS
  申请人：DR. AUGUST WOLFF GMBH & CO. KG ARZNEIMITTEL

  公开号：US20150111935A1

  公开（公告）日：2015-04-23

  The present invention relates to a novel class of 1,3-benzoxazol-2(3H)-ones and their use as a medicament, preferably as a dermatologic agent, and as a cosmetic. These novel compounds are particularly useful in treating and/or preventing inflammation, irritation, itching, pruritus, pain, oedema and/or pro-allergic or allergic conditions in a patient. Usually they are topically applied to the skin or mucosa in the form of a pharmaceutical or cosmetic composition comprising the compound and a pharmaceutically and/or cosmetically acceptable carrier.

  本发明涉及一种新型的1,3-苯并噁唑-2(3H)-酮类化合物及其作为药物的用途，尤其是作为皮肤科药剂和化妆品的用途。这些新型化合物在治疗和/或预防患者的炎症、刺激、瘙痒、瘙痒、疼痛、水肿和/或过敏症状方面特别有用。通常它们以药用或化妆品组合物的形式局部应用于皮肤或黏膜，包括该化合物和一种药学和/或化妆学可接受的载体。
• OIL RELEASE WITH AMINO ACID-BASED COMPOUNDS HAVING A LONG CHAIN N-ACYL GROUP
  申请人：Perry Michael P.

  公开号：US20130095562A1

  公开（公告）日：2013-04-18

  Chemical compounds that are N-acyl amino acids or derivatives thereof having long chain N-acyl groups were found to have oil-releasing activity. Solutions containing these compounds may be introduced into oil reservoirs or onto oil-contaminated surface sites to release oil from oil-coated surfaces. The released oil may be recovered for further processing or waste disposal.

  发现具有长链N-酰基基团的N-酰基氨基酸或其衍生物具有释放油的活性。含有这些化合物的溶液可以引入油藏或涂有油的表面上，以从油覆盖的表面释放油。释放的油可以被回收进行进一步处理或废物处理。
• Composition comprising a sulfur-containing, phosphorus-containing compound, and/or its salt, and uses thereof
  申请人：Afton Chemical Corporation

  公开号：EP1785470A2

  公开（公告）日：2007-05-16

  There is disclosed herein an additive composition including a compound of formula (III): wherein R1, R2, R3, R4, R5, R6, R7, R8, and R9 are independently selected from the group consisting of hydrogen, cyano, and hydrocarbyl groups comprising from about 1 to about 30 carbon atoms.

  本文公开了一种添加剂组合物，其中包括式（III）化合物： 其中 R1、R2、R3、R4、R5、R6、R7、R8 和 R9 独立地选自氢、氰基和包含约 1 至约 30 个碳原子的烃基组成的组。

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