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4aβ,7α,7aβ-Nepetalactone | 21651-53-6

中文名称
——
中文别名
——
英文名称
4aβ,7α,7aβ-Nepetalactone
英文别名
(4αR,7S,7αS)nepetalactone;cis,cis-Nepetalactone;cis-cis-nepetalactone;nepetalactone;(4aR,7S,7aS)-nepetalactone;4aR,7S,7aS-nepetalactone;Cyclopenta(c)pyran-1(4aH)-one, 5,6,7,7a-tetrahydro-4,7-dimethyl-, (4aR,7S,7aS)-;(4aR,7S,7aS)-4,7-dimethyl-5,6,7,7a-tetrahydro-4aH-cyclopenta[c]pyran-1-one
4aβ,7α,7aβ-Nepetalactone化学式
CAS
21651-53-6
化学式
C10H14O2
mdl
——
分子量
166.22
InChiKey
ZDKZHVNKFOXMND-XVYDVKMFSA-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

  • 保留指数:
    1360;1352;1357;1352;1355

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:68857f6d94ec41e55f1efee70c8f2384
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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

  • 作为反应物:
    描述:
    4aβ,7α,7aβ-Nepetalactone1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 xylene 为溶剂, 以7.2%的产率得到4aβ,7α,7aα-nepetalactone
    参考文献:
    名称:
    Simplified Isolation Procedure and Interconversion of the Diastereomers of Nepetalactone and Nepetalactol
    摘要:
    Three nepetalactones were isolated from Nepeta racemosa (mussinii) by traditional methods. An improved method was developed to isolate nepetalactones from N. faassenii. An epimerization procedure was used to prepare the fourth 7S-nepetalactone diastereomer. The cis-fused nepetalactols were prepared by reduction of the corresponding nepetalactones, while the trans-fused nepetalactols were unstable and found to undergo ring-opening reactions yielding iridodials. The characterizations and structural assignments by means of NMR agree with quantum chemical density functional calculations.
    DOI:
    10.1021/np049647d
  • 作为产物:
    描述:
    (3S,4R)-3-methyl-4-(3-oxobutyl)cyclopentan-1-one 在 palladium on activated charcoal potassium hydrogensulfate氢气对甲苯磺酸臭氧lithium diisopropyl amide 作用下, 以 四氢呋喃乙醇二氯甲烷环己烷甲苯 为溶剂, 反应 12.0h, 生成 4aβ,7α,7aβ-Nepetalactone
    参考文献:
    名称:
    The Potential of Semiochemicals for Control ofPhorodon humuli(Homoptera: Aphididae)
    摘要:
    Field experiments employing yellow water-traps with vials releasing methyl salicylate, butyl isothiocyanate, 4-pentenyl isothiocyanate and diethyltoluamide were conducted during the spring migration of Phorodon humuli (Schrank), with the aim of identifying substances which might be used in the field to deter landing on hop plants. Methyl salicylate and the two isothiocyanates reduced trap catches of P. humuli. During the spring of 1994 a slow-release formulation of methyl salicylate and a beta-acid-rich hop resin sprayed on to hop plants did not reduce aphid infestations significantly. In autumn cis,cis-nepetalactol the main component of P. humuli's sex pheromone, prepared by various synthetic routes, increased trap catches of males and gynoparae equally. Catches of males in pheromone traps situated in a hop garden decreased with increasing trap height. Catches of males in traps charged with increasing doses of the cis,cis-nepetalactol peaked at 1 mg and then plateaued, whereas catches of gynoparae peaked similarly at 1 mg and then decreased. The effects of kairomones from an extract of the primary host, sex pheromone and a visual cue from yellow compared with clear water-traps were additive. The prospects for developing a semiochemicals-based control strategy against P. humuli, using some or all of the above elements, are discussed.
    DOI:
    10.1002/(sici)1096-9063(199612)48:4<293::aid-ps479>3.0.co;2-5
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文献信息

  • [EN] INSECT REPELLENT COMPOSITIONS COMPRISING DIHYDRONEPETALACTONE<br/>[FR] COMPOSITIONS INSECTIFUGES COMPRENANT DU DIHYDRONEPETALACTONE
    申请人:DU PONT
    公开号:WO2005034626A1
    公开(公告)日:2005-04-21
    Dihydronepetalactone, a minor natural constituent of the essential oil of catmints (Nepeta spp.) such as Nepeta cataria, has been identified as an effective insect repellent compound. Synthesis of dihydronepetalactone may be achieved by hydrogenation of nepetalactone, the major constituent of catmint essential oils. This compound, which also has fragrance properties, may be used commercially for its insect repellent properties.
    二水合薄荷内酯是猫薄荷精油(Nepeta spp.)中的次要天然成分,例如在马齿苋属(Nepeta cataria)中发现,已被确认为有效的驱虫化合物。通过薄荷内酯的氢化反应可以合成二水合薄荷内酯,薄荷内酯是猫薄荷精油的主要成分。这种化合物除了具有芳香性质外,还可以商业化用于其驱虫性质。
  • Nepetalactol oxidoreductase in trichomes of the catmint Nepeta racemosa
    作者:David L. Hallahan、Jevon M. West、Diane W.M. Smiley、John A. Pickett
    DOI:10.1016/s0031-9422(98)00006-5
    日期:1998.6
    Abstract Isomers of (7 S )-nepetalactone are the principal constituents of the essential oil accumulated by plants of the genus Nepeta (catmints), with the cis , cis -isomer predominating in the catmint N. racemosa . An enzyme which catalyses the NAD + -dependent oxidation of cis , cis -nepetalactol to cis , cis -nepetalactone has been identified in cell-free extracts of N. racemosa leaves. This enzyme
    摘要 (7 S )-荆芥内酯的异构体是荆芥属植物(荆芥)积累的精油的主要成分,在荆芥总状荆芥中以顺式、顺式异构体为主。已在总状花椰菜叶的无细胞提取物中鉴定出一种酶,该酶催化 NAD + 依赖性氧化顺式,顺式 - 荆芥内酯为顺式,顺式 - 荆芥内酯。这种酶已被部分纯化,并已被证明位于该物种叶子表面的毛状体中。因为腺毛已被证明是荆芥内酯在总状花序草和卡塔利亚山楂中积累的场所,毛状体中存在这种活性表明荆芥内酯可能是荆芥内酯生物合成的中间体。
  • Uncoupled activation and cyclization in catmint reductive terpenoid biosynthesis
    作者:Benjamin R. Lichman、Mohamed O. Kamileen、Gabriel R. Titchiner、Gerhard Saalbach、Clare E. M. Stevenson、David M. Lawson、Sarah E. O’Connor
    DOI:10.1038/s41589-018-0185-2
    日期:2019.1
    NEPS1 provides nepetalactones, metabolites that are well known for both insect-repellent activity and euphoric effects in cats. Structural characterization of the NEPS3 cyclase reveals that it binds to NAD+ yet does not utilize it chemically for a non-oxidoreductive formal [4 + 2] cyclization. These discoveries will complement metabolic reconstructions of iridoid and monoterpene indole alkaloid biosynthesis
    萜烯合酶通常通过在单个酶活性位点中线性起始材料的协同活化和环化形成复杂的分子支架。在这里,我们显示环烯醚萜合酶,一种非典型的还原性萜烯合酶,催化其底物 8-氧代香叶醛活化为活性烯醇中间体,但不催化随后的环化为荆芥内醇。这一发现使我们从猫薄荷 ( Nepeta mussinii ) 中鉴定出一类与荆芥内醇相关的短链脱氢酶 (NEPS)) 捕获这种反应性中间体并催化立体选择性环化为不同的荆芥内酯立体异构体。NEPS1 对荆芥内酯的后续氧化提供荆芥内酯,这是众所周知的在猫中具有驱虫活性和欣快作用的代谢物。NEPS3 环化酶的结构表征表明它与 NAD +结合,但不会化学利用它进行非氧化还原形式的 [4 + 2] 环化。这些发现将补充环烯醚萜和单萜吲哚生物碱生物合成的代谢重建。
  • Biocatalytic Strategies towards [4+2] Cycloadditions
    作者:Benjamin R. Lichman、Sarah E. O'Connor、Hajo Kries
    DOI:10.1002/chem.201805412
    日期:2019.5.17
    problem in chemical synthesis. In a few cases, detailed pictures of the inner workings of these catalysts have emerged, but intense efforts to gain deeper understanding are underway by means of crystallography and computational modelling. This Minireview aims to shed light on the catalytic strategies that this highly diverse family of enzymes employs to accelerate and direct the course of [4+2] cycloadditions
    近年来,人们一直在追捧的 [4+2] 环化酶在众多生物合成途径中不断涌现,为环加成催化这一化学合成中的一个重要问题的生物催化解决方案带来了希望。在少数情况下,已经出现了这些催化剂内部运作的详细图片,但正在通过晶体学和计算建模进行深入了解的努力。这篇 Minireview 旨在阐明这一高度多样化的酶家族所采用的催化策略,以参考小分子催化剂和设计酶来加速和指导 [4+2] 环加成的过程。这些催化策略包括氧化或还原触发以及酶域的类似盖子的运动。
  • Soothing composition for animals, comprising at least one fatty acid and nepetalactone
    申请人:VIRBAC
    公开号:US10548867B2
    公开(公告)日:2020-02-04
    The invention relates to novel soothing compositions for animals, particularly for cats. It specifically relates to soothing compositions for non-human mammals, comprising between 1% and 50% w/w of at least one fatty acid comprising between 5 and 22 carbon atoms and between 0.01% and 5% w/w of nepetalactone, such that said at least one fatty acid and said nepetalactone are dissolved in a solvent. Said compositions are characterised in that they exhibit soothing properties for stressed animals and are stable for the entire period of use thereof.
    本发明涉及用于动物,特别是猫的新型舒缓组合物。本发明具体涉及用于非人类哺乳动物的舒缓组合物,其中包含重量百分比在 1%至 50%之间的至少一种由 5 至 22 个碳原子组成的脂肪酸和重量百分比在 0.01%至 5%之间的萘内酯,从而使所述至少一种脂肪酸和所述萘内酯溶解在溶剂中。所述组合物的特点是对受压动物具有舒缓特性,并在整个使用期间保持稳定。
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