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4-(3-aminopropyl)morpholine hydrochloride | 52198-68-2

中文名称
——
中文别名
——
英文名称
4-(3-aminopropyl)morpholine hydrochloride
英文别名
3-morpholin-4-yl-propylamine; hydrochloride;N-(aminopropyl)morpholine hydrochloride;4-Morpholinepropanamine, monohydrochloride;3-morpholin-4-ylpropan-1-amine;hydrochloride
4-(3-aminopropyl)morpholine hydrochloride化学式
CAS
52198-68-2
化学式
C7H16N2O*ClH
mdl
——
分子量
180.678
InChiKey
HCTBOZOAFWFRDH-UHFFFAOYSA-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):
    0.09
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    38.5
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    4-(3-aminopropyl)morpholine hydrochloride 在 trisodium thiophosphate 作用下, 生成 2-mercapto-N-(3-morpholin-4-yl-propyl)-acetamidine
    参考文献:
    名称:
    2-巯基乙acet及其衍生物为抗辐射剂。
    摘要:
    DOI:
    10.1021/jm00282a027
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文献信息

  • Chemical Derivatization of Peptide Carboxyl Groups for Highly Efficient Electron Transfer Dissociation
    作者:Brian L. Frey、Daniel T. Ladror、Samuel B. Sondalle、Casey J. Krusemark、April L. Jue、Joshua J. Coon、Lloyd M. Smith
    DOI:10.1007/s13361-013-0701-2
    日期:2013.11.1
    The carboxyl groups of tryptic peptides were derivatized with a tertiary or quaternary amine labeling reagent to generate more highly charged peptide ions that fragment efficiently by electron transfer dissociation (ETD). All peptide carboxyl groups—aspartic and glutamic acid side-chains as well as C-termini—were derivatized with an average reaction efficiency of 99 %. This nearly complete labeling avoids making complex peptide mixtures even more complex because of partially-labeled products, and it allows the use of static modifications during database searching. Alkyl tertiary amines were found to be the optimal labeling reagent among the four types tested. Charge states are substantially higher for derivatized peptides: a modified tryptic digest of bovine serum albumin (BSA) generates ~90% of its precursor ions with z  >  2, compared with less than 40 % for the unmodified sample. The increased charge density of modified peptide ions yields highly efficient ETD fragmentation, leading to many additional peptide identifications and higher sequence coverage (e.g., 70 % for modified versus only 43 % for unmodified BSA). The utility of this labeling strategy was demonstrated on a tryptic digest of ribosomal proteins isolated from yeast cells. Peptide derivatization of this sample produced an increase in the number of identified proteins, a >50 % increase in the sequence coverage of these proteins, and a doubling of the number of peptide spectral matches. This carboxyl derivatization strategy greatly improves proteome coverage obtained from ETD-MS/MS of tryptic digests, and we anticipate that it will also enhance identification and localization of post-translational modifications.
    使用叔胺或季胺标记试剂对胰蛋白酶肽的羧基进行衍生,以产生电荷更高的肽离子,从而通过电子转移解离(ETD)有效地进行碎裂。所有肽的羧基--天冬氨酸和谷氨酸侧链以及 C 端--都进行了衍生,平均反应效率为 99%。这种近乎完全的标记避免了因部分标记产物而使复杂的多肽混合物变得更加复杂,而且还可以在数据库搜索时使用静态修饰。在测试的四种试剂中,烷基叔胺是最佳的标记试剂。衍生肽的电荷状态要高得多:经修饰的牛血清白蛋白(BSA)胰蛋白酶消化物产生的前体离子中约有 90% 的 z > 2,而未经修饰的样品则不到 40%。修饰肽离子电荷密度的增加产生了高效的 ETD 片段,从而增加了许多肽的鉴定率和更高的序列覆盖率(例如,修饰肽离子的鉴定率为 70%,而未修饰 BSA 的鉴定率仅为 43%)。从酵母细胞中分离出来的核糖体蛋白质的胰蛋白酶消化物证明了这种标记策略的实用性。对该样本进行肽衍生处理后,鉴定出的蛋白质数量增加了,这些蛋白质的序列覆盖率提高了 50%以上,肽谱匹配的数量也增加了一倍。这种羧基衍生化策略大大提高了从胰蛋白酶消化物的 ETD-MS/MS 中获得的蛋白质组覆盖率,我们预计它还将提高翻译后修饰的鉴定和定位。
  • Chiti; Selleri, Farmaco, Edizione Scientifica, 1958, vol. 13, p. 261,282
    作者:Chiti、Selleri
    DOI:——
    日期:——
  • Synthesis, characterization and biological evaluation of fluorescent biphenyl–furocoumarin derivatives
    作者:Huaizhen He、Cheng Wang、Tao Wang、Nan Zhou、Zhenyi Wen、Sicen Wang、Langchong He
    DOI:10.1016/j.dyepig.2014.07.011
    日期:2015.2
    A series of new biphenyl furocoumarin derivatives were synthesized via Suzuki Miyaura reaction as a critical step. The structures were characterized by NMR, IR and HRMS. All the derivatives presented vasodilatory activity in different degree, especially 6b. Photoelectric properties of all derivatives were investigated by fluorescence, including the variation in different solvents and various pH of 6b. All the ground state molecular geometries from 6a-6j are fully optimized by Density Functional Theory (DFT) on gas phase, which was in accordance with the fluorescence detection. The results suggested cornpounds with biphenyl furocoumarin skeleton would serve as promising vasodilatory candidates as well as fluorescent indicators. (C) 2014 Elsevier Ltd. All rights reserved.
  • MIDDLETON, R. W.;PARRICK, J., J. HETEROCYCL. CHEM., 1985, 22, N 6, 1567-1572
    作者:MIDDLETON, R. W.、PARRICK, J.
    DOI:——
    日期:——
  • [EN] COMPOUNDS WITH GROWTH HORMONE RELEASING PROPERTIES<br/>[FR] COMPOSE FAVORISANT LA LIBERATION DE L'HORMONE DE CROISSANCE
    申请人:NOVO NORDISK A/S
    公开号:WO1996024587A1
    公开(公告)日:1996-08-15
    (EN) There are disclosed novel compounds of general formula (I) which compounds of formula (I) promote the release of growth hormone in humans and animals. This property can be utilized to promote the growth of food animals to render the production of edible meat products more efficient, and in humans, to increase the status of those afflicted with a lack of a normal secretion of natural growth hormone. Growth promoting compositions containing such compounds of formula (I) as the active ingredient thereof, methods of stimulating the release of growth hormone as well as use of such compounds of formula (I) are also disclosed.(FR) L'invention concerne des nouveaux composés de formule générale (I), qui favorisent la libération de l'hormone de croissance chez les humains et les animaux. Cette propriété peut être utilisée pour favoriser la croissance d'animaux destinés à l'alimentation, rendre la production de produits carnés comestibles plus efficace, et, chez les humains, améliorer l'état de ceux souffrant d'une sécrétion insuffisante de l'hormone de croissance naturelle. L'invention porte aussi sur des compositions favorisant la croissance, dont le principe actif est constitué desdits composés de formule I, sur des procédés de stimulation de la libération de l'hormone de croissance ainsi que sur l'utilisation des composés de formule I.
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