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1-己基-5-氧代-3-吡咯烷羧酸甲酯 | 71548-53-3

中文名称
1-己基-5-氧代-3-吡咯烷羧酸甲酯
中文别名
——
英文名称
1-Hexyl-4-methyloxycarbonyl-2-pyrrolidone
英文别名
Methyl N-n-hexyl-5-oxo-3-pyrrolidinylcarboxylat;1-hexyl-5-oxo-pyrrolidine-3-carboxylic acid methyl ester;methyl 1-hexyl-5-oxopyrrolidine-3-carboxylate
1-己基-5-氧代-3-吡咯烷羧酸甲酯化学式
CAS
71548-53-3
化学式
C12H21NO3
mdl
——
分子量
227.304
InChiKey
GJHNTLQYACBIND-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):
    1.6
  • 重原子数:
    16
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    46.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    Discovery of an orally efficaceous 4-phenoxypyrrolidine-based BACE-1 inhibitor
    摘要:
    Based on a lead compound identified from the patent literature, we developed patentably novel BACE-1 inhibitors by introducing a cyclic amine scaffold as embodied by la and 1b. Extensive SAR studies assessed a variety of isophthalamide replacements including substituted pyrrolidinones and ultimately led to the identification of 11. Due to its favorable overall profile, 11 has been extensively profiled in various in vivo settings. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.10.053
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文献信息

  • COMBINATION PEPTIDE-NANOPARTICLES AND DELIVERY SYSTEMS INCORPORATING SAME
    申请人:Midatech Limited
    公开号:US20150099698A1
    公开(公告)日:2015-04-09
    Nanoparticles having a core and a corona of ligands covalently linked to the core, wherein differing species of peptides are bound to the nanoparticles and incorporated into various dosage forms.
    纳米颗粒具有核心和与核心共价连接的配体环,其中不同种类的肽与纳米颗粒结合,并纳入各种剂型中。
  • FORMULATION FOR ENHANCED TRANSDERMAL ABSORPTION OF DRUG
    申请人:UNIST(ULSAN NATIONAL INSTITUTE OF SCIENCE AND TECHNOLOGY)
    公开号:US20190091168A1
    公开(公告)日:2019-03-28
    Provided is a transdermal formulation including a transdermal absorption enhancer including an aliphatic hydrocarbon derivative and a pyrrolidone derivative; and a benzene diamine derivative for preventing or treating dementia, Alzheimer's disease, and hair loss.
    提供的是一种透皮制剂,包括一种透皮吸收增强剂,其中包括一种脂肪族碳氢化合物衍生物和一种吡咯烷酮衍生物;以及一种苯二胺衍生物,用于预防或治疗痴呆症、阿尔茨海默病和脱发。
  • TRPV1 agonist compounds and methods for making and using the same
    申请人:Jamieson Curtis Gene
    公开号:US20060240097A1
    公开(公告)日:2006-10-26
    Described here are TRPV1 agonist compounds and their methods of synthesis and use. In addition to specifically identified compounds, capsaicin prodrugs, gemini dimers, and mutual prodrugs are also described. Formulations of the TRPV1 agonist compounds may be in the form of a liquid, tablets, capsules, gel, cream, emulsion, a patch, or the like. Methods for treating medical conditions using the compounds, compositions, or prodrugs described, are also provided.
    这里描述了TRPV1激动剂化合物及其合成和使用方法。除了具体识别的化合物外,还描述了辣椒素前药、双子星二聚体和相互前药。TRPV1激动剂化合物的配方可以是液体、片剂、胶囊、凝胶、乳霜、乳状液、贴片等形式。还提供了使用所述化合物、组合物或前药治疗医疗状况的方法。
  • [EN] USE OF CANNABIDIOL PRODRUGS IN TOPICAL AND TRANSDERMAL ADMINISTRATION WITH MICRONEEDLES<br/>[FR] UTILISATION DE PROMÉDICAMENTS DE CANNABIDIOL POUR ADMINISTRATION TOPIQUE ET TRANSDERMIQUE AVEC DES MICRO-AIGUILLES
    申请人:ALLTRANZ INC
    公开号:WO2011026144A1
    公开(公告)日:2011-03-03
    Described herein are microneedle drug delivery systems comprising a pharmaceutical compositions comprising pharmaceutically active agents (e.g., cannabidiol and prodrugs of cannabidiol) and microneedle arrays suitable for local and systemic delivery of the active agent to a mammal. Also described herein are methods of using a microneedle transdermal or topical drug delivery systems comprising pharmaceutical compositions, comprising cannabidiol and prodrugs of cannabidiol, and microneedle arrays in the treatment disease, including pancreatitis and pancreatic cancer.
    本文描述了微针药物递送系统,包括含有药物活性成分(例如大麻二酚和大麻二酚前药)的药物组合物和适用于将活性成分局部或全身性递送至哺乳动物的微针阵列。本文还描述了使用微针经皮或局部药物递送系统治疗疾病,包括胰腺炎和胰腺癌的方法,其中药物组合物包括大麻二酚和大麻二酚前药,并且使用微针阵列。
  • Compositions and methods for treatment of premature ejaculation
    申请人:NexMed (Holdings) Inc.
    公开号:US20040241245A1
    公开(公告)日:2004-12-02
    Compositions and methods for the treatment of premature ejaculation are provided wherein a composition comprising a topical anesthetic, a shear-thinning polymeric thickener, a lipophilic component that is selected from the group consisting of an aliphatic C 1 to C 8 alcohol, an aliphatic C 8 to C 30 ester, a liquid polyol and a mixture thereof, water and a buffer system that provides a buffered pH value for the composition in the range of about 3 to about 7.4 is administered to the penile meatus.
    提供了治疗早泄的组合物和方法,其中包括一种含有局部麻醉剂、剪切稀释聚合物增稠剂、选择自脂肪族C1到C8醇、脂肪族C8到C30酯、液态多元醇或其混合物的亲脂成分、水和缓冲系统的组合物,该缓冲系统为组合物提供了在约3至约7.4范围内的缓冲pH值,并将其用于阴茎尿道口。
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