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2-(二苄基氨基)-1-(4-羟基苯基)乙酮 | 88693-95-2

中文名称
2-(二苄基氨基)-1-(4-羟基苯基)乙酮
中文别名
——
英文名称
2-(dibenzylamino)-1-(4-hydroxyphenyl)ethanone
英文别名
2-Dibenzylamino-1-(4-hydroxy-phenyl)-aethanon;2-(Dibenzylamino)-1-(4-hydroxyphenyl)ethan-1-one
2-(二苄基氨基)-1-(4-羟基苯基)乙酮化学式
CAS
88693-95-2
化学式
C22H21NO2
mdl
MFCD30593051
分子量
331.414
InChiKey
IVYXQLYXYHJMEO-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):
    4.3
  • 重原子数:
    25
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.136
  • 拓扑面积:
    40.5
  • 氢给体数:
    1
  • 氢受体数:
    3

SDS

SDS:0e542c091f74fb7f1400d248e8adb661
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Discovery and SAR of hydantoin TACE inhibitors
    作者:Wensheng Yu、Zhuyan Guo、Peter Orth、Vincent Madison、Lei Chen、Chaoyang Dai、Robert J. Feltz、Vinay M. Girijavallabhan、Seong Heon Kim、Joseph A. Kozlowski、Brian J. Lavey、Dansu Li、Daniel Lundell、Xiaoda Niu、John J. Piwinski、Janeta Popovici-Muller、Razia Rizvi、Kristin E. Rosner、Bandarpalle B. Shankar、Neng-Yang Shih、M. Arshad Siddiqui、Jing Sun、Ling Tong、Shelby Umland、Michael K.C. Wong、De-yi Yang、Guowei Zhou
    DOI:10.1016/j.bmcl.2010.01.148
    日期:2010.3
    We disclose inhibitors of TNF-alpha converting enzyme (TACE) designed around a hydantoin zinc binding moiety. Crystal structures of inhibitors bound to TACE revealed monodentate coordination of the hydantoin to the zinc. SAR, X-ray, and modeling designs are described. To our knowledge, these are the first reported X-ray structures of TACE with a hydantoin zinc ligand. (C) 2010 Elsevier Ltd. All rights reserved.
  • COUCH, M. W.;GABRIELSEN, B. M.;MIDGLEY, J. M., J. LABELLED COMPOUNDS AND RADIOPHARM., 1983, 20, N 8, 933-949
    作者:COUCH, M. W.、GABRIELSEN, B. M.、MIDGLEY, J. M.
    DOI:——
    日期:——
  • BODY SCULPTING
    申请人:Brains Online Holding B.V.
    公开号:EP3206678A1
    公开(公告)日:2017-08-23
  • Body Sculpting
    申请人:Sculpt B.V.
    公开号:US20170231885A1
    公开(公告)日:2017-08-17
    The invention pertains to a pharmaceutical composition for topical administration, comprising a prodrug for an agonist and/or an antagonist for an adrenergic receptor, wherein the prodrug has an octanol/water partition coefficient of at least 0, for use in a method of shaping a mammalian body by modulation of subcutaneous fat tissue. The invention further pertains to cosmetic and therapeutic application of such prodrugs, such as their use in methods of shaping a mammalian body by locally modulating subcutaneous fat tissue. The invention also pertains to the prodrugs themselves, as well as to methods of making these prodrugs.
  • Simonoff; Hartung, Journal of the American Pharmaceutical Association (1912), 1946, vol. 35, p. 306,308
    作者:Simonoff、Hartung
    DOI:——
    日期:——
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