Ethyl 5-{(2S)-3-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}-2-hydroxybenzoate | 292836-01-2

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: Ethyl 5-{(2S)-3-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}-2-hydroxybenzoate
• 英文别名: ethyl 2-hydroxy-5-[(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-oxo-3-phenylmethoxypropyl]benzoate
• CAS: 292836-01-2
• 化学式: C₂₄H₂₉NO₇
• 分子量: 443.497
• InChiKey: BBMJNLRDFPYDBJ-IBGZPJMESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  32
• 可旋转键数：
  12
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  111
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  Ethyl 5-{(2S)-3-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}-2-hydroxybenzoate 在 palladium on activated charcoal sodium hydroxide 、 氢气 、 potassium carbonate 、 三乙胺 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 生成 5-{2-tert-Butoxycarbonylamino-2-[4-(2-methoxycarbonyl-3-hydroxy-phenoxy)-butylcarbamoyl]-ethyl}-2-(1-carboxy-ethoxy)-benzoic acid
  参考文献：
  名称：

  Discovery and SAR of novel, potent and selective protein tyrosine phosphatase 1B inhibitors

  摘要：

  A salicylate second site binder was linked to three classes of phosphotyrosine mimetics to produce potent protein tyrosine phosphatase 1B (PTP1B) inhibitors which exhibit significant selectivity against other phosphatases including the most homologous member, TCPTP.

  DOI：

  10.1016/s0960-894x(03)00725-x
• 作为产物：
  描述：

  Boc-l-3-碘酪氨酸 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 碳酸氢钠 作用下， 60.0 ℃ 、405.3 kPa 条件下， 生成 Ethyl 5-{(2S)-3-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}-2-hydroxybenzoate
  参考文献：
  名称：

  Discovery and SAR of novel, potent and selective protein tyrosine phosphatase 1B inhibitors

  摘要：

  A salicylate second site binder was linked to three classes of phosphotyrosine mimetics to produce potent protein tyrosine phosphatase 1B (PTP1B) inhibitors which exhibit significant selectivity against other phosphatases including the most homologous member, TCPTP.

  DOI：

  10.1016/s0960-894x(03)00725-x

文献信息

• Inhibitors of protein tyrosine phosphatase
  申请人：——

  公开号：US06410585B1

  公开（公告）日：2002-06-25

  The present invention comprises small molecular weight, non-peptidic inhibitors of formulae I-VII of Protein Tyrosine Phosphatase 1 (PTP1) which are useful for the treatment and/or prevention of Non-Insulin Dependent Diabetes Mellitus (NIDDM).

  本发明涉及蛋白酪氨酸磷酸酶1（PTP1）的式I-VII的小分子量、非肽类抑制剂，用于治疗和/或预防非胰岛素依赖型糖尿病（NIDDM）。
• INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE
  申请人：Pharmacia & Upjohn Aktiebolag

  公开号：EP1161421A1

  公开（公告）日：2001-12-12
• US6410585B1
  申请人：——

  公开号：US6410585B1

  公开（公告）日：2002-06-25
• [EN] INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE<br/>[FR] INHIBITEURS DE LA TYROSINE PHOSPHATASE
  申请人：PHARMACIA & UPJOHN AB

  公开号：WO2000053583A1

  公开（公告）日：2000-09-14

  The present invention comprises small molecular weight, non-peptidic inhibitors of formula (I) of Protein Tyrosine Phosphatase 1 (PTP1) which are useful for the treatment and/or prevention of Non-Insulin Dependent Diabetes Mellitus (NIDDM).
• Discovery and SAR of novel, potent and selective protein tyrosine phosphatase 1B inhibitors
  作者：Zhonghua Pei、Xiaofeng Li、Gang Liu、Cele Abad-Zapatero、Tom Lubben、Tianyuan Zhang、Stephen J. Ballaron、Charles W. Hutchins、James M. Trevillyan、Michael R. Jirousek

  DOI：10.1016/s0960-894x(03)00725-x

  日期：2003.10

  A salicylate second site binder was linked to three classes of phosphotyrosine mimetics to produce potent protein tyrosine phosphatase 1B (PTP1B) inhibitors which exhibit significant selectivity against other phosphatases including the most homologous member, TCPTP.