tert-butyl ((3S)-2-hydroxy-5-methylhexan-3-yl)carbamate

• 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: tert-butyl ((3S)-2-hydroxy-5-methylhexan-3-yl)carbamate
• 英文别名: tert-butyl N-[(3S)-2-hydroxy-5-methylhexan-3-yl]carbamate
• 化学式: C₁₂H₂₅NO₃
• 分子量: 231.335
• InChiKey: VSTFPUYIPVVPKP-AXDSSHIGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  16
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.92
• 拓扑面积：
  58.6
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  tert-butyl ((3S)-2-hydroxy-5-methylhexan-3-yl)carbamate 在 sodium hydroxide 、 TEA 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 生成 {(S)-1-[1-((S)-2-tert-Butoxycarbonylamino-1,4-dimethyl-pentyldisulfanyl)-ethyl]-3-methyl-butyl}-carbamic acid tert-butyl ester
  参考文献：
  名称：

  Synthesis of sulfur-containing analogs of bestatin. Inhibition of aminopeptidases by .alpha.-thiolbestatin analogs

  摘要：

  Sulfur-containing amino acid and peptide analogues of bestatin [((2S,3R)-3-amino-2-hydroxy-4-phenyl-butanoyl)-L-leucine] (1) have been synthesized and evaluated as inhibitors of aminopeptidase M (AP-M), leucine aminopeptidase (LAP), and aminopeptidase B (AP-B). The 2-thiolbestatin analogue (6) was found to be a potent inhibitor of all three aminopeptidases (AP-M, Ki = 4.4 microM; LAP, Ki = 0.55 microM; AP-B, Ki = 4.6 nM) but only a slightly better inhibitor of these aminopeptidases than the parent hydroxy-containing compound 1. Synthetic analogues of L-leucinethiol(4), a strong inhibitor of aminopeptidases, were prepared in which the carbon alpha to the thiol groups was substituted with methyl, methyl carboxylate, and carboxamide derivatives and found to be much weaker inhibitors of all aminopeptidases. A thioamide analogue of bestatin (49) is a modest inhibitor of AP-M (Ki = 40 microM), LAP (Ki = 0.33 microM), and AP-B (Ki = 2.4 microM). These results suggest that the sulfur atoms in 2-thiolbestatin and bestatin thioamide do not interact strongly with the active-site zinc atom of these aminopeptidases when the inhibitors are bound to the enzyme. These results are not consistent with proposed models for the inhibition of aminopeptidases by bestatin and related analogues.

  DOI：

  10.1021/jm00119a022
• 作为产物：
  描述：

  N-叔丁氧羰基-L-亮氨醇 在 戴斯-马丁氧化剂 作用下， 以 乙醚 、 二氯甲烷 为溶剂， 反应 18.0h， 生成 tert-butyl ((3S)-2-hydroxy-5-methylhexan-3-yl)carbamate
  参考文献：
  名称：

  [EN] ARYL LACTAM KINASE INHIBITORS
  [FR] INHIBITEURS D'ARYL-LACTAME KINASE

  摘要：

  本公开涉及一般可抑制AAK1（适配器相关激酶1）的化合物，包括这种化合物的组合物，以及抑制AAK1的方法。

  公开号：

  WO2015116060A1

文献信息

• SUBSTITUTED ISOQUINOLINEAND ISOQUINOLINONE DERIVATIVES
  申请人：Plettenburg Oliver

  公开号：US20120316152A1

  公开（公告）日：2012-12-13

  A method for the treatment or prevention in a mammal of a disease associated with Rho-kinase and/or Rho-kinase mediated phosphorylation of myosin light chain phosphatase comprising administering to the mammal in need thereof at least one compound of the formula (I)

  一种用于治疗或预防哺乳动物中与Rho-激酶和/或Rho-激酶介导的肌球蛋白轻链磷酸酶磷酸化相关的疾病的方法，包括向需要该方法的哺乳动物中至少给予一个式(I)的化合物。
• Aryl Lactam Kinase Inhibitors
  申请人：Bristol-Myers Squibb Company

  公开号：US20140038999A1

  公开（公告）日：2014-02-06

  The present disclosure is generally directed to compounds which can inhibit AAK1 (adaptor associated kinase 1), compositions comprising such compounds, and methods for inhibiting AAK1.

  本公开涉及一般用于抑制适配器相关激酶1（AAK1）的化合物、包含此类化合物的组合物以及抑制AAK1的方法。
• Aryl lactam kinase inhibitors
  申请人：Bristol-Myers Squibb Company

  公开号：US08901305B2

  公开（公告）日：2014-12-02

  The present disclosure is generally directed to compounds which can inhibit AAK1 (adaptor associated kinase 1), compositions comprising such compounds, and methods for inhibiting AAK1.

  本公开涉及能够抑制AAK1（适配器相关激酶1）的化合物，包括这些化合物的组合物和抑制AAK1的方法。
• JP2015528018A5
  申请人：——

  公开号：JP2015528018A5

  公开（公告）日：2015-09-24
• ARYL LACTAM KINASE INHIBITORS
  申请人：Bristol-Myers Squibb Company

  公开号：EP2880032B1

  公开（公告）日：2016-10-05