(S)-2-((S)-2-tert-Butoxycarbonylamino-propylamino)-3-methyl-butyric acid | 178734-55-9

• 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: (S)-2-((S)-2-tert-Butoxycarbonylamino-propylamino)-3-methyl-butyric acid
• 英文别名: L-Valine, N-[2-[[(1,1-dimethylethoxy)carbonyl]amino]propyl]-, (S)-；(2S)-3-methyl-2-[[(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]amino]butanoic acid
• CAS: 178734-55-9
• 化学式: C₁₃H₂₆N₂O₄
• 分子量: 274.36
• InChiKey: CEWLAJOLMTZZDP-UWVGGRQHSA-N

反应信息

• 作为产物：
  描述：

  (S)-2-((S)-2-tert-Butoxycarbonylamino-propylamino)-3-methyl-butyric acid methyl ester 在 lithium hydroxide 作用下， 生成 (S)-2-((S)-2-tert-Butoxycarbonylamino-propylamino)-3-methyl-butyric acid
  参考文献：
  名称：

  Dipeptide mimetics can substitute for the receptor activation domain resulting in highly potent analogues of hPTH(1–36)

  摘要：

  A series of hPTH(1-36) analogues were prepared to study the role of the first peptide bond between residues Ser(1)-Val(2). Some of these analogues were found to show high affinity binding in intact opossum kidney (OK-1) cells and were very active in their ability to stimulate adenylate cyclase production in intact OK-1 cells, rat UMR106-06 osteosarcoma cells, and SaOS-2 human osteosarcoma cells. (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0960-894x(96)00188-6