6α-Naloxol

CAS 20410-95-1 MFCD12031398

化学结构图

20410-95-1
SMILES: C=CCN1CC[C@@]23[C@H]4OC5C2=C(C[C@@H]1[C@]3(O)CC[C@@H]4O)C=CC=5O

化学属性

Mol. FormulaC19H23NO4
Mol. Weight329.394

别名和识别编码

Chemical Name6α-Naloxol
Chemical Name Translation
信息真实价格透明    资金保障    专业采购外包团队在线服务   
信息真实价格透明    资金保障    专业采购外包团队在线服务   
品牌质保精细包装    现货库存    一流品牌服务   

相关文献及参考

  • Volume 50, Issue 32, 1994, Pages 9757–9768.
  • [2]. Csaba Simon, et al. Stereoselective synthesis of β-naltrexol, β-naloxol β-naloxamine, β-naltrexamine and related compounds by the application of the mitsunobu reac. Tetrahedron
  • [3]. Schulteis G, et al. Relative potency of the opioid antagonists naloxone and 6-alpha-naloxol to precipitate withdrawal from acute morphine dependence varies with time post-antagonist. Pharmacol Biochem Behav. 2009 Mar;92(1):157-63.
  • Volume 50, Issue 32, 1994, Pages 9757–9768.
  • [1]. Weinstein SH, et al. Metabolites of naloxone in human urine. J Pharm Sci. 1971 Oct;60(10):1567-8.
  • [1]. Weinstein SH, et al. Metabolites of naloxone in human urine. J Pharm Sci. 1971 Oct;60(10):1567-8.
  • [2]. Csaba Simon, et al. Stereoselective synthesis of β-naltrexol, β-naloxol β-naloxamine, β-naltrexamine and related compounds by the application of the mitsunobu reac. Tetrahedron
  • [3]. Schulteis G, et al. Relative poten

系列性分类

  1. Medical Research Areas
  2. GPCR & G Protein
  3. Opioid Receptor  (阿片受体)

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