6α-Naloxol
CAS 20410-95-1 MFCD12031398
化学结构图
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. Formula | C19H23NO4 |
|---|---|
| Mol. Weight | 329.394 |
别名和识别编码
| Chemical Name | 6α-Naloxol |
|---|---|
| Chemical Name Translation |
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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
