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CAS 483-43-2 MFCD00483432
化学结构图
SMILES:
化学属性
| Mol. Formula | C20H21NO5 |
|---|---|
| Mol. Weight | 355.38 |
| Boiling Point | - |
| Flash Point | - |
别名和识别编码
| Chemical Name Translation | - |
|---|---|
| CAS Number | 483-43-2 |
| Synonym | Jatrorrhizine Hydroxide |
| Chemical Name | - |
| Canonical SMILES | OC1=C(OC)C=C2C(CC[N+]3=C2C=C(C=CC(OC)=C4OC)C4=C3)=C1.[OH-] |
| MDL Number | - |
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相关文献及参考
- [2]. Xiaofei Jiang, et al. Synthesis and Biological Evaluation of Novel Jatrorrhizine Derivatives with Amino Groups Linked at the 3-Position as Inhibitors of Acetylcholinesterase. Research Article Volume 2017
- [3]. C W Wright, et al. In vitro antiplasmodial, antiamoebic, and cytotoxic activities of some monomeric isoquinoline alkaloids. J Nat Prod. 2000 Dec;63(12):1638-40.
- [1]. Sun S, et al. Jatrorrhizine reduces 5-HT and NE uptake via inhibition of uptake-2 transporters and produces antidepressant-like action in mice. Xenobiotica. 2019 Oct;49(10):1237-1243.
- [1]. Sun S, et al. Jatrorrhizine reduces 5-HT and NE uptake via inhibition of uptake-2 transporters and produces antidepressant-like action in mice. Xenobiotica. 2019 Oct;49(10):1237-1243.
- [2]. Xiaofei Jiang, et al. Synthesis and Biological Evaluation of Novel Jatrorrhizine Derivatives with Amino Groups Linked at the 3-Position as Inhibitors of Acetylcholinesterase. Research Article Volume
