CAS: 28832-07-7; 5H-Benzo[g]-1,3-Benzodioxolo[6,5,4-De]Quinoline, 6,7,7A,8-Tetrahydro-10,11-Dimethoxy-7-Methyl-, (R)
该化合物是一种自然产生的超光速藻类,产自某些植物物种,特别是在劳拉塞氏家族内,它具有显著的药理特性,包括潜在的抗炎,止痛和抗肿瘤活动.其结构特征是:它的光柱骨,L-Dicentrine与多巴胺受体和血清素系统等各种生物目标相互作用,使其成为...
- 英文名称5H-Benzo[g]-1,3-Benzodioxolo[6,5,4-De]Quinoline, 6,7,7A,8-Tetrahydro-10,11-Dimethoxy-7-Methyl-, (R)
- 中文名称荷包牡丹碱
- IUPAC名称(R)-10,11-dimethoxy-7-methyl-6,7,7a,8-tetrahydro-5H-[1,3]dioxolo[4',5':4,5]benzo[1,2,3-de]benzo[g]quinoline
- 其它别名(R)-(-)-DICENTRINE; L-DICENTRINE; (7aR)-6,7,7a,8-Tetrahydro-10,11-dimethoxy-7-methyl-5H-benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline; Cepharanthine α-base; Eximine; 10,11-Dimethoxy-7-methyl-6,7,7A,8-tetrahydro-5H-benzo[G][1,3]benzodioxolo[6,5,4-de]quinoline; 5H-Benzo[G]-1,3-benzodioxolo[6,5,4-de]quinoline, 6,7,7A,8-tetrahydro-10,11-dimethoxy-7-methyl-; Inchi=1/C20H21no4/C1-21-5-4-11-7-17-20(25-10-24-17)19-13-9-16(23-3)15(22-2)8-12(13)6-14(21)18(11)19/H7-9,14H,4-6,10H2,1-3h
- CAS编号28832-07-7
- MFCD编号:MFCD00210492
- FDA UNII编号:5O9KK11109
- 分子式:C20H21NO4分子量:339.39
- 产品CID: 1269596
- 产品分类生物化工 → 提取物
物理性质
MSDS等安全信息
上下游产品
CAS号25368-02-9 (-)-phanostenine合成工艺路线路线简述
📜(-)-Phanostenine 反应生成荷包牡丹碱
参考文献:Tomita; Sirai,Yakugaku Zasshi,1943,Vol. 63,P. 233
标题:Tomita; Sirai,Yakugaku Zasshi,1943,Vol. 63,P. 233
海关参考信息
- 2902600000-乙苯
2905110000-甲醇
2907210001-间苯二酚
2908199090-其他酚的卤化衍生物 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
主要参考文献
1: Tiwari S, Awasthi M, Singh S, Pandey VP, Dwivedi UN. Modulation of interaction of mutant TP53 and wild type BRCA1 by alkaloids: a computational approach towards targeting protein-protein interaction as a futuristic therapeutic intervention strategy for breast cancer impediment. J Biomol Struct Dyn. 2017 Oct
23:1-12. doi: 10.1080/07391102.2017.1388286. [Epub ahead of print] eCollection 2015.
3: Lin HF, Huang HL, Liao JF, Shen CC, Huang RL. Dicentrine Analogue-Induced G2/M Arrest and Apoptosis through Inhibition of Topoisomerase II Activity in Human Cancer Cells. Planta Med. 2015 Jul;81(10):830-7. doi: 10.1055/s-0035-1546128. Epub 2015 Jul 9. doi: 10.1016/j.fitote.2015.05.019. Epub 2015 May 29. doi: 10.1016/j.mrgentox.2013.07.004. Epub 2013 Jul 24. doi: 10.1371/journal.pone.0067730. Print 2013.
合成参考文献
参考文献:10.1021/np50091a005
摘要:Likhitwitayawuid K, Angerhofer CK, Cordell GA, Pezzuto JM, Ruangrungsi N. Cytotoxic and antimalarial bisbenzylisoquinoline alkaloids from Stephania erecta. J Nat Prod. 1993 Jan;56(1):30–8. doi: 10.1021/np50091a005.
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