货品编码 | 规格 | 纯度 | 价格 (¥) | 现价(¥) | 特价(¥) | 库存描述 | 数量 | 总计 (¥) |
---|---|---|---|---|---|---|---|---|
TDZ004416-1g | 1g | 96.00%对照品 | ¥ 0.00 | ¥ 0.00 | backorder | ¥ 0.00 | ||
TDZ004416-5mg | 5mg | 96.00%对照品 | ¥ 4640.00 | ¥ 4640.00 | backorder | ¥ 0.00 |
中文别名 | Parvine |
英文别名 | Parvine |
CAS号 | 57103-51-2 |
SMILES | C1CN2C(=CC3=C(C2=O)C=NC=C3)C4=C1C5=CC=CC=C5N4 |
Inchi | InChI=1S/C18H13N3O/c22-18-14-10-19-7-5-11(14)9-16-17-13(6-8-21(16)18)12-3-1-2-4-15(12)20-17/h1-5,7,9-10,20H,6,8H2 |
InchiKey | GFQUYBVDVRJSP-UHFFFAOYSA-N |
分子式 Molecular Weight | C18H13N3O |
分子量 Formula | 287.3 |
闪点 FP | No data available |
熔点 Melting point | No data available |
沸点 Boiling point | No data available |
Polarizability极化度 | No data available |
密度 Density | No data available |
蒸汽压 Vapor Pressure | No data available |
溶解度Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. |
性状 | solid power;Yellow powder |
储藏条件 Storage conditions | -4℃存储更佳 |
产品说明 | |
Introduction | |
Application1 | |
Application2 | |
Application3 |
Naucline, a new indole alkaloid from the bark of Nauclea officinalis PMID 22469596; Molecules (Basel, Switzerland) 2012 Apr; 17(4):4028-36 |
Natural indole butyrylcholinesterase inhibitors from Nauclea officinalis PMID 25636869; Phytomedicine : international journal of phytotherapy and phytopharmacology 2015 Jan; 22(1):45-8 |
New indole alkaloids from Sarcocephalus latifolius PMID 11547422; Natural product letters 2001; 15(1):43-8 |
Naucline, a new indole alkaloid from the bark of Nauclea officinalis PMID 22469596; Molecules (Basel, Switzerland) 2012 Apr; 17(4):4028-36 |
Natural indole butyrylcholinesterase inhibitors from Nauclea officinalis PMID 25636869; Phytomedicine : international journal of phytotherapy and phytopharmacology 2015 Jan; 22(1):45-8 |
Naucline, a New Indole Alkaloid from the Bark of Nauclea officinalis.Molecules 2012, 17(4), 4028-4036;
Abstract:A new indole alkaloid, naucline (1) together with four known alkaloids, angustine (2), angustidine (3), nauclefine (4) and naucletine (5), were isolated from the bark of Nauclea officinalis. The structures of all isolated compounds were elucidated with various spectroscopic methods such as 1D- and 2D- NMR, IR, UV and LCMS-IT-TOF. In addition to that of alkaloid 1, the complete 13C-NMR data of naucletine (5) were also reported. Naucline (1) showed a moderate vasorelaxant activity (90% relaxation at 1 × 10−5 M) whereas, angustine (2), nauclefine (4), and naucletine (5) showed potent vasorelaxant activity (more than 90% relaxation at 1 × 10−5 M) on an isolated rat aorta.- 相关产品
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