Nauclefine|Nauclefine|57103-51-2|-范德生物科技公司

Nauclefine

Nauclefine
NMR and HPLC COA下载 MSDS下载
Names：
Nauclefine
CAS号：
57103-51-2
MDL Number：
MF(分子式)： C18H13N3O MW(分子量)： 287.3
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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

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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

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备注

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.

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