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Merck
CN

SMB00452

Sigma-Aldrich

水甘草碱

≥95% (HPLC)

别名:

(-)-Tabersonine, (5α,12β,19α)-2,3,6,7-Tetrahydro-aspidospermidine-3-carboxylic acid methyl ester, Tabersonin

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About This Item

经验公式(希尔记法):
C21H24N2O2
CAS号:
分子量:
336.43
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.25

方案

≥95% (HPLC)

表单

powder

应用

metabolomics
vitamins, nutraceuticals, and natural products

储存温度

2-8°C

SMILES字符串

COC(C1=C2NC3=CC=CC=C3[C@]24[C@]5([H])[C@](C=CCN5CC4)(CC)C1)=O

InChI

1S/C21H24N2O2/c1-3-20-9-6-11-23-12-10-21(19(20)23)15-7-4-5-8-16(15)22-17(21)14(13-20)18(24)25-2/h4-9,19,22H,3,10-13H2,1-2H3/t19-,20-,21-/m0/s1

InChI key

FNGGIPWAZSFKCN-ACRUOGEOSA-N

一般描述

Tabersonine is a terpenoid indole alkaloid (TIA) found in Amsonia elliptica.

生化/生理作用

Tabersonine shows hypotensive, anti-tumor, hypoglycemic, and diuretic activity.

象形图

Exclamation mark

警示用语:

Warning

危险声明

预防措施声明

危险分类

Acute Tox. 4 Oral

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

监管及禁止进口产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Amir Akhgari et al.
Molecules (Basel, Switzerland), 20(12), 22621-22634 (2015-12-24)
Rhazya stricta Decne. (Apocynaceae) contains a large number of terpenoid indole alkaloids (TIAs). This study focused on the composition of alkaloids obtained from transformed hairy root cultures of R. stricta employing ultra-performance liquid chromatography-mass spectrometry (UPLC-MS). In the UPLC-MS analyses
Hanqing Wang et al.
Food chemistry, 339, 128111-128111 (2020-11-07)
Licorice is known as a botanical source in medicine and a sweetening agent in food products. Commercial licorice is from the source of wild and cultivated G. uralensis. It was recognized that the material basis of wild and cultivated licorice
Claire Parage et al.
Plant physiology, 172(3), 1563-1577 (2016-10-01)
Expansion of the biosynthesis of plant specialized metabolites notably results from the massive recruitment of cytochrome P450s that catalyze multiple types of conversion of biosynthetic intermediates. For catalysis, P450s require a two-electron transfer catalyzed by shared cytochrome P450 oxidoreductases (CPRs)
Alison Edge et al.
Planta, 247(1), 155-169 (2017-09-13)
Monoterpenoid indole alkaloids (MIAs) have remarkable biological properties that have led to their medical uses for a variety of human diseases. Mutagenesis has been used to generate plants with new alkaloid profiles and a useful screen for rapid comparison of
Zerihun Demessie et al.
Phytochemistry, 140, 118-124 (2017-05-10)
Vinca minor is a herbaceous plant from the Apocynaceae family known to produce over 50 monoterpene indole alkaloids (MIAs). These include several biologically active MIAs that have a range of pharmaceutical activities. The present study shows that the MIAs, vincamine

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