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柚皮芸香苷

更新时间:2024-01-01 18:45:09

柚皮芸香苷结构式
柚皮芸香苷结构式
品牌特惠专场
常用名 柚皮芸香苷 英文名 Narirutin
CAS号 14259-46-2 分子量 580.535
密度 1.7±0.1 g/cm3 沸点 924.3±65.0 °C at 760 mmHg
分子式 C27H32O14 熔点 152-190ºC
MSDS 中文版 美版 闪点 307.3±27.8 °C

 柚皮芸香苷用途


Narirutin 是从 Citrus unshiu 中分离的活性成分之一,具有抗氧化和抗炎活性。Narirutin 是一种具有抗结核效力的 shikimate 激酶抑制剂。

 柚皮芸香苷名称

中文名 芸香柚皮苷
英文名 narirutin
中文别名 柚皮素-7-O-芸香糖苷 | 柚皮芸香苷
英文别名 更多

 柚皮芸香苷生物活性

描述 Narirutin 是从 Citrus unshiu 中分离的活性成分之一,具有抗氧化和抗炎活性。Narirutin 是一种具有抗结核效力的 shikimate 激酶抑制剂。
相关类别
参考文献

[1]. Sahu PK, et al. Structure-based Discovery of Narirutin as a Shikimate Kinase Inhibitor with Anti-tubercular Potency.Curr Comput Aided Drug Des. 2019 Oct 25.

[2]. Funaguchi N, et al. Narirutin inhibits airway inflammation in an allergic mouse model.Clin Exp Pharmacol Physiol. 2007 Aug;34(8):766-70.

 柚皮芸香苷物理化学性质

密度 1.7±0.1 g/cm3
沸点 924.3±65.0 °C at 760 mmHg
熔点 152-190ºC
分子式 C27H32O14
分子量 580.535
闪点 307.3±27.8 °C
精确质量 580.179199
PSA 225.06000
LogP 2.07
外观性状 灰白色粉末
蒸汽压 0.0±0.3 mmHg at 25°C
折射率 1.708
储存条件 室温

 柚皮芸香苷安全信息

安全声明 (欧洲) 22-24/25
危险品运输编码 NONH for all modes of transport
海关编码 29389090

 柚皮芸香苷文献2

更多文献
Berry and Citrus Phenolic Compounds Inhibit Dipeptidyl Peptidase IV: Implications in Diabetes Management.

Evid. Based. Complement. Alternat. Med. 2013 , 479505, (2013)

Beneficial health effects of fruits and vegetables in the diet have been attributed to their high flavonoid content. Dipeptidyl peptidase IV (DPP-IV) is a serine aminopeptidase that is a novel target ...

Huanglongbing modifies quality components and flavonoid content of 'Valencia' oranges.

J. Sci. Food Agric. 96 , 73-8, (2016)

In order to evaluate the effect of citrus greening disease, or Huanglongbing (HLB), on quality components and flavonoid contents of 'Valencia' oranges, fruit from non-infected trees (control), from in...

 柚皮芸香苷英文别名

(2S)-5-Hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl-6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 6-O-(6-deoxy-a-L-mannopyranosyl)-b-D-glucopyranoside
ISONARINGIN
Isonaringenin
Naringenin 7-O-rutinoside
4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-, (2S)-
Naringenin-7-rutinoside
(2S)-5-Hydroxy-2-(4-hydroxyphenyl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}methyl)tetrahydro-2H-pyran-2-yl]oxy}-2,3-dihydro-4H-chromen-4-one
Narirutin
(2S)-5-Hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside
(2S)-5-Hydroxy-2-(4-hydroxyphényl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-méthyltétrahydro-2H-pyran-2-yl]oxy}méthyl)tétrahydro-2H-pyran-2-yl]oxy}-2,3-dihydro-4H-chromén-4-one
Naringenin 7-rutinoside
(S)-7-((6-O-(6-Deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl)oxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
naringenin-7-O-rutinoside
Apigenin-7-rutinosid
(2S)-5-Hydroxy-2-(4-hydroxyphenyl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}methyl)tetrahydro-2H-pyran-2-yl]oxy}-2,3-dihydro-4H-chromen-4-on
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