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Merck
CN

08172

Sigma-Aldrich

环阿屯醇

≥90% (GC)

别名:

(3S,5R,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-二甲基-己-4-烯基)-4,4,13,14-四甲基十四氢环丙并[9,10]环戊二烯并[a]菲-3-醇, 9,19-环-24-羊毛甾烯-3β-醇, 汉地醇

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About This Item

经验公式(希尔记法):
C30H50O
CAS号:
分子量:
426.72
Beilstein:
2224850
UNSPSC代码:
12352211
NACRES:
NA.77

质量水平

方案

≥90% (GC)

表单

powder

SMILES字符串

O[C@@H]1C([C@H]2[C@@]3([C@]4([C@H]([C@]5([C@@]([C@H](CC5)[C@@H](CCC=C(C)C)C)(CC4)C)C)CC2)C3)CC1)(C)C

InChI

1S/C30H50O/c1-20(2)9-8-10-21(3)22-13-15-28(7)24-12-11-23-26(4,5)25(31)14-16-29(23)19-30(24,29)18-17-27(22,28)6/h9,21-25,31H,8,10-19H2,1-7H3/t21-,22-,23+,24+,25+,27-,28+,29-,30+/m1/s1

InChI key

ONQRKEUAIJMULO-YBXTVTTCSA-N

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应用

  • 全基因组氧化鲨烯环化酶基因研究揭示了茶树三萜生物合成的遗传基础- 通过对茶树氧化鲨烯环化酶的遗传研究,研究环阿屯醇的合成途径,为增强有益于人类健康的植物甾醇提供见解(Du et al., 2024)。

包装

无底玻璃瓶。内含物在插入的融合锥体内。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Anita Loeschcke et al.
PloS one, 12(12), e0189816-e0189816 (2017-12-28)
Cyclic triterpenes constitute one of the most diverse groups of plant natural products. Besides the intriguing biochemistry of their biosynthetic pathways, plant triterpenes exhibit versatile bioactivities, including antimicrobial effects against plant and human pathogens. While prokaryotes have been extensively used
Go Atsumi et al.
Scientific reports, 8(1), 14804-14804 (2018-10-06)
Secondary metabolites in plants play important roles in defence against biotic and abiotic stresses. Although the biosynthesis pathways of secondary metabolites have been extensively studied, the regulatory mechanism of gene expression involved in these pathways remains poorly understood. In this
Kiyoshi Ohyama et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(3), 725-730 (2009-01-14)
The differences between the biosynthesis of sterols in higher plants and yeast/mammals are believed to originate at the cyclization step of oxidosqualene, which is cyclized to cycloartenol in higher plants and lanosterol in yeast/mammals. Recently, lanosterol synthase genes were identified
Hideyuki Suzuki et al.
The Plant journal : for cell and molecular biology, 32(6), 1033-1048 (2002-12-21)
The saponins of the model legume Medicago truncatula are glycosides of at least five different triterpene aglycones: soyasapogenol B, soyasapogenol E, medicagenic acid, hederagenin and bayogenin. These aglycones are most likely derived from beta-amyrin, a product of the cyclization of
Augusta Caligiani et al.
Plant foods for human nutrition (Dordrecht, Netherlands), 65(3), 277-283 (2010-07-08)
The chemical fingerprinting of the unsaponifiable fraction of different Punica granatum seed oils was performed in order to evaluate their potential as a functional food ingredient. Qualitative and quantitative determinations of tocopherol, aliphatic alcohol (including policosanol), squalene, phytosterols and triterpene

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