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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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关于此项目

经验公式(希尔记法):
C30H50O
CAS Number:
分子量:
426.72
Beilstein:
2224850
UNSPSC代码:
12352211
NACRES:
NA.77
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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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Laurent F Wentzinger et al.
Plant physiology, 130(1), 334-346 (2002-09-13)
To get some insight into the regulatory mechanisms controlling the sterol branch of the mevalonate pathway, tobacco (Nicotiana tabacum cv Bright Yellow-2) cell suspensions were treated with squalestatin-1 and terbinafine, two specific inhibitors of squalene synthase (SQS) and squalene epoxidase
X Qi et al.
Proceedings of the National Academy of Sciences of the United States of America, 101(21), 8233-8238 (2004-05-19)
The evolution of the ability to synthesize specialized metabolites is likely to have been key for survival and diversification of different plant species. Oats (Avena spp.) produce antimicrobial triterpenoids (avenacins) that protect against disease. The oat beta-amyrin synthase gene AsbAS1
Wahid Herchi et al.
Plant physiology and biochemistry : PPB, 47(10), 880-885 (2009-07-21)
A comparative study was performed to determine the free sterols content and composition during the development of three varieties of linseed (H52, O116 and P129). Seed samples were collected at regular intervals from 7 to 60 days after flowering (DAF).
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
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

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