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Merck
CN

SML1016

Sigma-Aldrich

植保素

≥98% (HPLC), phytoalexin, powder

别名:

3-(噻唑-2-基)-1H-吲哚, Camalexine

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关于此项目

经验公式(希尔记法):
C11H8N2S
化学文摘社编号:
分子量:
200.26
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
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产品名称

植保素, ≥98% (HPLC)

方案

≥98% (HPLC)

表单

powder

颜色

white to light brown

溶解性

DMSO: 20 mg/mL, clear

储存温度

2-8°C

SMILES字符串

C12=CC=CC=C1NC=C2C3=NC=CS3

InChI

1S/C11H8N2S/c1-2-4-10-8(3-1)9(7-13-10)11-12-5-6-14-11/h1-7,13H

InChI key

IYODIJVWGPRBGQ-UHFFFAOYSA-N

应用

Camalexin已用于拟南芥叶片的定量和耐受性测定。

生化/生理作用

Camalexin是一种从十字花科植物中分离的植物抗毒素,具有抗细菌、抗真菌、抗增殖和癌症化学预防活性。
Camalexin是一种从十字花科植物中分离的植物抗毒素,具有抗细菌、抗真菌、抗增殖和癌症化学预防活性。很显然,camalexin可增加ROS的水平,并在表达高ROS水平的侵袭性前列腺癌细胞中更有效。在南芥中,camalexin和水杨酸赋予了其对辣椒疫霉的抗性。

特点和优势

这种化合物是凋亡研究的特色产品。点击此处发现更多特色凋亡产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。

象形图

Exclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Jhon Venegas-Molina et al.
Scientific reports, 10(1), 10319-10319 (2020-06-27)
The plant hormones salicylic acid (SA) and jasmonic acid (JA) regulate defense mechanisms capable of overcoming different plant stress conditions and constitute distinct but interconnected signaling pathways. Interestingly, several other molecules are reported to trigger stress-specific defense responses to biotic
Hector R Huarte et al.
Plants (Basel, Switzerland), 9(9) (2020-09-24)
The association among environmental cues, ethylene response, ABA signaling, and reactive oxygen species (ROS) homeostasis in the process of seed dormancy release is nowadays well-established in many species. Alternating temperatures are recognized as one of the main environmental signals determining
Camalexin quantification in Arabidopsis thaliana leaves infected with Botrytis cinerea
Savatin DV, et al.
Bio-protocol, 5(2), e1379-e1379 (2015)
Siva K Malka et al.
Frontiers in plant science, 8, 2131-2131 (2018-01-10)
Glucosinolates (GLS) are a group of plant secondary metabolites mainly found in Cruciferous plants, share a core structure consisting of a β-thioglucose moiety and a sulfonated oxime, but differ by a variable side chain derived from one of the several
Deepa Khare et al.
Proceedings of the National Academy of Sciences of the United States of America, 114(28), E5712-E5720 (2017-06-28)
Plant pathogens cause huge yield losses. Plant defense often depends on toxic secondary metabolites that inhibit pathogen growth. Because most secondary metabolites are also toxic to the plant, specific transporters are needed to deliver them to the pathogens. To identify

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