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Merck
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重要文件

SMB01039

Sigma-Aldrich

Murrayafoline A

≥90% (LC/MS-ELSD)

同義詞:

1-Methoxy-3-methyl-9H-carbazole

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About This Item

經驗公式(希爾表示法):
C14H13NO
CAS號碼:
分子量::
211.26
MDL號碼:
分類程式碼代碼:
12352205
NACRES:
NA.25

生物源

plant

化驗

≥90% (LC/MS-ELSD)

形狀

solid

分子量

211.26

溶解度

water: slightly soluble

應用

metabolomics
vitamins, nutraceuticals, and natural products

儲存溫度

−20°C

SMILES 字串

[nH]1c2c(c3c1cccc3)cc(cc2OC)C

InChI

1S/C14H13NO/c1-9-7-11-10-5-3-4-6-12(10)15-14(11)13(8-9)16-2/h3-8,15H,1-2H3

InChI 密鑰

HDETUOZJFUNSKG-UHFFFAOYSA-N

一般說明

Murrayafoline A, a carbazole alkaloid, is a bioactive natural compound commonly derived from plants such as Murraya euchrestifolia, Murraya kwangsiensis, Clausena excavata, Clausena dunniana, and Glycosmis stenocarpa. Current research indicates that this plant metabolite is an inhibitor and may possess diverse biological activities, including anticancer, antimalarial, cardioprotective and antifungal properties.

應用

Murrayafoline A is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

生化/生理作用

Murrayafoline A may be a potential chemotherapeutic agent for use in the treatment of colon cancer and may be useful in preventing the progression of vascular complications such as restenosis.

特點和優勢

  • Suitable for Biochemical and Biomedical research
  • Versatile and adaptable for wide variety of laboratory and research applications

其他說明

For additional information on our range of Biochemicals, please complete this form.

象形圖

Health hazard

訊號詞

Warning

危險聲明

危險分類

Aquatic Chronic 4 - Carc. 2 - Muta. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Joo-Hui Han et al.
The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology, 19(5), 421-426 (2015-09-04)
The increased potential for vascular smooth muscle cell (VSMC) growth is a key abnormality in the development of atherosclerosis and post-angioplasty restenosis. Abnormally high activity of platelet-derived growth factor (PDGF) is believed to play a central role in the etiology

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