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Merck

SML4104

Tomatine

new

≥95% (HPLC)

别名:

(3β,5α,22β,25S)-Spirosolan-3-yl O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside, Lycopersicin, NSC 234440, NSC 9223, Spirosolane, α-Tomatine, alpha-tomatine

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About This Item

经验公式(希尔记法):
C50H83NO21
CAS号:
分子量:
1034.19
UNSPSC代码:
12352200

生物来源

tomato

质量水平

方案

≥95% (HPLC)

表单

powder

颜色

white to beige

溶解性

DMSO: 2 mg/mL, clear (warmed)

储存温度

-10 to -25°C

SMILES字符串

N1[C@]2(O[C@@H]3[C@@H]([C@@]4([C@H]([C@H]5[C@@H]([C@@]6([C@H](C[C@H](CC6)O[C@@H]7O[C@@H]([C@@H]([C@@H]([C@H]7O)O)O[C@@H]8O[C@@H]([C@H]([C@@H]([C@H]8O[C@@H]%10O[C@@H]([C@H]([C@@H]([C@H]%10O)O)O)CO)O[C@@H]9OC[C@H]([C@@H]([C@H]9O)O)O)O)CO)CO)CC5)C)CC4)C3)C)[
C[C@@H]1[C@@]2(O[C@]3([H])[C@@]1([H])[C@]4(CC[C@]5([H])[C@@]6([C@@](C[C@@H](O[C@@H]7O[C@@H]([C@H](O[C@@H]8O[C@H](CO)[C@@H](O)[C@H](O[C@@H]9OC[C@@H](O)[C@H](O)[C@H]9O)[C@H]8O[C@H]%10[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O%10)[C@@H]([C@H]7O)O)CO)CC6)([H])CC[C@

InChI key

REJLGAUYTKNVJM-SGXCCWNXSA-N

生化/生理作用

Phytochemical from tomatoes; protects the plant from microbes; induces apoptosis in cancer cell lines.
Tomatine (Lycopersicin) is a natural glycoalkaloid from tomatoes that exhibits fungicidal, antimicrobial, and insecticidal properties. Tomatine induces apoptosis in cancer cell lines.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

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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Cesar Echeverría et al.
Frontiers in pharmacology, 13, 1003264-1003264 (2022-09-27)
Background: There is abundant ethnopharmacological evidence the uses of regarding Solanum species as antitumor and anticancer agents. Glycoalkaloids are among the molecules with antiproliferative activity reported in these species. Purpose: To evaluate the anticancer effect of the Solanum glycoalkaloid tomatine
Shin-Ichi Ito et al.
FEBS letters, 581(17), 3217-3222 (2007-06-26)
The tomato saponin alpha-tomatine has been proposed to kill sensitive cells by binding to cell membranes followed by leakage of cell components. However, details of the modes of action of the compound on fungal cells are poorly understood. In the

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