SMB01042

Allocryptopin

≥90% (LC/MS-ELSD)

• 别名: β-Allocryptopine, γ-Homochelidonine, Fagarine I
• 经验公式（希尔记法）: C₂₁H₂₃NO₅
• CAS号: 24240-04-8
• 分子量: 369.41
• MDL號碼: MFCD00022318
• 分類程式碼代碼: 12352205
• NACRES: NA.25

属性

• 生物源: plant
• 化驗: ≥90% (LC/MS-ELSD)
• 形狀: solid
• 分子量: 369.41
• 溶解度: water: slightly soluble
• 應用: metabolomics; vitamins, nutraceuticals, and natural products
• 儲存溫度: −20°C
• InChI: 1S/C21H23NO5/c1-22-7-6-14-9-19-20(27-12-26-19)10-15(14)17(23)8-13-4-5-18(24-2)21(25-3)16(13)11-22/h4-5,9-10H,6-8,11-12H2,1-3H3
• InChI 密鑰: HYBRYAPKQCZIAE-UHFFFAOYSA-N

说明

一般說明

Allocryptopin, an isoquinoline alkaliod, is a natural product commonly available from Allocryptopinus japonicus, Glaucium arabicum, Zanthoxylum beecheyanum, Berberis integerrima, and Macleaya cordata. This secondary metabolite derived from plant sources exhibits various biological activities such as anti-inflammatory, antiviral, and antitumor properties.

應用

It 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

Allocryptopine has been reported to possess strong antibacterial, anti-inflammatoty, antiparasitic, antineoplastic and anti-addictive activities. Allocryptopine inhibits human acetylcholinesterase and butyrylcholinesterase. It blocks hERG current in HEK293 cells. Allocryptopine strongly enhanced the I(peak) of the T353I channel by enhancing the plasma membrane (PM) expression of Nav1.5 and rescued defective trafficking after co-incubation with HEK293 cells that carry mutation channel 24 h.

特點和優勢

• High quality compound suitable for multiple research applications
• Compatible with HPLC and mass spectrometry techniques

其他說明

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安全信息

• 儲存類別代碼: 11 - Combustible Solids
• 閃點（°F）: Not applicable
• 閃點（°C）: Not applicable