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3,6-Dihydroxyxanthone Sale

目录号 : GC66212

3,6-Dihydroxyxanthone (compound 3) 是黄酮衍生物。3,6-Dihydroxyxanthone (compound 3) 具有抗癌活性。3,6-Dihydroxyxanthone (compound 3) 可用于癌症研究。

3,6-Dihydroxyxanthone Chemical Structure

Cas No.:1214-24-0

规格 价格 库存 购买数量
500mg
¥630.00
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1g
¥945.00
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Sample solution is provided at 25 µL, 10mM.

产品文档

Quality Control & SDS

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产品描述

3,6-Dihydroxyxanthone (compound 3) is a xanthone derivatives. 3,6-Dihydroxyxanthone (compound 3) has anticancer activity. 3,6-Dihydroxyxanthone (compound 3) can be used for cancer research[1].

3,6-Dihydroxyxanthone (compound 3) (3.906-1000 µg/mL; 24 hours) exhibits cytotoxic activity against WiDR and Vero cell lines with IC50 values of 785.58 and 1280.9 µM[1].

Cell Cytotoxicity Assay[1]

Cell Line: WiDR and Vero cell lines
Concentration: 3.906, 7.813, 15.625, 31.25, 62.5, 125, 250 and 500 µg/mL (WiDR cell line)7.813, 15.625, 31.25, 62.5, 125, 250, 500 and 1000 µg/mL (Vero cell line)
Incubation Time: 24 hours
Result: Inhibited cell activity and with IC50 values of 785.58 and 1,280.9 µM for WiDR and Vero cell lines.

Chemical Properties

Cas No. 1214-24-0 SDF Download SDF
分子式 C13H8O4 分子量 228.2
溶解度 储存条件 4°C, stored under nitrogen
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 4.3821 mL 21.9106 mL 43.8212 mL
5 mM 0.8764 mL 4.3821 mL 8.7642 mL
10 mM 0.4382 mL 2.1911 mL 4.3821 mL
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Research Update

gamma-Pyrone compounds. IV: Synthesis and antiplatelet effects of mono- and dioxygenated xanthones and xanthonoxypropanolamine

J Pharm Sci 1993 Jan;82(1):11-6.PMID:8429484DOI:10.1002/jps.2600820103.

Xanthodilol, mono- and dioxygenated xanthones, and 1,3-, 2,3-, 3,4-, 3,5-, 1,6-, 2,6- and 3,6-dioxygenated xanthones were synthesized from benzophenone precursors by Friedel-Crafts acylation and subsequent base-catalyzed cyclization to eliminate methanol. 3-Hydroxy-xanthone, xanthodilol, 2,3-dihydroxyxanthone diacetate, and 3,4-dihydroxyxanthone and its diacetate showed potent antiplatelet effects on arachidonate- and collagen-induced aggregation. 3,5-Dihydroxyxanthone and its diacetate, 1,6-dimethoxyxanthone, and 3,6-Dihydroxyxanthone and its diacetate showed potent antiplatelet effects on arachidonate-induced aggregation.