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5-Tricosylresorcinol Sale

(Synonyms: 5-二十三烷基间苯二酚) 目录号 : GC46079

An alkylresorcinol

5-Tricosylresorcinol Chemical Structure

Cas No.:70110-60-0

规格 价格 库存 购买数量
500μg
¥1,508.00
现货
1mg
¥2,861.00
现货
5mg
¥6,785.00
现货
10mg
¥12,215.00
现货

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Sample solution is provided at 25 µL, 10mM.

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产品描述

5-Tricosylresorcinol is an alkylresorcinol that has been found in wheat, rye, triticale, and barley.1 It reduces hydrogen peroxide-induced DNA damage in HT-29 cells when used at a concentration of 100 μM.2

|1. Ross, A.B., Shepherd, M.J., SchÜpphaus, M., et al. Alkylresorcinols in cereals and cereal products. J. Agric. Food Chem. 51(14), 4111-4118 (2003).|2. Parikka, K., Rowland, I.R., Welch, R.W., et al. In vitro antioxidant activity and antigenotoxicity of 5-n-alkylresorcinols. J. Agric. Food Chem. 54(5), 1646-1650 (2006).

Chemical Properties

Cas No. 70110-60-0 SDF
别名 5-二十三烷基间苯二酚
Canonical SMILES OC1=CC(O)=CC(CCCCCCCCCCCCCCCCCCCCCCC)=C1
分子式 C29H52O2 分子量 432.7
溶解度 Ethanol: soluble 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.3111 mL 11.5554 mL 23.1107 mL
5 mM 0.4622 mL 2.3111 mL 4.6221 mL
10 mM 0.2311 mL 1.1555 mL 2.3111 mL
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Research Update

The Impact of Some Natural Phenolic Compounds on α-Glucosidase and Sorbitol Dehydrogenase Enzymes, and Anti-leukemia Cancer Potential, Spin Density Distributions, and in silico Studies

J Oleo Sci 2022 Jun 3;71(6):863-873.PMID:35584958DOI:10.5650/jos.ess22029

In this study, some phenolic compounds including 4-Hexylresorcinol, 5-Pentadecylresorcinol, 5-Tricosylresorcinol, Bilobol, and Urushiol were tested against α-glycosidase enzyme from Saccharomyces cerevisiae and sorbitol dehydrogenase enzymes from sheep liver. These compounds determined good inhibition properties against α-glycosidase and sorbitol dehydrogenase (SDH) enzymes. IC50 values were record in the range of 1.45±0.20-24.532±3.83 μM for α-glycosidase and 6.20±0.96-108.22±18.02 μM for SDH. These inhibitor compounds can be selective drug candidates as anti-diabetic agents, because of they have inhibition properties against both enzymes. In this study, the anti-oxidant activities of the molecules were compared with density functional theory (DFT) calculations. Comparison was made with the experimental enzymes by molecular modeling calculations. In the cellular and molecular part of the recent study, the treated cells with some phenolic compounds were assessed by molecularly targeted therapy (MTT) assay for cytotoxicity and anti-acute lymphoblastic leukemia potentials on Clone 15 HL-60, HL-60, HL-60/MX1, and HL-60/MX2 cell lines. The IC50 of these compounds were µg/mL level against these cell lines.