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Vicenin 2 Sale

(Synonyms: 维采宁 2) 目录号 : GC37902

A flavonoid glycoside with diverse biological activities

Vicenin 2 Chemical Structure

Cas No.:23666-13-9

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产品描述

Vicenin-2 is a polyketide synthase-derived flavonoid glycoside that has been found in C. subternata and has diverse biological activities.1,2,3,4,5 It inhibits thrombin-induced aggregation of isolated mouse platelets when used at concentrations ranging from 2 to 30 ?M, as well as increases tail bleeding time in mice when administered at a dose of 35.7 ?g/animal.2 Vicenin-2 (1 mg/kg) reduces tumor growth in a PC3 prostate cancer mouse xenograft model.3 It decreases trabecular separation, as well as increases trabecular thickness and area, in an ovariectomized rat model of osteoporosis.4 Vicenin-2 (50 mg/kg) decreases ulceration and increases colon weight and length in a mouse model of colitis induced by dextran sulfate .5

1.Kitamura, K., Ando, Y., Matsumoto, T., et al.Total synthesis of aryl C-glycoside natural products: Strategies and tacticsChem. Rev.118(4)1495-1598(2018) 2.Lee, W., and Bae, J.-S.Antithrombotic and antiplatelet activities of vicenin-2Blood Coagul. Fibrinolysis26(6)628-634(2015) 3.Nagaprashantha, L.D., Vatsyayan, R., Singhal, J., et al.Anti-cancer effects of novel flavonoid vicenin-2 as a single agent and in synergistic combination with docetaxel in prostate cancerBiochem. Pharmacol.82(9)1100-1109(2011) 4.Zhang, Z., Zhao, Q., Liu, T., et al.Effect of vicenin-2 on ovariectomy-induced osteoporosis in ratsBiomed. Pharmacother.129110474(2020) 5.Yin, Y., Ye, L., Niu, Z., et al.Anti-inflammatory effects of Vicenin-2 on dextran sulfate sodium-induced colitis in miceDrug Dev. Res.80(5)546-555(2019)

Chemical Properties

Cas No. 23666-13-9 SDF
别名 维采宁 2
Canonical SMILES OC1=C([C@@H]([C@@H]([C@@H](O)[C@@H]2O)O)O[C@@H]2CO)C(O)=C3C(OC(C4=CC=C(O)C=C4)=CC3=O)=C1[C@@H]([C@@H]([C@@H](O)[C@@H]5O)O)O[C@@H]5CO
分子式 C27H30O15 分子量 594.52
溶解度 DMSO : 33.33 mg/mL (56.06 mM; Need ultrasonic); H2O : < 0.1 mg/mL (insoluble) 储存条件 4°C, protect from light
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1 mg 5 mg 10 mg
1 mM 1.682 mL 8.4101 mL 16.8203 mL
5 mM 0.3364 mL 1.682 mL 3.3641 mL
10 mM 0.1682 mL 0.841 mL 1.682 mL
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Research Update

Vicenin 2 isolated from Artemisia capillaris exhibited potent anti-glycation properties

Food Chem Toxicol 2014 Jul;69:55-62.PMID:24713265DOI:10.1016/j.fct.2014.03.042.

Vicenin 2, isolated from a traditionally used medicinal plant Artemisia capillaris, is a 6,8-di-C-glucoside of apigenin which has been previously reported to possess a wide variety of pharmacological activities including antioxidant, anti-inflammatory, anti-cancer, and hepatoprotective. However, there have not been any reports concerning its anti-diabetic potential until now. Therefore, in the present study, we evaluated the anti-diabetic potential of Vicenin 2 via α-glucosidase, protein tyrosine phosphatase 1B (PTP1B), rat lens aldose reductase (RLAR), and advanced glycation end products (AGE) formation inhibitory assays. Vicenin 2 strongly inhibited α-glucosidase, PTP1B, and RLAR in the corresponding assays. In addition, Vicenin 2 inhibited the formation of both fluorescent AGE and nonfluorescent AGE, e.g., CML, as well as the level of fructosamine in glucose-fructose-induced bovine serum albumin (BSA) glycation. In the test system, Vicenin 2 suppressed glycation-induced protein oxidation by attenuating the formation of protein carbonyl groups as well as by inhibiting the modification of protein thiol groups. Moreover, Vicenin 2 was found to be a potent inhibitor of glycation-induced formation of amyloid cross-β structures in BSA. Taken together, Vicenin 2 might be a useful lead for the development of multiple target-oriented therapeutic modalities for the treatment of diabetes and diabetes-associated complications.

Testing of Perilla frutescens extract and Vicenin 2 for their antispasmodic effect

Phytomedicine 2013 Mar 15;20(5):427-31.PMID:23357362DOI:10.1016/j.phymed.2012.12.018.

Gastrointestinal discomfort is frequently observed. The effects of Perilla frutescens extract and Vicenin 2 (a compound in this extract) were assayed in rat ileum with or without stimulation with acetylcholine or Ba(2+). Both had no direct spasmolytic effect, but both decreased acetylcholine- or Ba(2+)-induced contraction of rat ileum indicating an antispasmodic effect. This is valuable because effects were only observed when spasms were induced and may disturb the patient. The extract and the compound may be used to maintain and improve gut health.