alpha-AsaroneCAS# 2883-98-9 |
- beta-Asarone
Catalog No.:BCN5685
CAS No.:5273-86-9
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 2883-98-9 | SDF | Download SDF |
PubChem ID | 636822 | Appearance | White powder |
Formula | C12H16O3 | M.Wt | 208.25 |
Type of Compound | Phenylpropanoids | Storage | Desiccate at -20°C |
Synonyms | trans-Asarone; Asarum camphor; trans-Isoasarone | ||
Solubility | DMSO : 100 mg/mL (480.19 mM; Need ultrasonic) H2O : < 0.1 mg/mL (insoluble) | ||
Chemical Name | 1,2,4-trimethoxy-5-[(E)-prop-1-enyl]benzene | ||
SMILES | CC=CC1=CC(=C(C=C1OC)OC)OC | ||
Standard InChIKey | RKFAZBXYICVSKP-AATRIKPKSA-N | ||
Standard InChI | InChI=1S/C12H16O3/c1-5-6-9-7-11(14-3)12(15-4)8-10(9)13-2/h5-8H,1-4H3/b6-5+ | ||
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
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About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
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Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. |
Description | 1. Alpha-Asarone shows insecticidal activity. |
alpha-Asarone Dilution Calculator
alpha-Asarone Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 4.8019 mL | 24.0096 mL | 48.0192 mL | 96.0384 mL | 120.048 mL |
5 mM | 0.9604 mL | 4.8019 mL | 9.6038 mL | 19.2077 mL | 24.0096 mL |
10 mM | 0.4802 mL | 2.401 mL | 4.8019 mL | 9.6038 mL | 12.0048 mL |
50 mM | 0.096 mL | 0.4802 mL | 0.9604 mL | 1.9208 mL | 2.401 mL |
100 mM | 0.048 mL | 0.2401 mL | 0.4802 mL | 0.9604 mL | 1.2005 mL |
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. |
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Corrigendum: Oral Administration of alpha-Asarone Promotes Functional Recovery in Rats With Spinal Cord Injury.[Pubmed:30202415]
Front Pharmacol. 2018 Aug 30;9:949.
[This corrects the article DOI: 10.3389/fphar.2018.00445.].
Oral Administration of alpha-Asarone Promotes Functional Recovery in Rats With Spinal Cord Injury.[Pubmed:29867457]
Front Pharmacol. 2018 May 7;9:445.
alpha-Asarone, a bioactive compound found in Acorus plant species, has been shown to exhibit neuroprotective, anti-oxidative, anti-inflammatory, and cognitive-enhancing effects. However, the effects of alpha-Asarone on spinal cord injury (SCI) have not yet been elucidated. The present study investigated the effects of alpha-Asarone on the mRNA of pro-inflammatory cytokines, macrophage polarization toward an anti-inflammatory M2 phenotype, and angiogenesis in rats with compressive SCI. alpha-Asarone was orally administered (10 mg/kg) once per day for 14 days following moderate static compression SCI. Compared to controls, alpha-Asarone treatment significantly improved locomotor score, prevented neuroinflammation, and facilitated angiogenesis in the spinal cord at 14 days after SCI. Furthermore, alpha-Asarone significantly reduced the TNF-alpha, IL-1beta, IL-6, monocyte chemoattractant protein 1 (MCP-1), macrophage inflammatory protein 2 (MIP-2), and inducible nitric oxide synthase (iNOS) levels but increased the IL-4, IL-10, and arginase 1 levels at 24 h after SCI. At 7 and 14 days after SCI, immunohistochemistry showed reduced reactive gliosis and neuroinflammation and an increased expression of M2 macrophage markers and angiogenesis. The results suggest that the inhibition of pro-inflammatory cytokines, macrophage polarization toward an anti-inflammatory M2 phenotype, and angiogenesis by alpha-Asarone may be some of the mechanisms underlying the alpha-Asarone-mediated neuroprotective effects on an injured spinal cord.