Furanoeudesma 1,3-dieneCAS# 87605-93-4 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 87605-93-4 | SDF | Download SDF |
PubChem ID | 643237 | Appearance | Cream - beige waxy |
Formula | C15H18O | M.Wt | 214.3 |
Type of Compound | Sesquiterpenoids | Storage | Desiccate at -20°C |
Solubility | Soluble in ethanol and methan | ||
Chemical Name | (4aS,8aS)-3,5,8a-trimethyl-4a,9-dihydro-4H-benzo[f][1]benzofuran | ||
SMILES | CC1=CC=CC2(C1CC3=C(C2)OC=C3C)C | ||
Standard InChIKey | AUSAHAHDEVYCOC-DZGCQCFKSA-N | ||
Standard InChI | InChI=1S/C15H18O/c1-10-5-4-6-15(3)8-14-12(7-13(10)15)11(2)9-16-14/h4-6,9,13H,7-8H2,1-3H3/t13-,15+/m0/s1 | ||
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 | Reference standards. |
Furanoeudesma 1,3-diene Dilution Calculator
Furanoeudesma 1,3-diene Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 4.6664 mL | 23.3318 mL | 46.6636 mL | 93.3271 mL | 116.6589 mL |
5 mM | 0.9333 mL | 4.6664 mL | 9.3327 mL | 18.6654 mL | 23.3318 mL |
10 mM | 0.4666 mL | 2.3332 mL | 4.6664 mL | 9.3327 mL | 11.6659 mL |
50 mM | 0.0933 mL | 0.4666 mL | 0.9333 mL | 1.8665 mL | 2.3332 mL |
100 mM | 0.0467 mL | 0.2333 mL | 0.4666 mL | 0.9333 mL | 1.1666 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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The anti-dermatophyte activity of Commiphora molmol.[Pubmed:26427766]
Pharm Biol. 2016;54(4):720-5.
CONTEXT: Commiphora molmol Engl (Burseraceae) or myrrh has been traditionally used for the treatment of skin fungal infections. OBJECTIVE: This study evaluates the antifungal activity of myrrh ethanol extract and essential oil against skin dermatophytes. MATERIALS AND METHODS: The antifungal evaluations were performed by the food poisoning technique (250 ppm) and micro-broth dilution assay (800-6.25 microg/mL) against Trichophyton rubrum, T. mentagrophytes, Microsporum canis, M. gypseum, and T. verrucosum. The chemical composition of myrrh oil and ethanol extract was analyzed by GC and GC-MS. RESULTS: Furanoeudesma 1,3-diene and menthofuran were the main components of myrrh oil, while 2-tert-butyl-1,4-naphthoquinone, benzenemethanol,3-methoxy-alpha-phenyl, and curzerene were the main components of myrrh ethanol extract. The inhibitory effect of myrrh oil and ethanol extract against dermatophytes were 43.1-61.6% and 12.5-27.5%, respectively. The MIC and MFC values of myrrh oil were 25-100 and 25-200 microg/mL while these amounts for ethanol extract were 25-400 and 25-400 microg/mL, respectively. Therefore, myrrh oil had higher antifungal activity than that of the ethanol extract. Both extracts showed good anti-elastase activity. CONCLUSION: The results of our investigation confirmed the traditional uses of C. molmol as a poultice for the treatment of cutaneous fungal infections.