Moracin DCAS# 69120-07-6 |
Quality Control & MSDS
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| Cas No. | 69120-07-6 | SDF | Download SDF |
| PubChem ID | 641378 | Appearance | Powder |
| Formula | C19H16O4 | M.Wt | 308.3 |
| Type of Compound | Phenols | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 7-(6-hydroxy-1-benzofuran-2-yl)-2,2-dimethylchromen-5-ol | ||
| SMILES | CC1(C=CC2=C(O1)C=C(C=C2O)C3=CC4=C(O3)C=C(C=C4)O)C | ||
| Standard InChIKey | CHAAQDMHLLQJRO-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C19H16O4/c1-19(2)6-5-14-15(21)7-12(9-18(14)23-19)16-8-11-3-4-13(20)10-17(11)22-16/h3-10,20-21H,1-2H3 | ||
| 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. | ||
The root bark of Morus alba L.
| Description | 1. Moracin C and moracin D, new phytoalexins from diseased mulberry, are antifungal compounds. 2. Moracin may be protective influence in tumor promotion, utilization of Moracin may open a new avenue in the treatment of tumerigenesis. |
| Targets | COX | c-Myc | TNF-α | Antifection |
Moracin D Dilution Calculator
Moracin D Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 3.2436 mL | 16.218 mL | 32.4359 mL | 64.8719 mL | 81.0898 mL |
| 5 mM | 0.6487 mL | 3.2436 mL | 6.4872 mL | 12.9744 mL | 16.218 mL |
| 10 mM | 0.3244 mL | 1.6218 mL | 3.2436 mL | 6.4872 mL | 8.109 mL |
| 50 mM | 0.0649 mL | 0.3244 mL | 0.6487 mL | 1.2974 mL | 1.6218 mL |
| 100 mM | 0.0324 mL | 0.1622 mL | 0.3244 mL | 0.6487 mL | 0.8109 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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Inhibitory effects of constituents from Morus alba var. multicaulis on differentiation of 3T3-L1 cells and nitric oxide production in RAW264.7 cells.[Pubmed:21772233]
Molecules. 2011 Jul 19;16(7):6010-22.
A new arylbenzofuran, 3',5'-dihydroxy-6-methoxy-7-prenyl-2-arylbenzofuran (1), and 25 known compounds, including moracin R (2), moracin C (3), moracin O (4), moracin P (5), artoindonesianin O (6), Moracin D (7), alabafuran A (8), mulberrofuran L (9), mulberrofuran Y (10), kuwanon A (11), kuwanon C (12), kuwanon T (13), morusin (14), kuwanon E (15), sanggenon F (16), betulinic acid (17), uvaol (18), ursolic acid (19), beta-sitosterol (20), oxyresveratrol 2-O-beta-D-glucopyranoside (21), mulberroside A (22), mulberroside B (23), 5,7-dihydroxycoumarin 7-O-beta-D-glucopyranoside (24), 5,7-dihydroxycoumarin 7-O-beta-D-apiofuranosyl-(1-->6)-O-beta-D-glucopyranoside (25) and adenosine (26), were isolated from Morus alba var. multicaulis Perro. (Moraceae). Their structures were determined by spectroscopic methods. The prenyl-flavonoids 11-14, 16, triterpenoids 17,18 and 20 showed significant inhibitory activity towards the differentiation of 3T3-L1 adipocytes. The arylbenzofurans 1-10 and prenyl-flavonoids 11-16 also showed significant nitric oxide (NO) production inhibitory effects in RAW264.7 cells.
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