Dactylorhin ACAS# 256459-34-4 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 256459-34-4 | SDF | Download SDF |
| PubChem ID | 132472108 | Appearance | Powder |
| Formula | C40H56O22 | M.Wt | 888.9 |
| Type of Compound | Miscellaneous | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | bis[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl] 2-(2-methylpropyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanedioate | ||
| SMILES | CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O | ||
| Standard InChIKey | QUCKZYFUROTIBC-ZKVFJGDSSA-N | ||
| Standard InChI | InChI=1S/C40H56O22/c1-18(2)11-40(62-38-35(53)32(50)29(47)25(15-43)61-38,39(54)56-17-20-5-9-22(10-6-20)58-37-34(52)31(49)28(46)24(14-42)60-37)12-26(44)55-16-19-3-7-21(8-4-19)57-36-33(51)30(48)27(45)23(13-41)59-36/h3-10,18,23-25,27-38,41-43,45-53H,11-17H2,1-2H3/t23-,24-,25-,27-,28-,29-,30+,31+,32+,33-,34-,35-,36-,37-,38+,40?/m1/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. | ||
The tubers of Gymnadenia conopsea
| Description | Dactylorhin A exhibits moderate inhibitory effect on NO production effects in RAW 264.7 macrophage cells. |
| Targets | NO |
| In vitro | Chemical constituents from Bletilla striata and their NO production suppression in RAW 264.7 macrophage cells.[Pubmed: 28617053 ]J Asian Nat Prod Res. 2018 Apr;20(4):385-390.A novel glucoside bletilloside A (1) was isolated from the tubers of Bletilla striata, together with seven known compounds (2-8). |
Dactylorhin A Dilution Calculator
Dactylorhin A Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.125 mL | 5.6249 mL | 11.2499 mL | 22.4997 mL | 28.1246 mL |
| 5 mM | 0.225 mL | 1.125 mL | 2.25 mL | 4.4999 mL | 5.6249 mL |
| 10 mM | 0.1125 mL | 0.5625 mL | 1.125 mL | 2.25 mL | 2.8125 mL |
| 50 mM | 0.0225 mL | 0.1125 mL | 0.225 mL | 0.45 mL | 0.5625 mL |
| 100 mM | 0.0112 mL | 0.0562 mL | 0.1125 mL | 0.225 mL | 0.2812 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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Chemical constituents from Bletilla striata and their NO production suppression in RAW 264.7 macrophage cells.[Pubmed:28617053]
J Asian Nat Prod Res. 2018 Apr;20(4):385-390.
A novel glucoside bletilloside A (1) was isolated from the tubers of Bletilla striata, together with seven known compounds (2-8). Their structures were determined on the basis of extensive spectroscopic analyses. All compounds were evaluated for the inhibition on NO production effects in RAW 264.7 macrophage cells, while militarine (4) and Dactylorhin A (5) exhibited moderate inhibitory effects.
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