ChelidimerineCAS# 39110-99-1 |
Quality Control & MSDS
3D structure
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Number of papers citing our products
| Cas No. | 39110-99-1 | SDF | Download SDF |
| PubChem ID | 190990 | Appearance | Powder |
| Formula | C43H32N2O9 | M.Wt | 720.73 |
| Type of Compound | Alkaloids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 1-[(23~{S})-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaen-23-yl]-3-(24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaen-23-yl)propan-2-one | ||
| SMILES | CN1C(C2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6)CC(=O)CC7C8=C(C=CC9=C8OCO9)C1=C(N7C)C2=CC3=C(C=C2C=C1)OCO3 | ||
| Standard InChIKey | NIQFOSSBJJDEES-FSRLHOSWSA-N | ||
| Standard InChI | InChI=1S/C43H32N2O9/c1-44-30(38-24(7-9-32-42(38)53-19-47-32)26-5-3-21-11-34-36(51-17-49-34)15-28(21)40(26)44)13-23(46)14-31-39-25(8-10-33-43(39)54-20-48-33)27-6-4-22-12-35-37(52-18-50-35)16-29(22)41(27)45(31)2/h3-12,15-16,30-31H,13-14,17-20H2,1-2H3/t30-,31?/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. | ||
| Structure Identification | Zhongguo Zhong Yao Za Zhi. 2009 Jul;34(13):1683-6.Alkaloids from Macleaya cordata.[Pubmed: 19873781]To study the alkaloids of Macleaya cordata.
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Chelidimerine Dilution Calculator
Chelidimerine Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.3875 mL | 6.9374 mL | 13.8748 mL | 27.7496 mL | 34.6871 mL |
| 5 mM | 0.2775 mL | 1.3875 mL | 2.775 mL | 5.5499 mL | 6.9374 mL |
| 10 mM | 0.1387 mL | 0.6937 mL | 1.3875 mL | 2.775 mL | 3.4687 mL |
| 50 mM | 0.0277 mL | 0.1387 mL | 0.2775 mL | 0.555 mL | 0.6937 mL |
| 100 mM | 0.0139 mL | 0.0694 mL | 0.1387 mL | 0.2775 mL | 0.3469 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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[Alkaloids from Macleaya cordata].[Pubmed:19873781]
Zhongguo Zhong Yao Za Zhi. 2009 Jul;34(13):1683-6.
OBJECTIVE: To study the alkaloids of Macleaya cordata. METHOD: The alkaloids were isolated and purified by various column chromatography as well as recrystallization. Their structures were identified by physico-chemical properties and spectral analysis. RESULT: Thirteen alkaloids were isolated and identified as 6-methoxy-dihydrosanguinarine (1), norsanguinarine (2), 6-acetonyl-dihyrochelerythrine (3), 6-acetonyl-dihyrosanguinnarine (4), sanguidimerine (5), Chelidimerine (6), (+/-) -bocconarborine A (7), (+/-)-bocconarborine B (8), cryptopine (9), dihydrosanguinarine (10), dihydrochelerythrine (11), protopine (12), alpha-allocryptopine (13). CONCLUSION: Compounds 2, 3, 5 - 9 were firstly isolated from the genus Macleaya and compound 1 was obtained from M. cordata for the first time.
