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(-)-3-Demethylcolchicine

CAS# 7336-33-6

(-)-3-Demethylcolchicine

2D Structure

Catalog No. BCX1192----Order now to get a substantial discount!

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Quality Control of (-)-3-Demethylcolchicine

3D structure

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(-)-3-Demethylcolchicine

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Chemical Properties of (-)-3-Demethylcolchicine

Cas No. 7336-33-6 SDF Download SDF
PubChem ID 299664.0 Appearance Powder
Formula C21H23NO6 M.Wt 385.42
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name N-[(7S)-3-hydroxy-1,2,10-trimethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide
SMILES CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)O
Standard InChIKey JRRUSQGIRBEMRN-HNNXBMFYSA-N
Standard InChI InChI=1S/C21H23NO6/c1-11(23)22-15-7-5-12-9-17(25)20(27-3)21(28-4)19(12)13-6-8-18(26-2)16(24)10-14(13)15/h6,8-10,15,25H,5,7H2,1-4H3,(H,22,23)/t15-/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.
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.
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.

(-)-3-Demethylcolchicine Dilution Calculator

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(-)-3-Demethylcolchicine Molarity Calculator

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Preparing Stock Solutions of (-)-3-Demethylcolchicine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.5946 mL 12.9729 mL 25.9457 mL 51.8914 mL 64.8643 mL
5 mM 0.5189 mL 2.5946 mL 5.1891 mL 10.3783 mL 12.9729 mL
10 mM 0.2595 mL 1.2973 mL 2.5946 mL 5.1891 mL 6.4864 mL
50 mM 0.0519 mL 0.2595 mL 0.5189 mL 1.0378 mL 1.2973 mL
100 mM 0.0259 mL 0.1297 mL 0.2595 mL 0.5189 mL 0.6486 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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References on (-)-3-Demethylcolchicine

New colchicinoids from a native Jordanian meadow saffron, colchicum brachyphyllum: isolation of the first naturally occurring dextrorotatory colchicinoid.[Pubmed:15730238]

J Nat Prod. 2005 Feb;68(2):173-8.

As part of our continuing investigation of Jordanian Colchicum species, the biologically active components of Colchicum brachyphyllum were pursued. Using bioactivity-directed fractionation, nine colchicinoids were isolated and characterized. One of these has a novel ring system, to which we have ascribed the trivial name (+)-demecolcinone (9), and it represents the first naturally occurring dextrorotatory colchicinoid. Another isolated compound was a new colchicinoid analogue, (-)-2,3-didemethyldemecolcine (8), while the remaining seven known colchicinoids were new to the species: (-)-colchicine (1), (-)-3-Demethylcolchicine (2), (-)-cornigerine (3), beta-lumicolchicine (4), (-)-androbiphenyline (5), (-)-demecolcine (6), and (-)-3-demethyldemecolcine (7). The brine shrimp lethality test was used to direct the isolation of these colchicinoids. Moreover, all pure compounds were evaluated for cytotoxicity against a human cancer cell panel, for antimicrobial activity in an array of bacteria and fungi (including yeast), and for their potential to be allosteric modulators of the gamma-aminobutyric acid type A receptor.

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