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Dexamethasone dipropionate

CAS# 55541-30-5

Dexamethasone dipropionate

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Chemical structure

Dexamethasone dipropionate

3D structure

Chemical Properties of Dexamethasone dipropionate

Cas No. 55541-30-5 SDF Download SDF
PubChem ID 63049 Appearance Powder
Formula C28H37FO7 M.Wt 504.6
Type of Compound N/A Storage Desiccate at -20°C
Synonyms Methaderm
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [2-[(8S,9R,10S,11S,13S,14S,16R,17R)-9-fluoro-11-hydroxy-10,13,16-trimethyl-3-oxo-17-propanoyloxy-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] propanoate
SMILES CCC(=O)OCC(=O)C1(C(CC2C1(CC(C3(C2CCC4=CC(=O)C=CC43C)F)O)C)C)OC(=O)CC
Standard InChIKey CIWBQSYVNNPZIQ-PKWREOPISA-N
Standard InChI InChI=1S/C28H37FO7/c1-6-23(33)35-15-22(32)28(36-24(34)7-2)16(3)12-20-19-9-8-17-13-18(30)10-11-25(17,4)27(19,29)21(31)14-26(20,28)5/h10-11,13,16,19-21,31H,6-9,12,14-15H2,1-5H3/t16-,19+,20+,21+,25+,26+,27+,28+/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.
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.

Dexamethasone dipropionate Dilution Calculator

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Dexamethasone dipropionate Molarity Calculator

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Preparing Stock Solutions of Dexamethasone dipropionate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.9818 mL 9.9088 mL 19.8177 mL 39.6354 mL 49.5442 mL
5 mM 0.3964 mL 1.9818 mL 3.9635 mL 7.9271 mL 9.9088 mL
10 mM 0.1982 mL 0.9909 mL 1.9818 mL 3.9635 mL 4.9544 mL
50 mM 0.0396 mL 0.1982 mL 0.3964 mL 0.7927 mL 0.9909 mL
100 mM 0.0198 mL 0.0991 mL 0.1982 mL 0.3964 mL 0.4954 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 Dexamethasone dipropionate

Dexamethasone dipropionate loaded nanoparticles of alpha-elastin-g-PLGA for potential treatment of restenosis.[Pubmed:24206105]

Mol Pharm. 2013 Dec 2;10(12):4603-10.

A graft copolymer of alpha-elastin with poly(lactic-co-glycolic) acid (PLGA) has been synthesized and successfully employed to produce nanoparticles. Exploiting the known biological activity of alpha-elastin to promote the maintenance of smooth muscle cells (SMCs) contractile phenotype and the antiproliferative effect of glucocorticoids, the aim of this research was to produce drug-loaded nanoparticles suitable for potential treatment of restenosis. In particular, nanoparticles of alpha-elastin-g-PLGA with a mean size of 200 nm have been produced and loaded with Dexamethasone dipropionate (10% w/w), chosen as a model drug that inhibits proliferation of vascular SMCs. These nanoparticles are able to prolong the drug release and show a pronounced sensibility to elastase. Drug unloaded nanoparticles stimulate the differentiation of human umbilical artery smooth muscle cells (HUASMCs) toward the contractile phenotype as demonstrated by immunofluorescence, flow cytofluorimetric, and western blotting analyses. Finally, drug-loaded nanoparticles efficiently reduce viability of HUASMCs as evidenced by 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2- (4-sulfophenyl)-2H-tetrazolium, inner salt (MTS) assay.

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