Actinine

CAS# 407-64-7

Actinine

2D Structure

Catalog No. BCN1744----Order now to get a substantial discount!

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Quality Control of Actinine

3D structure

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Actinine

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Chemical Properties of Actinine

Cas No. 407-64-7 SDF Download SDF
PubChem ID 725 Appearance Powder
Formula C7H15NO2 M.Wt 145.2
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 4-(trimethylazaniumyl)butanoate
SMILES C[N+](C)(C)CCCC(=O)[O-]
Standard InChIKey JHPNVNIEXXLNTR-UHFFFAOYSA-N
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.

Source of Actinine

The herbs of Polyporus sulphureus

Biological Activity of Actinine

Description1. Actinine is the biosynthetic intermed, in synth. of Carnitine BDS79-T.

Actinine Dilution Calculator

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Actinine Molarity Calculator

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Preparing Stock Solutions of Actinine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 6.8871 mL 34.4353 mL 68.8705 mL 137.741 mL 172.1763 mL
5 mM 1.3774 mL 6.8871 mL 13.7741 mL 27.5482 mL 34.4353 mL
10 mM 0.6887 mL 3.4435 mL 6.8871 mL 13.7741 mL 17.2176 mL
50 mM 0.1377 mL 0.6887 mL 1.3774 mL 2.7548 mL 3.4435 mL
100 mM 0.0689 mL 0.3444 mL 0.6887 mL 1.3774 mL 1.7218 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 Actinine

[Expression of nephrin, podocin and a-actinine-4 in renal tissue of patients with proteinuria].[Pubmed:19936002]

Nefrologia. 2009;29(6):569-75.

INTRODUCTION: Slit diaphragm and/or podocyte's cytoskeleton alterations are related to proteinuria and nephrotic syndrome. In our population, focal and segmental glomerulosclerosis causing nephrotic syndrome is the more frequent biopsy demonstrated glomerulopathy. Our aim was search for alterations in some slit diaphragm-associated proteins in patients with nephrotic range proteinuria. METHODS: Renal tissue from 40 patients with nephrotic range proteinuria, 10 patients with non-nephrotic proteinuria, 3 with isolated hematuria, and 10 samples of normal renal tissue (deceased donors) were studied, by indirect immunofluorescence, for expression of nephrin, podocin, and alpha-actinin-4. RESULTS: Expression of these proteins was lineal, homogeneous, in the glomerular capillary walls in normal renal tissue and in patients with isolated hematuria. In nephrotic proteinuria this normal appearance was altered and immunostaining showed a fine granular appearance. In 18 cases (45%) of patients with nephrotic proteinuria and 3 cases (30%) of patients with non-nephrotic proteinuria there was loss of at least one of these proteins (p = 0.49). These alterations were found in the diverse glomerulopathies more frequently causing nephrotic syndrome. CONCLUSIONS: In nephrotic range proteinuria redistribution or loss of expression of slit diaphragm-associated proteins is very frequent. In many of our cases this fact could be more a consequence than a cause of proteinuria. These alterations can be also evidenced in patients with non-nephrotic proteinuria.

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