Helenien

CAS# 547-17-1

Helenien

Catalog No. BCN0154----Order now to get a substantial discount!

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Quality Control of Helenien

Number of papers citing our products

Chemical structure

Helenien

3D structure

Chemical Properties of Helenien

Cas No. 547-17-1 SDF Download SDF
PubChem ID 5281240 Appearance Powder
Formula C72H116O4 M.Wt 1045.7
Type of Compound Miscellaneous Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [(1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R,4R)-4-hexadecanoyloxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-yl] hexadecanoate
SMILES CCCCCCCCCCCCCCCC(=O)OC1CC(=C(C(C1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)OC(=O)CCCCCCCCCCCCCCC)C)C)C)C
Standard InChIKey YHGJHDJZIOYZIR-URPSFYETSA-N
Standard InChI InChI=1S/C72H116O4/c1-13-15-17-19-21-23-25-27-29-31-33-35-37-49-69(73)75-65-55-63(7)67(71(9,10)57-65)53-51-61(5)47-41-45-59(3)43-39-40-44-60(4)46-42-48-62(6)52-54-68-64(8)56-66(58-72(68,11)12)76-70(74)50-38-36-34-32-30-28-26-24-22-20-18-16-14-2/h39-48,51-55,65-67H,13-38,49-50,56-58H2,1-12H3/b40-39+,45-41+,46-42+,53-51+,54-52+,59-43+,60-44+,61-47+,62-48+/t65-,66+,67-/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.

Source of Helenien

The herbs of Tagetes erecta

Biological Activity of Helenien

DescriptionReference standards.

Helenien Dilution Calculator

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Helenien Molarity Calculator

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Preparing Stock Solutions of Helenien

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 0.9563 mL 4.7815 mL 9.563 mL 19.1259 mL 23.9074 mL
5 mM 0.1913 mL 0.9563 mL 1.9126 mL 3.8252 mL 4.7815 mL
10 mM 0.0956 mL 0.4781 mL 0.9563 mL 1.9126 mL 2.3907 mL
50 mM 0.0191 mL 0.0956 mL 0.1913 mL 0.3825 mL 0.4781 mL
100 mM 0.0096 mL 0.0478 mL 0.0956 mL 0.1913 mL 0.2391 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 Helenien

Effect of nilvadipine on central visual field in retinitis pigmentosa: a 30-month clinical trial.[Pubmed:20948238]

Ophthalmologica. 2011;225(2):120-6.

PURPOSE: To assess the effects of nilvadipine on the progression of central visual field defect in retinitis pigmentosa (RP). DESIGN: Prospective, randomized, nonmasked, single-center trial. METHODS: Patients with RP were randomly divided into a treated group receiving oral nilvadipine at 4 mg/day for >/=30 months and a control group receiving tocopherol nicotinate at 300 mg/day, Helenien at 15 mg/day or no medication for the same periods. Progression of RP was evaluated using the 10-2 SITA Fast Program of the Humphrey Visual Field Analyzer, and regression coefficients calculated from the time courses of mean deviation (MD slope) were compared between groups. RESULTS: Nineteen patients in the treated group and 14 patients in the control group completed the follow-up for >/=30 months. The mean (+/-standard deviation) duration of observation was 48.8 +/- 11.8 months (median 48 months, range 30-66 months) for the treated group and 49.2 +/- 18.1 months (median 48 months, range 30-90 months) for the control group (p = 0.94). Mean (+/-standard error of the mean, SEM) regression coefficients of the averaged MD values for the initial 30 months were -0.35 +/- 0.17 dB/year in the treated group and -0.75 +/- 0.06 dB/year in the control group (p < 0.01). Mean (+/-SEM) MD slopes for total observational periods were -0.49 +/- 0.17 dB/year in the treated group and -0.89 +/- 0.16 dB/year in the control group (mean +/- SEM, p = 0.042). CONCLUSION: Nilvadipine at 4 mg/day significantly retarded progression of central visual field defects in RP in this small patient series.

[Effects of cyaninoside chloride and Heleniene on mesopic and scotopic vision in myopia and night blindness].[Pubmed:6381579]

J Fr Ophtalmol. 1984;7(1):35-9.

A controlled, clinical trial, comparing cyaninoside chloride and Heleniene , was conducted on 31 out-patients suffering from functional disturbances of vision in low-luminance conditions. The evolution of photopic and mesopic visual acuities, electro- oculograms and adapto -electroretinograms was assessed for both treatment groups and controls. Both agents significantly improved photopic visual acuity (p less than 0.05). Only cyaninoside chloride treatment improved visual functions related to mesopic and scotopic vision (p less than 0.01). There were also significant differences between the two treatment groups regarding the velocity of visual adaptation in adapto -electroretinography. This study thus demonstrates the therapeutic value of cyaninoside chloride for the treatment of functional disturbances of mesopic and scotopic vision, especially in night blindness and myopia.

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