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1-Methoxyallocryptopine

CAS# 56743-52-3

1-Methoxyallocryptopine

Catalog No. BCN7454----Order now to get a substantial discount!

Product Name & Size Price Stock
1-Methoxyallocryptopine: 5mg $748 In Stock
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Quality Control of 1-Methoxyallocryptopine

Number of papers citing our products

Chemical structure

1-Methoxyallocryptopine

3D structure

Chemical Properties of 1-Methoxyallocryptopine

Cas No. 56743-52-3 SDF Download SDF
PubChem ID 363693 Appearance Powder
Formula C22H25NO6 M.Wt 399.44
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CN1CCC2=CC3=C(C(=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OC)OCO3
Standard InChIKey LLTCRRPEZHDFFY-UHFFFAOYSA-N
Standard InChI InChI=1S/C22H25NO6/c1-23-8-7-14-10-18-21(29-12-28-18)22(27-4)19(14)16(24)9-13-5-6-17(25-2)20(26-3)15(13)11-23/h5-6,10H,7-9,11-12H2,1-4H3
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 1-Methoxyallocryptopine

The herbs of Turkish Papaver curviscapum.

Biological Activity of 1-Methoxyallocryptopine

Description1-Methoxyallocryptopine is a natural product from Turkish Papaver curviscapum.

Protocol of 1-Methoxyallocryptopine

Structure Identification
Journal of Natural Products, 1983, 46(2):251-255.

The Stereochemistry and 13 C Nmr Spectra of Protopinium Salts.[Reference: WebLink]


METHODS AND RESULTS:
The 13C nmr spectra for protopine (1), allocryptopine (4), 1-Methoxyallocryptopine (5), hunnemanine (6), and thalictricine (7), were recorded in TFA-d solution. There is a predominance of the cis protopinium salt over the trans isomer, except in the case of thalictricine where the trans salt is the major isomer.
CONCLUSIONS:
The chemical shifts of C-6, C-13 and the N-methyl group are particularly diagnostic of the stereochemistry of the protopinium salts.

1-Methoxyallocryptopine Dilution Calculator

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1-Methoxyallocryptopine Molarity Calculator

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Preparing Stock Solutions of 1-Methoxyallocryptopine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.5035 mL 12.5175 mL 25.035 mL 50.0701 mL 62.5876 mL
5 mM 0.5007 mL 2.5035 mL 5.007 mL 10.014 mL 12.5175 mL
10 mM 0.2504 mL 1.2518 mL 2.5035 mL 5.007 mL 6.2588 mL
50 mM 0.0501 mL 0.2504 mL 0.5007 mL 1.0014 mL 1.2518 mL
100 mM 0.025 mL 0.1252 mL 0.2504 mL 0.5007 mL 0.6259 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 1-Methoxyallocryptopine

The Stereochemistry and 13 C Nmr Spectra of Protopinium Salts.

Journal of Natural Products, 1983, 46(2):251-255.

The 13C nmr spectra for protopine (1), allocryptopine (4), 1-Methoxyallocryptopine (5), hunnemanine (6), and thalictricine (7), were recorded in TFA-d solution. There is a predominance of the cis protopinium salt over the trans isomer, except in the case of thalictricine where the trans salt is the major isomer. The chemical shifts of C-6, C-13 and the N-methyl group are particularly diagnostic of the stereochemistry of the protopinium salts.

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