Norjuziphine

CAS# 74119-87-2

Norjuziphine

Catalog No. BCN3367----Order now to get a substantial discount!

Product Name & Size Price Stock
Norjuziphine: 5mg Please Inquire In Stock
Norjuziphine: 10mg Please Inquire In Stock
Norjuziphine: 20mg Please Inquire Please Inquire
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Quality Control of Norjuziphine

Number of papers citing our products

Chemical structure

Norjuziphine

3D structure

Chemical Properties of Norjuziphine

Cas No. 74119-87-2 SDF Download SDF
PubChem ID 15690955 Appearance Cryst.
Formula C17H19NO3 M.Wt 285.3
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (1R)-1-[(4-hydroxyphenyl)methyl]-7-methoxy-1,2,3,4-tetrahydroisoquinolin-8-ol
SMILES COC1=C(C2=C(CCNC2CC3=CC=C(C=C3)O)C=C1)O
Standard InChIKey BXWMZVREXWPYKF-CQSZACIVSA-N
Standard InChI InChI=1S/C17H19NO3/c1-21-15-7-4-12-8-9-18-14(16(12)17(15)20)10-11-2-5-13(19)6-3-11/h2-7,14,18-20H,8-10H2,1H3/t14-/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.

Source of Norjuziphine

The tuber of Corydalis incisa

Biological Activity of Norjuziphine

Description1. Norjuziphine has antiplatelet aggregation activity.

Norjuziphine Dilution Calculator

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Norjuziphine Molarity Calculator

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Preparing Stock Solutions of Norjuziphine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.5051 mL 17.5254 mL 35.0508 mL 70.1016 mL 87.6271 mL
5 mM 0.701 mL 3.5051 mL 7.0102 mL 14.0203 mL 17.5254 mL
10 mM 0.3505 mL 1.7525 mL 3.5051 mL 7.0102 mL 8.7627 mL
50 mM 0.0701 mL 0.3505 mL 0.701 mL 1.402 mL 1.7525 mL
100 mM 0.0351 mL 0.1753 mL 0.3505 mL 0.701 mL 0.8763 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 Norjuziphine

A new tetrahydroprotoberberine N-oxide alkaloid and anti-platelet aggregation constituents of Corydalis tashiroi.[Pubmed:11488455]

Planta Med. 2001 Jul;67(5):423-7.

A new tetrahydroprotoberberine N-oxide alkaloid, (-)-cis-isocorypalmine N-oxide (1), together with two known compounds, 6-methoxydihydrosanguinarine (2) and Norjuziphine (3), were isolated in continuing studies of the entire Formosan Corydalis tashiroi plant. The structures of these three compounds were determined through spectral analyses. In addition, compounds 1, 2, 3 and the seven alkaloids previously reported: (-)-cis-corydalmine N-oxide, (-)-trans-corydalmine N-oxide, (-)-trans-isocorypalmine N-oxide, scoulerine, protopine, oxysanguinarine and corydalmine, were found to possess antiplatelet aggregation activity.

Additional alkaloids of Pachygone ovata.[Pubmed:6481360]

J Nat Prod. 1984 May-Jun;47(3):459-64.

Pachygone ovata (Menispermaceae), indigenous to the sandy seashores of southern India, is a woody climber whose fruits have been used as a rodenticide and fish poison. Chromatography of the extract of the roots resulted in the reisolation of the alkaloids liriodenine, coclaurine, trilobine (1), and magnoflorine and the isolation of stepholidine, coreximine, isoboldine, Norjuziphine, and nortrilobine (2). Nortrilobine (2) is a new dibenzo-p-dioxin bisbenzylisoquinoline alkaloid whose structure was established by a consideration of spectral data and conversion to isotrilobine (3).

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