Gynuramide II

CAS# 295803-03-1

Gynuramide II

Catalog No. BCN5200----Order now to get a substantial discount!

Product Name & Size Price Stock
Gynuramide II: 5mg $374 In Stock
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Quality Control of Gynuramide II

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Chemical structure

Gynuramide II

3D structure

Chemical Properties of Gynuramide II

Cas No. 295803-03-1 SDF Download SDF
PubChem ID 76312320 Appearance Powder
Formula C42H83NO5 M.Wt 682.1
Type of Compound Cerebrosides Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (2R)-2-hydroxy-N-[(E,2S,3S,4R)-1,3,4-trihydroxyoctadec-8-en-2-yl]tetracosanamide
SMILES CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(CO)C(C(CCCC=CCCCCCCCCC)O)O)O
Standard InChIKey BIVGPKIBTGZJJH-BMAQVQEHSA-N
Standard InChI InChI=1S/C42H83NO5/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-26-28-30-32-34-36-40(46)42(48)43-38(37-44)41(47)39(45)35-33-31-29-27-25-16-14-12-10-8-6-4-2/h27,29,38-41,44-47H,3-26,28,30-37H2,1-2H3,(H,43,48)/b29-27+/t38-,39+,40+,41-/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 Gynuramide II

The herbs of Exochorda racemosa (Lindl.) Rehd

Protocol of Gynuramide II

Structure Identification
Zhongguo Zhong Yao Za Zhi. 2011 May;36(9):1198-201.

Chemical constituents from Exochorda racemosa.[Pubmed: 21842649]


METHODS AND RESULTS:
Twenty compounds were isolated and identified as N-p-coumaroyl-N'-caffeoylputrescine (1), sutherlandin trans-p-coumarate (2), apigenin 7-O-methylglucuronide (3), astragalin (4), nicotiflorin (5), kaempferol 3-neohesperidoside (6), rutin (7), apigenin (8), luteolin (9), linalool-1-oic acid (10), betulalbuside A (11), ursolic acid (12) , corosolic acid (13), Gynuramide II (14), beta-sitosterol (15), daucosterol (16), uridine (17), adenosine (18), syringin (19), and trans4-hydroxycinnamic acid (20), respectively.
CONCLUSIONS:
All compounds were obtained from this plant for the first time, moreover, 1 was reported as a new natural product, and 2 is a naturally rare cyanogenic glycoside.

Gynuramide II Dilution Calculator

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Gynuramide II Molarity Calculator

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Preparing Stock Solutions of Gynuramide II

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.4661 mL 7.3303 mL 14.6606 mL 29.3212 mL 36.6515 mL
5 mM 0.2932 mL 1.4661 mL 2.9321 mL 5.8642 mL 7.3303 mL
10 mM 0.1466 mL 0.733 mL 1.4661 mL 2.9321 mL 3.6652 mL
50 mM 0.0293 mL 0.1466 mL 0.2932 mL 0.5864 mL 0.733 mL
100 mM 0.0147 mL 0.0733 mL 0.1466 mL 0.2932 mL 0.3665 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 Gynuramide II

[Chemical constituents from Exochorda racemosa].[Pubmed:21842649]

Zhongguo Zhong Yao Za Zhi. 2011 May;36(9):1198-201.

OBJECTIVE: To study the chemical constituents of Exochorda racemosa. METHOD: Compounds were isolated and purified by silica gel, Sephadex LH-20, MCI gel and RP-18 column chromatography, and their structures were determined by spectroscopic analysis. RESULT: Twenty compounds were isolated and identified as N-p-coumaroyl-N'-caffeoylputrescine (1), sutherlandin trans-p-coumarate (2), apigenin 7-O-methylglucuronide (3), astragalin (4), nicotiflorin (5), kaempferol 3-neohesperidoside (6), rutin (7), apigenin (8), luteolin (9), linalool-1-oic acid (10), betulalbuside A (11), ursolic acid (12) , corosolic acid (13), Gynuramide II (14), beta-sitosterol (15), daucosterol (16), uridine (17), adenosine (18), syringin (19), and trans4-hydroxycinnamic acid (20), respectively. CONCLUSION: All compounds were obtained from this plant for the first time, moreover, 1 was reported as a new natural product, and 2 is a naturally rare cyanogenic glycoside.

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