Cinchonain IIa

CAS# 85081-23-8

Cinchonain IIa

Catalog No. BCN7716----Order now to get a substantial discount!

Product Name & Size Price Stock
Cinchonain IIa: 5mg $1098 In Stock
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Chemical structure

Cinchonain IIa

3D structure

Chemical Properties of Cinchonain IIa

Cas No. 85081-23-8 SDF Download SDF
PubChem ID 11765545 Appearance Powder
Formula C39H32O15 M.Wt 740.66
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (2R,3R,4S,10R)-2,10-bis(3,4-dihydroxyphenyl)-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5-dihydroxy-3,4,9,10-tetrahydro-2H-pyrano[2,3-h]chromen-8-one
SMILES C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C5C(CC(=O)OC5=CC(=C34)O)C6=CC(=C(C=C6)O)O)C7=CC(=C(C=C7)O)O)O)O)O)C8=CC(=C(C=C8)O)O)O
Standard InChIKey NWZBNZUABGSPSN-WRYDCQAKSA-N
Standard InChI InChI=1S/C39H32O15/c40-19-4-1-14(7-23(19)44)17-11-30(50)52-29-13-27(48)33-34(35(51)37(54-39(33)31(17)29)16-3-6-21(42)25(46)9-16)32-26(47)12-22(43)18-10-28(49)36(53-38(18)32)15-2-5-20(41)24(45)8-15/h1-9,12-13,17,28,34-37,40-49,51H,10-11H2/t17-,28-,34+,35-,36-,37-/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 Cinchonain IIa

The barks of Kandelia candel (L.) DRUCE.

Biological Activity of Cinchonain IIa

Description1. Cinchonain IIa has antioxidant activity, it shows high radical scavenging activity and reducing power.

Cinchonain IIa Dilution Calculator

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Cinchonain IIa Molarity Calculator

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Preparing Stock Solutions of Cinchonain IIa

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.3501 mL 6.7507 mL 13.5015 mL 27.0029 mL 33.7537 mL
5 mM 0.27 mL 1.3501 mL 2.7003 mL 5.4006 mL 6.7507 mL
10 mM 0.135 mL 0.6751 mL 1.3501 mL 2.7003 mL 3.3754 mL
50 mM 0.027 mL 0.135 mL 0.27 mL 0.5401 mL 0.6751 mL
100 mM 0.0135 mL 0.0675 mL 0.135 mL 0.27 mL 0.3375 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 Cinchonain IIa

Flavan-3-ol-phenylpropanoid conjugates from Anemopaegma arvense and their antioxidant activities.[Pubmed:17642036]

Planta Med. 2007 Aug;73(10):1107-11.

One of the species of commercially available catuaba was identified as Anemopaegma arvense by comparison of its micromorphological characteristics and TLC profile with six species of authenticated plants that are commonly referred to as catuaba. The bioactivity-guided fractionation of the ethyl acetate extract of the stem bark of this catuaba sample resulted in the isolation of one new (1, catuabin A) and three known flavan-3-ol type phenylpropanoids, cinchonain Ia (2), Cinchonain IIa (3), and kandelin A1 (4) with antioxidant activities. The structures of these compounds were determined by a combination of spectroscopic techniques. Additionally, these compounds were tested for their anti-inflammatory, cytotoxicity, antimalarial, and antimicrobial activities, where no activity was observed.

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