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Picfeltarraegenin I

CAS# 82145-63-9

Picfeltarraegenin I

Catalog No. BCX0823----Order now to get a substantial discount!

Product Name & Size Price Stock
Picfeltarraegenin I: 5mg Please Inquire In Stock
Picfeltarraegenin I: 10mg Please Inquire In Stock
Picfeltarraegenin I: 20mg Please Inquire Please Inquire
Picfeltarraegenin I: 50mg Please Inquire Please Inquire
Picfeltarraegenin I: 100mg Please Inquire Please Inquire
Picfeltarraegenin I: 200mg Please Inquire Please Inquire
Picfeltarraegenin I: 500mg Please Inquire Please Inquire
Picfeltarraegenin I: 1000mg Please Inquire Please Inquire

Quality Control of Picfeltarraegenin I

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Chemical structure

Picfeltarraegenin I

3D structure

Chemical Properties of Picfeltarraegenin I

Cas No. 82145-63-9 SDF Download SDF
PubChem ID 343254.0 Appearance Powder
Formula C30H44O5 M.Wt 484.67
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2-(3,16-dihydroxy-4,4,9,13,14-pentamethyl-11-oxo-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)-2-methyl-5-propan-2-ylfuran-3-one
SMILES CC(C)C1=CC(=O)C(O1)(C)C2C(CC3(C2(CC(=O)C4(C3CC=C5C4CCC(C5(C)C)O)C)C)C)O
Standard InChIKey NROSHSGZKWDRMB-UHFFFAOYSA-N
Standard InChI InChI=1S/C30H44O5/c1-16(2)20-13-23(33)30(8,35-20)25-19(31)14-27(5)21-11-9-17-18(10-12-22(32)26(17,3)4)29(21,7)24(34)15-28(25,27)6/h9,13,16,18-19,21-22,25,31-32H,10-12,14-15H2,1-8H3
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.

Picfeltarraegenin I Dilution Calculator

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Picfeltarraegenin I Molarity Calculator

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Preparing Stock Solutions of Picfeltarraegenin I

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.0633 mL 10.3163 mL 20.6326 mL 41.2652 mL 51.5815 mL
5 mM 0.4127 mL 2.0633 mL 4.1265 mL 8.253 mL 10.3163 mL
10 mM 0.2063 mL 1.0316 mL 2.0633 mL 4.1265 mL 5.1581 mL
50 mM 0.0413 mL 0.2063 mL 0.4127 mL 0.8253 mL 1.0316 mL
100 mM 0.0206 mL 0.1032 mL 0.2063 mL 0.4127 mL 0.5158 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 Picfeltarraegenin I

A new cucurbitacin from Picria fel-terrae.[Pubmed:16864449]

J Asian Nat Prod Res. 2006 Jun;8(4):367-71.

A new cucurbitacin, picfeltarraenone II (1) as well as four known cucurbitacins, Picfeltarraegenin I (2), picfeltarraenin IA (3), picfeltarraenin IB (4), and picfeltarraenin IV (5), have been isolated and characterized from the whole plant of Picria fel-terrae. The purity of picfeltarraenin IA has been determined by TLC and HPLC.

Complement-inhibiting cucurbitacin glycosides from Picria fel-terrae.[Pubmed:9644059]

J Nat Prod. 1998 Jun 26;61(6):757-61.

Four cucurbitacin glycosides were isolated from Picriafel-terrae and identified by MS and NMR spectroscopy as picfeltarraenin IA (1), picfeltarraenin IB (2), picfeltarraenin IV (4), and a new compound picfeltarraenin VI (3) (Picfeltarraegenin I 3-O-beta-D-xylopyranoside). All four compounds acted as inhibitors on both the classical and alternative pathways of the complement system, with compound 3 exhibiting the highest inhibitory activity (IC50 29 +/- 2 microM and 21 +/- 1 microM, respectively). Compounds 1-4 showed no antiviral, antibacterial, or antifungal activities. Picfeltarraenin IA and IB were tested in an in vitro human tumor cell line panel, but displayed no cytotoxic activity.

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