Pseudolarolide F

CAS# 412321-91-6

Pseudolarolide F

Catalog No. BCN6428----Order now to get a substantial discount!

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Quality Control of Pseudolarolide F

Number of papers citing our products

Chemical structure

Pseudolarolide F

3D structure

Chemical Properties of Pseudolarolide F

Cas No. 412321-91-6 SDF Download SDF
PubChem ID 134715230 Appearance Powder
Formula C30H42O7 M.Wt 514.65
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (1S,3'R,4R,5R,6R,8S,10R,12R,16R)-1-hydroxy-3',4,6,12,17,17-hexamethylspiro[9,18,24-trioxapentacyclo[19.2.1.04,12.05,10.016,22]tetracosa-20,22-diene-8,5'-oxolane]-2',19-dione
SMILES CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC5(C=C6C(CCCC4(C3)C)C(OC(=O)C=C6O5)(C)C)O)C
Standard InChIKey CGCRMQVWDAOCHS-SFOQKVPWSA-N
Standard InChI InChI=1S/C30H42O7/c1-17-13-30(14-18(2)25(32)37-30)35-22-16-27(5)9-7-8-20-19-15-29(33,11-10-28(27,6)24(17)22)34-21(19)12-23(31)36-26(20,3)4/h12,15,17-18,20,22,24,33H,7-11,13-14,16H2,1-6H3/t17-,18-,20-,22-,24+,27-,28-,29+,30+/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 Pseudolarolide F

The peel of Pseudolarix amabilis

Protocol of Pseudolarolide F

Structure Identification
J Asian Nat Prod Res. 2001;3(4):321-33.

A novel eleven-membered-ring triterpene dilactone, pseudolarolide F and A related compound, pseudolarolide E, from Pseudolarix kaempferi.[Pubmed: 11783586]


METHODS AND RESULTS:
A novel eleven-membered-ring triterpene dilactone, Pseudolarolide F (1), and a related compound, pseudolarolide E (2), were isolated from the seeds of Pseudolarix kaempferi, a plant indigenous to eastern China.
CONCLUSIONS:
Their structures and stereochemistry were established by spectroscopic studies, which included UV, IR, HREIMS, 2D NMR correlation methods (1H-1H COSY, 13C-H COSY, NOESY, HMQC, and HMBC), and single-crystal X-ray analysis.

Pseudolarolide F Dilution Calculator

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Pseudolarolide F Molarity Calculator

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Preparing Stock Solutions of Pseudolarolide F

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.9431 mL 9.7153 mL 19.4307 mL 38.8614 mL 48.5767 mL
5 mM 0.3886 mL 1.9431 mL 3.8861 mL 7.7723 mL 9.7153 mL
10 mM 0.1943 mL 0.9715 mL 1.9431 mL 3.8861 mL 4.8577 mL
50 mM 0.0389 mL 0.1943 mL 0.3886 mL 0.7772 mL 0.9715 mL
100 mM 0.0194 mL 0.0972 mL 0.1943 mL 0.3886 mL 0.4858 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 Pseudolarolide F

A novel eleven-membered-ring triterpene dilactone, pseudolarolide F and A related compound, pseudolarolide E, from Pseudolarix kaempferi.[Pubmed:11783586]

J Asian Nat Prod Res. 2001;3(4):321-33.

A novel eleven-membered-ring triterpene dilactone, Pseudolarolide F (1), and a related compound, pseudolarolide E (2), were isolated from the seeds of Pseudolarix kaempferi, a plant indigenous to eastern China. Their structures and stereochemistry were established by spectroscopic studies, which included UV, IR, HREIMS, 2D NMR correlation methods (1H-1H COSY, 13C-H COSY, NOESY, HMQC, and HMBC), and single-crystal X-ray analysis.

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