Mupinensisone

CAS# 152253-67-3

Mupinensisone

2D Structure

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Mupinensisone

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Chemical Properties of Mupinensisone

Cas No. 152253-67-3 SDF Download SDF
PubChem ID 158802 Appearance Powder
Formula C30H48O2 M.Wt 440.71
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (4aR,6aR,6bS,8aS,11R,12aR,14aR,14bR)-11-(hydroxymethyl)-4,4,6a,6b,8a,11,14b-heptamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one
SMILES CC1(C2CCC3(C(C2(CCC1=O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C
Standard InChIKey LZJSBKQYABASHG-OQYAAAAFSA-N
Standard InChI InChI=1S/C30H48O2/c1-25(2)22-10-13-30(7)23(28(22,5)12-11-24(25)32)9-8-20-21-18-26(3,19-31)14-15-27(21,4)16-17-29(20,30)6/h8,21-23,31H,9-19H2,1-7H3/t21-,22-,23+,26+,27+,28-,29+,30+/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 Mupinensisone

The herbs of Celastrus paniculatus

Biological Activity of Mupinensisone

DescriptionStandard reference

Protocol of Mupinensisone

Structure Identification
Yao Xue Xue Bao. 1993;28(9):684-9.

Studies on the chemical constituents of Euonymus mupinensis[Pubmed: 8010015]

Eight compounds have been isolated from Euonymus mupinensis.
METHODS AND RESULTS:
Their structures were identified by means of physico-chemical and spectral analysis. They are wilforlide A (I), wilforlide B (II), olean-12-en-3,29-diol (III), olean-3-oxo-29-ol (IV), stigmastan-3-one (V), stigmastan-3,6-dione (VI), beta-sistosterol (VII) and beta-sistosterol-3-O-beta-D-glucopyranoside (VIII).
CONCLUSIONS:
Compound IV is a new compound, named as Mupinensisone. Compounds I-VIII were isolated for the first time from this plant. 13C-NMR chemical shifts of compounds V and VI were assigned for the first time.

Mupinensisone Dilution Calculator

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Preparing Stock Solutions of Mupinensisone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.2691 mL 11.3453 mL 22.6907 mL 45.3813 mL 56.7266 mL
5 mM 0.4538 mL 2.2691 mL 4.5381 mL 9.0763 mL 11.3453 mL
10 mM 0.2269 mL 1.1345 mL 2.2691 mL 4.5381 mL 5.6727 mL
50 mM 0.0454 mL 0.2269 mL 0.4538 mL 0.9076 mL 1.1345 mL
100 mM 0.0227 mL 0.1135 mL 0.2269 mL 0.4538 mL 0.5673 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 Mupinensisone

[Studies on the chemical constituents of Euonymus mupinensis].[Pubmed:8010015]

Yao Xue Xue Bao. 1993;28(9):684-9.

Eight compounds have been isolated from Euonymus mupinensis. Their structures were identified by means of physico-chemical and spectral analysis. They are wilforlide A (I), wilforlide B (II), olean-12-en-3,29-diol (III), olean-3-oxo-29-ol (IV), stigmastan-3-one (V), stigmastan-3,6-dione (VI), beta-sistosterol (VII) and beta-sistosterol-3-O-beta-D-glucopyranoside (VIII). Compound IV is a new compound, named as Mupinensisone. Compounds I-VIII were isolated for the first time from this plant. 13C-NMR chemical shifts of compounds V and VI were assigned for the first time.

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