Blepharotriol

CAS# 849590-42-7

Blepharotriol

Catalog No. BCN8056----Order now to get a substantial discount!

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

Quality Control of Blepharotriol

Number of papers citing our products

Chemical structure

Blepharotriol

3D structure

Chemical Properties of Blepharotriol

Cas No. 849590-42-7 SDF Download SDF
PubChem ID 102207974 Appearance Powder
Formula C29H38O6 M.Wt 482.61
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl (2R,4aS,6aR,6aS,14aS,14bR)-9,10,11-trihydroxy-2,4a,6a,6a,14a-pentamethyl-8-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylate
SMILES CC12CCC(CC1C3(CCC4(C5=CC(=C(C(=C5C(=O)C=C4C3(CC2)C)O)O)O)C)C)(C)C(=O)OC
Standard InChIKey HQWIBPMOZRBBCQ-XOKHPUJZSA-N
Standard InChI InChI=1S/C29H38O6/c1-25-7-8-26(2,24(34)35-6)15-20(25)29(5)12-10-27(3)16-13-18(31)22(32)23(33)21(16)17(30)14-19(27)28(29,4)11-9-25/h13-14,20,31-33H,7-12,15H2,1-6H3/t20-,25-,26-,27+,28-,29+/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 Blepharotriol

The herbs of Tripterygium wilfordii

Biological Activity of Blepharotriol

TargetsAntifection

Blepharotriol Dilution Calculator

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Blepharotriol Molarity Calculator

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Preparing Stock Solutions of Blepharotriol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.0721 mL 10.3603 mL 20.7207 mL 41.4413 mL 51.8017 mL
5 mM 0.4144 mL 2.0721 mL 4.1441 mL 8.2883 mL 10.3603 mL
10 mM 0.2072 mL 1.036 mL 2.0721 mL 4.1441 mL 5.1802 mL
50 mM 0.0414 mL 0.2072 mL 0.4144 mL 0.8288 mL 1.036 mL
100 mM 0.0207 mL 0.1036 mL 0.2072 mL 0.4144 mL 0.518 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 Blepharotriol

New phenolic triterpenes from Maytenus blepharodes. Semisynthesis of 6-deoxoblepharodol from pristimerin

Tetrahedron, 2005, 61(9):2513-2519.

Four new phenolic triterpenes with a 24-nor-D:A-friedoleane skeleton, isoblepharodol, 7-oxoblepharodol, Blepharotriol and 6-deoxoblepharodol, were isolated from Maytenus blepharodes. Their structures were elucidated on the basis of spectroscopic analysis, including homo and heteronuclear correlation NMR experiments (COSY, ROESY, HSQC, and HMBC). The semisynthesis of 6-deoxoblepharodol and its epimer at C-8 was achieved by catalytic reduction of pristimerin, a quinone-methide triterpene present in the plant. The biosynthetic formation of the phenolic triterpenes isolated from this species is also discussed. The compounds were assayed for antimicrobial and cytotoxic activities.

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