Secaubrytriol

CAS# 925932-10-1

Secaubrytriol

2D Structure

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Quality Control of Secaubrytriol

3D structure

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Secaubrytriol

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Chemical Properties of Secaubrytriol

Cas No. 925932-10-1 SDF Download SDF
PubChem ID 16099421 Appearance Powder
Formula C30H50O5 M.Wt 490.7
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 3-[(1S,4R,5R,8S,9S,12R,13R)-5-[(2R,5R)-5,6-dihydroxy-6-methylheptan-2-yl]-12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid
SMILES CC(CCC(C(C)(C)O)O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)CO)C)C
Standard InChIKey NFSDEMPRAKPPFK-HIGWZERASA-N
Standard InChI InChI=1S/C30H50O5/c1-19(7-10-24(32)26(3,4)35)21-11-13-28(6)23-9-8-22(20(2)17-31)29(14-12-25(33)34)18-30(23,29)16-15-27(21,28)5/h19,21-24,31-32,35H,2,7-18H2,1,3-6H3,(H,33,34)/t19-,21-,22+,23+,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 Secaubrytriol

The fruits of Gardenia sootepensis

Protocol of Secaubrytriol

Structure Identification
J Nat Prod. 2006 Dec;69(12):1711-4.

seco-Cycloartane triterpenes from Gardenia aubryi.[Pubmed: 17190447]

Three new 3,4-seco-cycloartanes, secaubryenol (1), Secaubrytriol (2), and secaubryolide (3), were isolated from an exudate collected on the aerial parts of Gardenia aubryi, in addition to the known (24S)-cycloartane-24,25-diol-3-one, coccinetane A, herbacetin 3,8-dimethyl ether, hibiscetin 3,8,3',4'-tetramethyl ether, and conyzatin.
METHODS AND RESULTS:
The structures of 1 and 2 were established by mass spectrometry and NMR experiments, while the relative configuration of 2 was defined unequivocally using X-ray crystallography. The in vitro cytotoxic activity of compounds 1-3 was evaluated against four human solid tumor cell lines.

Secaubrytriol Dilution Calculator

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Secaubrytriol Molarity Calculator

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Preparing Stock Solutions of Secaubrytriol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.0379 mL 10.1895 mL 20.3791 mL 40.7581 mL 50.9476 mL
5 mM 0.4076 mL 2.0379 mL 4.0758 mL 8.1516 mL 10.1895 mL
10 mM 0.2038 mL 1.019 mL 2.0379 mL 4.0758 mL 5.0948 mL
50 mM 0.0408 mL 0.2038 mL 0.4076 mL 0.8152 mL 1.019 mL
100 mM 0.0204 mL 0.1019 mL 0.2038 mL 0.4076 mL 0.5095 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 Secaubrytriol

seco-Cycloartane triterpenes from Gardenia aubryi.[Pubmed:17190447]

J Nat Prod. 2006 Dec;69(12):1711-4.

Three new 3,4-seco-cycloartanes, secaubryenol (1), Secaubrytriol (2), and secaubryolide (3), were isolated from an exudate collected on the aerial parts of Gardenia aubryi, in addition to the known (24S)-cycloartane-24,25-diol-3-one, coccinetane A, herbacetin 3,8-dimethyl ether, hibiscetin 3,8,3',4'-tetramethyl ether, and conyzatin. The structures of 1 and 2 were established by mass spectrometry and NMR experiments, while the relative configuration of 2 was defined unequivocally using X-ray crystallography. The in vitro cytotoxic activity of compounds 1-3 was evaluated against four human solid tumor cell lines.

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